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Daniel P Gale

Showing results (71-80 of 115) with videos related to

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Kidney International|July 3, 2014
The 2014International Workshop on Alport SyndromeJeffrey H Miner, Colin Baigent, Frances Flinter, et al.
The Journal of Clinical Investigation|May 15, 2025
Genetic variants predisposing to increased risk of kidney stone diseaseCatherine E Lovegrove, Michelle Goldsworthy, Jeremy Haley, et al.
Kidney International Reports|August 7, 2023
Common Risk Variants in <i>AHI1</i> Are Associated With Childhood Steroid Sensitive Nephrotic SyndromeMallory L Downie, Sanjana Gupta, Catalin Voinescu, et al.
Pediatric Nephrology (Berlin, Germany)|November 10, 2022
Shared genetic risk across different presentations of gene test-negative idiopathic nephrotic syndromeMallory L Downie, Sanjana Gupta, Melanie M Y Chan, et al.
Kidney International|June 6, 2024
The role of complement in kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies ConferenceMarina Vivarelli, Jonathan Barratt, Laurence H Beck, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 19, 2026
The Alzheimer's Disease Diagnosis and Plasma Phospho-Tau217 (ADAPT) study stage 1: Validating clinical cut-points against CSF and amyloid PETAshvini Keshavan, Katharine Wiltshire, Ryan Wee, et al.
International Journal of Molecular Sciences|January 21, 2022
Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-OxidationYoussef Khalil, Sara Carrino, Fujun Lin, et al.
Lancet (London, England)|August 31, 2010
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritisDaniel P Gale, Elena Goicoechea de Jorge, H Terence Cook, et al.
Plos Genetics|March 8, 2017
Mutations in mitochondrial DNA causing tubulointerstitial kidney diseaseThomas M Connor, Simon Hoer, Andrew Mallett, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 14, 2024
Diagnosis, management and treatment of the Alport syndrome - 2024 guideline on behalf of ERKNet, ERA and ESPNRoser Torra, Beata Lipska-Ziętkiewicz, Frederic Acke, et al.
Pageof 12

Showing results (71-80 of 115) with videos related to

Sort By:
Pageof 12
Kidney International|July 3, 2014
The 2014International Workshop on Alport SyndromeJeffrey H Miner, Colin Baigent, Frances Flinter, et al.
The Journal of Clinical Investigation|May 15, 2025
Genetic variants predisposing to increased risk of kidney stone diseaseCatherine E Lovegrove, Michelle Goldsworthy, Jeremy Haley, et al.
Kidney International Reports|August 7, 2023
Common Risk Variants in <i>AHI1</i> Are Associated With Childhood Steroid Sensitive Nephrotic SyndromeMallory L Downie, Sanjana Gupta, Catalin Voinescu, et al.
Pediatric Nephrology (Berlin, Germany)|November 10, 2022
Shared genetic risk across different presentations of gene test-negative idiopathic nephrotic syndromeMallory L Downie, Sanjana Gupta, Melanie M Y Chan, et al.
Kidney International|June 6, 2024
The role of complement in kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies ConferenceMarina Vivarelli, Jonathan Barratt, Laurence H Beck, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 19, 2026
The Alzheimer's Disease Diagnosis and Plasma Phospho-Tau217 (ADAPT) study stage 1: Validating clinical cut-points against CSF and amyloid PETAshvini Keshavan, Katharine Wiltshire, Ryan Wee, et al.
International Journal of Molecular Sciences|January 21, 2022
Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-OxidationYoussef Khalil, Sara Carrino, Fujun Lin, et al.
Lancet (London, England)|August 31, 2010
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritisDaniel P Gale, Elena Goicoechea de Jorge, H Terence Cook, et al.
Plos Genetics|March 8, 2017
Mutations in mitochondrial DNA causing tubulointerstitial kidney diseaseThomas M Connor, Simon Hoer, Andrew Mallett, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 14, 2024
Diagnosis, management and treatment of the Alport syndrome - 2024 guideline on behalf of ERKNet, ERA and ESPNRoser Torra, Beata Lipska-Ziętkiewicz, Frederic Acke, et al.
Pageof 12