PUBLIKATIONEN (PDF)

2012  

Saygili E, Rana OR, Günzel C, Rackauskas G, Saygili E, Noor-Ebad F, Gemein C, Zink MD, Schwinger RH, Mischke K, Weis J, Marx N, Schauerte P. Rate and irregularity of electrical activation during atrial fibrillation affect myocardial NGF expression via different signalling routes. Cell Signal. 24(1): 99-105, 2012

Bozkurt A, Lassner F, O'Dey D, Deumens R, Böcker A, Schwendt T, Janzen C, Suschek CV, Tolba R, Kobayashi E, Sellhaus B, Tholl S, Eummelen L, Schügner F, Olde Damink L, Weis J, Brook GA, Pallua N. The role of microstructured and interconnected pore channels in a collagen-based nerve guide on axonal regeneration in peripheral nerves. Biomaterials. 33(5): 1363-75, 2012

Dreier A, Barth S, Goswami A, Weis J. Cetuximab induces mitochondrial translocalization of EGFRvIII, but not EGFR: involvement of mitochondria in tumor drug resistance? Tumour Biol. 33(1): 85-94, 2012

Parthey K, Kornhuber M, Kunze C, Wand D, Nolte KW, Nikolin S, Weis J, Schröder JM. SOX10 mutation with peripheral amyelination and developmental disturbance of axons. Muscle Nerve. 45(2): 284-90, 2012

De Paepe B, Creus KK, Weis J, De Bleecker JL. Heat shock protein families 70 and 90 in Duchenne muscular dystrophy and inflammatory myopathy: Balancing muscle protection and destruction. Neuromuscul Disord. 22(1): 26-33, 2012

Groh J, Weis J, Zieger H, Stanley ER, Heuer H, Martini R. Colony-stimulating factor-1 mediates macrophage-related neural damage in a model for Charcot-Marie-Tooth disease type 1X. Brain. 135(Pt 1): 88-104, 2012

Weis J, Brandner S, Lammens M, Sommer C, Vallat JM. Processing of nerve biopsies: A practical guide for neuropathologists. Clin Neuropathol. 31(1): 7-23, 2012

2011

Schwartz V, Krüttgen A, Weis J, Weber C, Ostendorf T, Lue H, Bernhagen J. Role for CD74 and CXCR4 in clathrin-dependent endocytosis of the cytokine MIF. Eur J Cell Biol. 2011 Oct 18. [Epub ahead of print]

Schröder JM, Klossok T, Weis J. Oculopharyngeal muscle dystrophy: fine structure and mRNA expression levels of PABPN1. Clin Neuropath.30(3): 94-103, 2011

Rana OR, Saygili E, Gemein C, Zink MD, Buhr A, Saygili E, Mischke K, Nolte KW, Weis J, Weber C, Marx N, Schauerte P. Chronic electrical neuronal stimulation increases cardiac parasympathetic tone by eliciting neurotrophic effects. Circ Res. 108(10): 1209-19, 2011

Saygili E, Kluttig R; Saygili Es, Rackauskas G, Weis J, Marx N, Schauerte P, Rana OR. Age-related regional differences in cardiac nerve growth factor expression. Age (Dordr). 2011 May 11. [Epub ahead of print]

Saygili E, Pekassa M, Saygili E, Rackauskas G, Hommes D, Noor-Ebad F, Gemein C, Zink MD, Schwinger RH, Weis J, Marx N, Schauerte P, Rana OR. Mechanical stretch of sympathetic neurons induces VEGF expression via a NGF and CNTF signaling pathway. Biochem Biophys Res Commun. 410(1): 62-7, 2011

Weis J*, Katona I*, Müller-Newen G, Sommer C, Necula G, Hendrich C, Ludolph AC, Sperfeld A-D. Small fiber neuropathy in ALS patients. Neurology. 76(23): 2024-9, 2011 *Equal contribution

Hanisch F, Müller T, Dietz A, Bitoun M, Kress W, Weis J, Stoltenburg G, Zierz S. Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations. J Neurol. 258(6): 1085-90, 2011

Guelly C, Zhu PP, Leonardis L, Papic L, Zidar J, Schabhüttl M, Strohmaier H, Weis J, Strom TM, Baets J, Willems J, De Jonghe P, Reilly MM, Fröhlich E, Hatz M, Trajanoski S, Pieber TR, Janecke AR, Blackstone C, Auer-Grumbach M. Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I. Am J Hum Genet. 88(1): 99-105, 2011

Doorschodt BM, Schreinemachers MC, Behbahani M, Floriquin S, Weis J, Staat M, Tolba RH. Hypothermic machine perfusion of kidney grafts: Which Pressure is Preferred? Ann Biomed Eng. 39(3): 1051-9, 2011

Saygili E, Schauerte P, Pekassa M, Saygilli E, Rackauskas G, Schwinger RH, Weis J, Weber C, Marx N, Rana OR. Sympathetic Neurons Express and Secrete MMP-2 and MT1-MMP to Control Nerve Sprouting via Pro-NFG Conversion. Cell Mol Neurobiol. 31(1): 17-25, 2011

Bozkurt A, Scheffel J, Brook GA, Joosten EA, Suschek CV, O'Dey DM, Pallua N, Deumens R. Aspects of static and dynamic motor function in peripheral nerve regeneration: SSI and CatWalk gait analysis. Behav Brain Res. 219(1): 55-62, 2011

Scholtes F, Theunissen E, Phan-Ba R, Adriaensens P, Brook G, Franzen R, Gelan J, Schoenen J, Martin D. Post-mortem assessment of rat spinal cord injury and white matter sparing using inversion recovery-supported proton density magnetic resonance imaging. Spinal Cord. 49(3): 345-51, 2011

Bockelmann J, Klinkhammer K, von Holst A, Seiler N, Faissner A, Brook GA, Klee D, Mey J. Functionalization of electrospun poly(ε-caprolactone) fibers with the extracellular matrix-derived peptide GRGDS improves guidance of schwann cell migration and axonal growth. Tissue Eng Part A. 17(3-4): 475-86, 2011

2010

Deumens R, Bozkurt A, Meek MF, Marcus M, Joosten E, Weis J, Brook GA. Repairing injured peripheral nerves: Bridging the gap. Prog Neurobiol. 92(3): 245-76, 2010 

Nachreiner T, Esser M, Tenten V, Troost D, Weis J, Krüttgen A. Novel splice variants of the amyotrophic lateral sclerosis-associated gene VAPB expressed in human tissues. Biochem Biophys Res Commun.394(3): 703-8, 2010 

Sommer CL, Brandner S, Dyck PJ, Harati Y, LaCroix C, Lammens M, Magy L, Mellgren SI, Morbin M, Navarro C, Powell HC, Schenone AE, Tan E, Urtizbera A, Weis J. Peripheral Nerve Society. Peripheral Nerve Society Guideline on processing and evaluation of nerve biopsies. J Peripher Nerv Syst. 15(3): 164-75, 2010 

Roehl AB, Hein M, Loetscher PD, Rossaint J, Weis J, Rossaint R, Coburn M. Neuroprotective properties of levosimendan in an in vitro model of traumatic brain injury. BMC Neurol. 10: 97, 2010

