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Items: 1 to 20 of 142

1.

Congenital myopathy with cytoplasmic bodies.

Goebel HH, Schloon H, Lenard HG.

Neuropediatrics. 1981 May;12(2):166-80.

PMID:
6267501
2.

Adult onset nemaline myopathy: a distinct nosologic entity?

Palmucci L, Doriguzzi C, Mongini T, Chiadò-Piat L.

Clin Neuropathol. 1993 May-Jun;12(3):153-5.

PMID:
8391957
3.

Nemaline myopathy and a mitochondrial neuromuscular disorder in one family.

Shapira YA, Yarom R, Blank A.

Neuropediatrics. 1981 May;12(2):152-65.

PMID:
6267500
4.

Zebra body myopathy: a second case of ultrastructurally distinct congenital myopathy.

Reyes MG, Goldbarg H, Fresco K, Bouffard A.

J Child Neurol. 1987 Oct;2(4):307-10.

PMID:
2821096
5.

Familial nemaline myopathy.

Scarlato G, Pellegrini G, Moggio M, Meola G, Cordone G, Minetti C, Lester A.

Neuropediatrics. 1982 Nov;13(4):211-5.

PMID:
6296713
6.

Congenital familial myopathy with type 2 fiber hypoplasia and type 1 fiber predominance.

Muranaka H, Osari S, Fujita H, Kimura Y, Goto A, Imoto C, Nonaka I.

Brain Dev. 1997 Jul;19(5):362-5.

PMID:
9253491
7.

A benign form of reducing body myopathy.

Oh SJ, Meyers GJ, Wilson ER Jr, Alexander CB.

Muscle Nerve. 1983 May;6(4):278-82. No abstract available.

PMID:
6306460
8.

A new myopathy with tubulomembranous inclusions.

Fukuhara N, Kumamoto T, Hirahara H, Tsubaki T.

J Neurol Sci. 1981 Apr;50(1):95-107.

PMID:
6262462
9.

Centronuclear myopathy with type I fibre hypotrophy and "fingerprint" inclusions associated with Marfan's syndrome.

Jadro-Santel D, Grcević N, Dogan S, Franjić J, Benc H.

J Neurol Sci. 1980 Feb;45(1):43-56.

PMID:
6244371
10.

Congenital myopathy with type 2A muscle fiber uniformity and smallness.

Gallanti A, Prelle A, Chianese L, Barbieri S, Jann S, Schiaffino S, Comini A, Scarpini E, Pellegrini G, Moggio M, et al.

Neuropediatrics. 1992 Feb;23(1):10-3.

PMID:
1565211
11.

[Infantile form of nemaline (rod inclusion) myopathy].

Berger W, Grisold W, Jellinger K.

Wien Klin Wochenschr. 1988 Jun 10;100(12):407-12. German.

PMID:
2841810
12.

Chronic neurogenic quadriceps amyotrophy.

Furukawa T, Akagami N, Maruyama S.

Ann Neurol. 1977 Dec;2(6):528-30.

PMID:
617595
13.

Intracytoplasmic inclusions in the atrophic muscle fibers in Werdnig-Hoffmann disease.

Miike T, Tamari H, Ohtani Y, Kondo Y.

Brain Dev. 1983;5(3):315-9.

PMID:
6311038
14.
15.

[Myotubular or centronuclear myopathy; report of a case and review of the literature].

Pereira de Sousa R, Miranda D, Perpetuo FO, Campos GB, Vuletin JC.

Arq Neuropsiquiatr. 1977 Sep;35(3):247-59. Portuguese.

PMID:
901263
16.

The spectrum of cytoplasmic body myopathy: report of a congenital severe case.

Mizuno Y, Nakamura Y, Komiya K.

Brain Dev. 1989;11(1):20-5.

PMID:
2538089
17.

Centronuclear myopathy with special consideration of the adult form.

Goebel HH, Meinck HM, Reinecke M, Schimrigk K, Mielke U.

Eur Neurol. 1984;23(6):425-34.

PMID:
6542524
18.

Fatal neonatal nemaline myopathy: a case report.

Tsujihata M, Shimomura C, Yoshimura T, Sato A, Ogawa T, Tsuji Y, Nagataki S, Matsuo T.

J Neurol Neurosurg Psychiatry. 1983 Sep;46(9):856-9.

19.

Fatal reducing body myopathy. Ultrastructural and immunohistochemical observations.

Kiyomoto BH, Murakami N, Kobayashi Y, Nihei K, Tanaka T, Takeshita K, Nonaka I.

J Neurol Sci. 1995 Jan;128(1):58-65.

PMID:
7722535
20.

Cytoplasmic body myopathy. Report on a family and review of the literature.

Patel H, Berry K, MacLeod P, Dunn HG.

J Neurol Sci. 1983 Aug;60(2):281-92.

PMID:
6886734

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