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JMIR Aging|February 4, 2025
Association of Subjective Cognitive Concerns With Performance on Mobile App-Based Cognitive Assessment in Cognitively Normal Older Adults: Observational StudyCaroline O Nester, Alyssa N De Vito, Sarah Prieto, et al.
Bone & Joint Open|April 13, 2025
The Inaugural UK National Hallux Valgus Think Tank : identification of key issues and strategies to improve clinical care for patient benefitThomas L Lewis, Abbas See, Martin Thomas, et al.
Journal of the American Society of Nephrology : JASN|August 3, 2013
Soluble CR1 therapy improves complement regulation in C3 glomerulopathyYuzhou Zhang, Carla M Nester, Danniele G Holanda, et al.
Molecular Immunology|August 5, 2016
Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion geneXue Xiao, Cybele Ghossein, Agustín Tortajada, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 9, 2021
Musculoskeletal Comorbidities and Quality of Life in ENPP1-Deficient Adults and the Response of Enthesopathy to Enzyme Replacement Therapy in Murine ModelsCarlos R Ferreira, Anenya Jai Ansh, Catherine Nester, et al.
Kidney International Reports|February 12, 2024
Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 GlomerulopathyJill J Hauer, Yuzhou Zhang, Renee Goodfellow, et al.
The Journal of Clinical Investigation|August 18, 2010
Epigenetic basis for aberrant upregulation of autoantigen genes in humans with ANCA vasculitisDominic J Ciavatta, Jiajin Yang, Gloria A Preston, et al.
Frontiers in Immunology|January 1, 2021
Factor H Autoantibodies and Complement-Mediated DiseasesYuzhou Zhang, Nicolo Ghiringhelli Borsa, Dingwu Shao, et al.
Molecular Cytogenetics|May 28, 2019
First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patientMaysoon Alsagob, Mustafa A Salih, Muddathir H A Hamad, et al.
Journal of the American Society of Nephrology : JASN|November 1, 2018
Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic SyndromeFengxiao Bu, Yuzhou Zhang, Kai Wang, et al.
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