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Maayan Kagan

Showing results (1-10 of 14) with videos related to

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Pediatric Nephrology (Berlin, Germany)|February 5, 2022
The genetic basis of congenital anomalies of the kidney and urinary tractMaayan Kagan, Oren Pleniceanu, Asaf Vivante
Pediatric Nephrology (Berlin, Germany)|November 19, 2022
HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract-ReplyMaayan Kagan, Oren Pleniceanu, Asaf Vivante
Harefuah|December 27, 2021
[THE GENETIC BASIS OF CHRONIC KIDNEY DISEASE IN CHILDREN AND YOUNG ADULTS]Maayan Kagan, Aviva Eliyahu, Yishay Ben Moshe, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|January 21, 2021
PD-L1 EXPRESSION IN NORMAL ENDOCRINE TISSUES IS NOT INCREASED DESPITE HIGH INCIDENCE OF PD-1 INHIBITOR-ASSOCIATED ENDOCRINOPATHIESRena Pollack, Maayan Kagan, Rivka Dresner-Pollak, et al.
BMC Nephrology|October 24, 2020
Cardiovascular outcomes following percutaneous coronary intervention with drug-eluting balloons in chronic kidney disease: a retrospective analysisMichael Jonas, Maayan Kagan, Gal Sella, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|April 24, 2019
BASELINE TSH LEVEL IS ASSOCIATED WITH RISK OF ANTI-PD-1-INDUCED THYROID DYSFUNCTIONRena M Pollack, Maayan Kagan, Michal Lotem, et al.
Pediatric Nephrology (Berlin, Germany)|September 27, 2021
Kidney and urinary tract findings among patients with Kabuki (make-up) syndromeRona Merdler-Rabinowicz, Ben Pode-Shakked, Asaf Vivante, et al.
Journal of Medical Genetics|July 3, 2021
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defectsYoav Bolkier, Ortal Barel, Dina Marek-Yagel, et al.
Frontiers in Genetics|January 26, 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disordersMaayan Kagan, Rotem Semo-Oz, Yishay Ben Moshe, et al.
Kidney International Reports|April 30, 2025
Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney FailureGuy Chowers, Dror Ben-Ruby, Danit Atias-Varon, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Pediatric Nephrology (Berlin, Germany)|February 5, 2022
The genetic basis of congenital anomalies of the kidney and urinary tractMaayan Kagan, Oren Pleniceanu, Asaf Vivante
Pediatric Nephrology (Berlin, Germany)|November 19, 2022
HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract-ReplyMaayan Kagan, Oren Pleniceanu, Asaf Vivante
Harefuah|December 27, 2021
[THE GENETIC BASIS OF CHRONIC KIDNEY DISEASE IN CHILDREN AND YOUNG ADULTS]Maayan Kagan, Aviva Eliyahu, Yishay Ben Moshe, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|January 21, 2021
PD-L1 EXPRESSION IN NORMAL ENDOCRINE TISSUES IS NOT INCREASED DESPITE HIGH INCIDENCE OF PD-1 INHIBITOR-ASSOCIATED ENDOCRINOPATHIESRena Pollack, Maayan Kagan, Rivka Dresner-Pollak, et al.
BMC Nephrology|October 24, 2020
Cardiovascular outcomes following percutaneous coronary intervention with drug-eluting balloons in chronic kidney disease: a retrospective analysisMichael Jonas, Maayan Kagan, Gal Sella, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|April 24, 2019
BASELINE TSH LEVEL IS ASSOCIATED WITH RISK OF ANTI-PD-1-INDUCED THYROID DYSFUNCTIONRena M Pollack, Maayan Kagan, Michal Lotem, et al.
Pediatric Nephrology (Berlin, Germany)|September 27, 2021
Kidney and urinary tract findings among patients with Kabuki (make-up) syndromeRona Merdler-Rabinowicz, Ben Pode-Shakked, Asaf Vivante, et al.
Journal of Medical Genetics|July 3, 2021
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defectsYoav Bolkier, Ortal Barel, Dina Marek-Yagel, et al.
Frontiers in Genetics|January 26, 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disordersMaayan Kagan, Rotem Semo-Oz, Yishay Ben Moshe, et al.
Kidney International Reports|April 30, 2025
Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney FailureGuy Chowers, Dror Ben-Ruby, Danit Atias-Varon, et al.
Pageof 2