Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yousra Benmakhlouf"'
Autor:
Yousra Benmakhlouf, Renaud Touraine, Ines Harzallah, Zeineb Zian, Kaoutar Ben Makhlouf, Amina Barakat, Naima Ghailani Nourouti, Mohcine Bennani Mechita
Publikováno v:
BMC Research Notes, Vol 14, Iss 1, Pp 1-5 (2021)
Abstract Objective Intellectual Disability (ID) represents a neuropsychiatric disorder, which its etiopathogenesis remains insufficiently understood. Mutations in the Aristaless Related Homeobox gene (ARX) have been identified to cause syndromic and
Externí odkaz:
https://doaj.org/article/0ca085e180954c6082b8abcd2187fb98
Autor:
Naima Ghailani Nourouti, Zeineb Zian, Mohcine Bennani Mechita, Amina Barakat, Yousra Benmakhlouf
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 21:569-576
Intellectual disability (ID), previously called mental retardation, is the most common neurodevelopmental disorder characterized by life-long intellectual and adaptive functioning impairments that have an impact on individuals, families, and society.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d166a177846dc1f9d10d7f31d2e08a6
https://doi.org/10.2174/1871530320666200628024944
https://doi.org/10.2174/1871530320666200628024944
Autor:
Yousra, Benmakhlouf, Zeineb, Zian, Kaoutar, Ben Makhlouf, Naima, Ghailani Nourouti, Amina, Barakat, Mohcine, Bennani Mechita
Publikováno v:
Innov Clin Neurosci
Objective: Intellectual disability (ID) is a heterogeneous group of disorders characterized by a congenital limitation in intellectual functioning and adaptive behaviour. Our present work aimed to describe the demographic and clinical characteristics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c08c68f284260740e54f7d23e15379de
https://pubmed.ncbi.nlm.nih.gov/33898095
https://pubmed.ncbi.nlm.nih.gov/33898095
Autor:
Zeineb Zian, Renaud Touraine, Naima Ghailani Nourouti, Amina Barakat, Kaoutar Ben Makhlouf, Ines Harzallah, Mohcine Bennani Mechita, Yousra Benmakhlouf
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 14, Iss 1, Pp 1-5 (2021)
BMC Research Notes, Vol 14, Iss 1, Pp 1-5 (2021)
Objective Intellectual Disability (ID) represents a neuropsychiatric disorder, which its etiopathogenesis remains insufficiently understood. Mutations in the Aristaless Related Homeobox gene (ARX) have been identified to cause syndromic and nonsyndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b1dac1126edc36d5492d99e0485816
https://pubmed.ncbi.nlm.nih.gov/33757564
https://pubmed.ncbi.nlm.nih.gov/33757564
Autor:
Ines Harzallah, Renaud Touraine, Yousra Benmakhlouf, Mohcine Bennani Mechita, Amina Barakat, Naima Ghailani Nourouti
Publikováno v:
Journal of Systems and Integrative Neuroscience. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d191c25375fbd500f83e77e214663947
https://doi.org/10.15761/jsin.1000204
https://doi.org/10.15761/jsin.1000204