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Results: 12

Related Articles by Review for PubMed (Select 623532)

1.

Investigations on the inheritance of nemaline myopathy.

Arts WF, Bethlem J, Dingemans KP, Eriksson AW.

Arch Neurol. 1978 Feb;35(2):72-7.

PMID:
623532
2.

Genetics of congenital nemaline myopathy.

Kondo K, Yuasa T.

Muscle Nerve. 1980 Jul-Aug;3(4):308-15. Review.

PMID:
6997732
3.

Centronuclear myopathy: clinical, morphological and genetic characters. A review of 288 cases.

De Angelis MS, Palmucci L, Leone M, Doriguzzi C.

J Neurol Sci. 1991 May;103(1):2-9. Review.

PMID:
1865227
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.

Quantitative histopathology in congenital myopathies.

Micaglio G, Ceccato MB, Trevisan C, Angelini C.

Riv Neurol. 1987 Jul-Aug;57(4):261-8. Review.

PMID:
3317765
6.

[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
7.

Clinical and histologic findings in autosomal centronuclear myopathy.

Jeannet PY, Bassez G, Eymard B, Laforêt P, Urtizberea JA, Rouche A, Guicheney P, Fardeau M, Romero NB.

Neurology. 2004 May 11;62(9):1484-90. Review.

PMID:
15136669
8.

Overview of distal myopathies: from the clinical to the molecular.

Barohn RJ, Amato AA, Griggs RC.

Neuromuscul Disord. 1998 Jun;8(5):309-16. Review.

PMID:
9673984
9.

The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies.

Wallgren-Pettersson C, Clarke A, Samson F, Fardeau M, Dubowitz V, Moser H, Grimm T, Barohn RJ, Barth PG.

J Med Genet. 1995 Sep;32(9):673-9. Review.

10.

[Cousins with X-linked recessive myotubular myopathy].

Mori Y, Kaneko S, Nakayama T, Date M, Nakamoto N, Kobayashi M, Sugiura M, Hashira S, Abe T, Hirokawa H, Nonaka I.

No To Hattatsu. 1997 Jul;29(4):310-4. Review. Japanese.

PMID:
9248291
11.

Nemaline myopathy: a clinical study of 143 cases.

Ryan MM, Schnell C, Strickland CD, Shield LK, Morgan G, Iannaccone ST, Laing NG, Beggs AH, North KN.

Ann Neurol. 2001 Sep;50(3):312-20. Review.

PMID:
11558787
12.

Mitochondrial myopathy: a genetic study of 71 cases.

Harding AE, Petty RK, Morgan-Hughes JA.

J Med Genet. 1988 Aug;25(8):528-35. Review.

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