J. Schröder

J. Schröder, 1994, European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery.

Changing ratio between myelin thickness and axon caliber in developing human facial nerves.

Pathomorphology of Regenerating Peripheral Nerves

J. Schröder, 1990 .

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

M. Pericak-Vance, S. Züchner, J. Vance, 2004, Nature Genetics.

X‐linked neuropathy of the Charcot–Marie–Tooth type

J. Senderek, J. Schröder, 2014 .

X-linked dominant Charcot-Marie-Tooth disease: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln)

V. Ramaekers, C. Bergmann, J. Senderek, 1998, Acta Neuropathologica.

Periaxin mutations cause a broad spectrum of demyelinating neuropathies

J. Lupski, P. Brophy, C. Boerkoel, 2002, Annals of neurology.

Perineurial cells are the first to traverse gaps of peripheral nerves in silicone tubes

J. Weis, J. Schröder, R. May, 1993, Clinical Neurology and Neurosurgery.

Quantitative Evaluation of Regenerated Nerve Fibers

J. Schröder, 1975 .

ALTERED RATIO BETWEEN AXON CALIBER AND MYELIN THICKNESS IN SURAL NERVES OF CHILDREN

J. Bohl, J. Schröder, 1978 .

Correlation of muscle fiber type measurements with clinical and molecular genetic data in Duchenne muscular dystrophy

J. Forst, Jian-Feng Wang, J. Schröder, 1999, Neuromuscular Disorders.

Adult polyglucosan body disease

K. Müller, J. Malin, T. Ziemssen, 2003, Neurology.

S-1 radiculopathy as a possible predisposing factor in focal myositis with unilateral hypertrophy of the calf muscles

R. Gobbelé, D. Vorwerk, J. Schröder, 1999, Journal of the Neurological Sciences.

Adult onset lipid storage in gastric mucosa and skeletal muscle fibers associated with gastric pain, progressive muscle weakness and partial deficiency of cytochrome C oxidase.

H. Reichmann, R. Weber, J. Schröder, 1991, Pathology, research and practice.

Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis)

M. Sigmund, Y. Shin, J. Schröder, 2004, Acta Neuropathologica.

Neuropathy Associated with Mitochondrial Disorders

J. Schröder, 1993, Brain pathology.

Renaut Bodies Contain Elastic Fiber Components

J. Weis, J. Schröder, M. Alexianu, 1993, Journal of neuropathology and experimental neurology.

Distribution of B-50(GAP-43) mRNA and protein in the normal adult human spinal cord

J. Noth, J. Weis, G. Brook, 1998, Acta Neuropathologica.

SOX10 mutation with peripheral amyelination and developmental disturbance of axons

M. Kornhuber, J. Weis, D. Wand, 2012, Muscle & nerve.

Infantile hypertrophic pyloric stenosis: myopathic type

J. Schröder, R. Dieler, H. Skopnik, 2004, Acta Neuropathologica.

Oculopharyngeal muscular dystrophy: clinical and morphological follow‐up study reveals mitochondrial alterations and unique nuclear inclusions in a severe autosomal recessive type

J. Weis, J. Schröder, B. Krabbe, 1995, Neuropathology and applied neurobiology.

Autosomal dominant burning feet syndrome

C. van Broeckhoven, V. Timmerman, J. Weis, 1999, Journal of neurology, neurosurgery, and psychiatry.

Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type.

K. Wessel, J. Peiffer, W. Roggendorf, 1988, Pathology, research and practice.

Multiple exercise-related mononeuropathy with abdominal colic

H. Freund, K. Toyka, K. Reiners, 1983, Journal of the Neurological Sciences.

Interrelationships between polyamines and nucleic acids

N. Seiler, J. Schröder, H. Fischer, 1972, Zeitschrift für Zellforschung und Mikroskopische Anatomie.

Correlation of histology, cytogenetics and proliferation fraction (Ki-67 and PCNA) quantitated by image analysis in meningiomas.

