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Items: 1 to 20 of 123

1.

[Congenital myopathy with type 1 fiber predominance in two children].

Luo MC, Li QX, Yin WF, Duan WW, Bi FF, Zhang N, Liang JH, Yang H.

Zhongguo Dang Dai Er Ke Za Zhi. 2011 Jun;13(6):499-502. Chinese.

2.
3.

[A case of congenital myopathy with the pathologic transformation from fiber type disproportion to type 1 fiber predominance myopathy].

Shibata R, Kusakawa I, Ozawa M, Ohya T, Nonaka I.

No To Hattatsu. 1998 Jul;30(4):307-11. Japanese.

PMID:
9695625
4.

Congenital fiber type disproportion: a rare type of congenital myopathy: a report of four cases.

Sharma MC, Ralte AM, Atri SK, Gulati S, Kalra V, Sarkar C.

Neurol India. 2004 Jun;52(2):254-6.

5.
6.

Spectrum of congenital myopathies: a single centre experience.

Uppin MS, Meena AK, Sundaram C.

Neurol India. 2013 May-Jun;61(3):254-9. doi: 10.4103/0028-3886.115064.

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.

[Clinical and biopsy-based myopathological features of 5 cases with centronuclear myopathy].

Li HH, Liu SP, Li W, Zhao YY, Wu JL, Li DN, Yan CZ.

Zhonghua Er Ke Za Zhi. 2008 Nov;46(11):856-9. Chinese.

PMID:
19099905
9.
10.

[Tubular aggregate congenital myopathy associated with neuromuscular block].

Zephir H, Stojkovic T, Maurage CA, Hurtevent JF, Vermersch P.

Rev Neurol (Paris). 2001 Oct;157(10):1293-6. French.

PMID:
11885525
11.

[Congenital myopathy with type 2 fiber hypoplasia].

Pavlovský Z, Lukás Z, Kuncíková M, Zakoutová A.

Cesk Patol. 2001 Apr;37(2):69-71. Czech.

PMID:
11455917
12.

Clinical and histologic changes in the follow-up of a congenital myopathy.

Camacho A, Villarejo A, Simón R, Mateos F, Cabello A.

Pediatr Neurol. 2005 Aug;33(2):139-41.

PMID:
16087062
13.

Congenital myopathy with tubular aggregates and tubulofilamentous IBM-type inclusions.

Fidziańska A, Kamińska A, Ryniewicz B.

Neuropediatrics. 2005 Feb;36(1):35-9.

PMID:
15776320
14.

Congenital myopathies.

D'Amico A, Bertini E.

Curr Neurol Neurosci Rep. 2008 Jan;8(1):73-9. Review.

PMID:
18367042
15.

Reducing body myopathy with cytoplasmic bodies and rigid spine syndrome: a mixed congenital myopathy.

Goebel HH, Halbig LE, Goldfarb L, Schober R, Albani M, Neuen-Jacob E, Voit T.

Neuropediatrics. 2001 Aug;32(4):196-205. Review.

PMID:
11571700
16.

Myotubular/centronuclear myopathy and central core disease.

Fujimura-Kiyono C, Racz GZ, Nishino I.

Neurol India. 2008 Jul-Sep;56(3):325-32. Review.

17.

Congenital myopathies: clinical and immunohistochemical study.

Thaha F, Gayathri N, Nalini A.

Neurol India. 2011 Nov-Dec;59(6):879-83. doi: 10.4103/0028-3886.91369.

PMID:
22234203
18.

Congenital fiber-type disproportion.

Clarke NF.

Semin Pediatr Neurol. 2011 Dec;18(4):264-71. doi: 10.1016/j.spen.2011.10.008. Review.

PMID:
22172422
19.

Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.

Sobrido MJ, Fernández JM, Fontoira E, Pérez-Sousa C, Cabello A, Castro M, Teijeira S, Alvarez S, Mederer S, Rivas E, Seijo-Martínez M, Navarro C.

Brain. 2005 Jul;128(Pt 7):1716-27. Epub 2005 Apr 27.

PMID:
15857933
20.

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

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