J. M. Schr�der

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)

J. M. Schr�der, Bernd Sellhaus, Johannes J�rg · Acta Neuropathologica · 1995 · 98 citations

Subcortical Infarcts, Neurological Disorder, Neuroanatomy +10

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

J. M. Schr�der, J. Böhl, K. Brodda · Acta Neuropathologica · 1978 · 86 citations

Developmental Biology, Axon Diameter, Peripheral Nerve Injury +10

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

J. M. Schr�der, R. May, Y. S. Shin et al. · Acta Neuropathologica · 1993 · 84 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body disease

Focke Ziemssen, E. Sindern, J. M. Schr�der et al. · Annals of Neurology · 2000 · 77 citations

Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn)

J. M. Schr�der, Hayley J. Durling, Nigel G. Laing · Acta Neuropathologica · 2004 · 60 citations

Mechanobiology, Medicine, Molecular Biology +8