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 *

457 related articles for article (PubMed ID: 20925031)

  • 21. A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies.
    Cetin N; Balci-Hayta B; Gundesli H; Korkusuz P; Purali N; Talim B; Tan E; Selcen D; Erdem-Ozdamar S; Dincer P
    J Med Genet; 2013 Jul; 50(7):437-43. PubMed ID: 23687351
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The muscular dystrophies.
    Bushby KM
    Baillieres Clin Neurol; 1994 Aug; 3(2):407-30. PubMed ID: 7952855
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Two novel CAV3 gene mutations in Japanese families.
    Sugie K; Murayama K; Noguchi S; Murakami N; Mochizuki M; Hayashi YK; Nonaka I; Nishino I
    Neuromuscul Disord; 2004 Dec; 14(12):810-4. PubMed ID: 15564037
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Ins and outs of therapy in limb girdle muscular dystrophies.
    Danièle N; Richard I; Bartoli M
    Int J Biochem Cell Biol; 2007; 39(9):1608-24. PubMed ID: 17339125
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Facioscapulohumeral muscular dystrophy and limb-girdle muscular dystrophy: "double trouble" overlapping syndrome?
    Simeoni S; Russo V; Gigli GL; Scalise A
    J Neurol Sci; 2015 Jan; 348(1-2):292-3. PubMed ID: 25528007
    [No Abstract]   [Full Text] [Related]  

  • 26. Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3.
    Jenne DE; Kley RA; Vorgerd M; Schröder JM; Weis J; Reimann H; Albrecht B; Nürnberg P; Thiele H; Müller CR; Meng G; Witt CC; Labeit S
    Biol Chem; 2005 Jan; 386(1):61-7. PubMed ID: 15843148
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.
    Au CG; Butler TL; Egan JR; Cooper ST; Lo HP; Compton AG; North KN; Winlaw DS
    Acta Neuropathol; 2008 Sep; 116(3):235-46. PubMed ID: 18392839
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF.
    Diers A; Carl M; Stoltenburg-Didinger G; Vorgerd M; Spuler S
    Neuromuscul Disord; 2007 Feb; 17(2):157-62. PubMed ID: 17129727
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Limb-girdle muscular dystrophies: heterogeneity of clinical phenotypes and pathogenetic mechanisms.
    Angelini C
    Acta Myol; 2004 Dec; 23(3):130-6. PubMed ID: 15938568
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locus.
    Kottlors M; Moske-Eick O; Huebner A; Krause S; Mueller K; Kress W; Schwarzwald R; Bornemann A; Haug V; Heitzer M; Kirschner J
    J Neurol Sci; 2010 Apr; 291(1-2):79-85. PubMed ID: 20116073
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients.
    Hermanová M; Zapletalová E; Sedlácková J; Chrobáková T; Letocha O; Kroupová I; Zámecník J; Vondrácek P; Mazanec R; Maríková T; Vohánka S; Fajkusová L
    Muscle Nerve; 2006 Mar; 33(3):424-32. PubMed ID: 16372320
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [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]  

  • 33. [Myopathology. New concept. New laboratory].
    Navarro C; Teijeira S
    Neurologia; 2004 May; 19(4):168-82. PubMed ID: 15131736
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Function and genetics of dystrophin and dystrophin-related proteins in muscle.
    Blake DJ; Weir A; Newey SE; Davies KE
    Physiol Rev; 2002 Apr; 82(2):291-329. PubMed ID: 11917091
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J.
    Udd B; Vihola A; Sarparanta J; Richard I; Hackman P
    Neurology; 2005 Feb; 64(4):636-42. PubMed ID: 15728284
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
    Nakamura A; Yoshida K; Ikeda S
    Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5.
    Penttilä S; Palmio J; Suominen T; Raheem O; Evilä A; Muelas Gomez N; Tasca G; Waddell LB; Clarke NF; Barboi A; Hackman P; Udd B
    Neurology; 2012 Mar; 78(12):897-903. PubMed ID: 22402862
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Epsilon-sarcoglycan compensates for lack of alpha-sarcoglycan in a mouse model of limb-girdle muscular dystrophy.
    Imamura M; Mochizuki Y; Engvall E; Takeda S
    Hum Mol Genet; 2005 Mar; 14(6):775-83. PubMed ID: 15689353
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Dystrophinopathies, congenital muscular dystrophy, limb-girdle dystrophies: updated classification].
    Teijeira-Bautista S; García-García D; Teijeiro-Ferreira A; Fernández-Hojas R; Fernández-Rodríguez JM; Navarro-Fernández-Balbuena C
    Rev Neurol; 1998 Jun; 26(154):1021-6. PubMed ID: 9658487
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dystrophinopathies and Limb-Girdle Muscular Dystrophies.
    Domingos J; Sarkozy A; Scoto M; Muntoni F
    Neuropediatrics; 2017 Aug; 48(4):262-272. PubMed ID: 28427100
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.