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Daniel Landau

Showing results (111-120 of 117) with videos related to

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Journal of the American Society of Nephrology : JASN|March 23, 2013
Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signalingAsaf Vivante, Michal Mark-Danieli, Miriam Davidovits, et al.
Pediatric Nephrology (Berlin, Germany)|May 13, 2014
An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndromeSally Johnson, Jelena Stojanovic, Gema Ariceta, et al.
Biomedicines|August 6, 2021
Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics AspectsHava Peretz, Ayala Lagziel, Florian Bittner, et al.
Pediatric Nephrology (Berlin, Germany)|April 11, 2015
An international consensus approach to the management of atypical hemolytic uremic syndrome in childrenChantal Loirat, Fadi Fakhouri, Gema Ariceta, et al.
Journal of the American Society of Nephrology : JASN|August 23, 2002
Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidusNannette Marr, Daniel G Bichet, Susan Hoefs, et al.
Nature Genetics|July 23, 2003
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationEdgar A Otto, Bernhard Schermer, Tomoko Obara, et al.
Nature Medicine|August 7, 2025
Geographical shifting of cholera burden in Africa and its implications for disease controlJavier Perez-Saez, Qulu Zheng, Joshua Kaminsky, et al.
Pageof 12

Showing results (111-120 of 117) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 117 results.
Journal of the American Society of Nephrology : JASN|March 23, 2013
Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signalingAsaf Vivante, Michal Mark-Danieli, Miriam Davidovits, et al.
Pediatric Nephrology (Berlin, Germany)|May 13, 2014
An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndromeSally Johnson, Jelena Stojanovic, Gema Ariceta, et al.
Biomedicines|August 6, 2021
Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics AspectsHava Peretz, Ayala Lagziel, Florian Bittner, et al.
Pediatric Nephrology (Berlin, Germany)|April 11, 2015
An international consensus approach to the management of atypical hemolytic uremic syndrome in childrenChantal Loirat, Fadi Fakhouri, Gema Ariceta, et al.
Journal of the American Society of Nephrology : JASN|August 23, 2002
Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidusNannette Marr, Daniel G Bichet, Susan Hoefs, et al.
Nature Genetics|July 23, 2003
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationEdgar A Otto, Bernhard Schermer, Tomoko Obara, et al.
Nature Medicine|August 7, 2025
Geographical shifting of cholera burden in Africa and its implications for disease controlJavier Perez-Saez, Qulu Zheng, Joshua Kaminsky, et al.
Pageof 12