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Items: 1 to 20 of 25

1.

Hyaline body myopathy.

Barohn RJ, Brumback RA, Mendell JR.

Neuromuscul Disord. 1994 May;4(3):257-62.

PMID:
7522681
2.

[Polysaccharide amylopectin-type storage myopathy].

Calore EE, Pellissier JF, Figarella-Branger D, de Barsy T, Pouget J, Serratrice G.

Rev Neurol (Paris). 1992;148(11):696-703. Review. French.

PMID:
1303560
3.
4.

Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients.

Kley RA, Hellenbroich Y, van der Ven PF, Fürst DO, Huebner A, Bruchertseifer V, Peters SA, Heyer CM, Kirschner J, Schröder R, Fischer D, Müller K, Tolksdorf K, Eger K, Germing A, Brodherr T, Reum C, Walter MC, Lochmüller H, Ketelsen UP, Vorgerd M.

Brain. 2007 Dec;130(Pt 12):3250-64. Review.

5.

[Slowly progressive myopathy with accumulation of tubular aggregates].

Figarella-Branger D, Pellissier JF, Perez-Castillo AM, Desnuelle C, Pouget J, Serratrice G.

Rev Neurol (Paris). 1991;147(8-9):586-94. Review. French.

PMID:
1962068
6.

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy.

Oldfors A, Tajsharghi H, Thornell LE.

Neurology. 2005 Feb 8;64(3):580-1; author reply 580-1. Review. No abstract available.

PMID:
15699411
7.

Polysaccharide storage myopathy--case report and literature review.

Miladi MI, Feki I, Choyakh F, Ben Hmida M, Zouari N, Mhiri C.

Clin Neuropathol. 2005 May-Jun;24(3):126-32. Review.

PMID:
15943164
8.

Adult polyglucosan body myopathy.

Goebel HH, Shin YS, Gullotta F, Yokota T, Alroy J, Voit T, Haller P, Schulz A.

J Neuropathol Exp Neurol. 1992 Jan;51(1):24-35. Review.

PMID:
1311021
9.

[Familial myopathy with "cytoplasmic body" (or "spheroid") type inclusions, disclosed by respiratory insufficiency].

Chapon F, Viader F, Fardeau M, Tomé F, Daluzeau N, Berthelin C, Thénint JP, Lechevalier B.

Rev Neurol (Paris). 1989;145(6-7):460-5. Review. French.

PMID:
2552561
10.

[Nemaline myopathy. General review apropos of 3 cases].

Pagès M, Ramos J, Pagès AM, Echenne B.

Ann Pathol. 1987;7(3):216-22. Review. French.

PMID:
3325069
11.

[Sporadic Z disk myopathy with accumulation of rods and cytoplasmic bodies].

Gérard JM, Telerman-Toppet N, Borenstein S, Flament-Durand J.

Rev Neurol (Paris). 1991;147(2):144-7. Review. French.

PMID:
2028148
12.

Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literature.

Wanschit J, Nakano S, Goudeau B, Ströbel T, Rinner W, Wimmer G, Resch H, Jaksch M, Akiguchi I, Vicart P, Budka H.

Clin Neuropathol. 2002 Sep-Oct;21(5):220-31. Review.

PMID:
12365725
13.

Juvenile hyaline fibromatosis: a report of two unrelated adult sibling cases and a literature review.

Senzaki H, Kiyozuka Y, Uemura Y, Shikata N, Ueda S, Tsubura A.

Pathol Int. 1998 Mar;48(3):230-6. Review.

PMID:
9589493
14.

Welander distal myopathy--an overview.

Borg K, Ahlberg G, Anvret M, Edström L.

Neuromuscul Disord. 1998 Apr;8(2):115-8. Review.

PMID:
9608565
15.

[Nemaline congenital myopathy:clinical features and histopathological findings in nine patients].

Botelho CH, Carod-Artal FJ, Kalil RK.

Rev Neurol. 2001 Feb 16-28;32(4):309-14. Review. Spanish.

PMID:
11333383
16.

[Congenital and other myopathies].

Goebel HH, Müller HD, Schröder R.

Pathologe. 2009 Sep;30(5):365-9. doi: 10.1007/s00292-009-1169-5. Review. German.

PMID:
19641920
17.

[Adult polysaccharide storage myopathy].

Ichikawa K, Komure O, Tsutsumi A, Hiyama K, Fujioka A.

Rinsho Shinkeigaku. 1989 Oct;29(10):1203-9. Review. Japanese.

PMID:
2691165
18.

Congenital myopathies with inclusion bodies: a brief review.

Goebel HH.

Neuromuscul Disord. 1998 May;8(3-4):162-8. Review.

PMID:
9631396
19.

Gene-related protein surplus myopathies.

Goebel HH, Warlo I.

Mol Genet Metab. 2000 Sep-Oct;71(1-2):267-75. Review.

PMID:
11001821
20.

Paraneoplastic necrotizing myopathy: clinical and pathological features.

Levin MI, Mozaffar T, Al-Lozi MT, Pestronk A.

Neurology. 1998 Mar;50(3):764-7. Review.

PMID:
9521271
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