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Michael Schröder

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TOP 3
J Michael Schröder
"Necklace" fibers as a late clue to the interpretation of the forgotten "trilaminar" fibers.
Kay W Nolte; Andreas R Janecke; Matthias Vorgerd; Joachim Weis; J Michael Schröder
Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 gene.
Kay W Nolte; Volkmar J Hans; Christoph Schattenfroh; Joachim Weis; J Michael Schröder
Perineurial cells filled with collagen in 'atypical' Cogan's syndrome.

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All Publications

2009: J Michael Schröder
"Necklace" fibers as a late clue to the interpretation of the forgotten "trilaminar" fibers.
Acta neuropathologica 2009;118(2):317-8; author reply 319-20.
2008: Kay W Nolte; Andreas R Janecke; Matthias Vorgerd; Joachim Weis; J Michael Schröder
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 neuropathologica 2008;116(5):491-506.
2008: Kay W Nolte; Volkmar J Hans; Christoph Schattenfroh; Joachim Weis; J Michael Schröder
Perineurial cells filled with collagen in 'atypical' Cogan's syndrome.
Acta neuropathologica 2008;115(5):589-96.
2007: Benedikt Schoser; J Michael Schröder; Timo Grimm; Damien Sternberg; Wolfram Kress
A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene.
Muscle & nerve 2007;35(5):599-606.
2006: J Michael Schröder
Neuropathology of Charcot-Marie-Tooth and related disorders.
Neuromolecular medicine 2006;8(1-2):23-42.
2005: J Michael Schröder; Stephan Zuchner; M Dichgans; Zoltán Nagy; Mária Judit Molnár
Peripheral nerve and skeletal muscle involvement in CADASIL.
Acta neuropathologica 2005;110(6):587-99.
2005: Jan Senderek; Michael Krieger; Claudia Stendel; Carsten Bergmann; Markus Moser; Nico Breitbach-Faller; Sabine Rudnik-Schöneborn; Astrid Blaschek; Nicole I Wolf; Inga Harting; Kathryn North; Janine Smith; Francesco Muntoni; Martin Brockington; Susana Quijano-Roy; Francis Renault; Ralf Herrmann; Linda M Hendershot; J Michael Schröder; Hanns Lochmüller; Haluk Topaloglu; Thomas Voit; Joachim Weis; Friedrich Ebinger; Klaus Zerres
Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy.
Nature genetics 2005;37(12):1312-4.
2005: J Michael Schröder
Ferritinopathy: diagnosis by muscle or nerve biopsy, with a note on other nuclear inclusion body diseases.
Acta neuropathologica 2005;109(1):109-14.
2004: J Michael Schröder; H Durling; N Laing
Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn).
Acta neuropathologica 2004;108(3):250-6.
2004: J Michael Schröder; V Hackel; R J A Wanders; G Göhlich-Ratmann; Thomas Voit
Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiency.
Acta neuropathologica 2004;108(2):154-67.
2004: Nisrine Bissar-Tadmouri; Eva Nelis; Stephan Zuchner; Yesim Parman; Feza Deymeer; Piraye Serdaroglu; Peter De Jonghe; Veerle Van Gerwen; Vincent Timmerman; J Michael Schröder; Esra Battaloglu
Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene.
Neurology 2004;62(9):1522-5.
2004: Stephan Zuchner; Irina V Mersiyanova; Maria Muglia; Nisrine Bissar-Tadmouri; Julie M Rochelle; Elena L Dadali; Mario Zappia; Eva Nelis; Alessandra Patitucci; Jan Senderek; Yesim Parman; Oleg V Evgrafov; Peter De Jonghe; Yuji Takahashi; Shoij Tsuji; Margaret Pericak-Vance; Aldo Quattrone; Esra Battaloglu; Alexander V Polyakov; Vincent Timmerman; J Michael Schröder; Jeffery Vance; Esra Battologlu
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Nature genetics 2004;36(5):449-51.
2004: Stephan Zuchner; Matthias Vorgerd; Eckhart Sindern; J Michael Schröder
The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy.
Neuromuscular disorders : NMD 2004;14(2):147-57.