Bremer J, O´Connor T, Tiberi C, Rehrauer H, Weis J, Aguzzi A. Ablation of Dicer from murine Schwann cells increases their proliferation while blocking myelination. PLoS One. 5(8): e12450, 2010 

Brücken A, Kaab AB, Kottmann K, Rossaint R, Nolte KW, Weis J, Fries M. Reducing the duration of 100% oxygen ventilation in the early reperfusion period after cardiopulmonary resuscitation decreases striatal brain damage. Resuscitation. 81(12): 1693-703, 2010 

Urban PP, Wellach I, Faiss S, Layer P, Rosenkranz T, Knop K, Weis J. Subacute axonal neuropathy in Parkinson´s disease with cobalamin and vitamin B6 deficiency under duodopa therapy. Mov Disord. 25(11): 1748-52, 2010 

Claeys KG, Pellissier JF, Garcia-Bragado F, Weis J, Urtizberea A, Poza JJ, Cobo AM, Stoltenburg G, Figarella-Branger D, Willems PJ, Depuydt CE, Kleiner W, Pouget J, Piraud M, Brochier G, Romero NB, Fardeau M, Goebel HH, Bönnemann CG, Voit T, Eymard B, Laforet P. Myopathy with hexogonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity. Neuromuscul Disord. 20(11): 701-8, 2010 

Brauers E, Dreier A, Roos A, Wormland B, Weis J, Krüttgen A. Differential effects of myopathy-associated caveolin 3-mutants on growth factor signaling. Am J Pathol. 177(1): 261-70, 2010 

Kaemmer D, Bozkurt A, Otto J, Junge K, Klinik C, Weis J, Sellhaus B, O´Dey DM Pallua N, Jansen M, Schumpelick V, Klinge U. Evaluation of tissue components in the peripheral nervous system using Sirius red staining and immunohistochemistry: A comparative study (human, pig, rat). J Neurosci Methods. 190: 112-6, 2010 

Rana OR, Schauerte P, Kluttig R, Schröder JW, Koenen RR, Weber C, Nolte KW, Weis J, Hoffmann R, Marx N, Saygili E. Acetylcholine as an age-dependent non-neuronal source in the heart. Auton Neurosci. 156(1-2): 82-9, 2010 

Meyer C, Rana OR, Saygili E, Gemein C, Becker M, Nolte K, Weis J, Schimpf T, Knackstedt C, Mischke K, Hoffmann R, Kelm M, Pauza D, Schauerte P. Augmentation of Left Ventricular Contractility by Cardiac Sympathetic Neural Stimulation. Circulation. 121(11): 1286-94, 2010 

Saygili E, Schauerte P, Küppers F, Heck L, Weis J, Weber C, Schwinger RH, Hoffmann R, Schröder JW, Marx N, Rana OR. Electrical stimulation of sympathetic neurons induces autocrine/paracrine effects of NGF mediated by TrkA. J Mol Cell Cardiol. 49(1): 79-87, 2010 

Reilich P, Schramm N, Schoser B, Schneiderat P, Strigl-Pill N, Müller-Höcker J, Kress W, Ferbert A, Rudnik-Schöneborn S, Noth J, Locjmüller H, Weis J, Walter MC. Fascioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy. J Neurol. 257(7): 1108-18, 2010 

Flohr S, Ewers P, Fink GR, Weis J, Krüttgen A. Impaired Neurotrophin-3 signaling in a TrkAII mutant associated with hereditary polyneuropathy. Exp Neurol. 224(1): 318-20, 2010 

Helfrich I, Scheffrahn I, Bartling S, Weis J, von Felbert V, Middleton M, Kato M, Ergün S, Schadendorf D. Resistance to antiangiogenetic therapy is directed by vascular phenotype, vessel stabilization, and maturation in malignant melanoma. J Exp Med. 207(3): 491-503, 2010 

Funke AD, Esser M, Krüttgen A, Weis J, Mitne-Neto M, Lazar M, Nishimura AL, Sperfeld AD, Trillenberg P, Senderek J, Krasnianski M, Zatz M, Zierz S, Deschauer M. The P56S mutation in the VAPB gen is not due to a single founder: the first European case. Clin Genet. 77(3): 302-3, 2010 

Bremer J, Baumann F, Tiberi C, Wessig C, Fischer H, Schwarz P, Steele AD, Toyka KV, Nave KA, Weis J, Aguzzi A. Axonal prion protein is required for peripheral myelin maintenance. Nature Neurosci. 13(3): 310-18, 2010 

Derwall M, Westerkamp M, Löwer C, Deike-Glindemann J, Schnorrenberger NK, Coburn M, Nolte KW, Gaisa N, Weis J, Siepmann K, Häusler M, Rossaint R, Fries M. Hydrogen sulfide does not oncrease resuscitability in a porcine model of prolonged cardiac arrest. Shock. 34(2): 190-5, 2010

Huttner HB, Richter G, Jünemann A, Kress W, Weis J, Schröder JM, Gal A, Doerfler A, Udd B, Schröder R. Incontinentia pigmenti-related myopathy or unsolved „double trouble"? Neuromuscul Disord. 20(2): 139-41, 2010

Evangelopoulos ME, Wüller S, Weis J, Krüttgen A. A role of nitric oxide in neurite outgrowth of neuroblastoma cells triggered by mevastatin or serum reduction. Neurosci Lett. 468(1): 28-33, 2010

Führmann T, Gerardo-Nava J, Brook GA. Tissue Engineering: Central Nervous System. In Tissue Engineering. Eds Pallua N, Suschek C. Springer Verlag, London, Heidelberg. 2010, in press

Deumens R, Bozkurt A, Brook GA. US Food and Drug Administration/Conformit Europe-approved absorbable nerve conduits for clinical repair of peripheral and cranial nerves. Commentary. Ann Plast Surg. 65(3): 371, 2010

Montzka K, Führmann T, Müller-Ehmsen J, Wöltje M, Brook GA. Growth factor and cytokine expression of human mesenchymal stromal cells is not altered in an in vitro model of tissue damage. Cytotherapy. 12(7): 870-80, 2010

Führmann T, Hillen LM, Montzka K, Wöltje M, Brook GA. Cell-cell interactions of human neural progenitor-derived astrocytes within a microstructured 3D-scaffold. Biomaterials. 31(30): 7705-15, 2010

Klinkhammer K, Bockelmann J, Simitzis C, Brook GA, Grafahrend D, Groll J, Möller M, Mey J, Klee D. Functionalization of electrospun fibers of poly(epsilon-caprolactone) with star shaped NCO-poly(ethylene glycol)-stat-poly(propylene glycol) for neuronal cell guidance. J Mater Sci Mater Med. 21(9): 2637-51, 2010

Führmann T, Montzka K, Hillen LM, Hodde D, Dreier A, Bozkurt A, Wöltje M, Brook GA. Axon growth-promoting properties of human bone marrow mesenchymal stromal cells. Neurosci Lett. 474(1): 37-41, 2010

