Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Pervasive development disorder"'
Autor:
Alshaimaa Alzahrani, Maha Alshalan, Mohammed Alfurayh, Abdulaziz Bin Akrish, Najlaa A. Alsubeeh, Fuad Al Mutairi
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundCalcium ions are involved in several human cellular processes; nevertheless, the relationship between calcium channelopathies (CCs) and autism spectrum disorder (ASD) or intellectual disability (ID) has been previously investigated. We deli
Externí odkaz:
https://doaj.org/article/7031d07d400a4fdc9017f3283953b37c
Autor:
Shimrit, Ochana
Publikováno v:
EcoSoEn. 2(1-2):171-179
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=830663
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2019)
Mutation of RPS6KA3 can induce Coffin–Lowry syndrome, an X-linked syndrome. The case here reported manifests its signature characteristic of short stature, facial dysmorphism, development retardation, hearing defect. The mutation of RPS6KA3 we dete
Externí odkaz:
https://doaj.org/article/239e974e97154f59b69e64cdc19d14cc
Akademický článek
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Publikováno v:
Cuadernos de Neuropsicologia, Vol 4, Iss 2, Pp 162-185 (2010)
Introduction: The last decades have brought great advances in the understanding of child neurodevelopment and knowledge of cognitive processes that occur in the brain from an early age. As a result and thanks to the large number of standardized and s
Externí odkaz:
https://doaj.org/article/31ce9c72e7b44ff0ab3cddd839b73976
Autor:
Marcos T. Mercadante, Elizeu C. Macedo, Patrícia M. Baptista, Cristiane S. Paula, José S. Schwartzman
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 64, Iss 3a, Pp 559-562 (2006)
OBJECTIVE: To verify differences in the visual scanning strategies between pervasive developmental disorders (PDD) and controls when they are observing social and non-social pictures. METHOD: PDD group (PDDG) comprised by 10 non-retarded subjects (ag
Externí odkaz:
https://doaj.org/article/183f32b0e30e493584b507e976e2f5ad
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2019)
Frontiers in Pediatrics
Frontiers in Pediatrics
Mutation of RPS6KA3 can induce Coffin–Lowry syndrome, an X-linked syndrome. The case here reported manifests its signature characteristic of short stature, facial dysmorphism, development retardation, hearing defect. The mutation of RPS6KA3 we dete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42e0299d8f9e94c0bff9b17c7d9a75ea
https://doi.org/10.3389/fped.2018.00430
https://doi.org/10.3389/fped.2018.00430
Akademický článek
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Autor:
Eiji Kirino
Publikováno v:
European Child & Adolescent Psychiatry
Aripiprazole (APZ) has a unique pharmacological profile, as a partial agonist at the dopamine D2 and serotonin 5HT1A receptors and an antagonist at the serotonin 5HT2A receptor; this drug has few side effects (such as extrapyramidal syndrome, hyperpr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab7b37f40596a9edd93a05d466135a2d
https://doi.org/10.1007/s00787-012-0270-0
https://doi.org/10.1007/s00787-012-0270-0
Autor:
J Gordon Millichap
Publikováno v:
Pediatric Neurology Briefs, Vol 9, Iss 6, Pp 42-42 (1995)
The interpretation of the literature on lead and child development is presented with open peer commentary from the Neuroepidemiology Unit, Children’s Hospital, Harvard Medical School, Boston, and other centers.
Externí odkaz:
https://doaj.org/article/18098e047b9a41709830e893089a5554