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4. Congenital nemaline myopathy with dilated cardiomyopathy: an autopsy study. Ishibashi-Ueda H; Imakita M; Yutani C; Takahashi S; Yazawa K; Kamiya T; Nonaka I Hum Pathol; 1990 Jan; 21(1):77-82. PubMed ID: 2295510 [TBL] [Abstract][Full Text] [Related]
5. [Nemaline myopathy: an unusual course]. Dóczy LC; Morscher M; Schmitzberger R; Willeit J; Haberfellner H Padiatr Padol; 1991; 26(1):49-51. PubMed ID: 1647515 [TBL] [Abstract][Full Text] [Related]
6. Congenital nemaline myopathy: two patients with consanguineous parents, one with a progressive course. Arts WF; de Groot CJ J Neurol; 1983; 230(2):123-30. PubMed ID: 6196458 [TBL] [Abstract][Full Text] [Related]
7. Fatal nemaline myopathy in infancy. McMenamin JB; Curry B; Taylor GP; Becker LE; Murphy EG Can J Neurol Sci; 1984 May; 11(2):305-9. PubMed ID: 6733612 [TBL] [Abstract][Full Text] [Related]
8. Heterogeneity of nemaline myopathy. A follow-up study of 13 cases. Shahar E; Tervo RC; Murphy EG Pediatr Neurosci; 1988; 14(5):236-40. PubMed ID: 3267818 [TBL] [Abstract][Full Text] [Related]
9. Congenital myopathy and cardiomyopathy with identical ultrastructural changes. Davis DG; Nelson KR; Markesbery WR Arch Neurol; 1990 Oct; 47(10):1141-4. PubMed ID: 2222249 [TBL] [Abstract][Full Text] [Related]
10. A case of nemaline myopathy with ophthalmoplegia and mitochondrial abnormalities. Fukunaga H; Osame M; Igata A J Neurol Sci; 1980 May; 46(2):169-77. PubMed ID: 6247453 [TBL] [Abstract][Full Text] [Related]
11. Fiber type disproportion in nemaline myopathy. Huang CC; Lee CC; Chen SS Zhonghua Yi Xue Za Zhi (Taipei); 1989 Apr; 43(4):229-32. PubMed ID: 2804774 [TBL] [Abstract][Full Text] [Related]
12. [Rod myopathy. A fatal neonatal case]. Netter JC; Laurent-Pellegrin M; Bildstein G; Chateauneuf R; Petrus M Arch Fr Pediatr; 1986 May; 43(5):327-9. PubMed ID: 3778091 [TBL] [Abstract][Full Text] [Related]
13. Nemaline myopathy: comparative muscle histochemistry in the severe neonatal, moderate congenital, and adult-onset forms. Shimomura C; Nonaka I Pediatr Neurol; 1989; 5(1):25-31. PubMed ID: 2712935 [TBL] [Abstract][Full Text] [Related]
14. A new case of severe congenital nemaline myopathy. Buonocore G; Balestri P; Toti P; Bagnoli F Acta Paediatr; 1993 Dec; 82(12):1082-4. PubMed ID: 8155933 [TBL] [Abstract][Full Text] [Related]
15. [Sibling cases of severe infantile form of nemaline myopathy with ACTA1-gene mutation]. Sudo A; Hayashi Y; Sano H; Kawamura N; Nishino I; Nonaka I No To Hattatsu; 2013 Nov; 45(6):452-6. PubMed ID: 24313005 [TBL] [Abstract][Full Text] [Related]
17. Complete external ophthalmoplegia in a patient with congenital myopathy without specific features (minimal change myopathy). Ohtaki E; Yamaguchi Y; Yamashita Y; Matsuishi T; Terasawa K; Katafuchi Y; Nonaka I Brain Dev; 1990; 12(4):427-30. PubMed ID: 2240464 [TBL] [Abstract][Full Text] [Related]
18. [A 34-year-old woman with delayed motor milestones, high arched palate, and proximal muscle weakness]. Yamamoto T; Kitada T; Hirasawa E; Mori H; Mizuno Y No To Shinkei; 1996 Jul; 48(7):677-84. PubMed ID: 8753005 [TBL] [Abstract][Full Text] [Related]
19. [An autopsy case of fatal neonatal nemaline myopathy]. Shimomura C; Nakashita Y; Ogawa T; Tsuji Y; Tsujihata M No To Hattatsu; 1983; 15(1):47-51. PubMed ID: 6821603 [No Abstract] [Full Text] [Related]
20. Nemaline myopathy in a newborn infant: a rare muscle disorder. Olukman O; Calkavur S; Diniz G; Unalp A; Atlihan F Neurol Neurochir Pol; 2013; 47(5):493-8. PubMed ID: 24166571 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]