Montzka K, Führmann T, Wöltje M, Brook GA. Expansion of human bone marrow-derived mesenchymal stromal cells: serum-reduced medium is better than conventional medium. Cytotherapy. 12(5): 587-92, 2010

Foret A, Quertainmont R, Botman O, Bouhy D, Amabili P, Brook G, Schoenen J, Franzen R. Stem cells in the adult rat spinal cord: plasticity after injury and treadmill training exercise. J Neurochem. 112(3): 762-72, 2010

van Neerven S, Joosten EAJ , Brook GA, Lambert CA, Mey J, Weis J, Marcus MA, Steinbusch HW, van Kleef M, Patijn J, Deumens R. Repetitive intrathecal VEGF 165 treatment has limited therapeutic effects after spinal cord injury in the rat. J. Neurotrauma. 27(10): 1781-91, 2010

Mischke K, Zarse M, Schmid M, Gemein C, Hatam N, Spillner J, Dohmen G, Rana O, Saygili E, Knackstedt C, Weis J, Pauza D, Bianchi S, Schauerte P. Chronic augmentation of the parasympathetic tone to the atrioventricular node: A nonthoracotomy neurostimulation technique for ventricular rate control during atrial fibrillation. J Cardiovasc Electrophysiol. 21(2): 193-9, 2010

Reinges MH, Krings T, Drexler AY, Ludolph A, Sellhaus B, Bovi M, Geibprasert S, Agid R, Scherer K, Hans FJ. Bare, bio-active and hydrogel-coated coils for endovascular treatment of experimentally induced aneurysms. Long-term histological and scanning electron microscopy results. Interv Neuroradiol. 16(2): 139-50. 2010

Geibprasert S, Krings T, Apitzsch J, Reinges MH, Nolte KW, Hans FJ. Subarachnoid hemorrhage following posterior spinal artery aneurysm. A case report and review of the literature. Interv Neuroradiol. 16(2): 183-90, 2010

Schilling S, Klotz P, Weis J, Gold R. Steroid responsive dementia syndrome and vasculitic polyneuritis. Akt Neurologie. 37(2): 80-2, 2010

2009

Loetscher PD, Rossaint J, Rossaint R, Weis J, Fries M, Fahlenkamp A, Ryang YM, Grottke O, Coburn M. Argon: neuroprotection in in vitro models of cerebral ischemia and traumatic brain injury. Crit Care. 13(6): R206, 2009

Weis J, Nolte K, Mader H, Schröder JM, Grehl H, Rada A, Zerres K, Senderek J. Late sporadic CMT4C-A new KIAA1985 mutation. Expert Consult: Companion to Peripheral Neuropathy. 171-173, 2009

Oertel M, Nolte K, Blaum M, Weis J, Gilsbach J, Korinth M. Primary intraventricular schwannomas. Clin Neurol Neurosurg. 111(9): 768-73, 2009

Schaakxs D, Bahm J, Sellhaus B, Weis J. Clinical and neuropathological study about the neurotization of the suprascapular nerve in obstetric brachial plexus lesions. J Brachial Plex Peripher Nerve Inj. 4: 15, 2009

Arnaud E, Zenker J, de Preux Charles AS, Stendel C, Roos A, Médard JJ, Tricaus N, Weis J, Suter U, Senderek J, Chrast R. SH3TC2/ KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system. Proc Natl Acad Sci USA106. (41): 17528-33, 2009

Moises T, Wüller S, Saxena S, Senderek J, Weis J, Krüttgen A. Proteasomal inhibition alters the trafficking of the neurotrophin receptor TrkA. Biochem Biophys Res Commun. 387(2): 360-4, 2009

Weis J, Nikolin S, Nolte K. Neurogenic muscular atrophy and selective fibre type atrophies: Crucial findings in the biopsy diagnosis of neuromuscular disease. Pathologe. 30(5): 379-83, 2009

Weis J. Myopathology: an update. Pathologe. 30(5):343-4, 2009

Weis J, Nolte K. Inflammatory and other myopathies and skeletal muscle vasculitis: The role of muscle and nerve biopsy. Z Rheumatol. 68(6): 459-64, 2009

Bergmann M, Weis J, Probst-Cousin S. Muscle biopsy: Indications and techniques. Pathologe. 30(5): 348-51, 2009

Weis J, Nikolin S, Nolte K. Muskel- und Nervenbiopsien: Aktuelle Aspekte. Nervenheilkunde. 9: 624-26, 2009

Senderek J, Garvey SM, Krieger M, Guergueltcheva V, Urtizberea A, Roos A, Elbracht M, Stendel C, Tournev I, Mihailova V, Feit H, Tramonte J, Hedera P, Crooks K, Bergmann C, Rudnik- Schöneborn S, Zerres K, Lochmüller H, Seboun E, Weis J, Beckmann JS, Hauser MA, Jackson CE. Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3. Am J Hum Genet. 84: 511-18, 2009

Schröder JM. "Necklace" fibers as a late clue to the interpretation of the forgotten "trilaminar" fibers. Acta Neuropathol. 118: 317-8, 2009

Roessler GF, Laube T, Brockmann C, Kirschkamp T, Mazinani BA, Goertz M, Koch C, Kirsch I, Sellhaus B, Trieu HK, Weis J, Bornfeld N, Roethgen H, Messner A, Mokwa W, Walter P. Implantation and explantation of a wireless epiretinal retina implant device: Observations during the EPIRET 3 prospective clinical trial. Invest Ophthalmol Vis Sci. 50(6): 3003-08, 2009

Rossaint J, Rossaint R, Weis J, Fries M, Rex S, Coburn M. Propofol: neuroprotection in an in vitro model of traumatic brain injury. Critical Care. 13(2): R61, 2009

Weis J. Stellenwert der Muskelbiopsie in der Diagnostik der Muskelerkrankungen. NeuroAktuell. 5: 21-25, 2009

Bahm J, Ocampo- Pavez C, Disselhorst-Klug C, Sellhaus B, Weis J. Obstetric brachial plexus palsy. Deutsches Ärzteblatt. 6: 83-90, 2009

Evangelopoulos M.E., Weis J, Krüttgen A. Mevastatin-induced neurite outgrowth of neuroblastoma cells via activation of EGFR. J Neuroscience Res. 87: 2138-44, 2009

Bozkurt A, Deumens R, Beckmann C, Olde Damink L, Schügner F, Heschel I, Sellhaus B, Weis J, Jahnen-Dechent W, Brook G, Pallua N. In vitro cell alignment obtained with a Schwann cell enriched microstructured nerve guide with longitudinal guidance channels. Biomaterials. 30(2): 169-79, 2009

Koopmans G, Deumens R, Buss A, Geoghegan L, Mu Myint A, Honig W, Kern N, Joosten E, Noth J, Brook G. Acute rolipram/thalidomide treatment improves tissue sparing and locomotion after experimental spinal cord injury. Exp Neurol. 216(2): 490-98, 2009

Derwall M., Coburn M, Rex S, Hein M, Rossaint R, Fries M. Xenon: recent developments and future perspectives. Minerva Anestesiol. 75(1-2): 37-45, 2009