K. Zang, J. Weis, U. Cremerius, 1996, Pathology, research and practice.

Novel TPM3 mutation in a family with cap myopathy and review of the literature

K. Claeys, T. Voit, J. Schulz, 2014, Neuromuscular Disorders.

Nuclear and mitochondrial changes of muscle fibers in AIDS after treatment with high doses of zidovudine

J. Schröder, M. Bertram, R. Schnabel, 2004, Acta Neuropathologica.

Nuclear and mitochondrial changes of co-cultivated spinal cord, spinal ganglia and muscle fibers following treatment with various doses of zidovudine

W. Piroth, J. Schröder, T. Kaldenbach, 1996, Acta Neuropathologica.

Ragged-red fibres detected in paraffin sections by a monoclonal antibody to inner mitochondrial membrane

W. Paulus, J. Peiffer, W. Roggendorf, 1989, Journal of Neurology.

Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies

Wolfram Kress, Jan Bürmann, Joachim Weis, 2014, Orphanet Journal of Rare Diseases.

Recommendations for the examination of peripheral nerve biopsies

J. Schröder, 1998, Virchows Archiv.

Peripheral nerve and skeletal muscle involvement in CADASIL

S. Züchner, M. Dichgans, J. Schröder, 2005, Acta Neuropathologica.

Mitochondrial abnormalities in human sural nerves: fine structural evaluation of cases with mitochondrial myopathy, hereditary and non-hereditary neuropathies, and review of the literature

C. Sommer, J. Schröder, 2004, Acta Neuropathologica.

Towards a functional pathology of hereditary neuropathies

I. Katona, K. Claeys, J. Weis, 2016, Acta Neuropathologica.

Electron Microscopic Observations on Different Models of Acute Experimental Brain Edema

K. Hossmann, P. Kleihues, J. Schröder, 1967 .

Altered ratio between axon diameter and myelin sheath thickness in regenerated nerve fibers.

J. Schröder, J M Schröder, 1972, Brain research.

Calcium potentials and tetrodotoxin-resistant sodium potentials in unmyelinated C fibres of biopsied human sural nerve

P. Grafe, J. Grosskreutz, J. Schröder, 1995, Neuroscience.

Abnormal sensory and motor reinnervation of rat muscle spindles following nerve transection and suture

J. Schröder, R. Dieler, 2004, Acta Neuropathologica.

Homozygous mutations in caveolin‐3 cause a severe form of rippling muscle disease

T. Brüning, J. Malin, H. Goebel, 2003, Annals of neurology.

Myopathy in Marinesco–Sjögren syndrome links endoplasmic reticulum chaperone dysfunction to nuclear envelope pathology

H. Goebel, C. Gatz, R. Zahedi, 2014, Acta Neuropathologica.

X-linked dominant Charcot–Marie–Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations 1 1 Presented in part at the 7th Annual Symposium of the European Charcot–Marie–Tooth Consortium, 3–5 July 1998, in Antwerp, Belgi

M. Bajbouj, B. Boroojerdi, M. Hungs, 1999, Journal of the Neurological Sciences.

PMP-22 gene duplications and deletions identified in archival, paraffin-embedded sural nerve biopsy specimens: correlation to structural changes

R. Thiex, J. Schröder, 1998, Acta Neuropathologica.

Merlin isoform 2 in neurofibromatosis type 2–associated polyneuropathy

M. Giovannini, D. Gutmann, S. Baader, 2013, Nature Neuroscience.

Primary eosinophilic granuloma of the oculomotor nerve. Case report.

A. Harders, J. Gilsbach, J. Schröder, 1994, Journal of neurosurgery.

A new type of distal myopathy in two brothers

J. Schröder, E. Kuhn, 2004, Journal of Neurology.

Oculopharyngeal muscle dystrophy: fine structure and mRNA expression levels of PABPN1.

J. Weis, J. Schröder, T. Klossok, 2011, Clinical neuropathology.

Multiple deletions of mtDNA remove the light strand origin of replication.

T. Soulimane, J. Schröder, G. Buse, 2000, Biochemical and biophysical research communications.

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

J. Weis, J. Schröder, R. May, 2004, Acta Neuropathologica.

Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD

T. Voit, V. Straub, R. Falsaperla, 2002, Neuromuscular Disorders.

Binding of swine IgM immunoglobulins to peripheral nerve myelin sheaths in electron microscopic immunocytochemistry

C. Sommer, J. Schröder, 2004, Acta Neuropathologica.

Colchicine myopathy in a case of familial mediterranean fever: immunohistochemical and ultrastructural study of accumulated tubulin-immunoreactive material

J. Schröder, F. Himmelmann, 2004, Acta Neuropathologica.

Perineurial cells filled with collagen in ‘atypical’ Cogan’s syndrome

J. Weis, J. Schröder, K. Nolte, 2008, Acta Neuropathologica.

Immune-mediated neuropathy and myopathy in post-streptococcal disease: electron-microscopical, morphometrical and immunohistochemical studies.

