Search research articles
Contact Us
Filters
Showing results (41-50 of 58) with videos related to
Page
of 6
Sort By:
Plos One
|
August 11, 2017
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
Beata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, et al.
Kidney International Reports
|
July 11, 2022
Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney Disease
Ramona Ajiri, Kathrin Burgmaier, Nurver Akinci, 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.
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.
Orphanet Journal of Rare Diseases
|
November 7, 2016
Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?
Marie Morimoto, Clara Myung, Kimberly Beirnes, et al.
Scientific Reports
|
September 30, 2020
Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)
Kathrin Burgmaier, Gema Ariceta, Martin Bald, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 5, 2025
COL4A1 and COL4A2-related disorders: Clinical features, diagnostic guidelines, and management
Diana Tambala, Rachel Vassar, John Snow, et al.
Scientific Reports
|
November 5, 2021
Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD
Kathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
April 21, 2018
Prevalence of Hypertension in Children with Early-Stage ADPKD
Laura Massella, Djalila Mekahli, Dušan Paripović, et al.
Kidney International
|
February 8, 2025
A risk score to predict kidney survival in patients with autosomal recessive polycystic kidney disease at the age of two months
Kathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
Plos One
|
August 11, 2017
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
Beata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, et al.
Kidney International Reports
|
July 11, 2022
Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney Disease
Ramona Ajiri, Kathrin Burgmaier, Nurver Akinci, 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.
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.
Orphanet Journal of Rare Diseases
|
November 7, 2016
Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?
Marie Morimoto, Clara Myung, Kimberly Beirnes, et al.
Scientific Reports
|
September 30, 2020
Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)
Kathrin Burgmaier, Gema Ariceta, Martin Bald, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 5, 2025
COL4A1 and COL4A2-related disorders: Clinical features, diagnostic guidelines, and management
Diana Tambala, Rachel Vassar, John Snow, et al.
Scientific Reports
|
November 5, 2021
Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD
Kathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
April 21, 2018
Prevalence of Hypertension in Children with Early-Stage ADPKD
Laura Massella, Djalila Mekahli, Dušan Paripović, et al.
Kidney International
|
February 8, 2025
A risk score to predict kidney survival in patients with autosomal recessive polycystic kidney disease at the age of two months
Kathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, et al.
Page
of 6