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Kidney International Reports
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March 19, 2026
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport Syndrome
Thomas M Oates, Moumita Barua, Susie Gear, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 5, 2017
X-Linked Glomerulopathy Due to COL4A5 Founder Variant
Moumita Barua, Rohan John, Lorenzo Stella, et al.
Journal of the American Society of Nephrology : JASN
|
August 27, 2024
Association of Genetically Predicted Skipping of COL4A4 Exon 27 with Hematuria and Albuminuria
Frida Lona-Durazo, Kohei Omachi, Damian Fermin, et al.
Diabetes
|
February 23, 2020
Erratum. Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease. Diabetes 2019;68:2235-2246
Priska Stahel, Avital Nahmias, Shawn K Sud, et al.
Diabetes
|
September 12, 2019
Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease
Priska Stahel, Avital Nahmias, Shawn K Sud, et al.
Canadian Journal of Kidney Health and Disease
|
April 22, 2022
The Canadian Glomerulonephritis Registry (CGNR) and Translational Research Initiative: Rationale and Clinical Research Protocol
Ainslie M Hildebrand, Moumita Barua, Sean J Barbour, et al.
Journal of the American Society of Nephrology : JASN
|
April 17, 2021
A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (<i>RCAN1</i>) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS
Brandon M Lane, Susan Murray, Katherine Benson, et al.
European Journal of Human Genetics : EJHG
|
January 23, 2023
Correction: The 2019 and 2021 International workshops on Alport syndrome
Sergio Daga, Jie Ding, Constantinos Deltas, et al.
European Journal of Human Genetics : EJHG
|
March 9, 2022
The 2019 and 2021 International Workshops on Alport Syndrome
Sergio Daga, Jie Ding, Constantinos Deltas, et al.
Journal of the American Society of Nephrology : JASN
|
March 29, 2014
Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS
Rasheed A Gbadegesin, Gentzon Hall, Adebowale Adeyemo, et al.
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Search research articles
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Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Kidney International Reports
|
March 19, 2026
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport Syndrome
Thomas M Oates, Moumita Barua, Susie Gear, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 5, 2017
X-Linked Glomerulopathy Due to COL4A5 Founder Variant
Moumita Barua, Rohan John, Lorenzo Stella, et al.
Journal of the American Society of Nephrology : JASN
|
August 27, 2024
Association of Genetically Predicted Skipping of COL4A4 Exon 27 with Hematuria and Albuminuria
Frida Lona-Durazo, Kohei Omachi, Damian Fermin, et al.
Diabetes
|
February 23, 2020
Erratum. Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease. Diabetes 2019;68:2235-2246
Priska Stahel, Avital Nahmias, Shawn K Sud, et al.
Diabetes
|
September 12, 2019
Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease
Priska Stahel, Avital Nahmias, Shawn K Sud, et al.
Canadian Journal of Kidney Health and Disease
|
April 22, 2022
The Canadian Glomerulonephritis Registry (CGNR) and Translational Research Initiative: Rationale and Clinical Research Protocol
Ainslie M Hildebrand, Moumita Barua, Sean J Barbour, et al.
Journal of the American Society of Nephrology : JASN
|
April 17, 2021
A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (<i>RCAN1</i>) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS
Brandon M Lane, Susan Murray, Katherine Benson, et al.
European Journal of Human Genetics : EJHG
|
January 23, 2023
Correction: The 2019 and 2021 International workshops on Alport syndrome
Sergio Daga, Jie Ding, Constantinos Deltas, et al.
European Journal of Human Genetics : EJHG
|
March 9, 2022
The 2019 and 2021 International Workshops on Alport Syndrome
Sergio Daga, Jie Ding, Constantinos Deltas, et al.
Journal of the American Society of Nephrology : JASN
|
March 29, 2014
Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS
Rasheed A Gbadegesin, Gentzon Hall, Adebowale Adeyemo, et al.
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of 5