메뉴 건너뛰기




Volumn 34, Issue 1, 2003, Pages 7-13

Neuropsychological assessment of a group of UK patients with Cohen syndrome

Author keywords

Autism; Cohen syndrome; Maladaptive behaviour; Mental retardation; Neuropsychology

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTISM; AUTOSOMAL RECESSIVE DISORDER; BEHAVIOR DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COHEN SYNDROME; COHORT ANALYSIS; FEMALE; FINLAND; GENETIC HETEROGENEITY; HUMAN; LEARNING DISORDER; MALADJUSTMENT; MALE; MENTAL DEFICIENCY; NEUROPSYCHOLOGICAL TEST; NEUROPSYCHOLOGY; PREVALENCE; PRIORITY JOURNAL; UNITED KINGDOM;

EID: 0346783431     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-38617     Document Type: Article
Times cited : (11)

References (30)
  • 2
    • 0017882399 scopus 로고
    • Confirmation of the Cohen syndrome
    • Carey JC, Hall BD. Confirmation of the Cohen syndrome. J Pediatr 1978; 93: 239-244
    • (1978) J Pediatr , vol.93 , pp. 239-244
    • Carey, J.C.1    Hall, B.D.2
  • 4
    • 0015831045 scopus 로고
    • A new syndrome with hypotonia, obesity, mental deficiency and facial, oral, ocular and limb anomalies
    • Cohen MM Jr, Hall BD, Smith DW, Graham CB, Lampert KJ. A new syndrome with hypotonia, obesity, mental deficiency and facial, oral, ocular and limb anomalies. J Pediatr 1973; 83: 280-284
    • (1973) J Pediatr , vol.83 , pp. 280-284
    • Cohen M.M., Jr.1    Hall, B.D.2    Smith, D.W.3    Graham, C.B.4    Lampert, K.J.5
  • 5
    • 0028021904 scopus 로고
    • The prevalence of autistic disorder among children with learning disability
    • Deb S, Prasad K. B. The prevalence of autistic disorder among children with learning disability. Br J Psychiatry 1994; 165: 395-399
    • (1994) Br J Psychiatry , vol.165 , pp. 395-399
    • Deb, S.1    Prasad, K.B.2
  • 7
    • 0034608284 scopus 로고    scopus 로고
    • Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: Redefining a clinical entity
    • Horn D, Krebsova A, Kunze J, Reis A. Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: redefining a clinical entity. Am J Med Genet 2000; 92: 285-292
    • (2000) Am J Med Genet , vol.92 , pp. 285-292
    • Horn, D.1    Krebsova, A.2    Kunze, J.3    Reis, A.4
  • 8
    • 0034763662 scopus 로고    scopus 로고
    • Autistic features in Cohen syndrome: A preliminary report
    • Howlin P. Autistic features in Cohen syndrome: a preliminary report. Dev Med Child Neurol 2001; 43; 692-696
    • (2001) Dev Med Child Neurol , vol.43 , pp. 692-696
    • Howlin, P.1
  • 10
    • 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 1998; 29: 298-301
    • (1998) Neuropediatrics , vol.29 , pp. 298-301
    • Kivitie-Kallio, S.1    Autti, T.2    Salonen, O.3    Norio, R.4
  • 12
    • 0032836335 scopus 로고    scopus 로고
    • Neurological and psychological findings in patients with Cohen syndrome: A study of 18 patients aged 11 months to 57 years
    • Kivitie-Kallio S, Larsen A, Kajasto K, Norio R. Neurological and psychological findings in patients with Cohen syndrome: A study of 18 patients aged 11 months to 57 years. Neuropediatrics 1999; 30: 181-189.
    • (1999) Neuropediatrics , vol.30 , pp. 181-189
    • Kivitie-Kallio, S.1    Larsen, A.2    Kajasto, K.3    Norio, R.4
  • 13
    • 0033756314 scopus 로고    scopus 로고
    • Opthalmologic findings in Cohen syndrome - A long term follow up
    • Kivitie-Kallio S, Summanen P, Raitta C, Norio R. Opthalmologic findings in Cohen syndrome - A long term follow up. Ophthalmology 2000; 107: 1737-1745
    • (2000) Ophthalmology , vol.107 , pp. 1737-1745
