Zobrazeno 1 - 10
of 208
pro vyhledávání: '"Causes of autism"'
Autor:
Tunkiewicz, Olga
Publikováno v:
Edukacja Humanistyczna / Humanistic Education. (1):165-176
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=793579
Publikováno v:
Materials Today: Proceedings. 80:2712-2715
Neurodevelopmental disorder, communication problems, and repetitive/stereotypic behaviour are all characteristics of autism, a severe developmental disorder. Even though the pathophysiological causes of autism are still unclear and contested in many
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8674e60238d4a9acbb68bd3a3995945e
https://doi.org/10.1016/j.matpr.2021.07.017
https://doi.org/10.1016/j.matpr.2021.07.017
Autor:
D.V. Maltsev
Publikováno v:
INTERNATIONAL NEUROLOGICAL JOURNAL. :5-19
Background. The genetic deficiency of folate cycle enzymes is considered today as one of the common causes of autism spectrum disorders in children, but the relationship between the genetic components of failures and clinical phenotype was not charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2608363f1c3f7279e1768c5534d6640
https://doi.org/10.22141/2224-0713.5.99.2018.142958
https://doi.org/10.22141/2224-0713.5.99.2018.142958
Publikováno v:
Sovremennye Issledovaniâ Socialʹnyh Problem, Vol 0, Iss 3, Pp 12-23 (2015)
Данная статья посвящена исследованию аутизма и изучению его с помощью системно-векторной методологии Юрия Бурлана. Системно-векторная
Externí odkaz:
https://doaj.org/article/48f5d40ace2147908c3117a0f77e17e7
Publikováno v:
Global Medical Genetics, Vol 08, Iss 04, Pp 144-148 (2021)
Global Medical Genetics
Global Medical Genetics
It is extremely important to understand the causes of autism spectrum disorder (ASD) which is a neurodevelopmental disease. Treatment and lifelong support of autism are also important to improve the patient's life quality. In this article, several fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c4ffe9f1c4a3fc5cca9a8b62f037d4b
https://doi.org/10.1055/s-0041-1735540
https://doi.org/10.1055/s-0041-1735540
Autor:
Laurent Mottron
Publikováno v:
Autism Research. 14:2213-2220
The evolution of autism diagnosis, from its discovery to its current delineation using standardized instruments, has been paralleled by a steady increase in its prevalence and heterogeneity. In clinical settings, the diagnosis of autism is now too va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6b57c19cfc8d09c29e954450901ea50
https://doi.org/10.1002/aur.2494
https://doi.org/10.1002/aur.2494
Autor:
Borzęcka, Anna
Publikováno v:
Konteksty Pedagogiczne / Pedagogical Context. 1(1):69-77
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=814281
Autor:
Sarah S. Mire, Eric Fombonne, Rachel M. Cunningham, Robin P. Goin-Kochel, Julie A. Boom, Leila C. Sahni, Charles G. Minard
Publikováno v:
Vaccine. 38:6327-6333
Vaccine hesitancy may be more common among parents of children with autism spectrum disorder (ASD). We examined factors associated with ASD-specific vaccine hesitancy among caregivers of children with ASD who participated in the SPARK study (Simons F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25b7c40a1f8b364a4e3be05ee20efb29
https://doi.org/10.1016/j.vaccine.2020.07.034
https://doi.org/10.1016/j.vaccine.2020.07.034
Autor:
Declan Murphy, Melissa Gilbert, Josephine Barbaro, Lauren Lawson, Darren Hedley, Kathy Leadbitter
Publikováno v:
Autism Research
David G. Amaral1 and Petrus J. de Vries2 1Department of Psychiatry and Behavioral Sciences, The MIND Institute, UC Davis, Sacramento, California, USA 2Centre for Autism Research in Africa, Division of Child and Adolescent Psychiatry, University of Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82cc1b9fffaf2955dcb66cfa075e631d
http://europepmc.org/articles/PMC7361219
http://europepmc.org/articles/PMC7361219
Publikováno v:
2021 2nd International Conference on Smart Electronics and Communication (ICOSEC).
Helsmoortel Van der Aa syndrome also known as ADNP syndrome is a neurological disorder which is caused by genetic changes in the ADNP gene. These genetic mutations occur impulsively in most patients, showing that there has been no family history of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::733f58bb8f3fb5d7f2797b30ee26ff3e
https://doi.org/10.1109/icosec51865.2021.9591933
https://doi.org/10.1109/icosec51865.2021.9591933