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.
5. [Problem of phenotypic polymorphism in hereditary neuromuscular diseases]. Badalian LO Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(3):257-61. PubMed ID: 571656 [No Abstract] [Full Text] [Related]
6. [Suspected muscular disease: what to do?]. Strozzi S; Steinlin M Ther Umsch; 2003 Jul; 60(7):399-406. PubMed ID: 12956033 [TBL] [Abstract][Full Text] [Related]
7. The muscular dystrophies--clarity or chaos? Dubowitz V N Engl J Med; 1997 Feb; 336(9):650-1. PubMed ID: 9032052 [No Abstract] [Full Text] [Related]
8. Correlation between electromyographic findings and muscle biopsy in ccases of neuromuscular diseease. Hausmanowa-Petrusewicz I; Jedrzejowska H J Neurol Sci; 1971 May; 13(1):85-106. PubMed ID: 5566111 [No Abstract] [Full Text] [Related]
9. Muscle MRI in inherited neuromuscular disorders: past, present, and future. Mercuri E; Pichiecchio A; Allsop J; Messina S; Pane M; Muntoni F J Magn Reson Imaging; 2007 Feb; 25(2):433-40. PubMed ID: 17260395 [TBL] [Abstract][Full Text] [Related]
10. Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype. Ignatieva E; Smolina N; Kostareva A; Dmitrieva R Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34298968 [TBL] [Abstract][Full Text] [Related]
11. [Electron microscopic study of the T-system in progressive muscular dystrophy and other neuromuscular diseases (author's transl)]. Oguchi K; Tsukagoshi H Rinsho Shinkeigaku; 1978 May; 18(5):266-72. PubMed ID: 699433 [No Abstract] [Full Text] [Related]
12. [Differential diagnosis of hereditary neuromuscular diseases and their phenocopies in children]. Gershman RN; Iakovleva SM Zh Nevropatol Psikhiatr Im S S Korsakova; 1985; 85(11):1639-42. PubMed ID: 4082831 [TBL] [Abstract][Full Text] [Related]
13. [Cardiomyopathy in Heredofamilial Neuromyopathies (author's transl)]. Sekiguchi M; Numao Y; Hiroe M Kokyu To Junkan; 1975 Mar; 23(3):209-24. PubMed ID: 1093249 [No Abstract] [Full Text] [Related]
14. Histochemical and immunohistological approach to comparative neuromuscular diseases. Paciello O; Papparella S Folia Histochem Cytobiol; 2009; 47(2):143-52. PubMed ID: 19995699 [TBL] [Abstract][Full Text] [Related]
15. The sick motoneurone hypothesis of muscular dystrophy. McComas AJ; Preswick G; Garner S Prog Neurobiol; 1988; 30(4):309-31. PubMed ID: 3278339 [No Abstract] [Full Text] [Related]
16. Radiation sensitivity of fibroblast strains from patients with Usher's syndrome, Duchenne muscular dystrophy, and Huntington's disease. Nove J; Tarone RE; Little JB; Robbins JH Mutat Res; 1987 Jul; 184(1):29-38. PubMed ID: 2955220 [TBL] [Abstract][Full Text] [Related]
17. [Heredity and neuromuscular diseases]. Zergollern L Neurologija; 1978; 26(1-4):29-36. PubMed ID: 754036 [No Abstract] [Full Text] [Related]
18. Clinical features for prediction of survival in neonatal muscle disease. Connolly MB; Roland EH; Hill A Pediatr Neurol; 1992; 8(4):285-8. PubMed ID: 1388418 [TBL] [Abstract][Full Text] [Related]