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22. Adult-onset Nemaline Myopathy Coexisting With Myasthenia Gravis: A Case Report. Cao L; Wang Y; Liu X; Hu Y; Li N; Qiu G; Luo Y; Li W Medicine (Baltimore); 2016 Jan; 95(4):e2527. PubMed ID: 26825889 [TBL] [Abstract][Full Text] [Related]
23. [An adulthood progressive case of congenital nemaline myopathy showing rimmed vacuoles in muscle biopsy and diffuse neurogenic changes on electromyography]. Ikezoe K; Murai H; Kawajiri M; Ohyagi Y; Kira J Rinsho Shinkeigaku; 2004 Jul; 44(7):450-3. PubMed ID: 15384708 [TBL] [Abstract][Full Text] [Related]
24. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report]. Oya Y; Segawa M; Ogawa M; Goto Y; Nonaka I; Kawai M Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727 [TBL] [Abstract][Full Text] [Related]
25. Two novel nebulin variants in an adult patient with congenital nemaline myopathy. Güttsches AK; Dekomien G; Claeys KG; von der Hagen M; Huebner A; Kley RA; Kirschner J; Vorgerd M Neuromuscul Disord; 2015 May; 25(5):392-6. PubMed ID: 25740301 [TBL] [Abstract][Full Text] [Related]
27. [Nemaline myopathy as a cause of neonatal hypotonia - with emphasis on personal experiences. Report of a family with two brothers affected]. Bojdo A; Obersztyn E; Wallgren-Pettersson C; Lehtokari V; Laing N; Davis M; Kułakowska Z Med Wieku Rozwoj; 2009; 13(1):5-10. PubMed ID: 19648653 [TBL] [Abstract][Full Text] [Related]
28. 'Amish Nemaline Myopathy' in 2 Italian siblings harbouring a novel homozygous mutation in Troponin-I gene. D'Amico A; Fattori F; Fiorillo C; Paglietti MG; Testa MBC; Verardo M; Catteruccia M; Bruno C; Bertini E Neuromuscul Disord; 2019 Oct; 29(10):766-770. PubMed ID: 31604653 [TBL] [Abstract][Full Text] [Related]
29. [A 22-year-old man with long-standing weakness and atrophy predominantly in the lower extremities]. Mori H; Sato K; Hirasawa E; Kondo T; Mizuno Y No To Shinkei; 1996 Aug; 48(8):763-71. PubMed ID: 8797213 [TBL] [Abstract][Full Text] [Related]
30. Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathy. Lehtokari VL; Pelin K; Herczegfalvi A; Karcagi V; Pouget J; Franques J; Pellissier JF; Figarella-Branger D; von der Hagen M; Huebner A; Schoser B; Lochmüller H; Wallgren-Pettersson C Neuromuscul Disord; 2011 Aug; 21(8):556-62. PubMed ID: 21724397 [TBL] [Abstract][Full Text] [Related]
31. Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred. Hutchinson DO; Charlton A; Laing NG; Ilkovski B; North KN Neuromuscul Disord; 2006 Feb; 16(2):113-21. PubMed ID: 16427282 [TBL] [Abstract][Full Text] [Related]
32. Sporadic late onset nemaline myopathy. Chahin N; Selcen D; Engel AG Neurology; 2005 Oct; 65(8):1158-64. PubMed ID: 16148261 [TBL] [Abstract][Full Text] [Related]
33. [Progressive external ophthalmoplegia and distal myopathy]. Damian C Oftalmologia; 1993; 37(1):65-7. PubMed ID: 8507616 [TBL] [Abstract][Full Text] [Related]
34. Adult-onset nemaline myopathy: a case report and review of the literature. Gyure KA; Prayson RA; Estes ML Arch Pathol Lab Med; 1997 Nov; 121(11):1210-3. PubMed ID: 9372751 [TBL] [Abstract][Full Text] [Related]
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