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Journal Abstract Search

136 related items for PubMed ID: 9693231

  • 1. 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
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  • 2. Alterations of the retino-cortical conduction in patients affected by classical congenital muscular dystrophy (CI-CMD) with merosin deficiency.
    Tormene AP, Trevisan C, Martinello F, Riva C, Pastorello E.
    Doc Ophthalmol; 1999 Jul; 98(2):127-38. PubMed ID: 10946999
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  • 3. Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophy.
    Mercuri E, Anker S, Philpot J, Sewry C, Dubowitz V, Muntoni F.
    Pediatr Neurol; 1998 May; 18(5):399-401. PubMed ID: 9650678
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  • 7. Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.
    Trevisan CP, Martinello F, Ferruzza E, Fanin M, Chevallay M, Tomé FM.
    Childs Nerv Syst; 1996 Oct; 12(10):604-10. PubMed ID: 8934020
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  • 10. Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRI.
    Leite CC, Lucato LT, Martin MG, Ferreira LG, Resende MB, Carvalho MS, Marie SK, Jinkins JR, Reed UC.
    Pediatr Radiol; 2005 Jun; 35(6):572-9. PubMed ID: 15750812
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  • 11. 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
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  • 14. 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
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  • 15. 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
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  • 16. Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain.
    Sewry CA, Naom I, D'Alessandro M, Sorokin L, Bruno S, Wilson LA, Dubowitz V, Muntoni F.
    Neuromuscul Disord; 1997 May; 7(3):169-75. PubMed ID: 9185180
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  • 17. [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
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  • 19. 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
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  • 20. 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 May; 4(3):109-14. PubMed ID: 10872105
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