Rana OR, Saygili E, Meyer C, Gemein C, Krüttgen A, Andrzejewski MG, Ludwig A, Schotten U, Schwinger RH, Weber C, Weis J, Mischke K, Rassaf T, Kelm M, Schauerte P. Regulation of nerve growth factor in the heart: the role of the calcineurin- NFAT pathway. J Mol Cell Cardiol. 46(4): 568- 78, 2009

Saygili E, Rana OR, Meyer C, Gemein C, Andrzejewski MG, Ludwig A, Weber C, Schotten U, Krüttgen A, Weis J, Schwinger RH, Mischke K, Rassaf T, Kelm M, Schauerte P. The angiotensin-calcineurin-NFAT pathway mediates stretch-induced up-regulation of matrix metalloproteinases-2/-9 in atrial myocytes. Basic Res Cardiol. 104(4): 435-448, 2009

Creus K, De Paepe B, Werbrouck B, Vervaet V, Weis J, De Bleecker J. Distribution of the NF-kB complex in the inflammatory exudates characterizing the idiopathic inflammatory myopathies. Ann NY Acad Sci. 1173: 370-7, 2009

De Paepe B, Creus K, Martin J, Weis J, De Bleecker J. A dual role for HSP90 and HSP70 in the inflammatory maopathies: from muscle fiber protection to active invasion by macrophages. Ann NY Acad Sci. 1173: 463-9, 2009

Montzka K, Lassonczyk N, Tschöke B, Neuss S, Führmann T, Franzen R, Smeets R, Brook G, Wöltje M. Neural differentiation potential of human bone marrow-derived mesenchymal stromal cells: misleading marker gene expression. BMC Neuroscience. 10:16, 2009

Möllers S, Heschel I, Olde Damink L, Schügner F, Deumens R, Müller B, Bozkurt A, Nava J, Noth J, Brook G. Cytocompatibility of a novel, longitudinally microstructured collagen scaffold intended for nerve tissue repair. Tissue Eng Part A. 15(3): 461-72, 2009

Gerado-Nava J, Führmann T, Klinkhammer K, Seiler N, Mey J, Klee D, Möller M, Dalton P, Brook G. Human neural cell interactions with orientated electrospun nanofibers in vitro. Nanomedicine. 4(1): 11-30, 2009

Klinkhammer K, Seiler N, Grafahrend D, Gerardo-Nava JL, Mey J, Brook, G., Möller M, Dalton PD, Klee D. Deposition of electrospun fibers on reactive substrates for in vitro investigations. Tissue Eng Part C Methods. 15(1): 77-85, 2009

Bozkurt A, Deumens R, Beckmann C, Olde Damink L, Schügner F, Heschel I, Sellhaus B, Weis J, Jahnen-Dechent W, Brook GA, Pallua N. In vitro cell alignment obtained with a Schwann cell enriched microstructured nerve guide with longitudinal guidance channels. Biomaterials. 30(2): 169-79, 2009

Andres RH, Guzman R, Weis J, Brekenfeld C, Fandino J, Seiler RW. Lhermitte-Duclos disease with atypical vascularization--case report and review of the literature. Clin Neuropathol. 28(2): 83-90, 2009

Fries M, Coburn M, Nolte KW, Timper A, Kottmann K, Kuru TH, Weis J, Rossaint R. Early administration of xenon or isoflurane may not improve functional outcome and cerebral alterations in a porcine model of cardiac arrest. Resuscitation. 80(5): 584-90, 2009

Balciūniene N, Tamasauskas A, Valanciūte A, Deltuva V, Vaitiekaitis G, Gudinaviciene I, Weis J, von Keyserlingk DG. Histology of human glioblastoma transplanted on chicken chorioallantoic membrane. Medicina (Kaunas). 45(2): 123-31, 2009

Buss A, Pech K, Kakulas BA, Didier M, Schoenen J, Noth J, Brook G. NG2 and phosphacan are present in the astroglial scar after human traumatic spinal cord injury. BMC Neurology. 9: 32, 2009

Rotthier A, Baets J, De Vriendt E, Jacobs A, Auer-Grumbach M, Le´vy N, Bonello-Palot N, Sebnem Kilic S, Weis J, Nascimento A, Swinkels M, Kruyt MC, Jordanova A, De Jonghe P, Timmerman V. Genes for hereditary sensory and autonomic neuropathies: a genotype--phenotype correlation. Brain. 132: 2699-711, 2009

Schroeder A, Ertl-Wagner B, Britsch S, Schröder J, Nikolin S, Weis J, Müller-Felber W, Koerte I, Stehr M, Berweck S, Borggraefe I, Heinen F. Muscle biopsy substantiates long-term MRI alterations one year after a single dose of botulinum toxin injected into the lateral gastrocnemius muscle of healthy volunteers. Mov Disord. 24(10): 1494-503, 2009

Weis J, Nolte K, Mader H, Schroder JM, Grehl H, Rada A, Zerres K, Senderek J. Late sporadic CMT4C -- a new KIAA 1985 mutation. Companion to Dyck an Thomas, Peripheral Neuropathy. Edited by Dyck PJ, Dyck PJB, Klein JC, Low PA, Amrami K, Spinner RJ. London and Amsterdam, Elsevier, 2009

2008

Weis J. Twenty-five years of the Neuromuscular Disease reference Center of the German Society for Neuroanatomy. Nervenarzt. 79: 958-60, 2008

Sommer C, Brandner S, Dyck PJ, Magy L, Mellgren SI, Morbin M, Schenone A, Tan E, Weis J. 147th ENMC international workshop: guideline on processing and evaluation of sural nerve biopsies, 15-17 December 2006, Naarden, The Netherlands. Neuromuscul Disord. 18: 90-96, 2008

Koy A, Ilkovski B, Laing N, North K, Weis J, Neuen-Jacob E, Maytepek E. Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H). Neuropediatrics. 39: 1-5, 2008

Fries M, Nolte K, Demir F, Kottmann K, Timper A, Coburn M, Weis J, Rossaint R. Neurocognitive performance after cardiopulmonary resuscitation in pigs. Critical Care Med. 36: 842-847, 2008

Nolte KW, Hans VJ, Schattenfroh C, Weis J, Schröder JM. Perineurial cells filled with collagen in „atypical" Cogan's syndrome. Acta Neuropathol. 115: 589-96, 2008

Urban PP, Kaczmarek E, Wellach I, Brüning R, Brüllke N, Schulte C, Knop K, Weis J. [Neurolymphomatosis : Subacute sensorimotor polyneuropathy as a first sign of non-Hodgkin's B cell lymphoma.] Nervenarzt. 79: 699-702, 2008

Guzman R, Altrichter S, El-Koussy M, Gralla J, Weis J, Barth A, Seiler RW, Schroth G, Lövblad KO. Contribution of the apparent diffusion coefficient in perilesional edema for the assessment of brain tumors. J Neuroradiol. 35(4): 224-9, 2008

Fries M, Nolte K, Timper A, Kottmann K, Weis J, Rossaint R. Xenon reduces neurohistopathological damage and improves the early neurological deficit after cardiac arrest in pigs. Critical Care Med. 36: 2420-26, 2008