    • Kivitie-Kallio, S.1    Summanen, P.2    Raitta, C.3    Norio, R.4
  • 14
    • 0035425580 scopus 로고    scopus 로고
    • Cohen syndrome: Essential features, natural history, and heterogeneity
    • Kivitie-Kallio S, Norio R. Cohen syndrome: Essential features, natural history, and heterogeneity. Am J Med Gen 2001; 102: 125-135
    • (2001) Am J Med Gen , vol.102 , pp. 125-135
    • Kivitie-Kallio, S.1    Norio, R.2
  • 16
    • 0025183027 scopus 로고
    • The Cohen syndrome: Does a mottled retina separate a Finnish and a Jewish type?
    • Kondo I, Nagataki S, Miyagi N. The Cohen syndrome: Does a mottled retina separate a Finnish and a Jewish type? Am J Med Genet 1990; 37: 109-13
    • (1990) Am J Med Genet , vol.37 , pp. 109-113
    • Kondo, I.1    Nagataki, S.2    Miyagi, N.3
  • 17
    • 0029983424 scopus 로고    scopus 로고
    • Autistic spectrum disorders in children with physical or mental disability or both I: Clinical and epidemiological aspects
    • Nordin V, Gillberg C. Autistic spectrum disorders in children with physical or mental disability or both I: Clinical and epidemiological aspects. Dev Med Child Neurol 1996; 38: 297-313
    • (1996) Dev Med Child Neurol , vol.38 , pp. 297-313
    • Nordin, V.1    Gillberg, C.2
  • 18
    • 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 1984; 25: 1-14
    • (1984) Clin Genet , vol.25 , pp. 1-14
    • Norio, R.1    Raitta, C.2    Lindahl, E.3
  • 19
    • 0021920419 scopus 로고
    • The clinical features of the Cohen syndrome: Further case reports
    • North C, Patton MA, Baraitser M, Winter R. The clinical features of the Cohen syndrome: further case reports. J Med Genet 1985; 22: 131-134
    • (1985) J Med Genet , vol.22 , pp. 131-134
    • North, C.1    Patton, M.A.2    Baraitser, M.3    Winter, R.4
  • 21
    • 0032513581 scopus 로고    scopus 로고
    • Cohen syndrome with high urinary excretion of hyaluronic acid
    • Okamoto N, Hatsukawa Y, Arai H, Goto M. Cohen syndrome with high urinary excretion of hyaluronic acid. Am J Med Genet 1998; 76: 387-388
    • (1998) Am J Med Genet , vol.76 , pp. 387-388
    • Okamoto, N.1    Hatsukawa, Y.2    Arai, H.3    Goto, M.4
  • 22
    • 0028085160 scopus 로고
    • Mild growth retardation and developmental delay, microcephaly, and a distinctive facial appearance
    • Partington M, Anderson D. Mild growth retardation and developmental delay, microcephaly, and a distinctive facial appearance. Am J Med Genet 1994; 49: 247-250
    • (1994) Am J Med Genet , vol.49 , pp. 247-250
    • Partington, M.1    Anderson, D.2
  • 23
    • 0022871182 scopus 로고
    • The Cohen syndrome in Israel
    • Sack J, Friedman E. The Cohen syndrome in Israel. Israel J Med Sci 1986; 22: 766-770
    • (1986) Israel J Med Sci , vol.22 , pp. 766-770
    • Sack, J.1    Friedman, E.2
  • 25
    • 0026044859 scopus 로고
    • Tapetoretinal degeneration in brothers with apparent Cohen syndrome: Nosology with Mirhosseini-Holmes-Walton syndrome
    • Steinlein O, Tariverdien G, Boll HU, Vogel F. Tapetoretinal degeneration in brothers with apparent Cohen syndrome: Nosology with Mirhosseini-Holmes-Walton syndrome. Am J Med Genet 1991; 41: 196-200
    • (1991) Am J Med Genet , vol.41 , pp. 196-200
    • Steinlein, O.1    Tariverdien, G.2    Boll, H.U.3    Vogel, F.4
  • 30
    • 0023222297 scopus 로고
    • Intrafamilial variation in Cohen syndrome
    • Young ID, Moore JR. Intrafamilial variation in Cohen syndrome. J Med Genet 1987; 24: 488-492
    • (1987) J Med Genet , vol.24 , pp. 488-492
    • Young, I.D.1    Moore, J.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.