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 *

209 related articles for article (PubMed ID: 15591603)

  • 21. Immunohistochemical evaluation of merosin deficiency in congenital muscular dystrophies.
    Brett FM; Loring P; Caesar A; Burke M; Brennan RP; King M; Farrell MA
    Arch Pathol Lab Med; 1998 Jan; 122(1):69-71. PubMed ID: 9448020
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular-eye-brain loci: report of three siblings.
    Ruggieri V; Lubieniecki F; Meli F; Diaz D; Ferragut E; Saito K; Brockington M; Muntoni F; Fukuyama Y; Taratuto AL
    Neuromuscul Disord; 2001 Sep; 11(6-7):570-8. PubMed ID: 11525887
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse.
    Matsumura K; Yamada H; Saito F; Sunada Y; Shimizu T
    Neuromuscul Disord; 1997 Jan; 7(1):7-12. PubMed ID: 9132144
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency.
    Reed UC; Marie SK; Vainzof M; Salum PB; Levy JA; Zatz M; Diament A
    Brain Dev; 1996; 18(1):53-8. PubMed ID: 8907344
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Congenital muscular dystrophy, white-matter abnormalities, and neuronal migration disorders: the expanding concept.
    Mackay MT; Kornberg AJ; Shield L; Phelan E; Kean MJ; Coleman LT; Dennett X
    J Child Neurol; 1998 Oct; 13(10):481-7. PubMed ID: 9796753
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.
    Triki C; Louhichi N; Méziou M; Choyakh F; Kéchaou MS; Jlidi R; Mhiri C; Fakhfakh F; Ayadi H
    Neuromuscul Disord; 2003 Jan; 13(1):4-12. PubMed ID: 12467726
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. [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]  

  • 30. Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping.
    Hillaire D; Leclerc A; Fauré S; Topaloglu H; Chiannilkulchaï N; Guicheney P; Grinas L; Legos P; Philpot J; Evangelista T
    Hum Mol Genet; 1994 Sep; 3(9):1657-61. PubMed ID: 7833925
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy.
    Shorer Z; Philpot J; Muntoni F; Sewry C; Dubowitz V
    J Child Neurol; 1995 Nov; 10(6):472-5. PubMed ID: 8576559
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Occidental-type cerebromuscular dystrophy versus congenital muscular dystrophy with merosin deficiency.
    Castro-Gago M
    Childs Nerv Syst; 1998 Oct; 14(10):531. PubMed ID: 9840374
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status.
    Mercuri E; Muntoni F; Berardinelli A; Pennock J; Sewry C; Philpot J; Dubowitz V
    Neuropediatrics; 1995 Feb; 26(1):3-7. PubMed ID: 7791947
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings.
    Topaloğlu H; Talim B; Vignier N; Helbling-Leclerc AH; Yetük M; Afşin IE; Cağlar M; Kale G; Guicheney P
    Neuromuscul Disord; 1998 May; 8(3-4):169-74. PubMed ID: 9631397
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients.
    Farina L; Morandi L; Milanesi I; Ciceri E; Mora M; Moroni I; Pantaleoni C; Savoiardo M
    Neuroradiology; 1998 Dec; 40(12):807-11. PubMed ID: 9877136
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [A unique case of congenital muscular dystrophy].
    Hermanová M; Vondrácek P; Lukás Z
    Cesk Patol; 2004 Apr; 40(2):57-62. PubMed ID: 15233018
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining.
    Connolly AM; Pestronk A; Planer GJ; Yue J; Mehta S; Choksi R
    Neurology; 1996 Mar; 46(3):810-14. PubMed ID: 8618688
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.