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Journal of Medical Genetics
|
July 2, 2010
Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome
Olivia Boyer, Geneviève Benoit, Olivier Gribouval, et al.
American Journal of Physiology. Renal Physiology
|
January 3, 2019
Heterozygous Pkhd1<sup>C642*</sup> mice develop cystic liver disease and proximal tubule ectasia that mimics radiographic signs of medullary sponge kidney
Dan Shan, Gabriel Rezonzew, Sean Mullen, et al.
Kidney International
|
September 24, 2017
Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
Ségolène Aymé, Detlef Bockenhauer, Simon Day, et al.
Journal of the American Society of Nephrology : JASN
|
June 22, 2007
Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease
Sandro Rossetti, Mark B Consugar, Arlene B Chapman, et al.
American Journal of Human Genetics
|
March 19, 2002
PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats
Luiz F Onuchic, Laszlo Furu, Yasuyuki Nagasawa, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
March 21, 2026
KDOQI US Commentary on the KDIGO 2025 Clinical Practice Guideline for the Evaluation, Management, and Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Neera K Dahl, Phyllis August, Whitney Besse, et al.
American Journal of Human Genetics
|
June 19, 1998
Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome
R Vargas-Poussou, D Feldmann, M Vollmer, et al.
Kidney International
|
November 25, 2003
Magnetic resonance measurements of renal blood flow as a marker of disease severity in autosomal-dominant polycystic kidney disease
Bernard F King, Vicente E Torres, Marijn E Brummer, et al.
Journal of the American Society of Nephrology : JASN
|
January 10, 2015
Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial
Jeffrey B Kopp, Cheryl A Winkler, Xiongce Zhao, et al.
The New England Journal of Medicine
|
May 19, 2006
Volume progression in polycystic kidney disease
Jared J Grantham, Vicente E Torres, Arlene B Chapman, et al.
Page
of 20
Search research articles
Search
Showing results (171-180 of 198) with videos related to
Sort By:
Page
of 20
Journal of Medical Genetics
|
July 2, 2010
Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome
Olivia Boyer, Geneviève Benoit, Olivier Gribouval, et al.
American Journal of Physiology. Renal Physiology
|
January 3, 2019
Heterozygous Pkhd1<sup>C642*</sup> mice develop cystic liver disease and proximal tubule ectasia that mimics radiographic signs of medullary sponge kidney
Dan Shan, Gabriel Rezonzew, Sean Mullen, et al.
Kidney International
|
September 24, 2017
Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
Ségolène Aymé, Detlef Bockenhauer, Simon Day, et al.
Journal of the American Society of Nephrology : JASN
|
June 22, 2007
Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease
Sandro Rossetti, Mark B Consugar, Arlene B Chapman, et al.
American Journal of Human Genetics
|
March 19, 2002
PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats
Luiz F Onuchic, Laszlo Furu, Yasuyuki Nagasawa, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
March 21, 2026
KDOQI US Commentary on the KDIGO 2025 Clinical Practice Guideline for the Evaluation, Management, and Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Neera K Dahl, Phyllis August, Whitney Besse, et al.
American Journal of Human Genetics
|
June 19, 1998
Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome
R Vargas-Poussou, D Feldmann, M Vollmer, et al.
Kidney International
|
November 25, 2003
Magnetic resonance measurements of renal blood flow as a marker of disease severity in autosomal-dominant polycystic kidney disease
Bernard F King, Vicente E Torres, Marijn E Brummer, et al.
Journal of the American Society of Nephrology : JASN
|
January 10, 2015
Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial
Jeffrey B Kopp, Cheryl A Winkler, Xiongce Zhao, et al.
The New England Journal of Medicine
|
May 19, 2006
Volume progression in polycystic kidney disease
Jared J Grantham, Vicente E Torres, Arlene B Chapman, et al.
Page
of 20