Bozkurt A.,Tholl S, Wehner S, Tank J, Cortese M, O'Dey D, Deumens R, Lassner F, Schügner F, Gröger A, Smeets R, Brook G,Pallua N. Evaluation of functional nerve recovery with Visual-SSI--a novel computerized approach for the. assessment of the static sciatic index (SSI). J Neurosci Methods. 170(1): 117-122, 2008

Bozkurt A, Deumens R, Scheffel J, O'Dey DM, Weis J, Joosten EA, Führmann T, Brook G, Pallua N.CatWalk gait analysis in assessment of functional recovery after sciatic nerve injury. J Neurosci Methods. 173(1): 91-98, 2008

Weis J. Stellenwert der Muskelbiopsie in der Diagnostik der Muskelerkrankungen. NeuroAktuell. : 501-03, 2008

Scholtes F, Phan-Ba R, Theunissen E, Adriaensens P, Brook G., Franzen R, Bouhy D, Gelan J, Martin D, Schoenen J .Rapid, postmortem 9.4T MRI of spinal cord injury: Correlation withhistology and survival times. J Neurosci Methods. 174(2): 157-67, 2008

Buss A, Pech K, Kakulas BA, Martin D, Schoenen J, Noth J, Brook G. TGF-beta1 and TGF-beta2 expressions after traumatic human spinal cord injury. Spinal Cord. 46(5): 364-71, 2008

Dafotakis M, Sparing R, Eickhoff SB, Boy C, Nikolin S, Fink GR. Postinfectious focal necrotizing myopathy. Clin Nucl Med. 33(7): 500-1, 2008

Nolte KW, Janecke AR, Vorgerd M, Weis J, Schröder JM. Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 gene. Acta Neuropathol. 116(5): 491-506, 2008

Rudnik-Schöneborn S, Weis J, Kress W, Häusler M, Zerres K. Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy - double trouble as an explanation for an atypical phenotype. Neuromuscul Disord. 18(11): 881-5, 2008

Jeub M, Bitoun M, Guicheney P, Kappes-Horn K, Strach K, Druschky KF, Weis J, Fischer D: Dynamin 2 related centronuclear myopathy: Clinical, histological and genetic aspects of further patients ans review of the literature. Clin Neuropathol. 27: 430-438, 2008

Roessler G, Laube T, Brockmann C, Kirschkamp T, Mazinani B, Goertz M, Koch C, Kirsch I, Sellhaus B, Trieu HK, Weis J, Bornfeld N, Röthgen H, Messner A, Mokwa W, Walter P. Implantation and explantation of a wireless epiretinal retina implant device in blind RP patients. Invest Ophthalmol Vissci. 50(6): 3003-8, 2008

Schröder J.M.: Congenital Fiber Type Disproportion In: Lang F. (Hrsg.) Encyclopedia of Molecular Mechanisms of Disease ISBN 978-3-540-33445-3, Springer Medizinverlag 2008 (2nd Edition)

Schröder J.M.: Ferritinopathy In: Lang F. (Hrsg.) Encyclopedia of Molecular Mechanisms of Disease ISBN 978-3-540-33445-3, Springer Medizinverlag 2008 (2nd Edition)

2007

Ponzoni M, Berger F, Chassagne-Clement C, Tinguely M, Jouvet A, Ferreri AJ, Dell'oro S, Terreni MR, Doglioni C, Weis J, Cerati M, Milani M, Iuzzolino P, Motta T, Carbone A, Pedrinis E, Sanchez J, Blay JY, Reni M, Conconi A, Bertoni F, Zucca E, Cavalli F, Borisch B; on Behalf of the International Extranodal Lymphoma Study Group (IELSG).Reactive perivascular T-cell infiltrate predicts survival in primary central nervous system B-cell lymphomas. Br J Haematol. 138(3): 316-23, 2007

Stendel C, Roos A, Deconinck T, Pereira J, Castagner F, Niemann A, Kirschner J, Korinthenberg R, Ketelsen UP, Battaloglu E, Parman Y, Nicholson G, Ouvrier R, Seeger J, Jonghe PD, Weis J, Krüttgen A, Rudnik-Schöneborn S, Bergmann C, Suter U, Zerres K, Timmerman V, Relvas JB, Senderek J. Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4. Am J Hum Genet. 81(1): 158-64, 2007

Buss A, Pech K, Kakulas BA, Martin D, Schoenen J, Noth J, Brook GA. Matrix metalloproteinases and their inhibitors in human traumatic spinal cord injury. BMC Neurology. 7: 17, 2007

Wühl E, Kogan J, Zurowska A, Matejas V, Vandevoorde RG, Aigner T, Wendler O, Lesniewska I, Bouvier R, Reis A, Weis J, Cochat P, Zenker M. Neurodevelopmental deficits in Pierson (microcoria-congenital nephrosis) syndrome. Am J Med Genet. A143A: 311-19, 2007

Thiex R, Weis J, Krings T, Barreiro S, Yakisikli-Alemi F, Gilsbach JM, Rohde V. Addition of intravenous N-methyl-D-aspartate receptor antagonists to local fibrinolytic therapy for the optimal treatment of experimental intracerebral hemorrhages. J Neurosurg. 106: 314-20, 2007

Smilowitz HM, Weissenberger J, Weis J, Brown JD, O'Neill RJ, Laissue JA. Orthotopic transplantation of v-src-expressing glioma cell lines into immunocompetent mice: establishment of a new transplantable in vivo model for malignant glioma. J Neurosurg. 106: 652-59, 2007

Schoser BGH, Schröder JM, Grimm T, Sternberg D., Kress W. A large german kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene. Muscle & Nerve. 35: 599-606, 2007

Yen K, Lovblad KO, Scheurer E, Ozdoba C, Thali MJ, Aghayev E, Jackowski C, Anon J, Frickey N, Zwygart K, Weis J, Dirnhofer R. Post-mortem forensic neuroimaging: Correlation of MSCT and MRI findings with autopsy results. Forensic Sci Int. 173: 21-35, 2007

Johann V, Schiefer J, Sass C, Mey J, Brook G, Krüttgen A, Schlangen C, Benreuther C, Schachner M, Dihne M, Kosinski CM. Time of transplantation and cell preparation determine neural stem cell survival in a mouse model of Huntington's disease. Exp Brain Res. 177(4): 458-70, 2007

Ramaekers VT, Weis J, Sequeira JM, Quadros EV, Blau N. Mitochondrial Complex I Encephalomyopathy and Cerebral 5-Methyltetrahydrofolate Deficiency. Neuropediatrics. 38: 1-4, 2007

Ueceyler N, Sellhaus B, Sommer C, Reiners K. Polyneuropathien bei Porphyrie. Nervenheilkunde. 26: 763-68, 2007

Deumens R, Lübbers M, Jaken RJP, Meijs MFL, Thurlings RM, Honig WMM, Schachner M, Brook GA, Joosten EAJ. Mice lacking L1 have reduced CGRP fibre in-growth into spinal transaction lesions. Neuroscience Letters. 420: 277--81, 2007

