메뉴 건너뛰기




Volumn 30, Issue 1, 2004, Pages 61-63

Cohen syndrome with insulin resistance and seizure

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; COHEN SYNDROME; CONNECTIVE TISSUE DISEASE; DIAGNOSTIC PROCEDURE; HUMAN; HYPERINSULINISM; INSULIN RESISTANCE; LABORATORY TEST; MALE; MENTAL DEFICIENCY; MULTIPLE MALFORMATION SYNDROME; MUSCLE HYPOTONIA; PATHOPHYSIOLOGY; PHYSIOLOGY; PRIORITY JOURNAL; SCHOOL CHILD; SEIZURE; SYNDROME;

EID: 0347761256     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(03)00309-6     Document Type: Article
Times cited : (10)

References (15)
  • 1
    • 0015831045 scopus 로고
    • A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular and limb anomalies
    • Cohen M.M. Jr, Hall B.D., Smith D.W., Graham C.B., Lampert K.J. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular and limb anomalies. J Pediatr. 83:1973;280-284.
    • (1973) J Pediatr , vol.83 , pp. 280-284
    • Cohen Jr., M.M.1    Hall, B.D.2    Smith, D.W.3    Graham, C.B.4    Lampert, K.J.5
  • 2
    • 0017882399 scopus 로고
    • Confirmation of the Cohen syndrome
    • Carey J.C., Hall B.D. Confirmation of the Cohen syndrome. J Pediatr. 93:1978;239-244.
    • (1978) J Pediatr , vol.93 , pp. 239-244
    • Carey, J.C.1    Hall, B.D.2
  • 3
    • 0022871182 scopus 로고
    • The Cohen syndrome in Israel
    • Sack L., Friedman E. The Cohen syndrome in Israel. Isr J Med Sci. 22:1986;766-770.
    • (1986) Isr J Med Sci , vol.22 , pp. 766-770
    • Sack, L.1    Friedman, E.2
  • 4
    • 0021360153 scopus 로고
    • Further delineation of the Cohen syndrome: Report on chorioretinal dystrophy, leukopenia and consanguinity
    • Norio R., Raitta C., Lindahl E. Further delineation of the Cohen syndrome Report on chorioretinal dystrophy, leukopenia and consanguinity . Clin Genet. 25:1984;1-14.
    • (1984) Clin Genet , vol.25 , pp. 1-14
    • Norio, R.1    Raitta, C.2    Lindahl, E.3
  • 5
    • 0025183027 scopus 로고
    • The Cohen syndrome: Does mottled retina separate a Finnish and a Jewish type?
    • Kondo L., Nagataki S., Miyagi N. The Cohen syndrome Does mottled retina separate a Finnish and a Jewish type? Am J Med Gen. 7:1990;109-113.
    • (1990) Am J Med Gen , vol.7 , pp. 109-113
    • Kondo, L.1    Nagataki, S.2    Miyagi, N.3
  • 6
    • 0032412407 scopus 로고    scopus 로고
    • MRI of the brain in the Cohen syndrome: A relatively large corpus callosum in patients with mental retardation and microcephaly
    • Kivitie-Kallio S., Autti T., Salonen O., Norio R. MRI of the brain in the Cohen syndrome A relatively large corpus callosum in patients with mental retardation and microcephaly . Neuropediatrics. 29:1998;298-301.
    • (1998) Neuropediatrics , vol.29 , pp. 298-301
    • Kivitie-Kallio, S.1    Autti, T.2    Salonen, O.3    Norio, R.4
  • 7
    • 0034749844 scopus 로고    scopus 로고
    • Fasting glucose insulin ratio: A useful measure of insulin resistance in girls with premature adrenarche
    • Vuguin P., Saenger P., Dimartino-Nardi J. Fasting glucose insulin ratio A useful measure of insulin resistance in girls with premature adrenarche . J Clin Endocrinol Metab. 86:2001;4615-4617.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 4615-4617
    • Vuguin, P.1    Saenger, P.2    Dimartino-Nardi, J.3
  • 9
    • 0027364613 scopus 로고
    • Report of the first international workshop on human chromosome 8 mapping
    • Wood S., Ben Othmane K., Bergerheim U.S.R., et al. Report of the first international workshop on human chromosome 8 mapping. Cytogenetic Cell Genet. 64:1993;134-141.
    • (1993) Cytogenetic Cell Genet , vol.64 , pp. 134-141
    • Wood, S.1    Ben Othmane, K.2    Bergerheim, U.S.R.3
  • 10
    • 0029980251 scopus 로고    scopus 로고
    • Cohen syndrome: The clinical symptoms and stigmata at young age
    • Fryns J.P., Legius E., Devrieudt K., et al. Cohen syndrome The clinical symptoms and stigmata at young age . Clin Genet. 49:1996;237-241.
    • (1996) Clin Genet , vol.49 , pp. 237-241
    • Fryns, J.P.1    Legius, E.2    Devrieudt, K.3
  • 12
    • 0021920419 scopus 로고
    • The clinical features of the Cohen syndrome: Further case reports
    • North C., Patton M.A., Baraitser M.İ., Winter R.M. The clinical features of the Cohen syndrome Further case reports . J Med Genet. 22:1985;131-134.
    • (1985) J Med Genet , vol.22 , pp. 131-134
    • North, C.1    Patton, M.A.2    Baraitser, M.I.3    Winter, R.M.4
  • 13
    • 0019966686 scopus 로고
    • Mental retardation, hypotonia, obesity, ocular, facial, dental and limb abnormalities (Cohen syndrome): Report of three patients
    • GoeckeT, Majewski F, Kauther KD, Sterzel U. Mental retardation, hypotonia, obesity, ocular, facial, dental and limb abnormalities (Cohen syndrome): Report of three patients. Eur J Pediatr 1982;138:338-40.
    • (1982) Eur J Pediatr , vol.138 , pp. 338-340
    • Goecke, T.1    Majewski, F.2    Kauther, K.D.3    Sterzel, U.4
  • 14
    • 0022222065 scopus 로고
    • The syndrome of retinal pigmentary degeneration, microcephally and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): Report of two patients
    • Mendes H.M.N., Paskulin G.A., Vallondro C. The syndrome of retinal pigmentary degeneration, microcephally and severe mental retardation (Mirhosseini-Holmes-Walton syndrome) Report of two patients . Am J Med Genet. 22:1985;223-228.
    • (1985) Am J Med Genet , vol.22 , pp. 223-228
    • Mendes, H.M.N.1    Paskulin, G.A.2    Vallondro, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.