2003: Harald D Müller; A Beckmann; J Michael Schröder
Inflammatory infiltrates in the spinal cord of patients with Guillain-Barré syndrome.
Acta neuropathologica 2003;106(6):509-17.
2003: Christian Mawrin; Anna Brunn; Christoph Röcken; J Michael Schröder
Peripheral neuropathy in systemic lupus erythematosus: pathomorphological features and distribution pattern of matrix metalloproteinases.
Acta neuropathologica 2003;105(4):365-72.
2003: Stephan Zuchner; Anne-Dorte Sperfeld; Jan Senderek; Bernd Sellhaus; C Oliver Hanemann; J Michael Schröder
A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier disease.
Brain : a journal of neurology 2003;126(Pt 4):920-7.
2003: Jan Senderek; Carsten Bergmann; Vincent T Ramaekers; Eva Nelis; Günther Bernert; Astrid Makowski; Stephan Zuchner; Peter De Jonghe; Sabine Rudnik-Schöneborn; Klaus Zerres; J Michael Schröder
Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy.
Brain : a journal of neurology 2003;126(Pt 3):642-9.
2002: Marcel Pilartz; Talke Jess; Dorit Indefrei; J Michael Schröder
Adoptive transfer-experimental allergic neuritis in newborn Lewis rats results in inflammatory infiltrates, mast cell activation, and increased Ia expression with only minor nerve fiber degeneration.
Acta neuropathologica 2002;104(5):513-24.
2002: Anna Brunn; W Nacimiento; Bernd Sellhaus; Harald D Müller; Armin Buss; J Michael Schröder
Acute onset of hemorrhagic leukoencephalomyelitis (Hurst) in the spinal cord.
Clinical neuropathology 2002;21(5):214-9.
2002: Carsten Bergmann; Klaus Zerres; Sabine Rudnik-Schöneborn; Thomas Eggermann; J Michael Schröder; Jan Senderek
Allelic variants in the 5' non-coding region of the connexin32 gene: possible pitfalls in the diagnosis of X linked Charcot-Marie-Tooth neuropathy (CMTX).
Journal of medical genetics 2002;39(9):e58.
2001: Christian Mawrin; G Schütz; J Michael Schröder
Correlation between the number of epineurial and endoneurial blood vessels in diseased human sural nerves.
Acta neuropathologica 2001;102(4):364-72.
2001: Harald D Müller; S Vielhaber; Anna Brunn; J Michael Schröder
Dominantly inherited myopathy with novel tubular aggregates containing 1-21 tubulofilamentous structures.
Acta neuropathologica 2001;102(1):27-35.
2001: Carsten Bergmann; J Michael Schröder; Sabine Rudnik-Schöneborn; Klaus Zerres; Jan Senderek
A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany.
Brain research. Molecular brain research 2001;88(1-2):183-5.
2001: Benita Hermanns; Anna Brunn; Ernst R Schwarz; Jörg S Sachweh; Ingrid M Seipelt; J Michael Schröder; U Vogel; Friedrich A Schoendube; Reinhard Buettner
Fulminant toxoplasmosis in a heart transplant recipient.
Pathology, research and practice 2001;197(3):211-5.
2000: C Bank; Tewfik Soulimane; J Michael Schröder; Gerhard Buse; Stefanie Zanssen
Multiple deletions of mtDNA remove the light strand origin of replication.
Biochemical and biophysical research communications 2000;279(2):595-601.
2000: Lothar Mayfrank; Y Kim; J Kissler; P Delsing; Joachim M Gilsbach; J Michael Schröder; J Weis
Morphological changes following experimental intraventricular haemorrhage and intraventricular fibrinolytic treatment with recombinant tissue plasminogen activator.
Acta neuropathologica 2000;100(5):561-7.
2000: Andreas B Schmitt; Armin Buss; Sebastian Breuer; Gary A Brook; Katrin Pech; Didier Martin; Jean Schoenen; Johannes Noth; S Love; J Michael Schröder; Georg W Kreutzberg; W Nacimiento
Major histocompatibility complex class II expression by activated microglia caudal to lesions of descending tracts in the human spinal cord is not associated with a T cell response.
Acta neuropathologica 2000;100(5):528-36.