Fathi AR, Vassella E, Arnold M, Curschmann J, Reinert M, Vajtai I, Weis J, Deiana G, Mariani L. Objective response to radiation therapy and long-term survival of patients with WHO grade II astrocytic gliomas with known LOH 1p/19q status. Strahlenther Onkol. 183(9): 517-22, 2007

Andres RH, Guzman R, Weis J, Schroth G, Barth A. Granuloma formation and occlusion of an unruptured aneurysm after wrapping. Acta Neurochir. 149(9): 953-58, 2007

Bronfman FC, Escudero CA, Weis J, Krüttgen A. Endosomal transport of neurotrophins: roles in signaling and neurodegenerative diseases. Dev Neurobiol. 67(9): 1183-203, 2007

Häusler M, Sellhaus B, Scheithauer S, Gaida B, Kuropka S, Siepmann K, Panek A, Berg W, Teubner A, Ritter K, Kleines M. Myocarditis in newborn wild-type BALB/c mice infected with the murine gamma herpesvirus MHV-68. Cardiovascular Research. 76: 323-30, 2007

Moises T, Dreier A, Flohr S, Esser M, Brauers E, Reiss K, Merken D, Weis J, Kruttgen A. Tracking TrkA's Trafficking: NGF Receptor Trafficking Controls NGF Receptor Signaling. Mol Neurobiol. 35(2): 151-9, 2007

Hehr U, Bauer P, Winner B, Schuele R, Olmez A, Koehler W, Uyanik G, Engel A, Lenz D, Seibel A, Hehr A, Ploetz S, Gamez J, Rolfs A, Weis J, Ringer TM, Bonin M, Schuierer G, Marienhagen J, Bogdahn U, Weber BHF, Topaloglu H, Schoels L, Riess O, Winkler J. Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia. Ann Neurol. 62: 656-65, 200

Bozkurt A, Brook GA, Moellers S, Lassner F, Sellhaus B, Weis J, Woeltje M, Tank J, Beckmann C, Fuchs P, Olde Daminik L, Schügner F, Heschel I, Pallua N. In vitro assessment of axonal growth using dorsal root ganglia explants in a novel three-dimensional collagen matrix. Tiss Eng. 13(12): 2971-79, 2007

Buss A, Pech K, Kakulas BA, Martin D, Schoenen J, Noth J, Brook GA. Growth-modulating molecules are associated with invading Schwann cells and not astrocytes in human traumatic spinal cord injury. Brain. 130: 940-53, 2007

Kosinski CM, Schlangen C, Gellerich FN, Gizatullina Z, Deschauer M, Schiefer J, Young AB, Landwehrmeyer GB, Toyka KV, Sellhaus B, Lindenberg KS .Myopathy as a first symptom of Huntington's disease in a Marathon runner. Mov Disord. 22: 1637-40, 2007

Wirths O, Weis J, Kayed R, Saido TC, Bayer TA. Age-dependent axonal degeneration in an Alzheimer mouse model. Neurobiol Aging. 28: 1689-99, 2007

Koopmans GC, Deumens R, Brook G, Gerver J, Honig WM, Hamers FP, Joosten EA. Strain and locomotor speed affect over-ground locomotion in intact rats. Physiol Behav. 92: 993-1001, 2007

Wuhl E, Kogan J, Zurowska A, Matejas V, Vandevoorde RG, Aigner T, Wendler O, Lesniewska I, Bouvier R, Reis A, Weis J, Cochat P, Zenker M. Neurodevelopmental deficits in Prierson ( microcoria- congenital nephrosis) syndrom. Am J Med Genet A. 143(4): 311-319, 2007

2006

Fries M, Weis J, Rossaint R. Is Xenon really neuroprotective after cardiac arrest? Anesthesiology. 104: 211, 2006

Yen K, Lövblad KO, Scheurer E, Ozdoba C, Thali MJ, Aghayev E, Jackowski C, Anon J, Frickey N, Weis J, Zwygart K, Bratzke H, Dirnhofer R. Line scan diffusion tensor imaging of the post-traumatic brainstem: Changes with neuropathological correlation. AJNR Am J Neuroradiol. 27: 70-3, 2006

Wirths O, Weis J, Szczygielski J, Multhaup G, Bayer TA. Axonopathy in an APP/PS1 transgenic mouse model of Alzheimer's disease. Acta Neuropathol. 111: 312-19, 2006

Ramelli G, Joncourt F, Luetschg J, Weis J, Tolnay M, Burgunder J. Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series. Swiss Med Wkly. 136: 189-93, 2006

Möller JC, Krüttgen A, Burmester R, Weis J, Oertel WH, Shooter EM. Release of interleukin-6 via the regulated secretory pathway in PC12 cells. Neurosci Lett. 400: 75-9, 2006

Landolt HP, Glatzel M, Blättler Th, Achermann P, Roth C, Mathis J, Weis J, Tobler I, Aguzzi A, Bassetti CL. Sleep-wake disturbances in sporadic Creutzfeldt-Jakob Disease. Neurology. 66: 1418-24, 2006

Hergersberg M, Mariani L, Vassella E, Murtin C, Weis J, Moschopulos M, Laeng H, Landolt H, Huber A, Roelcke U. Age at diagnosis and loss of heterozygosity on chromosome 1p and 19 q in oligodendroglial tumors . J NeuroOncol. 80:215-17, 2006

Verhoeven K, Claeys KG, Züchner S, Schröder JM, Weis J, Ceuterick C, Jordanova A, Nelis E, De Vriendt E, Van Hul M, Seeman P, Mazanec R, Saifi GM, Szigeti K, Mancias P, Butler IJ, Kochanski A, Ryniewicz B, De Bleecker J, Van den Bergh P, Verellen C, Van Coster R, Goeman N, Robberecht W, Rasic VM, Nevo Y, Tournev I, Guergueltcheva V, Roelens F, Vieregge P, Vinci P, Moreno MT, Christen HJ, Shy ME, Lupski JR, Vance JM, De Jonghe P, Timmerman V. MFN2 mutation distribution an d genotype/phenotype correlation in Charcot-Marie-Tooth type 2. Brain. 129: 2093-102, 2006

Mariani L, Deiana G, Vassella E, Fathi AR, Murtin C, Arnold M, Vajtai I, Weis J, Siegenthaler P, Schobesberger M, Reinert MM. Loss of heterozygosity 1p36 and 19q13 is a prognostic factor for overall survival in patients with diffuse WHO grade 2 gliomas treated without chemotherapy. J Clin Oncol. 24: 4758-63, 2006

Ramelli G. P., Gallati S., Weis J., Krähenbühl S., Burgunder J.-M. Point Mutation tRNASer(UCN) in a Child With Hearing Loss and Myoclonus Epilepsy. J Child Neurol. 21: 253-55, 2006

Wirths O, Weis J, Kayed R, Saido TC, Bayer TA. Age-dependent axonal degeneration in an Alzheimer mouse model. Neurobiol Aging. 28(11): 1689-99, 2006

Krings T, Busch C, Sellhaus B, Drexler AY, Bovi M, Hermanns-Sachweh B, Scherer K, Gilsbach JM, Thron A, Hans FJ. Long-term histological and scanning electron microscopy results of endovascular and operative treatments of experimentally induced aneurysms in the rabbit. Neurosurgery. 400(1-2): 911-23, 2006

