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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 9845765)

  • 1. [Identification of adhalin gene mutation in limb-girdle muscular dystrophy in Chinese].
    Sun G; Wu Y; Zhang K; Zhang X; Jin C; Sun K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Dec; 15(6):351-3. PubMed ID: 9845765
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. [Adhalin(alpha-sarcoglycan) gene mutations in patients with malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi)].
    Endo T; Kawai H
    Nihon Rinsho; 1997 Dec; 55(12):3159-64. PubMed ID: 9436428
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Gene analysis in patients with muscular dystrophy: alpha-sarcoglycan (adhalin) gene mutations in patients with malignant limb-girdle muscular dystrophy].
    Akaike M; Kawai H
    Rinsho Byori; 1997 Feb; 45(2):136-40. PubMed ID: 9120997
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adhalin gene mutations and autosomal recessive limb-girdle muscular dystrophy.
    Campbell KP
    Ann Neurol; 1995 Sep; 38(3):353-4. PubMed ID: 7668818
    [No Abstract]   [Full Text] [Related]  

  • 6. [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]  

  • 7. 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]  

  • 8. [Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation].
    Eirís-Puñal J; Pintos-Martínez E; Lasa A; Gallano P; Castro-Gago M
    Rev Neurol; 2002 Mar 1-15; 34(5):486-9. PubMed ID: 12040521
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.
    Dinçer P; Leturcq F; Richard I; Piccolo F; Yalnizoglu D; de Toma C; Akçören Z; Broux O; Deburgrave N; Brenguier L; Roudaut C; Urtizberea JA; Jung D; Tan E; Jeanpierre M; Campbell KP; Kaplan JC; Beckmann JS; Topaloglu H
    Ann Neurol; 1997 Aug; 42(2):222-9. PubMed ID: 9266733
    [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. 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]  

  • 12. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12.
    Lim LE; Duclos F; Broux O; Bourg N; Sunada Y; Allamand V; Meyer J; Richard I; Moomaw C; Slaughter C
    Nat Genet; 1995 Nov; 11(3):257-65. PubMed ID: 7581448
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan gene.
    Lasa A; Piccolo F; de Diego C; Jeanpierre M; Colomer J; Rodríguez MJ; Urtizberea JA; Baiget M; Kaplan J; Gallano P
    Eur J Hum Genet; 1998; 6(4):396-9. PubMed ID: 9781048
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. [Muscular dystrophy due to a mutation in the gene of alpha-sarcoglycan subunit of dystrophin associated protein complex].
    Urtasun M; Poza JJ; Gallano P; Lasa A; Sáenz A; Cobo AM; Leturcq F; López de Munain A; García-Bragado F
    Med Clin (Barc); 1998 Apr; 110(14):538-42. PubMed ID: 9646269
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Limb girdle muscular dystrophy: use of dHPLC and direct sequencing to detect sarcoglycan gene mutations in a New Zealand cohort.
    Love DR
    Clin Genet; 2004 Jan; 65(1):55-60. PubMed ID: 15032976
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. C283Y mutation and other C-terminal nucleotide changes in the gamma-sarcoglycan gene in the Bulgarian Gypsy population.
    Todorova A; Ashikov A; Beltcheva O; Tournev I; Kremensky I
    Hum Mutat; 1999; 14(1):40-4. PubMed ID: 10447257
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Complete deficiency of adhalin (50 kDa DAG) in skeletal muscle of malignant limb-girdle muscular dystrophy].
    Kawai H; Inui T; Mitsui T; Campbell KP; Shimizu T; Matsumura K
    Rinsho Shinkeigaku; 1995 Feb; 35(2):184-9. PubMed ID: 7781237
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.