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Similar articles for PubMed (Select 14076166)

1.
2.

[Centronuclear myopathy with autosomal dominant inheritance(author's transl)].

Mortier W, Michaelis E, Becker J, Gerhard L.

Humangenetik. 1975;27(3):199-215. German.

PMID:
1150240
3.

Multicore myopathy--a case report.

Myong NH, Kang YK, Chi JG, Suk SI.

J Korean Med Sci. 1993 Aug;8(4):312-7.

4.

[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
5.

The syndrome of continuous muscle fibre activity: light and electron microscopic studies in muscle and nerve biopsies.

Ono S, Munakata S, Nagao K, Shimizu N, Shimizu N.

J Neurol. 1989 Oct;236(7):377-81.

PMID:
2809637
6.

Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration.

Sugie H, Hanson R, Rasmussen G, Verity MA.

J Neurol Neurosurg Psychiatry. 1982 Jun;45(6):507-12.

7.

Sarcomere and filament lengths in passive muscle fibres with wavy myofibrils.

Brown LM, González-Serratos H, Huxley AF.

J Muscle Res Cell Motil. 1984 Jun;5(3):293-314.

PMID:
6611352
8.
9.

Postnatal centralization of muscle fibre nuclei in centronuclear myopathy.

van der Ven PF, Jap PH, Wetzels RH, ter Laak HJ, Ramaekers FC, Stadhouders AM, Sengers RC.

Neuromuscul Disord. 1991;1(3):211-20.

PMID:
1822797
10.
11.

[Centronuclear (myotubular) myopathy: a case report].

Reed UC, Tsanaclis AM, Ferreira LM, Carvalho MS, Diament A, Levy JA.

Rev Hosp Clin Fac Med Sao Paulo. 1992 Sep-Oct;47(5):237-9. Review. Portuguese.

PMID:
1340609
12.

[The importance of muscle biopsy in the diagnosis of neuromuscular diseases].

Bleggi-Torres LF, de Noronha L.

Arq Neuropsiquiatr. 1994 Sep;52(3):370-5. Portuguese.

PMID:
7893212
13.
14.

Congenital myopathy with focal loss of cross striations: a case report with morphologic and immunohistochemical study.

Yun Y, Bergmann M, Klein H, Sternowsky HJ.

Gen Diagn Pathol. 1995 Oct;141(2):155-60.

PMID:
8548596
15.

X-linked myotubular myopathy: clinical and pathological findings in a family.

Oldfors A, Kyllerman M, Wahlström J, Darnfors C, Henriksson KG.

Clin Genet. 1989 Jul;36(1):5-14. Review.

PMID:
2670345
16.

Congenital myopathy with type II muscle fiber hypoplasia.

Castro-Gago M, Novo-Rodríguez I, Martínez EP, Iglesias AB, Puñal JE.

Childs Nerv Syst. 1996 May;12(5):262-5.

PMID:
8737802
17.

Familial multicore disease with focal loss of cross-striations and ophthalmoplegia.

Swash M, Schwartz MS.

J Neurol Sci. 1981 Oct;52(1):1-10.

PMID:
7299413
18.

Mixed nemaline-mitochondrial "myopathy".

Kornfeld M.

Acta Neuropathol. 1980;51(3):185-9.

PMID:
6255722
19.

42-year-old man with discoid lupus and progressive weakness.

Stevens MA, Yeaney GA, Lacomis D.

Brain Pathol. 2009 Jan;19(1):153-6. doi: 10.1111/j.1750-3639.2008.00238.x.

PMID:
19076781
20.

[Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)].

Pongratz D, Hübner G, Deufel T, Wieland O, Pongratz E, Liphardt R.

Klin Wochenschr. 1979 Sep 17;57(18):927-36. German.

PMID:
502358
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