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.
146 related articles for article (PubMed ID: 9044410)
1. Muscle pathology and clinical features of the sarcolemmopathies. Fadic R; Waclawik AJ; Lewandoski PJ; Lotz BP Pediatr Neurol; 1997 Jan; 16(1):79-82. PubMed ID: 9044410 [TBL] [Abstract][Full Text] [Related]
2. Sarcolemmal defect and subsarcolemmal lesion in a patient with gamma-sarcoglycan deficiency. Li M; Dickson DW; Spiro AJ Neurology; 1998 Mar; 50(3):807-9. PubMed ID: 9521284 [TBL] [Abstract][Full Text] [Related]
3. Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle. Cohn RD; Mayer U; Saher G; Herrmann R; van der Flier A; Sonnenberg A; Sorokin L; Voit T J Neurol Sci; 1999 Mar; 163(2):140-52. PubMed ID: 10371075 [TBL] [Abstract][Full Text] [Related]
5. The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instability. Mendell JR; Sahenk Z; Prior TW J Child Neurol; 1995 Mar; 10(2):150-9. PubMed ID: 7782608 [TBL] [Abstract][Full Text] [Related]
6. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. Higuchi I; Yamada H; Fukunaga H; Iwaki H; Okubo R; Nakagawa M; Osame M; Roberds SL; Shimizu T; Campbell KP J Clin Invest; 1994 Aug; 94(2):601-6. PubMed ID: 8040315 [TBL] [Abstract][Full Text] [Related]
7. Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy. Durbeej M; Sawatzki SM; Barresi R; Schmainda KM; Allamand V; Michele DE; Campbell KP Proc Natl Acad Sci U S A; 2003 Jul; 100(15):8910-5. PubMed ID: 12851463 [TBL] [Abstract][Full Text] [Related]
8. Loss of sarcolemma nNOS in sarcoglycan-deficient muscle. Crosbie RH; Barresi R; Campbell KP FASEB J; 2002 Nov; 16(13):1786-91. PubMed ID: 12409321 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
11. [Significance of merosin and sarcoglycan in manifestations of certain forms of muscular dystrophy]. Medić S; Rakocević-Stojanović V Srp Arh Celok Lek; 1998; 126(1-2):34-9. PubMed ID: 9525081 [TBL] [Abstract][Full Text] [Related]
12. Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin. Tachi N; Ohya K; Chiba S; Matsuo M; Patria SY; Matsumura K Neurology; 1997 Aug; 49(2):579-83. PubMed ID: 9270600 [TBL] [Abstract][Full Text] [Related]
13. Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy. Fadic R; Sunada Y; Waclawik AJ; Buck S; Lewandoski PJ; Campbell KP; Lotz BP N Engl J Med; 1996 Feb; 334(6):362-6. PubMed ID: 8538707 [No Abstract] [Full Text] [Related]
14. New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency. Higuchi I; Iwaki H; Kawai H; Endo T; Kunishige M; Fukunaga H; Nakagawa M; Arimura K; Osame M J Neurol Sci; 1997 Dec; 153(1):100-5. PubMed ID: 9455986 [TBL] [Abstract][Full Text] [Related]
15. Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects. Handa V; Mital A; Gupta M; Goyle S Neurol India; 2001 Mar; 49(1):19-24. PubMed ID: 11303236 [TBL] [Abstract][Full Text] [Related]
16. Sarcoglycans in muscular dystrophy. Hack AA; Groh ME; McNally EM Microsc Res Tech; 2000 Feb 1-15; 48(3-4):167-80. PubMed ID: 10679964 [TBL] [Abstract][Full Text] [Related]
17. A novel insert mutation in gamma-sarcoglycan gene leads to severe childhood autosomal recessive muscular dystrophy. Lin S; Ramelli GP; Moser H; Gallati S; Burgunder JM J Neurol; 2002 Nov; 249(11):1608-11. PubMed ID: 12532930 [No Abstract] [Full Text] [Related]
18. [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]
19. Confocal analysis of the dystrophin protein complex in muscular dystrophy. Draviam R; Billington L; Senchak A; Hoffman EP; Watkins SC Muscle Nerve; 2001 Feb; 24(2):262-72. PubMed ID: 11180210 [TBL] [Abstract][Full Text] [Related]