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.
104 related articles for article (PubMed ID: 494906)
1. [Variant of the facial-scapular-humeral-gluteal-femoral form of primary myopathy in children]. Grinio LP Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(10):1338-41. PubMed ID: 494906 [TBL] [Abstract][Full Text] [Related]
2. [Facial-scapular-humeral myodystrophy (genetic and clinical features)]. Bogorodinskiĭ DK; Znoĭko ZV; Kazakov VM; Skoromets AA Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):801-9. PubMed ID: 4753589 [No Abstract] [Full Text] [Related]
3. [Rapidly progressing facio-scapulo-humero-femoro-peroneal muscular dystrophy with sensorineural deafness]. Badalian LO; Temin PA; Mukhin KIu; Nikanorova MIu; Bulaeva NV; Kret LA; Lysov VL Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(9):5-8. PubMed ID: 1664615 [TBL] [Abstract][Full Text] [Related]
4. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease. Jackson CE; Strehler DA Pediatrics; 1968 Feb; 41(2):495-502. PubMed ID: 5637795 [No Abstract] [Full Text] [Related]
6. [Some data on the characteristics of myopathy in the Orenburg region]. Shtil' RG Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1461-5. PubMed ID: 4257931 [No Abstract] [Full Text] [Related]
8. [Malate dehydrogenase activity in children with myopathy]. Gil'manov VKh Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):829-31. PubMed ID: 4753593 [No Abstract] [Full Text] [Related]
9. [Clinico-morphologic characteristics of X-linked pseudohypertrophic myopathy]. Demidov PV; Kop'eva TN; Potomskaia IZ; Grinio LP; Kopylova EN Zh Nevropatol Psikhiatr Im S S Korsakova; 1976; 76(5):641-6. PubMed ID: 936862 [TBL] [Abstract][Full Text] [Related]
15. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia]. Ben Hamida M; Attia N; Chabouni H; Fardeau M Rev Neurol (Paris); 1983; 139(4):289-97. PubMed ID: 6612142 [TBL] [Abstract][Full Text] [Related]
16. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood. Gamstorp I Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129 [TBL] [Abstract][Full Text] [Related]
17. [Duchenne-Becker congenital myopathy]. Segers M; Vanderstraeten G; Schuermans P Acta Belg Med Phys; 1987; 10(1):29-35. PubMed ID: 2956810 [No Abstract] [Full Text] [Related]
18. [Ocular myopathy. A familial case of oculo-pharyngeal and skeletal muscular dystrophy with late onset]. Manigand G; Lucsko M; Deparis M Sem Hop; 1969 Nov; 45(45):2803-8. PubMed ID: 4312491 [No Abstract] [Full Text] [Related]
19. [Identification of primary and secondary forms of progressive muscular dystrophy, from data of clinico-genetic and biochemical studies]. Bondarenko ES; Tamarkina AD; Zakoshchikova LV Vestn Akad Med Nauk SSSR; 1973; 28(7):38-44. PubMed ID: 4786657 [No Abstract] [Full Text] [Related]
20. [Pseudohypertrophic proximal progressive muscular dystrophy with a malignant course manifesting itself in adolescence]. Badalian LO; Temin PA; Saidbegov DG; Nikitin MV; Arkhipov BA Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(3):113-20. PubMed ID: 2728733 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]