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Volumn 47, Issue 5, 2012, Pages 375-378

Vici syndrome associated with sensorineural hearing loss and laryngomalacia

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTATE AMINOTRANSFERASE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CEFTRIAXONE; CREATINE KINASE; MUSCLE ENZYME;

EID: 84867311766     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2012.07.007     Document Type: Article
Times cited : (26)

References (10)
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    • 33846004224 scopus 로고    scopus 로고
    • Siblng cases of Vici syndrome: Sleep abnormalities and complications of renal tubularacidosis
    • R. Miyata, M. Hayashi, and H. Sato Siblng cases of Vici syndrome: Sleep abnormalities and complications of renal tubularacidosis Am J Med Genet 143 2007 189 194
    • (2007) Am J Med Genet , vol.143 , pp. 189-194
    • Miyata, R.1    Hayashi, M.2    Sato, H.3
  • 2
    • 0037089941 scopus 로고    scopus 로고
    • Sister and brother with Vici syndrome: Agenesis of the corpus callosum, albinism, and recurrent infections
    • T. Chiyonobu, T. Yoshihara, and Y. Fukushima Sister and brother with Vici syndrome: Agenesis of the corpus callosum, albinism, and recurrent infections Am J Med Genet 109 2002 61 66
    • (2002) Am J Med Genet , vol.109 , pp. 61-66
    • Chiyonobu, T.1    Yoshihara, T.2    Fukushima, Y.3
  • 3
    • 0033609847 scopus 로고    scopus 로고
    • Albinism and agenesis of the corpus callosum with profound developmental delay: Vici syndrome, evidence for autosomal recessive inheritance
    • M. Del Campo, B.D. Hall, and A. Aeby Albinism and agenesis of the corpus callosum with profound developmental delay: Vici syndrome, evidence for autosomal recessive inheritance Am J Med Genet 85 1999 479 485
    • (1999) Am J Med Genet , vol.85 , pp. 479-485
    • Del Campo, M.1    Hall, B.D.2    Aeby, A.3
  • 4
    • 0023845505 scopus 로고
    • Agenesis of the corpus callosum, combined immunodeficiency, bilateral cataract, and hypopigmentation in two brothers
    • C.D. Vici, G. Sabetta, and M. Gambarara Agenesis of the corpus callosum, combined immunodeficiency, bilateral cataract, and hypopigmentation in two brothers Am J Med Genet 29 1988 1 8
    • (1988) Am J Med Genet , vol.29 , pp. 1-8
    • Vici, C.D.1    Sabetta, G.2    Gambarara, M.3
  • 5
    • 84856157292 scopus 로고    scopus 로고
    • Immunodeficiency in Vici syndrome: A heterogeneous phenotype
    • A. Finocchi, G. Angelino, and N. Cantarutti Immunodeficiency in Vici syndrome: A heterogeneous phenotype Am J Med Genet [A] 158 2012 434 439
    • (2012) Am J Med Genet [A] , vol.158 , pp. 434-439
    • Finocchi, A.1    Angelino, G.2    Cantarutti, N.3
  • 6
    • 84856173454 scopus 로고    scopus 로고
    • Vici syndrome: A rapidly progressive neurodegenerative disorder with hypopigmentation, immunodeficiency, and myopathic changes on muscle biopsy
    • E. Said, D. Soler, and C. Sewry Vici syndrome: A rapidly progressive neurodegenerative disorder with hypopigmentation, immunodeficiency, and myopathic changes on muscle biopsy Am J Med Genet [A] 158 2012 440 444
    • (2012) Am J Med Genet [A] , vol.158 , pp. 440-444
    • Said, E.1    Soler, D.2    Sewry, C.3
  • 7
    • 77954123367 scopus 로고    scopus 로고
    • Vici syndrome associated with unilateral lung hypoplasia and myopathy
    • M. Al-Owain, A. Al-Hashem, and M. Al-Muhaizea Vici syndrome associated with unilateral lung hypoplasia and myopathy Am J Med Genet [A] 152 2010 1849 1853
    • (2010) Am J Med Genet [A] , vol.152 , pp. 1849-1853
    • Al-Owain, M.1    Al-Hashem, A.2    Al-Muhaizea, M.3
  • 8
    • 77649202003 scopus 로고    scopus 로고
    • Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy
    • V. McClelland, T. Cullup, and I. Bodi Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy Am J Med Genet [A] 152 2010 741 747
    • (2010) Am J Med Genet [A] , vol.152 , pp. 741-747
    • McClelland, V.1    Cullup, T.2    Bodi, I.3
  • 9
    • 0034564663 scopus 로고    scopus 로고
    • Congenital laryngomalacia in children
    • M. Grzegorowski, and B. Pucher Congenital laryngomalacia in children Otolaryngol Pol 54 2000 561 565
    • (2000) Otolaryngol Pol , vol.54 , pp. 561-565
    • Grzegorowski, M.1    Pucher, B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.