C. Sommer, J. Schröder, 1992, Clinical neuropathology.

Lacunar dilatations of intrafusal and extrafusal terminal cisternae, annulate lamellae, confronting cisternae and tubulofilamentous inclusions within the spectrum of muscle and nerve fiber changes in myotonic dystrophy.

J. Schröder, R. Dieler, 1990, Pathology, research and practice.

Hereditary motor and sensory neuropathy with optic atrophy. Ultrastructural and morphometric observations on nerve fibers, mitochondria, and dense-cored vesicles.

C. Sommer, J. Schröder, 1989, Archives of neurology.

Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene

S. Züchner, Y. Parman, E. Battaloğlu, 2004, Neurology.

The fine structure of de-and reinnervated muscle spindles

J. Schröder, 2004, Acta Neuropathologica.

The fine structure of denervated and reinnervated muscle spindles: Morphometric study of intrafusal muscle fibers

J. Schröder, L. Scholz, P. Kemme, 1979, Acta Neuropathologica.

The fine structure of de- and reinnervated muscle spindles

J. Schröder, 2004, Acta Neuropathologica.

Proliferation of epineurial capillaries and smooth muscle cells in angiopathic peripheral neuropathy

J. Schröder, 2004, Acta Neuropathologica.

Reconstruction of the spinal accessory nerve with an anastomosis to the dorsal C3 branch: technical note.

V. Braun, H. Richter, J. Schröder, 1996, Neurosurgery.

Significance of degenerating endoneurial cells in peripheral neuropathy

J. Schröder, H. Grehl, 2004, Acta Neuropathologica.

Changes of the ratio between myelin thickness and axon diameter in the human developing sural nerve

K. Brodda, J. M. Schröder, J. Bohl, 1978, Acta Neuropathologica.

Granular nuclear inclusion body disease: Fine structure of tibial muscle and sural nerve

H. Hopf, J. Schröder, Klaus Günter Krämer, 1985, Muscle & nerve.

Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions

J. Schröder, M. Molnár, 1998, Acta Neuropathologica.

Distribution of Nerve Fibres in the Extra-Temporal Branches of the Facial Nerve

M. Samii, J. Schröder, I. Søgard, 1981 .

Amyloid neuropathy: immunocytochemical localization of intra- and extracellular immunoglobulin light chains

C. Sommer, J. Schröder, 2004, Acta Neuropathologica.

Mitochondrial abnormalities and intrafamilial variability of sural nerve biopsy findings in adrenomyeloneuropathy

J. Weis, J. Schröder, M. Mayer, 1996, Acta Neuropathologica.

Polyneuropathy with osmiophilic membrane-bound, cytoplasmic inclusions in Schwann cells (POMCIS)

J. Malin, J. Schröder, E. Sindern, 1999, Acta Neuropathologica.

Comparative morphometric evaluation of peripheral nerves and muscle fibers in myotonic dystrophy

J. Schröder, J. -. Wang, 2000, Acta Neuropathologica.

Phrenic nerves and diaphragms in sudden infant death syndrome.

J. Weis, J. Schröder, R. Lemke, 1998, Forensic Science International.

Incontinetia pigmenti-related myopathy or unsolved “double trouble”?

A. Doerfler, A. Jünemann, W. Kress, 2010, Neuromuscular Disorders.

Spinal schwannoma mimicking lower limb SMA.

A. Brunn, J. Reul, D. Fischer, 2002, Neurology.

Ferritinopathy: diagnosis by muscle or nerve biopsy, with a note on other nuclear inclusion body diseases

J. Schröder, J. Michael Schröder, 2005, Acta Neuropathologica.

Scanning electron microscopy of teased intrafusal muscle fibers from rat muscle spindles

J. Schröder, C. Verres, Herbert Bodden, 1989, Muscle & nerve.

Fasting improves discrimination of grade 1 and atypical or malignant meningioma in FDG-PET.

J. Gilsbach, J. Weis, O. Sabri, 1997, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

Limitation of Neuroma Formation by Fat Tissue

J. Weis, J. Schröder, 1990 .

The influence of fat tissue on neuroma formation.

