BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

424 related articles for article (PubMed ID: 11938437)

  • 1. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin).
    Allamand V; Guicheney P
    Eur J Hum Genet; 2002 Feb; 10(2):91-4. PubMed ID: 11938437
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.
    Helbling-Leclerc A; Zhang X; Topaloglu H; Cruaud C; Tesson F; Weissenbach J; Tomé FM; Schwartz K; Fardeau M; Tryggvason K
    Nat Genet; 1995 Oct; 11(2):216-8. PubMed ID: 7550355
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian families.
    Louhichi N; Richard P; Triki CH; Meziou M; Ayadi H; Guicheney P; Fakhfakh F
    Arch Inst Pasteur Tunis; 2006; 83(1-4):19-23. PubMed ID: 19388593
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers.
    Vainzof M; Richard P; Herrmann R; Jimenez-Mallebrera C; Talim B; Yamamoto LU; Ledeuil C; Mein R; Abbs S; Brockington M; Romero NB; Zatz M; Topaloglu H; Voit T; Sewry C; Muntoni F; Guicheney P; Tomé FM
    Neuromuscul Disord; 2005 Oct; 15(9-10):588-94. PubMed ID: 16084089
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Merosin and congenital muscular dystrophy.
    Miyagoe-Suzuki Y; Nakagawa M; Takeda S
    Microsc Res Tech; 2000 Feb 1-15; 48(3-4):181-91. PubMed ID: 10679965
    [TBL] [Abstract][Full Text] [Related]  

  • 6. LAMA2 stop-codon mutation: merosin-deficient congenital muscular dystrophy with occipital polymicrogyria, epilepsy and psychomotor regression.
    Vigliano P; Dassi P; Di Blasi C; Mora M; Jarre L
    Eur J Paediatr Neurol; 2009 Jan; 13(1):72-6. PubMed ID: 18406646
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Merosin-deficient congenital muscular dystrophy type 1A.
    Buteică E; Roşulescu E; Burada F; Stănoiu B; Zăvăleanu M
    Rom J Morphol Embryol; 2008; 49(2):229-33. PubMed ID: 18516331
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy.
    Pegoraro E; Mancias P; Swerdlow SH; Raikow RB; Garcia C; Marks H; Crawford T; Carver V; Di Cianno B; Hoffman EP
    Ann Neurol; 1996 Nov; 40(5):782-91. PubMed ID: 8957020
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin alpha-2 gene.
    Coral-Vazquez RM; Rosas-Vargas H; Meza-Espinosa P; Mendoza I; Huicochea JC; Ramon G; Salamanca F
    J Hum Genet; 2003; 48(2):91-5. PubMed ID: 12601554
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2.
    Helbling-Leclerc A; Topaloglu H; Tomé FM; Sewry C; Gyapay G; Naom I; Muntoni F; Dubowitz V; Barois A; Estournet B
    C R Acad Sci III; 1995 Dec; 318(12):1245-52. PubMed ID: 8745640
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
    Taniguchi M; Kurahashi H; Noguchi S; Sese J; Okinaga T; Tsukahara T; Guicheney P; Ozono K; Nishino I; Morishita S; Toda T
    Biochem Biophys Res Commun; 2006 Apr; 342(2):489-502. PubMed ID: 16487936
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe congenital muscular dystrophy in a LAMA2-mutated case.
    Di Blasi C; van Alfen N; Colleoni F; ter Laak H; Mora M
    Pediatr Neurol; 2007 Sep; 37(3):212-4. PubMed ID: 17765811
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination.
    Patton BL; Wang B; Tarumi YS; Seburn KL; Burgess RW
    J Cell Sci; 2008 May; 121(Pt 10):1593-604. PubMed ID: 18430779
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Merosin-deficient congenital muscular dystrophy: A novel homozygous mutation in the laminin-2 gene.
    Turner C; Mein R; Sharpe C; Love DR
    J Clin Neurosci; 2015 Dec; 22(12):1983-5. PubMed ID: 26249246
    [TBL] [Abstract][Full Text] [Related]  

  • 15. LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients.
    Oliveira J; Santos R; Soares-Silva I; Jorge P; Vieira E; Oliveira ME; Moreira A; Coelho T; Ferreira JC; Fonseca MJ; Barbosa C; Prats J; Aríztegui ML; Martins ML; Moreno T; Heinimann K; Barbot C; Pascual-Pascual SI; Cabral A; Fineza I; Santos M; Bronze-da-Rocha E
    Clin Genet; 2008 Dec; 74(6):502-12. PubMed ID: 18700894
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetically confirmed patients with merosin-deficient congenital muscular dystrophy in China.
    Yuan J; Takashima H; Higuchi I; Arimura K; Li N; Zhao Z; Shen H; Hu J
    Neuropediatrics; 2008 Oct; 39(5):264-7. PubMed ID: 19294599
    [TBL] [Abstract][Full Text] [Related]  

  • 17. LAMA2 mRNA processing alterations generate a complete deficiency of laminin-alpha2 protein and a severe congenital muscular dystrophy.
    Siala O; Louhichi N; Triki C; Morinière M; Fakhfakh F; Baklouti F
    Neuromuscul Disord; 2008 Feb; 18(2):137-45. PubMed ID: 18053718
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].
    Fardeau M; Tomé FM; Helbling-Leclerc A; Evangelista T; Ottolini A; Chevallay M; Barois A; Estournet B; Harpey JP; Fauré S; Guicheney P; Hillaire D
    Rev Neurol (Paris); 1996 Jan; 152(1):11-9. PubMed ID: 8729391
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice.
    Gawlik K; Miyagoe-Suzuki Y; Ekblom P; Takeda S; Durbeej M
    Hum Mol Genet; 2004 Aug; 13(16):1775-84. PubMed ID: 15213105
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P
    Rev Neurol; 1999 Jan 16-31; 28(2):141-9. PubMed ID: 10101782
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.