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2. Deficiency of adhalin in a patient with muscular dystrophy and cardiomyopathy. McNally EM; Bönnemann CG; Kunkel LM; Bhattacharya SK N Engl J Med; 1996 Jun; 334(24):1610-1. PubMed ID: 8628353 [No Abstract] [Full Text] [Related]
3. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. Bueno MR; Moreira ES; Vainzof M; Chamberlain J; Marie SK; Pereira L; Akiyama J; Roberds SL; Campbell KP; Zatz M Hum Mol Genet; 1995 Jul; 4(7):1163-7. PubMed ID: 8528203 [TBL] [Abstract][Full Text] [Related]
4. Understanding the heterogeneity of the limb-girdle muscular dystrophies. Bushby K Biochem Soc Trans; 1996 May; 24(2):489-96. PubMed ID: 8736790 [No Abstract] [Full Text] [Related]
5. The limb-girdle muscular dystrophies--proposal for a new nomenclature. Bushby KM; Beckmann JS Neuromuscul Disord; 1995 Jul; 5(4):337-43. PubMed ID: 7580247 [No Abstract] [Full Text] [Related]
6. 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]
7. From adhalinopathies to alpha-sarcoglycanopathies: an overview. Jeanpierre M; Carrié A; Piccolo F; Leturcq F; Azibi K; De Toma C; Beldjord C; Merlini L; Voit T; Romero N; Sunada Y; Tomé FM; Fardeau M; Campbell KP; Kaplan JC Neuromuscul Disord; 1996 Dec; 6(6):463-5. PubMed ID: 9027856 [No Abstract] [Full Text] [Related]
9. Genetic medicine and the muscular dystrophies: triumphs and tribulations. Hoffman EP; Chen YW Dev Med Child Neurol; 2002 Feb; 44(2):136-40. PubMed ID: 11848111 [No Abstract] [Full Text] [Related]
10. 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]
11. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families. Passos-Bueno MR; Moreira ES; Marie SK; Bashir R; Vasquez L; Love DR; Vainzof M; Iughetti P; Oliveira JR; Bakker E; Strachan T; Bushby K; Zatz M J Med Genet; 1996 Feb; 33(2):97-102. PubMed ID: 8929943 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. [The frequency of patients with adhalin deficiency in a muscular dystrophy patient population]. Hayashi YK; Arahata K Nihon Rinsho; 1997 Dec; 55(12):3165-8. PubMed ID: 9436429 [TBL] [Abstract][Full Text] [Related]
14. [Clinicopathological characteristics and molecular genetics of adhalin deficiency (severe childhood autosomal recessive muscular dystrophy/SCARMD)]. Matsumura K Nihon Rinsho; 1997 Dec; 55(12):3154-8. PubMed ID: 9436427 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. Prenatal diagnosis of limb-girdle muscular dystrophy type 2C. Dinçer P; Piccolo F; Leturcq F; Kaplan JC; Jeanpierre M; Topaloğlu H Prenat Diagn; 1998 Dec; 18(12):1300-3. PubMed ID: 9885023 [TBL] [Abstract][Full Text] [Related]
17. 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]