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Journal of Immunology (Baltimore, Md. : 1950)|January 22, 2004
p47phox deficiency impairs NF-kappa B activation and host defense in Pseudomonas pneumoniaRuxana T Sadikot, Heng Zeng, Fiona E Yull, et al.
Blood|May 21, 2026
Biallelic loss-of-function mutations in BPNT1 cause vitamin B12-dependent megaloblastic anemiaYi-Heng Zeng, Yun-Hong Li, Ru-Ying Yuan, et al.
Clinical Genetics|March 21, 2019
Identification of SLC20A2 deletions in patients with primary familial brain calcificationXin-Xin Guo, Hui-Zhen Su, Xiao-Huan Zou, et al.
BMJ Open|January 12, 2022
Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort studyYu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, et al.
Annals of Clinical and Translational Neurology|November 1, 2024
Progressive myoclonic ataxia as an initial symptom of typical type I sialidosis with NEU1 mutationJingjing Lin, Yun-Lu Li, Bo-Li Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2023
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular CharacterizationXiang Lin, Jun-Yi Jiang, Dao-Jun Hong, et al.
Annals of Neurology|June 14, 2022
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal MyopathyYi-Heng Zeng, Kang Yang, Gan-Qin Du, et al.
Journal of Human Genetics|June 12, 2024
Characteristics of tandem repeat inheritance and sympathetic nerve involvement in GAA-FGF14 ataxiaZe-Hong Zheng, Chun-Yan Cao, Bi Cheng, et al.
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