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Neurogenetics

Showing results (831-840 of 949) with videos related to

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Neurogenetics|July 2, 2021
Secondary biogenic amine deficiencies: genetic etiology, therapeutic interventions, and clinical effectsClara D van Karnebeek, Ingrid Blydt-Hansen, Allison M Matthews, et al.
Neurogenetics|January 22, 2013
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disordersJ J T van Harssel, S Weckhuysen, M J A van Kempen, et al.
Neurogenetics|February 8, 2013
MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathwaysAlex R Paciorkowski, Ryan N Traylor, Jill A Rosenfeld, et al.
Neurogenetics|March 28, 2013
Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiencyCélia Nogueira, José Barros, Maria José Sá, et al.
Neurogenetics|August 31, 2013
Chromosomal rearrangements in Tourette syndrome: implications for identification of candidate susceptibility genes and review of the literatureBirgitte Bertelsen, Nanette Mol Debes, Lena E Hjermind, et al.
Neurogenetics|September 21, 2013
Homozygous dystroglycan mutation associated with a novel muscle-eye-brain disease-like phenotype with multicystic leucodystrophyTobias Geis, Klaus Marquard, Tanja Rödl, et al.
Neurogenetics|December 11, 2012
Comprehensive cytogenomic profile of the in vitro neuronal model SH-SY5YMohammed Yusuf, Kay Leung, Keith J Morris, et al.
Neurogenetics|April 25, 2012
Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephalyAyse Guven, Aysegul Gunduz, Tarik M Bozoglu, et al.
Neurogenetics|June 5, 2012
A novel binding protein of single-minded 2: the mitotic arrest-deficient protein MAD2BXianfang Meng, Xiujuan Tian, Xiaolan Wang, et al.
Neurogenetics|May 29, 2012
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onsetMaría del Mar O'Callaghan, Sonia Emperador, Ester López-Gallardo, et al.
Pageof 95

Showing results (831-840 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|July 2, 2021
Secondary biogenic amine deficiencies: genetic etiology, therapeutic interventions, and clinical effectsClara D van Karnebeek, Ingrid Blydt-Hansen, Allison M Matthews, et al.
Neurogenetics|January 22, 2013
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disordersJ J T van Harssel, S Weckhuysen, M J A van Kempen, et al.
Neurogenetics|February 8, 2013
MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathwaysAlex R Paciorkowski, Ryan N Traylor, Jill A Rosenfeld, et al.
Neurogenetics|March 28, 2013
Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiencyCélia Nogueira, José Barros, Maria José Sá, et al.
Neurogenetics|August 31, 2013
Chromosomal rearrangements in Tourette syndrome: implications for identification of candidate susceptibility genes and review of the literatureBirgitte Bertelsen, Nanette Mol Debes, Lena E Hjermind, et al.
Neurogenetics|September 21, 2013
Homozygous dystroglycan mutation associated with a novel muscle-eye-brain disease-like phenotype with multicystic leucodystrophyTobias Geis, Klaus Marquard, Tanja Rödl, et al.
Neurogenetics|December 11, 2012
Comprehensive cytogenomic profile of the in vitro neuronal model SH-SY5YMohammed Yusuf, Kay Leung, Keith J Morris, et al.
Neurogenetics|April 25, 2012
Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephalyAyse Guven, Aysegul Gunduz, Tarik M Bozoglu, et al.
Neurogenetics|June 5, 2012
A novel binding protein of single-minded 2: the mitotic arrest-deficient protein MAD2BXianfang Meng, Xiujuan Tian, Xiaolan Wang, et al.
Neurogenetics|May 29, 2012
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onsetMaría del Mar O'Callaghan, Sonia Emperador, Ester López-Gallardo, et al.
Pageof 95