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Neurogenetics

Showing results (551-560 of 1,081) with videos related to

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Neurogenetics|November 6, 2023
Lethal variant in the C2A domain may cause severe SYT1-associated neurodevelopmental disorder in the newbornsWendi Huang, Ying Yang, Fengyu Che, et al.
Neurogenetics|March 14, 2026
Targeting ABC transporters in glioma: farnesiferols as potent agents against chemotherapy resistanceHamidreza Jamali, Mohamad Vosough Ghanbari, Fatemeh B Rassouli
Neurogenetics|September 5, 2023
A biallelic loss-of-function variant in TMEM147 causes profound intellectual disability and spasticityTahereh Ghorashi, Hossein Darvish, Somayeh Bakhtiari, et al.
Neurogenetics|August 16, 2023
Clinical and functional study of two de novo variations of CDKL5 geneYang You, Xinyi Men, Wenjuan Wu, et al.
Neurogenetics|October 26, 2023
Two novel cases of biallelic SMPD4 variants with brain structural abnormalitiesShintaro Aoki, Kazuki Watanabe, Mitsuhiro Kato, et al.
Neurogenetics|July 15, 2023
Novel mutations and molecular pathways identified in patients with brain iron accumulation disordersLianghao Si, Zhanjun Wang, Xu-Ying Li, et al.
Neurogenetics|July 19, 2023
Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature reviewZeyu Zhu, Wenzhe Hou, Yuwen Cao, et al.
Neurogenetics|May 28, 2002
Sequence analysis of two nuclear encoded subunits (10 and 51 kDa) of mitochondrial complex I in Parkinson diseaseEva M Grasbon-Frodl, P Mehraein
Neurogenetics|April 17, 2003
Gene expression profiling of Duchenne muscular dystrophy skeletal muscleJudith N Haslett, Despina Sanoudou, Alvin T Kho, et al.
Neurogenetics|November 21, 2001
Linkage and association analysis of chromosome 19q13 in multiple sclerosisM A Pericak-Vance, J B Rimmler, E R Martin, et al.
Pageof 109

Showing results (551-560 of 1,081) with videos related to

Sort By:
Pageof 109
Neurogenetics|November 6, 2023
Lethal variant in the C2A domain may cause severe SYT1-associated neurodevelopmental disorder in the newbornsWendi Huang, Ying Yang, Fengyu Che, et al.
Neurogenetics|March 14, 2026
Targeting ABC transporters in glioma: farnesiferols as potent agents against chemotherapy resistanceHamidreza Jamali, Mohamad Vosough Ghanbari, Fatemeh B Rassouli
Neurogenetics|September 5, 2023
A biallelic loss-of-function variant in TMEM147 causes profound intellectual disability and spasticityTahereh Ghorashi, Hossein Darvish, Somayeh Bakhtiari, et al.
Neurogenetics|August 16, 2023
Clinical and functional study of two de novo variations of CDKL5 geneYang You, Xinyi Men, Wenjuan Wu, et al.
Neurogenetics|October 26, 2023
Two novel cases of biallelic SMPD4 variants with brain structural abnormalitiesShintaro Aoki, Kazuki Watanabe, Mitsuhiro Kato, et al.
Neurogenetics|July 15, 2023
Novel mutations and molecular pathways identified in patients with brain iron accumulation disordersLianghao Si, Zhanjun Wang, Xu-Ying Li, et al.
Neurogenetics|July 19, 2023
Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature reviewZeyu Zhu, Wenzhe Hou, Yuwen Cao, et al.
Neurogenetics|May 28, 2002
Sequence analysis of two nuclear encoded subunits (10 and 51 kDa) of mitochondrial complex I in Parkinson diseaseEva M Grasbon-Frodl, P Mehraein
Neurogenetics|April 17, 2003
Gene expression profiling of Duchenne muscular dystrophy skeletal muscleJudith N Haslett, Despina Sanoudou, Alvin T Kho, et al.
Neurogenetics|November 21, 2001
Linkage and association analysis of chromosome 19q13 in multiple sclerosisM A Pericak-Vance, J B Rimmler, E R Martin, et al.
Pageof 109