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Neurogenetics

Showing results (251-260 of 1,080) with videos related to

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Neurogenetics|November 22, 2024
Expansion of phenotypic and genotypic data in autism spectrum disorders due to variants in the CHD8 geneMariia A Parfenenko, Ilya S Dantsev, Sergei V Bochenkov, et al.
Neurogenetics|May 29, 2026
Genetic spectrum of rare neurogenetic and neurometabolic disorders in a clinically heterogeneous cohort: insights from whole-exome sequencingJasodhara Chaudhuri, Dipanwita Sadhukhan, Amrita Karmakar, et al.
Neurogenetics|March 23, 2026
Expanding mutational and phenotypic spectrum of CST3-related leukoencephalopathy: a novel family and literature reviewShaoping Zhong, Yangye Lian, Jingzhen Liang, et al.
Neurogenetics|July 31, 2023
A novel heterozygous ZBTB18 missense mutation in a family with non-syndromic intellectual disabilityNana Li, Hong Kang, Yanna Zou, et al.
Neurogenetics|May 8, 2026
Multicenter experience of Kabuki syndrome: a case series of eight patients including three novel KMT2D variants and a brief reviewFirat Ozcelik, Nilgun Duman, Aslihan Kiraz, et al.
Neurogenetics|June 25, 2026
Correction to: Identification of critical genes and drug repurposing targets in entorhinal cortex of Alzheimer's diseaseArghavan Hosseinpouri, Khadijeh Sadegh, Zeinab Zarei-Behjani, et al.
Neurogenetics|August 5, 2003
Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2U Finckh, K van Hadeln, T Müller-Thomsen, et al.
Neurogenetics|May 9, 2003
Immunoglobulin KM genes in Guillain-Barré syndromeJanardan P Pandey, Christian A Vedeler
Neurogenetics|January 5, 2011
Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1Mariana Ferreira, Alessandra Torraco, Teresa Rizza, et al.
Neurogenetics|December 22, 2010
Hydroxyurea enhances SMN2 gene expression through nitric oxide releaseCheng Xu, Xin Chen, Susanna M Grzeschik, et al.
Pageof 108

Showing results (251-260 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|November 22, 2024
Expansion of phenotypic and genotypic data in autism spectrum disorders due to variants in the CHD8 geneMariia A Parfenenko, Ilya S Dantsev, Sergei V Bochenkov, et al.
Neurogenetics|May 29, 2026
Genetic spectrum of rare neurogenetic and neurometabolic disorders in a clinically heterogeneous cohort: insights from whole-exome sequencingJasodhara Chaudhuri, Dipanwita Sadhukhan, Amrita Karmakar, et al.
Neurogenetics|March 23, 2026
Expanding mutational and phenotypic spectrum of CST3-related leukoencephalopathy: a novel family and literature reviewShaoping Zhong, Yangye Lian, Jingzhen Liang, et al.
Neurogenetics|July 31, 2023
A novel heterozygous ZBTB18 missense mutation in a family with non-syndromic intellectual disabilityNana Li, Hong Kang, Yanna Zou, et al.
Neurogenetics|May 8, 2026
Multicenter experience of Kabuki syndrome: a case series of eight patients including three novel KMT2D variants and a brief reviewFirat Ozcelik, Nilgun Duman, Aslihan Kiraz, et al.
Neurogenetics|June 25, 2026
Correction to: Identification of critical genes and drug repurposing targets in entorhinal cortex of Alzheimer's diseaseArghavan Hosseinpouri, Khadijeh Sadegh, Zeinab Zarei-Behjani, et al.
Neurogenetics|August 5, 2003
Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2U Finckh, K van Hadeln, T Müller-Thomsen, et al.
Neurogenetics|May 9, 2003
Immunoglobulin KM genes in Guillain-Barré syndromeJanardan P Pandey, Christian A Vedeler
Neurogenetics|January 5, 2011
Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1Mariana Ferreira, Alessandra Torraco, Teresa Rizza, et al.
Neurogenetics|December 22, 2010
Hydroxyurea enhances SMN2 gene expression through nitric oxide releaseCheng Xu, Xin Chen, Susanna M Grzeschik, et al.
Pageof 108