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Volumn 18, Issue 5, 2008, Pages 258-259

Psychiatric comorbidity in a girl with Saethre-Chotzen syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ACROCEPHALOSYNDACTYLY; AUTISM; CASE REPORT; CHROMOSOME 7P; CLINICAL FEATURE; COMORBIDITY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LETTER; OBSESSIVE COMPULSIVE DISORDER; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 55049107701     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/YPG.0b013e328306c989     Document Type: Letter
Times cited : (1)

References (10)
  • 1
    • 0004235298 scopus 로고    scopus 로고
    • American Psychiatric Association , 4th ed. Text revision. Washington, DC: American Psychiatric Association
    • American Psychiatric Association (2000). Diagnostic and statistical manual of mental disorders DSM-IV-TR. 4th ed. Text revision. Washington, DC: American Psychiatric Association.
    • (2000) Diagnostic and statistical manual of mental disorders DSM-IV-TR
  • 2
    • 0034583691 scopus 로고    scopus 로고
    • Saethre-Chotzen syndrome: Review of the literature and report of a case
    • Clauser L, Galie M, Hassanipour A, Calabrese O (2000). Saethre-Chotzen syndrome: review of the literature and report of a case. J Craniofac Surg 11:480-486.
    • (2000) J Craniofac Surg , vol.11 , pp. 480-486
    • Clauser, L.1    Galie, M.2    Hassanipour, A.3    Calabrese, O.4
  • 4
    • 33748076432 scopus 로고    scopus 로고
    • Attention-deficit hyperactivity disorder (ADHD) comorbidity: A case for 'pure' Tourette syndrome?
    • Denckla MB (2006). Attention-deficit hyperactivity disorder (ADHD) comorbidity: a case for 'pure' Tourette syndrome? J Child Neurol 21:701-703.
    • (2006) J Child Neurol , vol.21 , pp. 701-703
    • Denckla, M.B.1
  • 6
    • 0032231374 scopus 로고    scopus 로고
    • A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
    • Johnson D, Horsley SW, Moloney DM, Oldridge M, Twigg SR, Walsh S, et al. (1998). A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1. Am J Hum Genet 63:1282-1293.
    • (1998) Am J Hum Genet , vol.63 , pp. 1282-1293
    • Johnson, D.1    Horsley, S.W.2    Moloney, D.M.3    Oldridge, M.4    Twigg, S.R.5    Walsh, S.6
  • 7
    • 0029865979 scopus 로고    scopus 로고
    • Case study: Comorbidity among Tourette's syndrome, autistic disorder, and bipolar disorder
    • Kerbeshian J, Burd L (1996). Case study: comorbidity among Tourette's syndrome, autistic disorder, and bipolar disorder. J Am Acad Child Adolesc Psychiatry 35:681-685.
    • (1996) J Am Acad Child Adolesc Psychiatry , vol.35 , pp. 681-685
    • Kerbeshian, J.1    Burd, L.2
  • 8
    • 0028819689 scopus 로고
    • Comorbid Tourette's disorder and bipolar disorder: An etiologic perspective
    • Kerbeshian J, Burd L, Klug MG (1995). Comorbid Tourette's disorder and bipolar disorder: an etiologic perspective. Am J Psychiatry 152:1646-1651.
    • (1995) Am J Psychiatry , vol.152 , pp. 1646-1651
    • Kerbeshian, J.1    Burd, L.2    Klug, M.G.3
  • 9
    • 0034615073 scopus 로고    scopus 로고
    • Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation
    • Kerbeshian J, Severud R, Burd L, Larson L (2000). Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation. Am J Med Genet 96:69-73.
    • (2000) Am J Med Genet , vol.96 , pp. 69-73
    • Kerbeshian, J.1    Severud, R.2    Burd, L.3    Larson, L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.