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Plant Disease
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February 17, 2019
Phenotypic and Genetic Analysis of Epiphytic Pseudomonas syringae Populations from Sweet Cherry in Michigan
Lisa J Renick, Andrea G Cogal, George W Sundin
Clinical Nephrology. Case Studies
|
May 13, 2021
Bariatric surgery in a patient with cystinuria
Melissa R Nemati, Peter C Harris, Andrea G Cogal, et al.
Clinical Kidney Journal
|
August 28, 2025
Global genetic prevalence estimates of primary hyperoxaluria are greater than previously reported
Giorgia Mandrile, Gill Rumsby, Veronica Sciannameo, et al.
Kidney International Reports
|
June 11, 2020
Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) <i>AGXT</i> Gene Mutation
Prince Singh, Fouad T Chebib, Andrea G Cogal, et al.
Journal of Inherited Metabolic Disease
|
June 11, 2025
A Minor Haplotype Variant Determines the Pathogenicity of the p.Ile279Thr Substitution in the Primary Hyperoxaluria Type 1 Gene, AGXT
Luana Ruta, Andrea G Cogal, Gioena Pampalone, et al.
Kidney International Reports
|
June 7, 2023
The Site and Type of
Muhammad G Arnous, Jennifer Arroyo, Andrea G Cogal, et al.
BMC Research Notes
|
November 1, 2017
The first Sri Lankan family with Dent disease-1 due to a pathogenic variant in the CLCN5 gene: a case report
Randula Ranawaka, Nirmala Dushyanthi Sirisena, Kavinda Chandimal Dayasiri, et al.
Physiological Reports
|
April 28, 2016
Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patients
Xiaojing Tang, Matthew R Brown, Andrea G Cogal, et al.
Journal of the American Society of Nephrology : JASN
|
February 4, 2015
Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria
Katharina Hopp, Andrea G Cogal, Eric J Bergstralh, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
October 28, 2008
Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis
Carla G Monico, Adam Weinstein, Zhirong Jiang, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Plant Disease
|
February 17, 2019
Phenotypic and Genetic Analysis of Epiphytic Pseudomonas syringae Populations from Sweet Cherry in Michigan
Lisa J Renick, Andrea G Cogal, George W Sundin
Clinical Nephrology. Case Studies
|
May 13, 2021
Bariatric surgery in a patient with cystinuria
Melissa R Nemati, Peter C Harris, Andrea G Cogal, et al.
Clinical Kidney Journal
|
August 28, 2025
Global genetic prevalence estimates of primary hyperoxaluria are greater than previously reported
Giorgia Mandrile, Gill Rumsby, Veronica Sciannameo, et al.
Kidney International Reports
|
June 11, 2020
Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) <i>AGXT</i> Gene Mutation
Prince Singh, Fouad T Chebib, Andrea G Cogal, et al.
Journal of Inherited Metabolic Disease
|
June 11, 2025
A Minor Haplotype Variant Determines the Pathogenicity of the p.Ile279Thr Substitution in the Primary Hyperoxaluria Type 1 Gene, AGXT
Luana Ruta, Andrea G Cogal, Gioena Pampalone, et al.
Kidney International Reports
|
June 7, 2023
The Site and Type of
Muhammad G Arnous, Jennifer Arroyo, Andrea G Cogal, et al.
BMC Research Notes
|
November 1, 2017
The first Sri Lankan family with Dent disease-1 due to a pathogenic variant in the CLCN5 gene: a case report
Randula Ranawaka, Nirmala Dushyanthi Sirisena, Kavinda Chandimal Dayasiri, et al.
Physiological Reports
|
April 28, 2016
Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patients
Xiaojing Tang, Matthew R Brown, Andrea G Cogal, et al.
Journal of the American Society of Nephrology : JASN
|
February 4, 2015
Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria
Katharina Hopp, Andrea G Cogal, Eric J Bergstralh, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
October 28, 2008
Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis
Carla G Monico, Adam Weinstein, Zhirong Jiang, et al.
Page
of 2