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Volumn 40, Issue 5, 2003, Pages 418-423

Fowler-like syndrome with extreme oligohydramnios, growth restriction and without muscular hypoplasia

Author keywords

Fowler Syndrome; Oligohydramnios

Indexed keywords

IMMUNOGLOBULIN G; IMMUNOGLOBULIN M;

EID: 0037911380     PISSN: 00196061     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (7)
  • 1
    • 0015325063 scopus 로고
    • Congenital hydrocephalus-hydrencephaly in five siblings, with autopsy studies; a new disease
    • Fowler M, Dow R, White TA, Greer CH. Congenital hydrocephalus-hydrencephaly in five siblings, with autopsy studies; a new disease. Dev Med Child Neurol 1972; 14: 173-188.
    • (1972) Dev Med Child Neurol , vol.14 , pp. 173-188
    • Fowler, M.1    Dow, R.2    White, T.A.3    Greer, C.H.4
  • 2
    • 0020534980 scopus 로고
    • Proliferative vasculopathy and an hydrencephalic-hydrocephalic syndrome: A neuropathological study of two siblings
    • Harper C, Hockey A. Proliferative vasculopathy and an hydrencephalic-hydrocephalic syndrome: a neuropathological study of two siblings. Dev Med Child Neurol: 1983; 25: 232-244.
    • (1983) Dev Med Child Neurol , vol.25 , pp. 232-244
    • Harper, C.1    Hockey, A.2
  • 3
    • 0024363871 scopus 로고
    • Fetal neuropathology of proliferative vasculopathy and hydrencephaly-hydrocephaly with multiple limb pterigia
    • Norman MG, McGillivray B. Fetal neuropathology of proliferative vasculopathy and hydrencephaly-hydrocephaly with multiple limb pterigia. Pediatr Neurosci 1988; 14: 301-306.
    • (1988) Pediatr Neurosci , vol.14 , pp. 301-306
    • Norman, M.G.1    McGillivray, B.2
  • 4
    • 0028960804 scopus 로고
    • The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly; immunocytochemical and ultrastructural evidence for endothelial proliferation
    • Harding BN, Ramani P, Thurley P. The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly; immunocytochemical and ultrastructural evidence for endothelial proliferation. Neuropathol App Neurobiol 1995; 21: 61-67.
    • (1995) Neuropathol App Neurobiol , vol.21 , pp. 61-67
    • Harding, B.N.1    Ramani, P.2    Thurley, P.3
  • 5
    • 0035218325 scopus 로고    scopus 로고
    • Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: A possible relation with mitochondrial dysfunction
    • Castro-Gago M, Pintos-Martinez E, Forteza-Vila J, Iglesias-Diz M, Ucieda-Somoza R, Silva-Villar I, et al. Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: a possible relation with mitochondrial dysfunction. J Child Neurol 2001; 16: 858-862.
    • (2001) J Child Neurol , vol.16 , pp. 858-862
    • Castro-Gago, M.1    Pintos-Martinez, E.2    Forteza-Vila, J.3    Iglesias-Diz, M.4    Ucieda-Somoza, R.5    Silva-Villar, I.6
  • 6
    • 0037082978 scopus 로고    scopus 로고
    • Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: Further evidence for autosomal recessive inheritance of hydranencephaly, Fowler type
    • Witters I, Moerman P, devriendt K, Braet P, Van Schoubroeck D, Van Assche FA, et al. Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: Further evidence for autosomal recessive inheritance of hydranencephaly, Fowler type. Am J Med Genet 2002; 108: 41-44.
    • (2002) Am J Med Genet , vol.108 , pp. 41-44
    • Witters, I.1    Moerman, P.2    Devriendt, K.3    Braet, P.4    Van Schoubroeck, D.5    Van Assche, F.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.