BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 16541798)

  • 1. [Four siblings with becker muscular dystrophy (BMD) manifesting severe mental retardation].
    Futamura N; Kawamoto K; Takahashi K; Funakawa I; Jinnai K
    Rinsho Shinkeigaku; 2006 Jan; 46(1):62-5. PubMed ID: 16541798
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Therapy of Duchenne muscular dystrophy with umbilical cord blood stem cell transplantation].
    Zhang C; Feng HY; Huang SL; Fang JP; Xiao LL; Yao XL; Chen C; Ye X; Zeng Y; Lu XL; Wen JM; Zhang WX; Li Z; Feng SW; Xu HG; Huang K; Zhou DH; Chen W; Xie YM; Xi J; Zhang M; Li Y; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):399-405. PubMed ID: 16086277
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cognitive and psychological profile of males with Becker muscular dystrophy.
    Young HK; Barton BA; Waisbren S; Portales Dale L; Ryan MM; Webster RI; North KN
    J Child Neurol; 2008 Feb; 23(2):155-62. PubMed ID: 18056690
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case of Becker muscular dystrophy presenting cardiac failure as an initial symptom].
    Sakata C; Sunohara N; Nonaka I; Arahata K; Sugita H
    Rinsho Shinkeigaku; 1990 Feb; 30(2):210-3. PubMed ID: 2190744
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pseudoexon activation in the DMD gene as a novel mechanism for Becker muscular dystrophy.
    Tuffery-Giraud S; Saquet C; Chambert S; Claustres M
    Hum Mutat; 2003 Jun; 21(6):608-14. PubMed ID: 12754707
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of deletion in the dystrophin gene of a patient with quadriceps myopathy.
    Kumari D; Gupta M; Goyle S
    Neurol India; 2000 Mar; 48(1):68-71. PubMed ID: 10751817
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.
    Rudnik-Schöneborn S; Weis J; Kress W; Häusler M; Zerres K
    Neuromuscul Disord; 2008 Nov; 18(11):881-5. PubMed ID: 18684626
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A case of Becker muscular dystrophy with schizophrenic symptoms].
    Abe M; Arai M; Maehara K; Arikawa E; Arahata K
    No To Shinkei; 1990 Nov; 42(11):1061-6. PubMed ID: 2076351
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [A rare case of adult-onset Becker muscular dystrophy diagnosed by dystrophin staining].
    Ujike H; Tomita J; Kuroda S; Otsuki S; Arahata K
    No To Shinkei; 1991 Oct; 43(10):975-9. PubMed ID: 1724729
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Coinheritance of Noonan syndrome and Becker muscular dystrophy.
    Dinopoulos A; Papadopoulou A; Manta P; Kekou K; Kanelopoulos T; Fretzayas A; Kitsiou S
    Neuromuscul Disord; 2010 Jan; 20(1):61-3. PubMed ID: 19875288
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype.
    Witting N; Duno M; Vissing J
    Acta Myol; 2011 Dec; 30(3):182-4. PubMed ID: 22616200
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion.
    Ferreiro V; Giliberto F; Muñiz GM; Francipane L; Marzese DM; Mampel A; Roqué M; Frechtel GD; Szijan I
    Muscle Nerve; 2009 Feb; 39(2):239-43. PubMed ID: 19012301
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
    Pikó H; Vancsó V; Nagy B; Bán Z; Herczegfalvi A; Karcagi V
    Neuromuscul Disord; 2009 Feb; 19(2):108-12. PubMed ID: 19084397
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Detection of the gene-deleted female carriers of Duchenne/Becker muscular dystrophy using a fluorescent in situ hybridization based method].
    Qi QW; Sun NH; Hao N
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):350-2. PubMed ID: 12903051
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal.
    Hallwirth Pillay KD; Bill PL; Madurai S; Mubaiwa L; Rapiti P
    J Neurol Sci; 2007 Jan; 252(1):1-3. PubMed ID: 17141273
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions.
    Torelli S; Brown SC; Jimenez-Mallebrera C; Feng L; Muntoni F; Sewry CA
    Neuropathol Appl Neurobiol; 2004 Oct; 30(5):540-5. PubMed ID: 15488030
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A manifesting carrier of Duchenne muscular dystrophy presenting mosaic distribution of dystrophin negative and positive muscle fibers].
    Kikumoto O; Yoshinaga J; Sasaki T; Ideshita H; Hikiji A; Arahata K
    Rinsho Shinkeigaku; 1990 Jan; 30(1):107-9. PubMed ID: 2184962
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Female carrier of Duchenne muscular dystrophy presenting with secondary dilated cardiomyopathy: a case report].
    Hiramatsu S; Maekawa K; Hioka T; Takagaki K; Shoji K
    J Cardiol; 2001 Jul; 38(1):35-40. PubMed ID: 11496434
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A case of Down syndrome complicated with Becker muscular dystrophy].
    Sakai K; Kojima S; Matsumura T; Takagi A; Arahata K
    Rinsho Shinkeigaku; 1993 Nov; 33(11):1201-3. PubMed ID: 8124883
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27.
    Tsuda T; Fitzgerald K; Scavena M; Gidding S; Cox MO; Marks H; Flanigan KM; Moore SA
    J Hum Genet; 2015 Mar; 60(3):151-5. PubMed ID: 25537791
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.