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 *

143 related articles for article (PubMed ID: 7580244)

  • 21. [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]  

  • 22. Immunohistochemical study of merosin-negative congenital muscular dystrophy: laminin alpha 2 deficiency in skin biopsy.
    Marbini A; Bellanova MF; Ferrari A; Lodesani M; Gemignani F
    Acta Neuropathol; 1997 Aug; 94(2):103-8. PubMed ID: 9255383
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Congenital muscular dystrophy and merosin deficiency].
    Werneck LC; Scola RH; Iwamoto FM
    Arq Neuropsiquiatr; 1997 Dec; 55(4):780-7. PubMed ID: 9629338
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging.
    Philpot J; Cowan F; Pennock J; Sewry C; Dubowitz V; Bydder G; Muntoni F
    Neuromuscul Disord; 1999 Mar; 9(2):81-5. PubMed ID: 10220862
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy.
    Matsumura K; Nonaka I; Campbell KP
    Lancet; 1993 Feb; 341(8844):521-2. PubMed ID: 8094772
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies.
    Jones KJ; Kim SS; North KN
    J Med Genet; 1998 May; 35(5):379-86. PubMed ID: 9610800
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. [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]  

  • 29. Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities.
    Mora M; Moroni I; Uziel G; di Blasi C; Barresi R; Farina L; Morandi L
    Neuromuscul Disord; 1996 Oct; 6(5):377-81. PubMed ID: 8938702
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Severe classical congenital muscular dystrophy and merosin expression.
    Vajsar J; Chitayat D; Becker LE; Ho M; Ben-Zeev B; Jay V
    Clin Genet; 1998 Sep; 54(3):193-8. PubMed ID: 9788720
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter.
    Echenne B; Rivier F; Jellali AJ; Azais M; Mornet D; Pons F
    Neuromuscul Disord; 1997 May; 7(3):187-90. PubMed ID: 9185183
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Expression of laminin subunits in human fetal skeletal muscle.
    Sewry CA; Chevallay M; Tomé FM
    Histochem J; 1995 Jul; 27(7):497-504. PubMed ID: 7591842
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Dystrophin-glycoproteins associated in congenital muscular dystrophy: immunohistochemical analysis of 59 Brazilian cases.
    Ferreira LG; Marie SK; Liu EC; Resende MB; Carvalho MS; Scaff M; Reed UC
    Arq Neuropsiquiatr; 2005 Sep; 63(3B):791-800. PubMed ID: 16258658
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Evidence of left ventricular dysfunction in children with merosin-deficient congenital muscular dystrophy.
    Spyrou N; Philpot J; Foale R; Camici PG; Muntoni F
    Am Heart J; 1998 Sep; 136(3):474-6. PubMed ID: 9736139
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
    Vainzof M; Passos-Bueno MR; Canovas M; Moreira ES; Pavanello RC; Marie SK; Anderson LV; Bonnemann CG; McNally EM; Nigro V; Kunkel LM; Zatz M
    Hum Mol Genet; 1996 Dec; 5(12):1963-9. PubMed ID: 8968750
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review.
    Jones KJ; Morgan G; Johnston H; Tobias V; Ouvrier RA; Wilkinson I; North KN
    J Med Genet; 2001 Oct; 38(10):649-57. PubMed ID: 11584042
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy.
    Sewry CA; Philpot J; Sorokin LM; Wilson LA; Naom I; Goodwin F; D'Alessandro M; Dubowitz V; Muntoni F
    Lancet; 1996 Mar; 347(9001):582-4. PubMed ID: 8596321
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy.
    Martinello F; Angelini C; Trevisan CP
    Eur Neurol; 1998 Jul; 40(1):37-45. PubMed ID: 9693231
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.
    Brockington M; Yuva Y; Prandini P; Brown SC; Torelli S; Benson MA; Herrmann R; Anderson LV; Bashir R; Burgunder JM; Fallet S; Romero N; Fardeau M; Straub V; Storey G; Pollitt C; Richard I; Sewry CA; Bushby K; Voit T; Blake DJ; Muntoni F
    Hum Mol Genet; 2001 Dec; 10(25):2851-9. PubMed ID: 11741828
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.