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Volumn 47, Issue 2, 2012, Pages 129-132

Galloway-Mowat syndrome: Neurologic features in two sibling pairs

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN; PHENOBARBITAL; PHENYTOIN; PREDNISONE;

EID: 84863308565     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2012.04.011     Document Type: Article
Times cited : (8)

References (15)
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    • W.H. Galloway, and A.P. Mowat Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs J Med Genet 5 1968 319 321
    • (1968) J Med Genet , vol.5 , pp. 319-321
    • Galloway, W.H.1    Mowat, A.P.2
  • 2
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    • Association of early-onset nephrotic syndrome and microcephaly: Apropos of four cases in two families [in French]
    • J. Gaudelus, G. Leverger, and G. Rault Association of early-onset nephrotic syndrome and microcephaly: Apropos of four cases in two families [in French] Arch Fr Pediatr 41 1984 409 415
    • (1984) Arch Fr Pediatr , vol.41 , pp. 409-415
    • Gaudelus, J.1    Leverger, G.2    Rault, G.3
  • 3
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    • Congenital microcephaly, infantile spasms, psychomotor retardation, and nephrotic syndrome in two sibs
    • R.A.C. Roos, P.D. Maaswinkel-Mooy, and H.H.H. Kanhai Congenital microcephaly, infantile spasms, psychomotor retardation, and nephrotic syndrome in two sibs Eur J Pediatr 146 1987 532 536
    • (1987) Eur J Pediatr , vol.146 , pp. 532-536
    • Roos, R.A.C.1    Maaswinkel-Mooy, P.D.2    Kanhai, H.H.H.3
  • 4
    • 0036370272 scopus 로고    scopus 로고
    • Another autosomal recessive form of focal glomerulosclerosis with neurologic findings
    • H. Nakazato, S. Hattori, and S. Karashima Another autosomal recessive form of focal glomerulosclerosis with neurologic findings Pediatr Nephrol 17 2002 16 19
    • (2002) Pediatr Nephrol , vol.17 , pp. 16-19
    • Nakazato, H.1    Hattori, S.2    Karashima, S.3
  • 6
    • 76549106531 scopus 로고    scopus 로고
    • Galloway-Mowat syndrome: An early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature
    • M. Pezzella, N.S. Yeghiazaryan, and P. Veggiotti Galloway-Mowat syndrome: An early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature Seizure 19 2010 132 135
    • (2010) Seizure , vol.19 , pp. 132-135
    • Pezzella, M.1    Yeghiazaryan, N.S.2    Veggiotti, P.3
  • 8
    • 0027296792 scopus 로고
    • Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy
    • B.G. Cooperstone, A. Friedman, and B.S. Kaplan Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy Am J Med Genet 47 1993 250 254
    • (1993) Am J Med Genet , vol.47 , pp. 250-254
    • Cooperstone, B.G.1    Friedman, A.2    Kaplan, B.S.3
  • 9
    • 61449229729 scopus 로고    scopus 로고
    • Recurrence of Galloway-Mowat syndrome and associated prenatal imaging findings
    • A.L. Horton, J.K. Smith, and R.A. Strauss Recurrence of Galloway-Mowat syndrome and associated prenatal imaging findings Prenat Diagn 29 2009 280 282
    • (2009) Prenat Diagn , vol.29 , pp. 280-282
    • Horton, A.L.1    Smith, J.K.2    Strauss, R.A.3
  • 10
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    • Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome
    • J.O. Steiss, S. Gross, B.A. Neubauer, and A. Hahn Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome Neuropediatrics 36 2005 332 335
    • (2005) Neuropediatrics , vol.36 , pp. 332-335
    • Steiss, J.O.1    Gross, S.2    Neubauer, B.A.3    Hahn, A.4
  • 12
    • 0020554785 scopus 로고
    • Pachygyria and congenital nephrosis: Disorder of migration and neuronal orientation
    • O. Robain, and T. Deonna Pachygyria and congenital nephrosis: Disorder of migration and neuronal orientation Acta Neuropathol (Berl) 60 1983 137 141
    • (1983) Acta Neuropathol (Berl) , vol.60 , pp. 137-141
    • Robain, O.1    Deonna, T.2
  • 13
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    • Nephrotic syndrome, microcephaly, and developmental delay: Three separate syndromes
    • K.E.C. Meyers, P. Kaplan, and B.S. Kaplan Nephrotic syndrome, microcephaly, and developmental delay: Three separate syndromes Am J Med Genet 82 1999 257 260
    • (1999) Am J Med Genet , vol.82 , pp. 257-260
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  • 15
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    • Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome
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    • Dietrich, A.1    Matejas, V.2    Bitzan, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.