Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Atypical bipolar disorder"'
Publikováno v:
Genes, Brain and Behavior. 15(4):395-404
Phelan-McDermid syndrome presents with specific deficits in neurocognition, cerebellar regulatory functioning and enhanced vulnerability for the development of atypical bipolar disorder.Phelan-McDermid syndrome (PMS) or 22q13.3 deletion syndrome is c
Autor:
Egger, J.I.M., Zwanenburg, R.J., Ravenswaaij-Arts, C.M.A. van, Kleefstra, T., Verhoeven, W.M.A.
Publikováno v:
Genes, Brain and Behavior, 15, 4, pp. 395-404
Genes, Brain and Behavior, 15(4), 395-404. Wiley-Blackwell
Genes, Brain and Behavior, 15, 395-404
Genes, Brain and Behavior, 15(4), 395-404. Wiley-Blackwell
Genes, Brain and Behavior, 15, 395-404
Phelan-McDermid syndrome presents with specific deficits in neurocognition, cerebellar regulatory functioning and enhanced vulnerability for the development of atypical bipolar disorder. Phelan-McDermid syndrome (PMS) or 22q13.3 deletion syndrome is
Akademický článek
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Publikováno v:
Journal of Clinical Sleep Medicine. 13:923-924
We report the case of a 50-year-old man with disabling recurrent hypersomnia with autonomic instability due to catatonia in the setting of atypical bipolar disorder. Treatment with valproic acid for bipolar disorder resulted in complete resolution of
Publikováno v:
Journal of Intellectual Disability Research. 34:205-210
A case report of a 33-year-old woman wich atypical bipolar disorder, autistic disorder, profound mental retardation and a chromosomal anomaly is presented. This patient is behaviourally similar to a patient reported by Akuffo et al. (1986), who appar
Publikováno v:
American Journal of Medical Genetics. Part A, 161, 158-161
American Journal of Medical Genetics. Part A, 161A, 1, pp. 158-61
American Journal of Medical Genetics Part A, 161A(1), 158-161. Wiley-Liss Inc.
American Journal of Medical Genetics. Part A, 161, 1, pp. 158-161
American Journal of Medical Genetics Part A, 161A(1), 158-161
American Journal of Medical Genetics. Part A, 161A, 158-61
American Journal of Medical Genetics. Part A, 161A, 1, pp. 158-61
American Journal of Medical Genetics Part A, 161A(1), 158-161. Wiley-Liss Inc.
American Journal of Medical Genetics. Part A, 161, 1, pp. 158-161
American Journal of Medical Genetics Part A, 161A(1), 158-161
American Journal of Medical Genetics. Part A, 161A, 158-61
Item does not contain fulltext PhelanMcDermid or 22q13.3 deletion syndrome is characterized by global intellectual disability, childhood hypotonia, severely delayed or absent speech, features of autism spectrum disorder, without any major dysmorphism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3a5bc44c6483557fef7867322041a73
https://hdl.handle.net/1887/102690
https://hdl.handle.net/1887/102690
Publikováno v:
Bipolar Disorders ISBN: 9780521835176
This chapter longitudinally compares patients diagnosed as having acute and transient psychotic disorder (ATPD) from the Halle Study on Brief and Acute Psychotic Disorder (HASBAP) with patients diagnosed as having affective or schizoaffective mixed s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d3d5e2b4a5501133445674700f10e7c
https://doi.org/10.1017/cbo9780511544019.010
https://doi.org/10.1017/cbo9780511544019.010
Akademický článek
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Autor:
Linda L Keeler, Ekkehard Othmer
Publikováno v:
Psychiatric Annals. 17:21-27
Autor:
Atul C. Pande
Publikováno v:
Psychosomatics. 29:333-335