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.
100 related articles for article (PubMed ID: 8631523)
1. Clinical and molecular pathological features of severe childhood autosomal recessive muscular dystrophy in Saudi Arabia. Salih MA; Mahdi AH; al-Rikabi AC; al-Bunyan M; Roberds SL; Anderson RD; Campbell KP Dev Med Child Neurol; 1996 Mar; 38(3):262-70. PubMed ID: 8631523 [TBL] [Abstract][Full Text] [Related]
2. Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency. Romero NB; Tomé FM; Leturcq F; el Kerch FE; Azibi K; Bachner L; Anderson RD; Roberds SL; Campbell KP; Fardeau M C R Acad Sci III; 1994 Jan; 317(1):70-6. PubMed ID: 7987694 [TBL] [Abstract][Full Text] [Related]
3. Dystrophin analysis in the differential diagnosis of autosomal recessive muscular dystrophy of childhood and Duchenne muscular dystrophy. Tachi N; Tachi M; Sasaki K; Nagata N; Chiba S Pediatr Neurol; 1990; 6(4):265-8. PubMed ID: 2206159 [TBL] [Abstract][Full Text] [Related]
4. Severe autosomal recessive muscular dystrophy in an extended Sudanese kindred. Salih MA; Omer MI; Bayoumi RA; Karrar O; Johnson M Dev Med Child Neurol; 1983 Feb; 25(1):43-52. PubMed ID: 6832497 [TBL] [Abstract][Full Text] [Related]
5. [Adhalin gene mutations in malignant limb-girdle muscular dystrophy and clinical features in adhalin-deficient muscular dystrophy]. Endo T; Akaike M; Kawai H; Matsumura K; Saito S Rinsho Shinkeigaku; 1996 Mar; 36(3):415-22. PubMed ID: 8741343 [TBL] [Abstract][Full Text] [Related]
6. Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency. Kawai H; Akaike M; Endo T; Adachi K; Inui T; Mitsui T; Kashiwagi S; Fujiwara T; Okuno S; Shin S J Clin Invest; 1995 Sep; 96(3):1202-7. PubMed ID: 7657792 [TBL] [Abstract][Full Text] [Related]
7. Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity. Piccolo F; Roberds SL; Jeanpierre M; Leturcq F; Azibi K; Beldjord C; Carrié A; Récan D; Chaouch M; Reghis A Nat Genet; 1995 Jun; 10(2):243-5. PubMed ID: 7663524 [TBL] [Abstract][Full Text] [Related]
8. Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features. Cupler EJ; Bohlega S; Hessler R; McLean D; Stigsby B; Ahmad J Neuromuscul Disord; 1998 Jun; 8(5):321-6. PubMed ID: 9673986 [TBL] [Abstract][Full Text] [Related]
9. Childhood neuromuscular disorders: a decade's experience in Saudi Arabia. Salih MA; Mahdi AH; al-Jarallah AA; al Jarallah AS; al-Saadi M; Hafeez MA; Aziz SA Ann Trop Paediatr; 1996 Dec; 16(4):271-80. PubMed ID: 8985523 [TBL] [Abstract][Full Text] [Related]
10. Becker-like muscular dystrophy in sisters. Diószeghy P; Molnár M; Mechler F Eur Arch Psychiatry Clin Neurosci; 1995; 245(6):326-30. PubMed ID: 8527470 [TBL] [Abstract][Full Text] [Related]
11. [Clinical and genetic heterogeneity of limb-girdle muscular dystrophy]. Kozłowska M Neurol Neurochir Pol; 1995; 29(4):569-75. PubMed ID: 8544936 [TBL] [Abstract][Full Text] [Related]
20. Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin. Ljunggren A; Duggan D; McNally E; Boylan KB; Gama CH; Kunkel LM; Hoffman EP Ann Neurol; 1995 Sep; 38(3):367-72. PubMed ID: 7668821 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]