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Journal Abstract Search

119 related items for PubMed ID: 2290477

  • 1. 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
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  • 2. 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 Nov; 4(3):109-14. PubMed ID: 10872105
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  • 3. 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
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  • 4. Congenital muscular dystrophy of non-Fukuyama type with characteristic CT images.
    Yoshioka M, Kuroki S, Mizue H.
    Brain Dev; 1987 Jul; 9(3):316-8. PubMed ID: 3661912
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  • 5. Congenital muscular dystrophy.
    Huang FL, Mak SC, Chi CS.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Feb; 63(2):165-9. PubMed ID: 10677931
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  • 6. [2 autopsy cases of congenital muscular dystrophy of Fukuyama type--a typical and an atypical cases].
    Koga M, Abe M, Tateishi J, Antoku Y, Iwashita H, Miyoshino S.
    No To Shinkei; 1984 Nov; 36(11):1103-8. PubMed ID: 6525323
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  • 7. A case of Fukuyama-type congenital muscular dystrophy with a very mild mental deficit.
    Hino-Fukuyo N, Haginoya K, Hayashi YK, Nishino I, Murakami T, Nonaka I, Togashi K, Tanaka S, Takayanagi M, Yokoyama H, Sakamoto O, Abe T, Toda T, Iinuma K.
    Neuromuscul Disord; 2006 Apr; 16(4):274-6. PubMed ID: 16545565
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  • 8. Congenital muscular dystrophy with cerebral involvement--report of a case of "occidental type cerebromuscular dystrophy"?
    Topaloglu H, Yalaz K, Kale G, Ergin M.
    Neuropediatrics; 1990 Feb; 21(1):53-4. PubMed ID: 2314559
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  • 10. CNS in congenital muscular dystrophy without mental retardation.
    Pihko H, Louhimo T, Valanne L, Donner M.
    Neuropediatrics; 1992 Jun; 23(3):116-22. PubMed ID: 1641078
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  • 12. 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
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  • 13. Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up.
    Trevisan CP, Martinello F, Ferruzza E, Angelini C.
    Eur Neurol; 1995 Jun; 35(4):230-5. PubMed ID: 7671985
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  • 16. 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
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  • 18. Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?
    Mercuri E, Sewry CA, Brown SC, Brockington M, Jungbluth H, DeVile C, Counsell S, Manzur A, Muntoni F.
    Neuropediatrics; 2000 Aug; 31(4):186-9. PubMed ID: 11071142
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  • 19. Merosin-positive congenital muscular dystrophy: a large inbred family.
    Mahjneh I, Bushby K, Anderson L, Muntoni F, Tolvanen-Mahjneh H, Bashir R, Pizzi A, Brockington M, Marconi G.
    Neuropediatrics; 1999 Feb; 30(1):22-8. PubMed ID: 10222457
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