2000: A Beckmann; J Michael Schröder
Screening for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsy in archival nerve biopsy samples by direct-double-differential PCR.
Acta neuropathologica 2000;100(5):459-63.
2000: B Hermanns; Mária Judit Molnár; J Michael Schröder
Peripheral neuropathy associated with hereditary and sporadic inclusion body myositis: confirmation by electron microscopy and morphometry.
Journal of the neurological sciences 2000;179(S 1-2):92-102.
2000: Harald D Müller; M Mugler; Vincent T Ramaekers; J Michael Schröder
Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy (HMSN-ADM).
Journal of the peripheral nervous system : JPNS 2000;5(3):147-57.
2000: Carsten Bergmann; Jan Senderek; B Hermanns; A Jauch; Bart Janssen; J Michael Schröder; D Karch
Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathy.
Muscle & nerve 2000;23(5):818-23.
2000: Stefanie Zanssen; Mária Judit Molnár; Gerhard Buse; J Michael Schröder
Novel cluster of tRNALeu(UUR) mutations in a sporadic case of infantile myopathy restricted to muscle tissue.
Neuropediatrics 2000;31(2):93-6.
2000: Jan Senderek; B Hermanns; U Lehmann; Carsten Bergmann; G Marx; C Kabus; V Timmerman; G Stoltenburg-Didinger; J Michael Schröder
Charcot-Marie-Tooth neuropathy type 2 and P0 point mutations: two novel amino acid substitutions (Asp61Gly; Tyr119Cys) and a possible "hotspot" on Thr124Met.
Brain pathology (Zurich, Switzerland) 2000;10(2):235-48.
2000: J F Wang; J Michael Schröder
Comparative morphometric evaluation of peripheral nerves and muscle fibers in myotonic dystrophy.
Acta neuropathologica 2000;99(1):39-47.
1999: René Gobbelé; S W Schoen; J Michael Schröder; D Vorwerk; M Schwarz
S-1 radiculopathy as a possible predisposing factor in focal myositis with unilateral hypertrophy of the calf muscles.
Journal of the neurological sciences 1999;170(1):64-8.
1999: J Michael Schröder; J F Wang; Eckhart Sindern; Jean-Pierre Malin
Polyneuropathy with osmiophilic membrane-bound, cytoplasmic inclusions in Schwann cells (POMCIS).
Acta neuropathologica 1999;98(4):427-32.
1999: J Michael Schröder; J D Rollnik; M Schubert; R Dengler
Demyelinating sensorimotor neuropathy with congenital cataract, mental retardation, and unique, dysplastic perineurial cells within the endoneurium.
Acta neuropathologica 1999;98(4):421-6.
1999: Jan Senderek; B Hermanns; Carsten Bergmann; Babak Boroojerdi; Malek Bajbouj; Marcel Hungs; Vincent T Ramaekers; S Quasthoff; D Karch; J Michael Schröder
X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1).
Journal of the neurological sciences 1999;167(2):90-101.
1999: J F Wang; Juergen Forst; S Schröder; J Michael Schröder
Correlation of muscle fiber type measurements with clinical and molecular genetic data in Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1999;9(3):150-8.
1998: Stefanie Zanssen; Mária Judit Molnár; Gerhard Buse; J Michael Schröder
Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.
Clinical neuropathology 1998;17(6):291-6.
1998: Joachim Weis; DC Lie; U Ragoss; Stephan Zuchner; J Michael Schröder; G Karpati; TJ Farruggella; Neil stahl; George D Yancopoulos; P S DiStefano
Increased expression of CNTF receptor alpha in denervated human skeletal muscle.
Journal of neuropathology and experimental neurology 1998;57(9):850-7.
1998: Mária Judit Molnár; J Michael Schröder
Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions.
Acta neuropathologica 1998;96(1):41-51.
1998: R Thiex; J Michael Schröder
PMP-22 gene duplications and deletions identified in archival, paraffin-embedded sural nerve biopsy specimens: correlation to structural changes.
Acta neuropathologica 1998;96(1):13-21.
1998: Jan Senderek; Carsten Bergmann; S Quasthoff; Vincent T Ramaekers; J Michael Schröder
X-linked dominant Charcot-Marie-Tooth disease: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln).
