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Journal Abstract Search

191 related items for PubMed ID: 24113355

  • 1. Leigh syndrome with Fukuyama congenital muscular dystrophy: a case report.
    Kondo H, Tanda K, Tabata C, Hayashi K, Kihara M, Kizaki Z, Taniguchi-Ikeda M, Mori M, Murayama K, Ohtake A.
    Brain Dev; 2014 Sep; 36(8):730-3. PubMed ID: 24113355
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  • 5. The gross motor function measure is valid for Fukuyama congenital muscular dystrophy.
    Sato T, Adachi M, Nakamura K, Zushi M, Goto K, Murakami T, Ishiguro K, Shichiji M, Saito K, Ikai T, Osawa M, Kondo I, Nagata S, Ishigaki K.
    Neuromuscul Disord; 2017 Jan; 27(1):45-49. PubMed ID: 27818010
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  • 6. Developmental changes of radiological findings in Fukuyama-type congenital muscular dystrophy.
    Kato Z, Morimoto M, Orii KE, Kato T, Kondo N.
    Pediatr Radiol; 2010 Dec; 40 Suppl 1():S127-9. PubMed ID: 20571791
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  • 7. A Portuguese case of Fukuyama congenital muscular dystrophy caused by a multi-exonic duplication in the fukutin gene.
    Costa C, Oliveira J, Gonçalves A, Santos R, Bronze-da-Rocha E, Rebelo O, Pais RP, Fineza I.
    Neuromuscul Disord; 2013 Jul; 23(7):557-61. PubMed ID: 23582336
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  • 8. MRI findings in Fukuyama congenital muscular dystrophy: a rare case report.
    Jakkani RK, Sureka J, Shyam S, Mani S.
    Acta Neurol Belg; 2012 Dec; 112(4):401-3. PubMed ID: 22553003
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  • 11. Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophy.
    Yamamoto T, Taniguchi-Ikeda M, Awano H, Matsumoto M, Lee T, Harada R, Imanishi T, Hayashi N, Sakai Y, Morioka I, Takeshima Y, Iijima K, Saegusa J, Toda T.
    Brain Dev; 2017 Nov; 39(10):861-868. PubMed ID: 28578814
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  • 12. Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients.
    Yang H, Kobayashi K, Wang S, Jiao H, Xiao J, Toda T, Wu X, Xiong H.
    Brain Dev; 2015 Oct; 37(9):880-6. PubMed ID: 25814170
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