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Laura Massella

Showing results (41-50 of 58) with videos related to

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Plos One|August 11, 2017
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasiaBeata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, et al.
Kidney International Reports|July 11, 2022
Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney DiseaseRamona Ajiri, Kathrin Burgmaier, Nurver Akinci, et al.
European Journal of Human Genetics : EJHG|March 9, 2022
The 2019 and 2021 International Workshops on Alport SyndromeSergio 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 syndromeSergio 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 managementDiana 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 ARPKDKathrin 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 ADPKDLaura 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 monthsKathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Plos One|August 11, 2017
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasiaBeata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, et al.
Kidney International Reports|July 11, 2022
Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney DiseaseRamona Ajiri, Kathrin Burgmaier, Nurver Akinci, et al.
European Journal of Human Genetics : EJHG|March 9, 2022
The 2019 and 2021 International Workshops on Alport SyndromeSergio 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 syndromeSergio 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 managementDiana 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 ARPKDKathrin 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 ADPKDLaura 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 monthsKathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, et al.
Pageof 6