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4. [Muscular disease of X-linked autosomal recessive transmission with early muscular retractions and cardiac conduction disorders]. Serratrice G; Pouget J; Pellissier JF; Gastaut JL; Cros D Rev Neurol (Paris); 1982; 138(10):713-24. PubMed ID: 6891495 [No Abstract] [Full Text] [Related]
5. Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation. Abbadi N; Philippe C; Chery M; Gilgenkrantz H; Tome F; Collin H; Theau D; Recan D; Broux O; Fardeau M Am J Med Genet; 1994 Aug; 52(2):198-206. PubMed ID: 7802009 [TBL] [Abstract][Full Text] [Related]
9. [Peculiar type of congenital muscular dystrophy (Fukuyama type) (author's transl)]. Itagaki Y; Sakamoto Y; Nishitani Y Rinsho Shinkeigaku; 1980 Nov; 20(11):897-903. PubMed ID: 7249470 [No Abstract] [Full Text] [Related]
10. Merosin-deficient congenital muscular dystrophy type 1A. Buteică E; Roşulescu E; Burada F; Stănoiu B; Zăvăleanu M Rom J Morphol Embryol; 2008; 49(2):229-33. PubMed ID: 18516331 [TBL] [Abstract][Full Text] [Related]
11. Investigation on healthy individuals from families of patients with Duchenne type muscular dystrophy. Hausmanowa-Petrusewicz I; Prot J; Niebrój-Dobosz I; Emeryk B; Wasowicz B; Slucka C; Hetnarska L; Bendarzewska B; Pucek Z Pol Med J; 1968; 7(1):228-37. PubMed ID: 5652928 [No Abstract] [Full Text] [Related]
12. The detection of female carriers of pseudohypertrophic muscular dystrophy. Kakulas BA; Knight JO; Gubbay SS; Mastaglia FL Proc Aust Assoc Neurol; 1968; 5(3):545-51. PubMed ID: 5709982 [No Abstract] [Full Text] [Related]
13. Quantitative measurements in female siblings and mothers of boys with Duchenne dystrophy. Fowler WM; Gardner GW; Taylor RG; Scavarda A; Busheikin JB Arch Phys Med Rehabil; 1969 Jun; 50(6):301-10. PubMed ID: 5788486 [No Abstract] [Full Text] [Related]
14. [Case of ectopic accessory bone in the gluteal muscles]. RUMENOV I Khirurgiia (Sofiia); 1954; 7(10):623-4. PubMed ID: 14382264 [No Abstract] [Full Text] [Related]
15. Congenital muscular dystrophy. (A case report). Magotra ML; Likhare RS; Sircar PK Indian Pediatr; 1980 Dec; 17(12):983-5. PubMed ID: 7251126 [No Abstract] [Full Text] [Related]
16. [On Becker's benign muscular dystrophy: study of a family with 10 affected members in 6 generations]. Caruso G; Campanella G Acta Neurol (Napoli); 1968; 23(4):709-31. PubMed ID: 5747395 [No Abstract] [Full Text] [Related]
17. Maturational defect of regenerating muscle fibers in cases with Duchenne and congenital muscular dystrophies. Miike T Muscle Nerve; 1983 Oct; 6(8):545-52. PubMed ID: 6196637 [TBL] [Abstract][Full Text] [Related]
18. [Gene hunting for Fukuyama type congenital muscular dystrophy]. Toda T No To Shinkei; 1996 Apr; 48(4):315-22. PubMed ID: 8679327 [No Abstract] [Full Text] [Related]
19. [The place of electromyography in the diagnosis of myopathy in children]. Raimbault J; Renault F; Laget P Ann Pediatr (Paris); 1977; 24(6-7):451-8. PubMed ID: 16211924 [No Abstract] [Full Text] [Related]
20. [Fukuyama type congenital muscular dystrophy]. Calzada-Sierra DJ Rev Neurol; 2002 Jan 1-15; 34(1):98. PubMed ID: 11988898 [No Abstract] [Full Text] [Related] [Next] [New Search]