BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 12868400)

  • 1. [Merosin-positive congenital muscular dystrophy, white matter abnormalities, and bilateral posterior occipital cortical dysplasia].
    Ribeiro VT; Moreira NC; Teixeira J; Guimarães A; Cruz R; Lima L
    Acta Med Port; 2003; 16(3):189-92. PubMed ID: 12868400
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.
    van der Knaap MS; Smit LM; Barth PG; Catsman-Berrevoets CE; Brouwer OF; Begeer JH; de Coo IF; Valk J
    Ann Neurol; 1997 Jul; 42(1):50-9. PubMed ID: 9225685
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Brain MRI features of merosin-negative congenital muscular dystrophy.
    Ibrahim Abdulla JK; Vattoth S; Al Tawari AA; Pandey T; Abubacker S
    Australas Radiol; 2007 Dec; 51 Suppl():B221-3. PubMed ID: 17991069
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Non-Fukuyama type congenital muscular dystrophy--merosin deficient and positive forms].
    Nonaka I
    Nihon Rinsho; 1997 Dec; 55(12):3176-80. PubMed ID: 9436431
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Merosin positive congenital muscular dystrophy with severe involvement of the central nervous system.
    De Stefano N; Dotti MT; Villanova M; Scarano G; Federico A
    Brain Dev; 1996; 18(4):323-6. PubMed ID: 8879654
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy.
    Sewry CA; D'Alessandro M; Wilson LA; Sorokin LM; Naom I; Bruno S; Ferlini A; Dubowitz V; Muntoni F
    Neuropediatrics; 1997 Aug; 28(4):217-22. PubMed ID: 9309712
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy.
    Voit T; Sewry CA; Meyer K; Hermann R; Straub V; Muntoni F; Kahn T; Unsöld R; Helliwell TR; Appleton R
    Neuropediatrics; 1995 Jun; 26(3):148-55. PubMed ID: 7477753
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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]  

  • 11. Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy.
    Philpot J; Pennock J; Cowan F; Sewry CA; Dubowitz V; Bydder G; Muntoni F
    Eur J Paediatr Neurol; 2000; 4(3):109-14. PubMed ID: 10872105
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?
    Mercuri E; Sewry CA; Brown SC; Brockington M; Jungbluth H; DeVile C; Counsell S; Manzur A; Muntoni F
    Neuropediatrics; 2000 Aug; 31(4):186-9. PubMed ID: 11071142
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. Congenital muscular dystrophy with merosin deficiency.
    Tomé FM; Evangelista T; Leclerc A; Sunada Y; Manole E; Estournet B; Barois A; Campbell KP; Fardeau M
    C R Acad Sci III; 1994 Apr; 317(4):351-7. PubMed ID: 8000914
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Occipito-temporal polymicrogyria and subclinical muscular dystrophy.
    Zolkipli Z; Hartley L; Brown S; Rutherford M; Cowan F; Mercuri E; Muntoni F
    Neuropediatrics; 2003 Apr; 34(2):92-5. PubMed ID: 12776231
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Merosin-negative congenital muscular dystrophy: diffusion-weighted imaging findings of brain.
    Alkan A; Sigirci A; Kutlu R; Aslan M; Doganay S; Yakinci C
    J Child Neurol; 2007 May; 22(5):655-9. PubMed ID: 17690079
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations.
    Vainzof M; Marie SK; Reed UC; Schwartzman JS; Pavanello RC; Passos-Bueno MR; Zatz M
    Neuropediatrics; 1995 Dec; 26(6):293-7. PubMed ID: 8719743
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Merosin-negative congenital muscular dystrophy: magnetic resonance spectroscopy findings.
    Aslan M; Alkan A; Yakinci C; Sonmezgoz E; Bicak U; Zorludemir S
    Brain Dev; 2005 Jun; 27(4):308-10. PubMed ID: 15862197
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.
    Longman C; Brockington M; Torelli S; Jimenez-Mallebrera C; Kennedy C; Khalil N; Feng L; Saran RK; Voit T; Merlini L; Sewry CA; Brown SC; Muntoni F
    Hum Mol Genet; 2003 Nov; 12(21):2853-61. PubMed ID: 12966029
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.