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Neurogenetics

Showing results (401-410 of 1,080) with videos related to

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Neurogenetics|April 25, 2006
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in TaiwanAlessio Di Fonzo, Yah-Huei Wu-Chou, Chin-Song Lu, et al.
Neurogenetics|March 26, 2004
Towards a transcriptome definition of microglial cellsL B Moran, D C Duke, F E Turkheimer, et al.
Neurogenetics|October 2, 2004
Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotypeSofia A Oliveira, William K Scott, Fengyu Zhang, et al.
Neurogenetics|March 3, 2005
NR2A and NR2B receptor gene variations modify age at onset in Huntington diseaseLarissa Arning, Peter H Kraus, Sandra Valentin, et al.
Neurogenetics|August 9, 2005
X-linked creatine transporter deficiency: clinical description of a patient with a novel SLC6A8 gene mutationMaria C Schiaffino, Carlo Bellini, Laura Costabello, et al.
Neurogenetics|November 7, 2009
Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-ICAmanda J DuBose, Karen A Johnstone, Emily Y Smith, et al.
Neurogenetics|October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosisK Poirier, D Lacombe, B Gilbert-Dussardier, et al.
Neurogenetics|January 25, 2026
Clinical and neuroimaging features in a case of cerebrotendinous xanthomatosis with a CYP27A1 genotype newly identified in morocco: a literature review of African casesAmal Ouskri, Hajar Ihlal, Oumayma Lahjouji, et al.
Neurogenetics|February 14, 2026
A novel homozygous in-frame deletion variant in TPRKB causing Galloway-Mowat syndrome 5Namanpreet Kaur, Khushbu Shirsat, Vivekananda Bhat, et al.
Neurogenetics|February 12, 2026
Probable cerebral amyloid angiopathy - related inflammation in a 32-year-old woman with down syndromeThales Pardini Fagundes, Gustavo Maximiano Alves, Mateus Gustavo Favaro, et al.
Pageof 108

Showing results (401-410 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|April 25, 2006
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in TaiwanAlessio Di Fonzo, Yah-Huei Wu-Chou, Chin-Song Lu, et al.
Neurogenetics|March 26, 2004
Towards a transcriptome definition of microglial cellsL B Moran, D C Duke, F E Turkheimer, et al.
Neurogenetics|October 2, 2004
Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotypeSofia A Oliveira, William K Scott, Fengyu Zhang, et al.
Neurogenetics|March 3, 2005
NR2A and NR2B receptor gene variations modify age at onset in Huntington diseaseLarissa Arning, Peter H Kraus, Sandra Valentin, et al.
Neurogenetics|August 9, 2005
X-linked creatine transporter deficiency: clinical description of a patient with a novel SLC6A8 gene mutationMaria C Schiaffino, Carlo Bellini, Laura Costabello, et al.
Neurogenetics|November 7, 2009
Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-ICAmanda J DuBose, Karen A Johnstone, Emily Y Smith, et al.
Neurogenetics|October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosisK Poirier, D Lacombe, B Gilbert-Dussardier, et al.
Neurogenetics|January 25, 2026
Clinical and neuroimaging features in a case of cerebrotendinous xanthomatosis with a CYP27A1 genotype newly identified in morocco: a literature review of African casesAmal Ouskri, Hajar Ihlal, Oumayma Lahjouji, et al.
Neurogenetics|February 14, 2026
A novel homozygous in-frame deletion variant in TPRKB causing Galloway-Mowat syndrome 5Namanpreet Kaur, Khushbu Shirsat, Vivekananda Bhat, et al.
Neurogenetics|February 12, 2026
Probable cerebral amyloid angiopathy - related inflammation in a 32-year-old woman with down syndromeThales Pardini Fagundes, Gustavo Maximiano Alves, Mateus Gustavo Favaro, et al.
Pageof 108