112 related articles for article (PubMed ID: 7811489)
1. [Congenital muscular dystrophy: report on 10 cases].
Olivé M; Roig M; Bonaventura I; Navarro C
Neurologia; 1994 Nov; 9(9):387-92. PubMed ID: 7811489
[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. Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changes.
Mercuri E; Dubowitz L; Berardinelli A; Pennock J; Jongmans M; Henderson S; Muntoni F; Sewry C; Philpot J; Dubowitz V
Neuropediatrics; 1995 Jun; 26(3):156-62. PubMed ID: 7477754
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. [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]
7. 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]
8. New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.
Yanagisawa A; Bouchet C; Van den Bergh PY; Cuisset JM; Viollet L; Leturcq F; Romero NB; Quijano-Roy S; Fardeau M; Seta N; Guicheney P
Neurology; 2007 Sep; 69(12):1254-60. PubMed ID: 17634419
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Merosin-deficient congenital muscular dystrophy in Korea.
Chae JH; Lee JS; Hwang H; Kim KJ; Hwang YS; Park JD; Cheon JE; Kim IO; Choe GY; Park SH
Brain Dev; 2009 May; 31(5):341-6. PubMed ID: 18723302
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Changes in cerebral white matter in a case of congenital muscular dystrophy (non-Fukuyama type).
Tanaka J; Mimaki T; Okada S; Fujimura H
Neuropediatrics; 1990 Nov; 21(4):183-6. PubMed ID: 2290477
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.
Moore SA; Saito F; Chen J; Michele DE; Henry MD; Messing A; Cohn RD; Ross-Barta SE; Westra S; Williamson RA; Hoshi T; Campbell KP
Nature; 2002 Jul; 418(6896):422-5. PubMed ID: 12140559
[TBL] [Abstract][Full Text] [Related]
16. Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?
Seidahmed MZ; Sunada Y; Ozo CO; Hamid F; Campbell KP; Salih MA
Neuropediatrics; 1996 Dec; 27(6):305-10. PubMed ID: 9050048
[TBL] [Abstract][Full Text] [Related]
17. Two cases of Walker-Warburg syndrome complicated by hydrocephalus.
Preuss M; Heckmann M; Stein M; Nestler U
Pediatr Neurosurg; 2010; 46(1):34-8. PubMed ID: 20516736
[TBL] [Abstract][Full Text] [Related]
18. Congenital muscular dystrophy.
Huang FL; Mak SC; Chi CS
Zhonghua Yi Xue Za Zhi (Taipei); 2000 Feb; 63(2):165-9. PubMed ID: 10677931
[TBL] [Abstract][Full Text] [Related]
19. Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophy.
Di Rocco M; Leveratto L; Cama A; Bado M; Tortori Donati P; Andreussi L; Borrone C
Genet Couns; 1993; 4(4):295-8. PubMed ID: 8110418
[TBL] [Abstract][Full Text] [Related]
20. Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study.
Flanigan KM; Kerr L; Bromberg MB; Leonard C; Tsuruda J; Zhang P; Gonzalez-Gomez I; Cohn R; Campbell KP; Leppert M
Ann Neurol; 2000 Feb; 47(2):152-61. PubMed ID: 10665485
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