Schröder JM: Neuropathology of Charcot-Marie-Tooth and Related Disorders NeuroMolecular Medicine. 8: 23-42, 2006

Krüttgen A, Schneider I, Weis J. The dark side of the NGF family: Neurotrophins in neoplasias. Brain Pathol. 16: 304-10, 2006

2005

Yen K, Sonnenschein M, Thali MJ, Ozdoba C, Weis J, Zwygart K, Aghayev E, Jackowski C, Dirnhofer R. Postmortem multislice computed tomography and magnetic resonance imaging of odontoid fractures, atlantoaxial distractions and ascending medullary edema. Int J Legal Med. 119: 129-36, 2005

Walther LE, Ilgner J, Oehme A, Schmidt P, Sellhaus B, Gudziol H, Beleites E, Westhofen M. Infectious mononucleosis. HNO. 53: 383-94, 2005

von Felbert V, Córdoba F, Weissenberger J, Vallan C, Kato M, Nakashima I, Braathen LR, Weis J. Interleukin-6 gene ablation in a transgenic mouse model of spontaneous malignant skin melanoma. Am J Pathol. 166: 831-41, 2005

Thiex R, Hans FJ, Krings T, Sellhaus B, Gilsbach JM. Technical pitfalls in a porcine brain retraction model. The impact of brain spatula on the retracted brain tissue in a porcine model: a feasibility study and its technical pitfalls. Neuroradiology. 47: 765-73, 2005

Szurman P, Warga M, Roters S, Grisanti S, Heimann U, Aisenbrey S, Rohrbach JM, Sellhaus B, Ziemssen F, Bartz-Schmidt KU. Experimental implantation and long-term testing of an intraocular vision aid in rabbits. Arch Ophthalmol. 123: 964-69, 2005

Schröder JM. Ferritinopathy: diagnosis by muscle or nerve biopsy, with a note on other nuclear inclusion body diseases. Acta Neuropathol (Berl). 109: 109-14, 2005

Saxena S, Howe CL, Cosgaya JM, Steiner P, Hirling H, Chan JR, Weis J, Krüttgen A. Differential endocytic sorting of p75NTR and TrkA in response to NGF: a role for the ubiquitin/proteasome system in trafficking of TrkA into multivesicular bodies. Mol Cell Neurosci. 28: 571-87, 2005

Ozdoba C, Weis J, Plattner T, Dirnhofer R, Yen K. Fatal scuba diving incident with massive gas embolism in cerebral and spinal arteries. Neuroradiology. 47: 411-16, 2005

Mawrin C, Schneider T, Firsching R, Wiedemann FR, Dietzmann K, Bornemann A, Romeike BF, Sellhaus B, von Deimling A. Assessment of tumor cell invasion factors in gliomatosis cerebri. J Neurooncol. 73: 109-15, 2005

Mawrin C, Kirches E, Schneider-Stock R, Boltze C, Vorwerk CK, Mawrin A, von Deimling A, Stoltenburg-Didinger G, Bornemann A, Romeike B, Sellhaus B, Dietzmann K. Alterations of cell cycle regulators in gliomatosis cerebri. J Neurooncol. 72: 115-22, 2005

Marcao AM, Wiest R, Schindler K, Wiesmann U, Weis J, Schroth G, Miranda MSC, Sturzenegger M, Gieselmann V. Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: a new mutation in the ARSA gene. Arch Neurol. 62: 309-13, 2005

Loeffler S, Fayard B, Weis J, Weissenberger J. Interleukin-6 induces vascular endothelial growth factor (VEGF) expression in the mouse brain: evidence that IL-6 induces VEGF promoter activity via STAT3 and Sp1. Int J Cancer. 115: 202-13, 2005

Kaindl AM, Jakubiczka S, Luecke T, Bartsch O, Weis J, Stoltenburg-Didinger G, Aksu F, Oexle K, Koehler K, Huebner A. A homozygous microdeletion of chromosome 4q11-q12 causes severe limb girdle muscular dystrophy type 2E with joint hyperlaxity and contractures. Hum Mutat. 26: 279-80, 2005

Jenne DE, Kley RA, Vorgerd M, Schröder JM, Weis J, Reimann H, Albrecht B, Nürnberg P, Thiele H, Müller CR, Meng G, Witt CC, Labeit S. Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3. Biol Chem. 386: 61-7, 2005

Hoelzinger DB, Mariani L, Weis J, Woyke T, Berens TJ, McDonough WS, Sloan A, Coons SW, Berens ME. Gene expression profile of glioblastoma multiforme invasive phenotype points to new therapeutic targets. Neoplasia. 7: 7-16, 2005

Häusler M, Sellhaus B, Scheithauer S, Engler M, Alberg E, Teubner A, Ritter K, Kleines M: Murine gammaherpesvirus-68 infection of mice: A new model for human cerebral Epstein-Barr virus infection. Ann Neurol. 57: 600-3, 2005

Fries M, Bickenbach J, Henzler D, Beckers S, Dembinski R, Sellhaus B, Rossaint R, Kuhlen R. S-100 protein and neurohistopathologic changes in a porcine model of acute lung injury. Anesthesiology. 102: 761-7, 2005

Fayard B, Loeffler S, Weis J, Vogelin E, Krüttgen A. The secreted brain-derived neurotrophic factor precursor pro-BDNF binds to TrkB and p75NTR but not to TrkA or TrkC. J Neurosci Res. 80: 18-28, 2005

Evangelopoulos ME, Weis J, Krüttgen A. Signalling pathways leading to neuroblastoma differentiation after serum withdrawal: HDL blocks neuroblastoma differentiation by inhibition of EGFR. Oncogene. 24: 3309-18, 2005

Di Martino E, Sellhaus B, Haensel J, Schlegel JG, Westhofen M, Prescher A. Fallopian canal dehiscences: a survey of clinical and anatomical findings. Eur Arch Otorhinolaryngol. 262: 120-6, 2005

Cordoba F, Braathen LR, Weissenberger J, Vallan C, Kato M, Nakashima I, Weis J, von Felbert V. 5 aminolaevulinic acid photodynamic therapy in a transgenic mouse model of skin melanoma. Exp Dermatol. 14: 429-37, 2005

Buss A, Sellhaus B, Wolmsley A, Noth J, Schwab ME, Brook GA. Expression pattern of NOGO-A protein in the human nervous system. Acta Neuropathol (Berl). 110: 113-9, 2005

Hans FJ, Reinges MH, Nolte K, Reipke P, Krings T. Primary lymphoma of the skull base. Neuroradiology. 47: 539-42, 2005

Saxena S, Bucci C, Weis J, Krüttgen A. The small GTPase Rab7 controls the endosomal trafficking and neurotogenic signalling of the NGF receptor TrkA. J Neurosci. 25:10930-40, 2005

