Zobrazeno 1 - 10
of 507
pro vyhledávání: '"Verhoeven, W.m.a."'
Publikováno v:
CLINICAL NEUROPSYCHIATRY, 17(3), 175-180. GIOVANNI FIORITI EDITORE
Neurosyphilis may imitate a wide range of neurological and psychiatric diseases, including autoimmune encephalitis. To avoid further cognitive decline and morbidity, early recognition and adequate treatment are of particular importance in both neuros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::86adfa803537eb2d03420a3fe88371bb
https://hdl.handle.net/1887/3182776
https://hdl.handle.net/1887/3182776
Publikováno v:
In Epilepsy and Behavior 2007 11(2):218-221
Publikováno v:
In European Neuropsychopharmacology January 2006 16(1):71-77
Autor:
van der Heijden, F.M.M.A. *, Tuinier, S., Fekkes, D., Sijben, A.E.S., Kahn, R.S., Verhoeven, W.M.A.
Publikováno v:
In European Neuropsychopharmacology 2004 14(3):259-265
Publikováno v:
Tijdschrift voor Psychiatrie, 59, 7, pp. 433-437
Tijdschrift voor Psychiatrie, 59, 433-437
Tijdschrift voor Psychiatrie, 59, 433-437
Item does not contain fulltext Many of the patients who attend the outpatient mental health clinics already have a long history of psychiatric problems. Their symptoms seem easy to classify, but the misdiagnosis of the patients' underlying problems c
Autor:
Vogels, A., Verhoeven, W.M.A. *, Tuinier, S., DeVriendt, K., Swillen, A., Curfs, L.M.G., Frijns, J.P.
Publikováno v:
In Annales de genetique 2002 45(2):89-95
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
Publikováno v:
In European Psychiatry 2001 16(2):104-108
Publikováno v:
Clinical Neuropsychiatry, 15, 306-310
Clinical Neuropsychiatry, 15, 5, pp. 306-310
Clinical Neuropsychiatry, 15, 5, pp. 306-310
Contains fulltext : 197326.pdf (Publisher’s version ) (Open Access) Objective: One of the most prevalent deletion syndromes is the common 22q11.2 deletion syndrome (22q11.2DS) that has a highly variable somatic and behavioural phenotype with differ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::aa2b544b48903831740e9cd93cf9511d
http://hdl.handle.net/2066/197326
http://hdl.handle.net/2066/197326
Publikováno v:
Clinical Neuropsychiatry, 14, 2, pp. 135-140
Clinical Neuropsychiatry, 14, 135-140
Clinical Neuropsychiatry, 14, 135-140
Contains fulltext : 170486.pdf (Publisher’s version ) (Open Access) Objective: While modern genetic techniques have substantially increased the knowledge regarding causes of intellectual disabilities and related neuropsychiatric disorders, a marked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e4121d1da25442be9ff5302f54bb1363
https://hdl.handle.net/2066/170486
https://hdl.handle.net/2066/170486