Acta neuropathologica 1998;95(5):443-9.
1998: Gary A Brook; Andreas B Schmitt; W Nacimiento; J Weis; J Michael Schröder; Johannes Noth
Distribution of B-50(GAP-43) mRNA and protein in the normal adult human spinal cord.
Acta neuropathologica 1998;95(4):378-86.
1998: Joachim Weis; U Weber; J Michael Schröder; R Lemke; H Althoff
Phrenic nerves and diaphragms in sudden infant death syndrome.
Forensic science international 1998;91(2):133-46.
1998: J F Wang; J Michael Schröder
Morphometric evaluation of paraneoplastic neuropathies associated with carcinomas, lymphomas, and dysproteinemias.
Journal of the peripheral nervous system : JPNS 1998;3(4):259-66.
1997: G Schütz; J Michael Schröder
Number and size of epineurial blood vessels in normal and diseased human sural nerves.
Cell and tissue research 1997;290(1):31-7.
1997: J Michael Schröder; Mária Judit Molnár
Mitochondrial abnormalities and peripheral neuropathy in inflammatory myopathy, especially inclusion body myositis.
Molecular and cellular biochemistry 1997;174(1-2):277-81.
1997: Stefanie Zanssen; Mária Judit Molnár; J Michael Schröder; Gerhard Buse
Multiple mitochondrial tRNA(Leu[UUR]) mutations associated with infantile myopathy.
Molecular and cellular biochemistry 1997;174(1-2):231-6.
1996: J Michael Schröder
Developmental and pathological changes at the node and paranode in human sural nerves.
Microscopy research and technique 1996;34(5):422-35.
1996: J Michael Schröder; M Mayer; Joachim Weis
Mitochondrial abnormalities and intrafamilial variability of sural nerve biopsy findings in adrenomyeloneuropathy.
Acta neuropathologica 1996;92(1):64-9.
1996: Mária Judit Molnár; Stefanie Zanssen; Gerhard Buse; J Michael Schröder
A large-scale deletion of mitochondrial DNA in a case with pure mitochondrial myopathy and neuropathy.
Acta neuropathologica 1996;91(6):654-8.
1995: Mária Judit Molnár; S Neudecker; J Michael Schröder
Increase of mitochondria in vasa nervorum of cases with mitochondrial myopathy, Kearns-Sayre syndrome, progressive external ophthalmoplegia and MELAS.
Neuropathology and applied neurobiology 1995;21(5):432-9.
1995: J Weis; Wilfried Dimpfel; J Michael Schröder
Nerve conduction changes and fine structural alterations of extra- and intrafusal muscle and nerve fibers in streptozotocin diabetic rats.
Muscle & nerve 1995;18(2):175-84.
1995: J Michael Schröder; B Krabbe; Joachim Weis
Oculopharyngeal muscular dystrophy: clinical and morphological follow-up study reveals mitochondrial alterations and unique nuclear inclusions in a severe autosomal recessive type.
Neuropathology and applied neurobiology 1995;21(1):68-73.
1995: J Michael Schröder; B Sellhaus; J Jörg
Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
Acta neuropathologica 1995;89(2):116-21.
1995: J Michael Schröder; K V Toyka; H P Hartung
11th meeting of the Peripheral Nerve Study Group (PNSG). "Klostergut Jakobsberg", Boppard, Germany 29 July-1 August 1993.
Neuromuscular disorders : NMD 1995;5(1):75-7.
1995: J Michael Schröder; B Sellhaus; T Wöhrmann; B Kögel; K Zwingenberger
Inhibitory effects of thalidomide on cellular proliferation, endoneurial edema and myelin phagocytosis during early wallerian degeneration.
Acta neuropathologica 1995;89(5):415-9.
1994: M Hardenack; A Völker; J Michael Schröder; Joachim M Gilsbach; Albrecht Harders
Primary eosinophilic granuloma of the oculomotor nerve. Case report.
Journal of neurosurgery 1994;81(5):784-7.
