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Journal Abstract Search

153 related items for PubMed ID: 2314559

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Congenital muscular dystrophy of a non-Fukuyama type with white matter hyperlucency on CT scan.
    Kao KP, Lin KP.
    Brain Dev; 1992 Nov; 14(6):420-2. PubMed ID: 1492657
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  • 4. Congenital muscular dystrophy (non-Fukuyama type): a case report.
    Ju TH, Kao KP, Kwan SY, Chen CC, Chi CS, Lee YC.
    Zhonghua Yi Xue Za Zhi (Taipei); 1995 Apr; 55(4):331-4. PubMed ID: 7796362
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  • 5. 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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  • 6. Analysis of "pure" congenital muscular dystrophies in thirty-eight cases. How different is the classical type 1 from the occidental type cerebromuscular dystrophy?
    Topaloğlu H, Kale G, Yalnizoğlu D, Taşdemir AH, Karaduman A, Topçu M, Kotiloğlu E.
    Neuropediatrics; 1994 Apr; 25(2):94-100. PubMed ID: 8072682
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  • 8. Congenital muscular dystrophy of non-Fukuyama type with characteristic CT images.
    Yoshioka M, Kuroki S, Mizue H.
    Brain Dev; 1987 Apr; 9(3):316-8. PubMed ID: 3661912
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  • 9. [Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder].
    Castro-Gago M, Novo-Rodríguez MI, Pintos-Martínez E, Alonso-Martín A, Morales-Redondo R, Eirís-Puñal J.
    Rev Neurol; 1998 Sep; 27(157):459-62. PubMed ID: 9774819
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  • 10. Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsies.
    Leyten QH, ter Laak HJ, Gabreëls FJ, Renier WO, Renkawek K, Sengers RC.
    Acta Neuropathol; 1993 Sep; 86(4):386-92. PubMed ID: 8256590
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  • 12. Congenital muscular dystrophy with leukoencephalopathy.
    Streib EW, Lucking CH.
    Eur Neurol; 1989 Sep; 29(4):211-5. PubMed ID: 2759146
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  • 14. 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 Sep; 18(1):53-8. PubMed ID: 8907344
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  • 15. 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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  • 16. Central nervous system involvement in progressive muscular dystrophy.
    Yoshioka M, Okuno T, Honda Y, Nakano Y.
    Arch Dis Child; 1980 Aug; 55(8):589-94. PubMed ID: 7436514
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  • 17. 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 Aug; 4(3):109-14. PubMed ID: 10872105
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  • 18. Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie Infantile.
    Echenne B, Arthuis M, Billard C, Campos-Castello J, Castel Y, Dulac O, Fontan D, Gauthier A, Kulakowski S, De Meuron G.
    J Neurol Sci; 1986 Aug; 75(1):7-22. PubMed ID: 3091775
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  • 20. [Cranial X-ray CT and MRI in congenital muscular dystrophy].
    Horikawa H, Konishi T, Konagaya M, Mano Y, Takayanagi T.
    Rinsho Shinkeigaku; 1988 Jan; 28(1):102-6. PubMed ID: 3383509
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