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Annals of Clinical Biochemistry|October 6, 2001
Diagnosis and clinical biochemistry of inherited tubulopathiesJ A Sayer, S H Pearce
International Journal of Molecular Sciences|January 16, 2020
Nephrocalcinosis: A Review of Monogenic Causes and Insights They Provide into This Heterogeneous ConditionFay J Dickson, John A Sayer
Journal of Cell Science|October 27, 2025
Tackling ciliary specialization to understand phenotypic variability in human primary ciliopathiesRuxandra Bachmann-Gagescu, John A Sayer
Current Opinion in Genetics & Development|August 17, 2019
Renal ciliopathiesLaura A Devlin, John A Sayer
Clinical Endocrinology|October 4, 2019
The challenges of diagnosis and management of Gitelman syndromeStephanie Urwin, Jamie Willows, John A Sayer
Kidney & Blood Pressure Research|May 8, 2008
Urinary concentration defects and mechanisms underlying nephronophthisisRajesh Krishnan, Lorraine Eley, John A Sayer
The Journal of Head Trauma Rehabilitation|November 19, 2011
Evaluation of the Veterans Health Administration traumatic brain injury screening program in the upper MidwestNina A Sayer, Dave Nelson, Sean Nugent
Journal of Rare Diseases (Berlin, Germany)|March 3, 2025
GLP-1 receptor agonists-another promising therapy for Alport syndrome?Jan Boeckhaus, Holly Mabillard, John A Sayer
Journal of Rare Diseases (Berlin, Germany)|December 26, 2022
UMOD and you! Explaining a rare disease diagnosisHolly Mabillard, Eric Olinger, John A Sayer
Kidney360|July 2, 2026
Anti-Glomerular Basement Membrane Nephritis Post-Renal Transplant in Alport Syndrome PatientsLucy Hong, Holly Mabillard, John A Sayer
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