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 *

133 related articles for article (PubMed ID: 12235836)

  • 21. [Dysferlin expression in limb-girdle muscular dystrophy and Miyoshi myopathy: analysis of 45 cases].
    Ren SC; Yan CZ; Li MX; Liu SP; Wu JL; Zhao YY; Li W; Li DN
    Zhonghua Yi Xue Za Zhi; 2007 Jun; 87(21):1486-90. PubMed ID: 17785089
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The 10 autosomal recessive limb-girdle muscular dystrophies.
    Zatz M; de Paula F; Starling A; Vainzof M
    Neuromuscul Disord; 2003 Sep; 13(7-8):532-44. PubMed ID: 12921790
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Limb-girdle muscular dystrophy: an immunohistochemical diagnostic approach.
    Comerlato EA; Scola RH; Werneck LC
    Arq Neuropsiquiatr; 2005 Jun; 63(2A):235-45. PubMed ID: 16100969
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Epidemiological and Molecular Characterization of a Mexican Population Isolate with High Prevalence of Limb-Girdle Muscular Dystrophy Type 2A Due to a Novel Calpain-3 Mutation.
    Pantoja-Melendez CA; Miranda-Duarte A; Roque-Ramirez B; Zenteno JC
    PLoS One; 2017; 12(1):e0170280. PubMed ID: 28103310
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The sarcoglycan complex in limb-girdle muscular dystrophy.
    Lim LE; Campbell KP
    Curr Opin Neurol; 1998 Oct; 11(5):443-52. PubMed ID: 9847993
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [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]  

  • 27. Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers.
    Olby NJ; Sharp NJ; Anderson LV; Kunkel LM; Bönnemann CG
    Neuromuscul Disord; 2001 Jan; 11(1):41-9. PubMed ID: 11166165
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Positional cloning of the gene for Miyoshi myopathy and limb-girdle muscular dystrophy].
    Aoki M; Arahata K; Brown RH
    Rinsho Shinkeigaku; 1999 Dec; 39(12):1272-5. PubMed ID: 10791095
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family].
    Horváth R; Walter MC; Lochmüller H; Hübner A; Karcagi V; Pikó H; Timár L; Komoly S
    Ideggyogy Sz; 2005 Jan; 58(1-2):52-8. PubMed ID: 15884399
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Limb-girdle muscular dystrophy in a 71-year-old woman with an R27Q mutation in the CAV3 gene.
    Figarella-Branger D; Pouget J; Bernard R; Krahn M; Fernandez C; Lévy N; Pellissier JF
    Neurology; 2003 Aug; 61(4):562-4. PubMed ID: 12939441
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: The yield and the pitfalls.
    Fanin M; Angelini C
    Muscle Nerve; 2015 Aug; 52(2):163-73. PubMed ID: 25900067
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [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]  

  • 33. [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]  

  • 34. The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more.
    Gordon ES; Hoffman EP
    Curr Opin Neurol; 2001 Oct; 14(5):567-73. PubMed ID: 11562567
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients.
    Guglieri M; Magri F; D'Angelo MG; Prelle A; Morandi L; Rodolico C; Cagliani R; Mora M; Fortunato F; Bordoni A; Del Bo R; Ghezzi S; Pagliarani S; Lucchiari S; Salani S; Zecca C; Lamperti C; Ronchi D; Aguennouz M; Ciscato P; Di Blasi C; Ruggieri A; Moroni I; Turconi A; Toscano A; Moggio M; Bresolin N; Comi GP
    Hum Mutat; 2008 Feb; 29(2):258-66. PubMed ID: 17994539
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Limb-girdle muscular dystrophy; update].
    Sunada Y
    Rinsho Shinkeigaku; 2004 Nov; 44(11):995-7. PubMed ID: 15651352
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Limb-Girdle Muscular Dystrophy Type 2A Resulting From c.C479G and c.G1818A Mutations in the Calpain-3 Gene.
    Ramos E; Pardo S; Mas Rodríguez MF; Vélez J
    J Clin Neuromuscul Dis; 2015 Dec; 17(2):59-62. PubMed ID: 26583491
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Dysferlin deficiency: the cause of limb-girdle muscular dystrophy 2B and Miyoshi myopathy in a Chinese pedigree].
    Sun S; Fan Q; Wu H; Leturcq F; Zhang B; Yu W; Deburgrave N; Liu M; Song Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):128-31. PubMed ID: 15079794
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies.
    Inashkina I; Jankevics E; Stavusis J; Vasiljeva I; Viksne K; Micule I; Strautmanis J; Naudina MS; Cimbalistiene L; Kucinskas V; Krumina A; Utkus A; Burnyte B; Matuleviciene A; Lace B
    BMC Musculoskelet Disord; 2016 May; 17():200. PubMed ID: 27142102
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.