1994: Joachim Weis; R May; J Michael Schröder
Fine structural and immunohistochemical identification of perineurial cells connecting proximal and distal stumps of transected peripheral nerves at early stages of regeneration in silicone tubes.
Acta neuropathologica 1994;88(2):159-65.
1993: J Michael Schröder; G Heide; Vincent T Ramaekers; Wilhelm Mortier
Subtotal aplasia of myelinated nerve fibers in the sural nerve.
Neuropediatrics 1993;24(5):286-91.
1993: Joachim Weis; M E Alexianu; G Heide; J Michael Schröder
Renaut bodies contain elastic fiber components.
Journal of neuropathology and experimental neurology 1993;52(5):444-51.
1993: J Michael Schröder; R May; J Weis
Perineurial cells are the first to traverse gaps of peripheral nerves in silicone tubes.
Clinical neurology and neurosurgery 1993;95 Suppl():S78-83.
1993: J Michael Schröder; R May; Y S Shin; M Sigmund; S Nase-Hüppmeier
Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).
Acta neuropathologica 1993;85(4):419-30.
1992: R Dieler; A Völker; J Michael Schröder
Scanning electron microscopic study of denervated and reinnervated intrafusal muscle fibers in rats.
Muscle & nerve 1992;15(4):433-41.
1992: Claudia Sommer; J Michael Schröder
Immune-mediated neuropathy and myopathy in post-streptococcal disease: electron-microscopical, morphometrical and immunohistochemical studies.
Clinical neuropathology 1992;11(2):77-86.
1992: J Michael Schröder; F Himmelmann
Fine structural evaluation of altered Schmidt-Lanterman incisures in human sural nerve biopsies.
Acta neuropathologica 1992;83(2):120-33.
1992: J Michael Schröder
[Pathomorphology of epineural and endoneural blood vessels in diabetic polyneuropathy].
VASA. Supplementum 1992;35():29.
1992: J Michael Schröder; B Huffmann; V Braun; H P Richter
Spasmodic torticollis: severe compression neuropathy in rami dorsales of cervical nerves C1-6.
Acta neuropathologica 1992;84(4):416-24.
1991: H Grehl; J Michael Schröder
Significance of degenerating endoneurial cells in peripheral neuropathy.
Acta neuropathologica 1991;81(6):680-5.
1990: R Dieler; J Michael Schröder
Increase of elastic fibres in muscle spindles of rats following single or repeated denervation with or without reinnervation.
Virchows Archiv. A, Pathological anatomy and histopathology 1990;417(3):213-21.
1989: J Weis; J Michael Schröder
The influence of fat tissue on neuroma formation.
Journal of neurosurgery 1989;71(4):588-93.
1989: Claudia Sommer; J Michael Schröder
Hereditary motor and sensory neuropathy with optic atrophy. Ultrastructural and morphometric observations on nerve fibers, mitochondria, and dense-cored vesicles.
Archives of neurology 1989;46(9):973-7.
1989: J Weis; J Michael Schröder
Differential effects of nerve, muscle, and fat tissue on regenerating nerve fibers in vivo.
Muscle & nerve 1989;12(9):723-34.
1989: J Michael Schröder; H Bodden; A Hamacher; C Verres
Scanning electron microscopy of teased intrafusal muscle fibers from rat muscle spindles.
Muscle & nerve 1989;12(3):221-32.
1989: R Dieler; J Michael Schröder
Myenteric plexus neuropathy in infantile hypertrophic pyloric stenosis.
Acta neuropathologica 1989;78(6):649-61.
1988: Joachim Weis; J Michael Schröder
Adult polyglucosan body myopathy with subclinical peripheral neuropathy: case report and review of diseases associated with polyglucosan body accumulation.
Clinical neuropathology 1988;7(6):271-9.
1988: J Michael Schröder; J Bohl; U von Bardeleben
Changes of the ratio between myelin thickness and axon diameter in human developing sural, femoral, ulnar, facial, and trochlear nerves.
Acta neuropathologica 1988;76(5):471-83.
1988: Claudia Sommer; J Michael Schröder
Binding of swine IgM immunoglobulins to peripheral nerve myelin sheaths in electron microscopic immunocytochemistry.
Acta neuropathologica 1988;77(1):100-3.