Senderek J, Krieger M, Stendel C, Bergmann C, Moser M, Breitbach-Faller N, Rudnik-Schöneborn S, Blaschek A, Wolf NI, Harting I, North K, Smith J, Muntoni F, Brockington M, Quijano-Roy S, Renault F, Herrmann R, Hendershot LM, Schröder JM, Lochmüller H, Topaloglu H, Voit T, Weis J, Ebinger F, Zerres K. Mutations in SIL1 cause Marinesco Sjögren syndrome, a cerebellar ataxia with cataract and myopathy. Nature Genetics. 37:1312-14, 2005

Schröder JM, Züchner S, Dichgans M, Nagy Z, Molnar MJ. Peripheral nerve and skeletal muscle involvement in CADASIL. Acta Neuropathol (Berl). 110: 587-99, 2005

Goebel HH, Kiefer R, Pongratz D, Schröder JM, von Moers A. Indikation und Qualifikationskriterien für die Biopsie und präparative Aufarbeitung von Muskel- und Nervengewebeproben. Nervenheilkunde. 24: 933-35, 2005

Block F, Weis J: Periphere Neuropathie, Kap. 17, S. 303 -- 328. In: Block F, Prüter C (Hrsg.) Medikamentös induzierte neurologische und psychiatrische Störungen, Springer Medizinverlag Heidelberg, 2006

Block R, Weis J: Myopathie, Kap. 19, S. 343 -- 357. In: Block F, Prüter C (Hrsg.) Medikamentös induzierte neurologische und psychiatrische Störungen, Springer Medizinverlag Heidelberg, 2006

2004

Züchner S, Vorgerd M, Sindern E, Schröder JM. The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie Tooth neuropathy. Neuromuscul Disord. 14: 147-57, 2004

Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, Rochelle J, Dadali EL, Zappia M, Nelis E, Patitucci A, Senderek J, Parman Y, Evgrafov O, Jonghe PD, Takahashi Y, Tsuji S, Pericak-Vance MA, Quattrone A, Battaloglu E, Polyakov AV, Timmerman V, Schröder JM, Vance JM. Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A. Nature Genetics. 36: 449-51, 2004

Wu YJ, Krüttgen A, Moller JC, Shine D, Chan JR, Shooter EM, Cosgaya JM. Nerve growth factor, brain-derived neurotrophic factor, and neurotrophin-3 are sorted to dense-core vesicles and released via the regulated pathway in primary rat cortical neurons. J Neurosci Res. 75: 825-34, 2004

Weissenberger J, Loeffler S, Kappeler A, Kopf M, Lukes A, Afanasieva TA, Aguzzi A, Weis J: IL-6 is required for glioma development in a mouse model. Oncogene. 23: 3308-16, 2004

Weigel R, Senn P, Weis J, Krauss JK. Severe complications after intrathecal methotrexate (MTX) for treatment of primary central nervous system lymphoma (PCNSL). Clin Neurol Neurosurg. 106: 82-7, 2004

Vielhaber S, Feistner H, Weis J, Kreuder J, Sailer M, Schröder JM, Kunz WS. Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical course. J Clin Neurosci. 11(8): 919-24, 2004

Saxena S, Howe CL, Cosgaya JM, Hu M, Weis J, Krüttgen A. Differences in the surface binding and endocytosis of neurotrophins by p75NTR. Mol Cell Neurosci. 26: 292-307, 2004

Rohde V, Reinacher P, Patz E, Sellhaus B, Gilsbach JM. Spinal cord compression by a cervical oseteocartilaginous exostosis: surgical strategy aspects. Z Orthop Grenzgeb. 142: 179-83, 2004

Mariani L, Siegenthaler P, Guzman R, Friedrich D, Fathi AR, Ozdoba C, Weis J, Ballinari P, Seiler RW. The impact of tumour volume and surgery on the outcome of adults with supratentorial WHO grade II astrocytic tumors. Acta Neurochir (Wien). 146: 441-48, 2004

Mariani L, Schaller B, Weis J, Ozdoba C, Seiler RW. Esthesioneuroblastoma of the pituitary gland: a clinicopathological entity? Case report and review of the literature. J Neurosurg. 101: 1049-52, 2004

Evangelopoulos ME, Weis J, Krüttgen A. Neurotrophin effects on neuroblastoma cells: Correlation with Trk and p75NTR expression and influence of Trk receptor bodies. J NeuroOncol. 66: 101-10, 2004

De Paepe B, Schröder JM, Martin JJ, Racz GZ, De Bleecker JL. Localization of the alpha-chemokine SDF-1 and its receptor CXCR4 in idiopathic inflammatory myopathies. Neuromuscul Disord. 14: 265-73, 2004

Christiansen S, Demircan L, Kwant PB, Akdis M, Rex S, Buhre W, Langebartels G, Kuruc N, Nikolin S, Reul H, Autschbach R. Experimental testing of a new left ventricular assist device - the microdiagonal blood pump. Asaio J. 50: 200-4, 2004

Chen L, Schaerer M, Lu ZH, Lang D, Joncourt F, Weis J, Fritschi J, Kappeler L, Gallati S, Sigel E, Burgunder JM. Exon 17 skipping in CLCN1 leads to recessive myotonia congenita. Muscle Nerve. 29: 670-6, 2004

Buss A, Assmus A, Weidemann J, Sellhaus B, Lorenzen J, Block F. Diagnosis of an initial infratentorial central nervous system B-cell lymphoma during prolonged cortisone medication. Nervenarzt. 75: 1217-21, 2004

Bissar-Tadmouri N, Nelis E, Züchner S, Parman Y, Deymeer F, Serdaroglu P, De Jonghe P, Van Gerwen V, Timmerman V, Schröder JM, Battaloglu E. Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene. Neurology. 62: 1522-5, 2004

Bahm J, Becker M, Disselhorst-Klug C, Williams S, Meinecke L, Müller H, Sellhaus B, Schröder JM, Rau G. Surgical Strategy in Obstetric Brachial Plexus Palsy: The Aachen Experience. Seminars in Plastic Surgery. 18: 285-99, 2004

Korinth MC, Kapser A, Nolte K, Gilsbach JM. Cervical diastematomyelia associated with an intradural epidermoid cyst between the hemicords and multiple vertebral body anomalies. Pediatr Neurosurg. 40: 253-6, 2004

De Paepe B, Racz GZ, Schröder JM, De Bleecker JL. Expression and distribution of the nitric oxide synthases in idiopathic inflammatory myopathies. Acta Neuropathol (Berl). 108: 37-42, 2004

Schröder JM, Durling H, Laing N. Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn). Acta Neuropathol (Berl). 108: 250-56, 2004

Schröder JM, Hackel V, Wanders RJ, Gohlich-Ratmann G, Voit T. Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiency. Acta Neuropathol (Berl). 108: 154-67, 2004

Gossrau G, Gestrich B, Koch R, Wunderlich C, Schröder JM, Schroeder S, Reichmann H, Lampe JB. Apolipoprotein E and alpha-1-antichymotrypsin polymorphisms in sporadic inclusion body myositis. Eur Neurol. 51: 215-20, 2004

Schaller B, Weis J, Brekenfeldt K, Seiler R, Mariani L. Esthesioneuroblastoma of the pituitary gland: a clinicopathological entity? J Neurosurg. 101: 1049-52, 2004