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Results: 1 to 20 of 97

Similar articles for PubMed (Select 24060078)

1.

[Nemaline myopathy: report of a case].

Wu HR, Liu X, Sun LY, Bu Y, Guo YS, Wu DX, Song XQ.

Zhonghua Bing Li Xue Za Zhi. 2013 Jun;42(6):407-8. doi: 10.3760/cma.j.issn.0529-5807.2013.06.013. Chinese. No abstract available.

PMID:
24060078
2.

Nemaline rod myopathy: a rare form of myopathy.

Sharma MC, Gulati S, Atri S, Seth R, Kalra V, Das TK, Sarkar C.

Neurol India. 2007 Jan-Mar;55(1):70-4.

3.

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
4.

Nemaline cardiomyopathy in a young adult: an ultraimmunohistochemical study and review of the literature.

Müller-Höcker J, Schäfer S, Mendel B, Lochmüller H, Pongratz D.

Ultrastruct Pathol. 2000 Nov-Dec;24(6):407-16. Review.

PMID:
11206338
5.

Idiopathic adult-onset nemaline myopathy presenting with isolated respiratory failure.

Whitaker J, Love S, Williams AP, Plummeridge M.

Muscle Nerve. 2009 Mar;39(3):406-8. doi: 10.1002/mus.21234.

PMID:
19208402
6.

Skeletal muscle repair in a mouse model of nemaline myopathy.

Sanoudou D, Corbett MA, Han M, Ghoddusi M, Nguyen MA, Vlahovich N, Hardeman EC, Beggs AH.

Hum Mol Genet. 2006 Sep 1;15(17):2603-12. Epub 2006 Jul 28.

7.

Clinical course correlates poorly with muscle pathology in nemaline myopathy.

Ryan MM, Ilkovski B, Strickland CD, Schnell C, Sanoudou D, Midgett C, Houston R, Muirhead D, Dennett X, Shield LK, De Girolami U, Iannaccone ST, Laing NG, North KN, Beggs AH.

Neurology. 2003 Feb 25;60(4):665-73.

PMID:
12601110
8.

Intranuclear rod myopathy, a rare and morphologically striking variant of nemaline rod myopathy.

Weeks DA, Nixon RR, Kaimaktchiev V, Mierau GW.

Ultrastruct Pathol. 2003 May-Jun;27(3):151-4.

PMID:
12775505
9.

Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathy.

Suwa K, Mizuguchi M, Momoi MY, Nakamura M, Arima K, Komaki H, Nonaka I.

Neuropathology. 2002 Dec;22(4):294-8.

PMID:
12564770
10.

Histopathologic progression and a novel mutation in a child with nemaline myopathy.

Ladha S, Coons S, Johnsen S, Sambuughin N, Bien-Wilner R, Sivakumar K.

J Child Neurol. 2008 Jul;23(7):813-7. doi: 10.1177/0883073808314363. Epub 2008 May 16.

PMID:
18487519
11.

Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene.

Ilkovski B, Cooper ST, Nowak K, Ryan MM, Yang N, Schnell C, Durling HJ, Roddick LG, Wilkinson I, Kornberg AJ, Collins KJ, Wallace G, Gunning P, Hardeman EC, Laing NG, North KN.

Am J Hum Genet. 2001 Jun;68(6):1333-43. Epub 2001 Apr 27.

12.

Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy.

Wallgren-Pettersson C, Jasani B, Newman GR, Morris GE, Jones S, Singhrao S, Clarke A, Virtanen I, Holmberg C, Rapola J.

Neuromuscul Disord. 1995 Mar;5(2):93-104.

PMID:
7767098
13.

Nemaline bodies of skeletal muscle fibers of the neck in a case of pharyngeal cancer.

Kimura M, Furuta T, Hiruma S, Otsuka K, Teramura K, Maekura S, Satou T, Hashimoto S.

Pathol Int. 1997 Apr;47(4):256-9.

PMID:
9103217
14.

Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1).

Ohlsson M, Tajsharghi H, Darin N, Kyllerman M, Oldfors A.

Neuromuscul Disord. 2004 Sep;14(8-9):471-5.

PMID:
15336687
15.

Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene.

Jungbluth H, Sewry CA, Brown SC, Nowak KJ, Laing NG, Wallgren-Pettersson C, Pelin K, Manzur AY, Mercuri E, Dubowitz V, Muntoni F.

Neuromuscul Disord. 2001 Jan;11(1):35-40.

PMID:
11166164
16.

Severe infantile congenital myopathy with nemaline and cytoplasmic bodies: a case report.

Itakura Y, Ogawa Y, Murakami N, Nonaka I.

Brain Dev. 1998 Mar;20(2):112-5.

PMID:
9545182
17.

Nemaline myopathy: clinical, histochemical and immunohistochemical features.

Youssef NC, Scola RH, Lorenzoni PJ, Werneck LC.

Arq Neuropsiquiatr. 2009 Sep;67(3B):886-91.

18.

Nemaline myopathy: description of an adult onset case.

Ginanneschi F, Mondelli M, Malandrini A, Gambelli S, Dotti MT, Federico A.

J Submicrosc Cytol Pathol. 2002 Jan;34(1):105-8.

PMID:
11989852
19.

[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
20.

Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H).

Koy A, Ilkovski B, Laing N, North K, Weis J, Neuen-Jacob E, Mayatepek E, Voit T.

Neuropediatrics. 2007 Dec;38(6):282-6. doi: 10.1055/s-2008-1065356.

PMID:
18461503
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