Schröder JM - Search Results

1

Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3.

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. Jenne DE, et al. Among authors: schroder jm. Biol Chem. 2005 Jan;386(1):61-7. doi: 10.1515/BC.2005.008. Biol Chem. 2005. PMID: 15843148

2

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

Schröder JM, Krabbe B, Weis J. Schröder JM, et al. Neuropathol Appl Neurobiol. 1995 Feb;21(1):68-73. doi: 10.1111/j.1365-2990.1995.tb01030.x. Neuropathol Appl Neurobiol. 1995. PMID: 7770123

3

The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy.

Züchner S, Vorgerd M, Sindern E, Schröder JM. Züchner S, et al. Among authors: schroder jm. Neuromuscul Disord. 2004 Feb;14(2):147-57. doi: 10.1016/j.nmd.2003.10.003. Neuromuscul Disord. 2004. PMID: 14733962

4

Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 gene.

Nolte KW, Janecke AR, Vorgerd M, Weis J, Schröder JM. Nolte KW, et al. Among authors: schroder jm. Acta Neuropathol. 2008 Nov;116(5):491-506. doi: 10.1007/s00401-008-0417-8. Epub 2008 Jul 26. Acta Neuropathol. 2008. PMID: 18661138

5

Morphological spectrum and clinical features of myopathies with tubular aggregates.

Funk F, Ceuterick-de Groote C, Martin JJ, Meinhardt A, Taratuto AL, De Bleecker J, Van Coster R, De Paepe B, Schara U, Vorgerd M, Häusler M, Koppi S, Maschke M, De Jonghe P, Van Maldergem L, Noel S, Zimmermann CW, Wirth S, Isenmann S, Stadler R, Schröder JM, Schulz JB, Weis J, Claeys KG. Funk F, et al. Among authors: schroder jm. Histol Histopathol. 2013 Aug;28(8):1041-54. doi: 10.14670/HH-28.1041. Epub 2013 Mar 12. Histol Histopathol. 2013. PMID: 23479431

6

Adult polyglucosan body myopathy with subclinical peripheral neuropathy: case report and review of diseases associated with polyglucosan body accumulation.

Weis J, Schröder JM. Weis J, et al. Among authors: schroder jm. Clin Neuropathol. 1988 Nov-Dec;7(6):271-9. Clin Neuropathol. 1988. PMID: 2852083 Review.

7

Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy.

Dohrn MF, Röcken C, De Bleecker JL, Martin JJ, Vorgerd M, Van den Bergh PY, Ferbert A, Hinderhofer K, Schröder JM, Weis J, Schulz JB, Claeys KG. Dohrn MF, et al. Among authors: schroder jm. J Neurol. 2013 Dec;260(12):3093-108. doi: 10.1007/s00415-013-7124-7. Epub 2013 Oct 8. J Neurol. 2013. PMID: 24101130

8

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

Kubisch C, Schoser BG, von Düring M, Betz RC, Goebel HH, Zahn S, Ehrbrecht A, Aasly J, Schroers A, Popovic N, Lochmüller H, Schröder JM, Brüning T, Malin JP, Fricke B, Meinck HM, Torbergsen T, Engels H, Voss B, Vorgerd M. Kubisch C, et al. Among authors: schroder jm. Ann Neurol. 2003 Apr;53(4):512-20. doi: 10.1002/ana.10501. Ann Neurol. 2003. PMID: 12666119

9

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

Schröder JM, Klossok T, Weis J. Schröder JM, et al. Clin Neuropathol. 2011 May-Jun;30(3):94-103. doi: 10.5414/npp30094. Clin Neuropathol. 2011. PMID: 21545772

10

The influence of fat tissue on neuroma formation.

Weis J, Schröder JM. Weis J, et al. Among authors: schroder jm. J Neurosurg. 1989 Oct;71(4):588-93. doi: 10.3171/jns.1989.71.4.0588. J Neurosurg. 1989. PMID: 2795177

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