These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
176 related articles for article (PubMed ID: 9093960)
41. Pregnancy in a patient with nemaline myopathy. Eskandar OS; Eckford SD Obstet Gynecol; 2007 Feb; 109(2 Pt2):501-4. PubMed ID: 17267873 [TBL] [Abstract][Full Text] [Related]
42. Severe congenital nemaline myopathy with primary pulmonary lymphangiectasia: unusual clinical presentation and review of the literature. Waisayarat J; Suriyonplengsaeng C; Khongkhatithum C; Rochanawutanon M Diagn Pathol; 2015 Apr; 10():27. PubMed ID: 25890230 [TBL] [Abstract][Full Text] [Related]
43. Adult nemaline myopathy with trabecular muscle fibers. Irodenko VS; Lee HS; de Armond SJ; Layzer RB Muscle Nerve; 2009 Jun; 39(6):871-5. PubMed ID: 19229965 [TBL] [Abstract][Full Text] [Related]
44. A case of neuromuscular mimicry. Bos MM; Overeem S; van Engelen BG; Scheffer H; van den Elzen C; Ter Laak H; Lammens M; Schelhaas HJ; Zwarts MJ Neuromuscul Disord; 2006 Aug; 16(8):510-3. PubMed ID: 16919950 [TBL] [Abstract][Full Text] [Related]
45. 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. PubMed ID: 15336687 [TBL] [Abstract][Full Text] [Related]
46. [Diagnostic and therapeutic problems in chronic progressive external ophthalmoplegia (CPEO)]. Sommer F; Fötzsch R; Pillunat LE; Wollensak G Klin Monbl Augenheilkd; 2003 May; 220(5):315-9. PubMed ID: 12766819 [TBL] [Abstract][Full Text] [Related]
48. Sporadic late onset nemaline myopathy and immunoglobulin deposition disease. Doppler K; Knop S; Einsele H; Sommer C; Wessig C Muscle Nerve; 2013 Dec; 48(6):983-8. PubMed ID: 23873431 [TBL] [Abstract][Full Text] [Related]
49. The dropped head sign: an unusual presentation of congenital myopathy. Riggs JE; Bodensteiner JB; Schochet SS J Child Neurol; 1994 Jul; 9(3):330-1. PubMed ID: 7930416 [No Abstract] [Full Text] [Related]
50. Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene. Lehtokari VL; Gardberg M; Pelin K; Wallgren-Pettersson C Neuromuscul Disord; 2018 Apr; 28(4):323-326. PubMed ID: 29433794 [TBL] [Abstract][Full Text] [Related]
51. [Mitochondrial myopathy: two case reports]. Grebos SP; Almeida Td; Barbosa KH; Buquera MA; Moreira AT Arq Bras Oftalmol; 2005; 68(5):675-8. PubMed ID: 16322868 [TBL] [Abstract][Full Text] [Related]
52. [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. PubMed ID: 11333383 [TBL] [Abstract][Full Text] [Related]
53. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature. Moreno CAM; Abath Neto O; Donkervoort S; Hu Y; Reed UC; Oliveira ASB; Bönnemann C; Zanoteli E Pediatr Neurol; 2017 Oct; 75():11-16. PubMed ID: 28780987 [TBL] [Abstract][Full Text] [Related]
54. Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy. Nguyen MA; Joya JE; Kee AJ; Domazetovska A; Yang N; Hook JW; Lemckert FA; Kettle E; Valova VA; Robinson PJ; North KN; Gunning PW; Mitchell CA; Hardeman EC Brain; 2011 Dec; 134(Pt 12):3516-29. PubMed ID: 22067542 [TBL] [Abstract][Full Text] [Related]
55. Intranuclear rod myopathy, a rare and morphologically striking variant of nemaline rod myopathy. Weeks DA; Nixon RR; Kaimaktchiev V; Mierau GW Ultrastruct Pathol; 2003; 27(3):151-4. PubMed ID: 12775505 [TBL] [Abstract][Full Text] [Related]
59. Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation. Kim SY; Park YE; Kim HS; Lee CH; Yang DH; Kim DS J Neurol Sci; 2011 Aug; 307(1-2):171-3. PubMed ID: 21570694 [TBL] [Abstract][Full Text] [Related]