J. Weis, J. Schröder, 1989, Journal of neurosurgery.

[Light and electron microscopic studies of late stages of thalidomide polyneuropathy].

J. Schröder, E. Gibbels, W. Krücke, 1971, Fortschritte der Neurologie, Psychiatrie, und ihrer Grenzgebiete.

Increase of mitochondria in vasa nervorum of cases with mitochondrial myopathy, Kearns‐Sayre syndrome, progressive externaI ophthalmoplegia and MEWS *

J. Schröder, M. Molnár, S. Neudecker, 1995, Neuropathology and applied neurobiology.

Peripheral neuropathy associated with hereditary and sporadic inclusion body myositis: confirmation by electron microscopy and morphometry

J. Schröder, M. Molnár, B. Hermanns, 2000, Journal of the Neurological Sciences.

Number and size of epineurial blood vessels in normal and diseased human sural nerves

J. Schröder, G. Schütz, 1997, Cell and Tissue Research.

Mitochondrial abnormalities and peripheral neuropathy in inflammatory myopathy, especially inclusion body myositis.

J. Schröder, M. Molnár, 1997 .

A large-scale deletion of mitochondrial DNA in a case with pure mitochondrial myopathy and neuropathy

J. Schröder, M. Molnár, G. Buse, 1996, Acta Neuropathologica.

Multiple mitochondrial tRNA(Leu[UUR]) mutations associated with infantile myopathy.

J. Schröder, M. Molnár, G. Buse, 1997 .

A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany.

K. Zerres, S. Rudnik-Schöneborn, C. Bergmann, 2001, Brain research. Molecular brain research.

Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.

J. Schröder, M. Molnár, G. Buse, 1998, Clinical neuropathology.

Fine structural evaluation of altered Schmidt-Lanterman incisures in human sural nerve biopsies

J. Schröder, F. Himmelmann, 2004, Acta Neuropathologica.

Fulminant toxoplasmosis in a heart transplant recipient.

A. Brunn, R. Buettner, J. Sachweh, 2001, Pathology, research and practice.

The human dorsal spinocerebellar tract: myelinated fiber spectrum and fiber density in controls, autosomal dominant spinocerebellar atrophy, Huntington's chorea, radiation myelopathy, and diseases with peripheral sensory nerve involvement.

E. Ringelstein, J. Schröder, 1982, Clinical neuropathology.

Pathology of Peripheral Nerves: An Atlas of Structural and Molecular Pathological Changes

J. Schröder, 2001 .

Spasmodic torticollis: severe compression neuropathy in rami dorsales of cervical nerves C1–6

V. Braun, H. Richter, J. Schröder, 2004, Acta Neuropathologica.

Immunohistochemical and electrophysiological evidence for ω-conotoxin-sensitive calcium channels in unmyelinated C-fibres of biopsied human sural nerve

H. Adelsberger, T. Arzberger, J. Schröder, 1996, Brain Research.

Myelin protein zero mutation‐related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohort

I. Katona, B. Sellhaus, J. Weis, 2023, Brain pathology.

Structure of the nodes and paranodes in peripheral nerves, Part I. Introduction.

J. Schröder, 1996, Microscopy research and technique.

Oculopharyngeal muscular dystrophy: clinical and morphological follow‐up study reveals mitochondrial alterations and unique nuclear inclusions in a severe autosomal recessive type

J. Weis, J. Schröder, B. Krabbe, 1995 .

Apolipoprotein E and Alpha-1-Antichymotrypsin Polymorphisms in Sporadic Inclusion Body Myositis

H. Reichmann, H. Reichmann, J. Schröder, 2004, European Neurology.

Multiple mitochondrial tRNAMLeu[UUR] mutations associated with infantile myopathy

J. Schröder, M. Molnár, G. Buse, 2004, Molecular and Cellular Biochemistry.

Mitochondrial changes in muscle phosphoglycerate kinase deficiency.

H. Reichmann, R. Dodel, J. Weis, 1996, Clinical neuropathology.

Scanning Electron Microscopic Identification of Motor and Sensory Endings on Teased Intrafusal Muscle Fibers

J. Schröder, A. Hamacher, C. Verres, 1988 .

Desmin and actin associated with cytoplasmic bodies in skeletal muscle fibers: immunocytochemical and fine structural studies, with a note on unusual 18- to 20-nm filaments

C. Sommer, J. Schröder, B. Schmidt, 2004, Acta Neuropathologica.