194 related articles for article (PubMed ID: 9131648)
1. Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency.
Tan E; Topaloglu H; Sewry C; Zorlu Y; Naom I; Erdem S; D'Alessandro M; Muntoni F; Dubowitz V
Neuromuscul Disord; 1997 Mar; 7(2):85-9. PubMed ID: 9131648
[TBL] [Abstract][Full Text] [Related]
2. Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy.
Naom I; D'Alessandro M; Sewry CA; Philpot J; Manzur AY; Dubowitz V; Muntoni F
Neuromuscul Disord; 1998 Oct; 8(7):495-501. PubMed ID: 9829280
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Early white matter changes on brain magnetic resonance imaging in a newborn affected by merosin-deficient congenital muscular dystrophy.
Mercuri E; Rutherford M; De Vile C; Counsell S; Sewry C; Brown S; Bydder G; Dubowitz V; Muntoni F
Neuromuscul Disord; 2001 Apr; 11(3):297-9. PubMed ID: 11297945
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Merosin-deficient congenital muscular dystrophy and cortical dysplasia.
Brett FM; Costigan D; Farrell MA; Heaphy P; Thornton J; King MD
Eur J Paediatr Neurol; 1998; 2(2):77-82. PubMed ID: 10724100
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci.
Talim B; Ferreiro A; Cormand B; Vignier N; Oto A; Göğüş S; Cila A; Lehesjoki AE; Pihko H; Guicheney P; Topaloğlu H
Neuromuscul Disord; 2000 Dec; 10(8):548-52. PubMed ID: 11053680
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Limb girdle muscular dystrophy due to
Magri F; Brusa R; Bello L; Peverelli L; Del Bo R; Govoni A; Cinnante C; Colombo I; Fortunato F; Tironi R; Corti S; Grimoldi N; Sciacco M; Bresolin N; Pegoraro E; Moggio M; Comi GP
Acta Myol; 2020 Jun; 39(2):67-82. PubMed ID: 32904964
[TBL] [Abstract][Full Text] [Related]
14. Clinical and pathological heterogeneity in late-onset partial merosin deficiency.
Rajakulendran S; Parton M; Holton JL; Hanna MG
Muscle Nerve; 2011 Oct; 44(4):590-3. PubMed ID: 21922472
[TBL] [Abstract][Full Text] [Related]
15. Abnormal expression of laminin beta 1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy.
Li M; Dickson DW; Spiro AJ
Arch Neurol; 1997 Dec; 54(12):1457-61. PubMed ID: 9400354
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.
Naom IS; D'Alessandro M; Topaloglu H; Sewry C; Ferlini A; Helbling-Leclerc A; Guicheney P; Weissenbach J; Schwartz K; Bushby K; Philpot J; Dubowitz V; Muntoni F
J Med Genet; 1997 Feb; 34(2):99-104. PubMed ID: 9039983
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. 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]
[Next] [New Search]
