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Pornprot Limprasert

Showing results (31-40 of 38) with videos related to

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Genetic Testing and Molecular Biomarkers|May 17, 2014
Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorderSupaporn Yangngam, Oradawan Plong-On, Thanya Sripo, et al.
Cytogenetic and Genome Research|August 30, 2014
A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literatureChariyawan Charalsawadi, Worathai Maisrikhaw, Verayuth Praphanphoj, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 22, 2011
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivityUtcharee Intusoma, Fadell Hayeeduereh, Oradawan Plong-On, et al.
Human Molecular Genetics|September 9, 2006
Beta-synuclein modulates alpha-synuclein neurotoxicity by reducing alpha-synuclein protein expressionYuxin Fan, Pornprot Limprasert, Ian V J Murray, et al.
Archives of Neurology|October 11, 2002
Familial dementia with lewy bodies: a clinical and neuropathological study of 2 familiesDebby W Tsuang, Aaron M Dalan, Charisma J Eugenio, et al.
Scientific Reports|September 23, 2017
Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorderAreerat Hnoonual, Weerin Thammachote, Thipwimol Tim-Aroon, et al.
The HUGO Journal|April 20, 2016
A genome wide pattern of population structure and admixture in peninsular Malaysia MalaysWan Isa Hatin, Ab Rajab Nur-Shafawati, Ali Etemad, et al.
Journal of Geriatric Psychiatry and Neurology|March 19, 2003
Familial dementia with Lewy bodies with an atypical clinical presentationLauren T Bonner, Debby W Tsuang, Monique M Cherrier, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Genetic Testing and Molecular Biomarkers|May 17, 2014
Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorderSupaporn Yangngam, Oradawan Plong-On, Thanya Sripo, et al.
Cytogenetic and Genome Research|August 30, 2014
A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literatureChariyawan Charalsawadi, Worathai Maisrikhaw, Verayuth Praphanphoj, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 22, 2011
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivityUtcharee Intusoma, Fadell Hayeeduereh, Oradawan Plong-On, et al.
Human Molecular Genetics|September 9, 2006
Beta-synuclein modulates alpha-synuclein neurotoxicity by reducing alpha-synuclein protein expressionYuxin Fan, Pornprot Limprasert, Ian V J Murray, et al.
Archives of Neurology|October 11, 2002
Familial dementia with lewy bodies: a clinical and neuropathological study of 2 familiesDebby W Tsuang, Aaron M Dalan, Charisma J Eugenio, et al.
Scientific Reports|September 23, 2017
Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorderAreerat Hnoonual, Weerin Thammachote, Thipwimol Tim-Aroon, et al.
The HUGO Journal|April 20, 2016
A genome wide pattern of population structure and admixture in peninsular Malaysia MalaysWan Isa Hatin, Ab Rajab Nur-Shafawati, Ali Etemad, et al.
Journal of Geriatric Psychiatry and Neurology|March 19, 2003
Familial dementia with Lewy bodies with an atypical clinical presentationLauren T Bonner, Debby W Tsuang, Monique M Cherrier, et al.
Pageof 4