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 *

61 related articles for article (PubMed ID: 11915708)

  • 1. [Clinical polymorphism, genetic heterogeneity and primary myopathy pathogenesis problems].
    Shishkin SS; Shakhovskaia NI; Krakhmaleva IN
    Zh Nevrol Psikhiatr Im S S Korsakova; 2002; 102(2):54-60. PubMed ID: 11915708
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [The genetic basis of muscle disease].
    Bindoff L; Gilhus NE
    Tidsskr Nor Laegeforen; 2003 Sep; 123(18):2588-92. PubMed ID: 14714051
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Muscular dystrophies and other genetic myopathies.
    Shieh PB
    Neurol Clin; 2013 Nov; 31(4):1009-29. PubMed ID: 24176421
    [TBL] [Abstract][Full Text] [Related]  

  • 4. COL6A1 genomic deletions in Bethlem myopathy and Ullrich muscular dystrophy.
    Pepe G; Lucarini L; Zhang RZ; Pan TC; Giusti B; Quijano-Roy S; Gartioux C; Bushby KM; Guicheney P; Chu ML
    Ann Neurol; 2006 Jan; 59(1):190-5. PubMed ID: 16278855
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.
    Nowak KJ; Wattanasirichaigoon D; Goebel HH; Wilce M; Pelin K; Donner K; Jacob RL; Hübner C; Oexle K; Anderson JR; Verity CM; North KN; Iannaccone ST; Müller CR; Nürnberg P; Muntoni F; Sewry C; Hughes I; Sutphen R; Lacson AG; Swoboda KJ; Vigneron J; Wallgren-Pettersson C; Beggs AH; Laing NG
    Nat Genet; 1999 Oct; 23(2):208-12. PubMed ID: 10508519
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patients.
    Chaturvedi LS; Mukherjee M; Srivastava S; Mittal RD; Mittal B
    Exp Mol Med; 2001 Dec; 33(4):251-6. PubMed ID: 11795488
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Preferential deletion of exons in Duchenne and Becker muscular dystrophies.
    Forrest SM; Cross GS; Speer A; Gardner-Medwin D; Burn J; Davies KE
    Nature; 1987 Oct 15-21; 329(6140):638-40. PubMed ID: 2821406
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical polymorphism of X-linked myopathies].
    Grinio LP
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(3):321-9. PubMed ID: 4466264
    [No Abstract]   [Full Text] [Related]  

  • 9. Dystrophinopathy mimicking metabolic myopathies.
    Liewluck T; Tian X; Wong LJ; Pestronk A
    Neuromuscul Disord; 2015 Aug; 25(8):653-7. PubMed ID: 25998609
    [TBL] [Abstract][Full Text] [Related]  

  • 10. History and current difficulties in classifying inherited myopathies and muscular dystrophies.
    Mathis S; Tazir M; Magy L; Duval F; Le Masson G; Duchesne M; Couratier P; Ghorab K; Solé G; Lacoste I; Goizet C; Vallat JM
    J Neurol Sci; 2018 Jan; 384():50-54. PubMed ID: 29249377
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
    Li H; Ding J; Wang W; Chen Y; Lu W; Shao H; Wu BL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Becker muscular dystrophy severity is linked to the structure of dystrophin.
    Nicolas A; Raguénès-Nicol C; Ben Yaou R; Ameziane-Le Hir S; Chéron A; Vié V; Claustres M; Leturcq F; Delalande O; Hubert JF; Tuffery-Giraud S; Giudice E; Le Rumeur E;
    Hum Mol Genet; 2015 Mar; 24(5):1267-79. PubMed ID: 25348330
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Polymorphism of exon 4 in the CANP-3 gene in patients with primary myopathies].
    Lipatova NA; Krakhmaleva IN; Shishkin SS; Shakhovskaia NI; Podnikova NI; Lunga IN; Tarksh MA; Gerasimova NL
    Genetika; 1999 Dec; 35(12):1713-7. PubMed ID: 10687099
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies.
    Stockley TL; Akber S; Bulgin N; Ray PN
    Genet Test; 2006; 10(4):229-43. PubMed ID: 17253928
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis.
    Murugan S; Chandramohan A; Lakshmi BR
    Indian J Med Res; 2010 Sep; 132():303-11. PubMed ID: 20847377
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
    Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F
    Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frameshift deletion mechanisms in Egyptian Duchenne and Becker muscular dystrophy families.
    Elhawary NA; Shawky RM; Hashem N
    Mol Cells; 2004 Oct; 18(2):141-9. PubMed ID: 15528988
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Analysis of the polymorphism of primary myopathies with recessive X-linked inheritance].
    Grinio LP
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(11):1621-4. PubMed ID: 7324662
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy.
    Ruggieri A; Brancati F; Zanotti S; Maggi L; Pasanisi MB; Saredi S; Terracciano C; Antozzi C; D Apice MR; Sangiuolo F; Novelli G; Marshall CR; Scherer SW; Morandi L; Federici L; Massa R; Mora M; Minassian BA
    Acta Neuropathol Commun; 2015 Jul; 3():44. PubMed ID: 26205529
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.