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Daniel Landau

Showing results (91-100 of 117) with videos related to

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Annals of Human Genetics|April 13, 2019
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type IDaniel Halperin, Vadim Dolgin, Michael Geylis, et al.
The Pediatric Infectious Disease Journal|August 12, 2021
Clinical Outcomes and Antibody Response in COVID-19-Positive Pediatric Solid Organ Transplant RecipientsEfrat Talgam-Horshi, Yael Mozer-Glassberg, Orit Waisbourd-Zinman, et al.
Annals of the American Thoracic Society|September 28, 2022
Inhaled Nitric Oxide for the Treatment of Acute Bronchiolitis: A Multicenter Randomized Controlled Clinical Trial to Evaluate Dose ResponseAviv Goldbart, Moran Lavie, Ronit Lubetzky, et al.
Pediatric Nephrology (Berlin, Germany)|September 25, 2024
An innocent bystander or a predisposing culprit? Kidney injury following pediatric liver transplantationAdi Glass, Ori Goldberg, Yael Mozer-Glassberg, et al.
Transplantation|August 12, 2021
Serological Response to the BNT162b2 COVID-19 mRNA Vaccine in Adolescent and Young Adult Kidney Transplant RecipientsOrly Haskin, Liat Ashkenazi-Hoffnung, Noa Ziv, et al.
Pediatric Transplantation|June 20, 2012
Post-transplantation lymphoproliferative disorder in pediatric kidney-transplant recipients - a national studyRoxana Cleper, Efrat Ben Shalom, Daniel Landau, et al.
American Journal of Human Genetics|November 2, 2010
Hyperchlorhidrosis caused by homozygous mutation in CA12, encoding carbonic anhydrase XIIMaya Feldshtein, Suliman Elkrinawi, Baruch Yerushalmi, et al.
Harefuah|November 21, 2024
[A NEW TRANSITION PROGRAM FOR KIDNEY TRANSPLANTED YOUNG ADULTS FROM PEDIATRIC TO ADULT CARE SERVICES]Yael Borovitz, Neomi Zanhendler, Noga Katz, et al.
Nephron. Physiology|August 19, 2011
Familial autosomal recessive renal tubular acidosis: importance of early diagnosisAsaf Vivante, Danny Lotan, Naomi Pode-Shakked, et al.
The Journal of Clinical Investigation|October 23, 2019
Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenaseMax Drabkin, Yuval Yogev, Lior Zeller, et al.
Pageof 12

Showing results (91-100 of 117) with videos related to

Sort By:
Pageof 12
Annals of Human Genetics|April 13, 2019
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type IDaniel Halperin, Vadim Dolgin, Michael Geylis, et al.
The Pediatric Infectious Disease Journal|August 12, 2021
Clinical Outcomes and Antibody Response in COVID-19-Positive Pediatric Solid Organ Transplant RecipientsEfrat Talgam-Horshi, Yael Mozer-Glassberg, Orit Waisbourd-Zinman, et al.
Annals of the American Thoracic Society|September 28, 2022
Inhaled Nitric Oxide for the Treatment of Acute Bronchiolitis: A Multicenter Randomized Controlled Clinical Trial to Evaluate Dose ResponseAviv Goldbart, Moran Lavie, Ronit Lubetzky, et al.
Pediatric Nephrology (Berlin, Germany)|September 25, 2024
An innocent bystander or a predisposing culprit? Kidney injury following pediatric liver transplantationAdi Glass, Ori Goldberg, Yael Mozer-Glassberg, et al.
Transplantation|August 12, 2021
Serological Response to the BNT162b2 COVID-19 mRNA Vaccine in Adolescent and Young Adult Kidney Transplant RecipientsOrly Haskin, Liat Ashkenazi-Hoffnung, Noa Ziv, et al.
Pediatric Transplantation|June 20, 2012
Post-transplantation lymphoproliferative disorder in pediatric kidney-transplant recipients - a national studyRoxana Cleper, Efrat Ben Shalom, Daniel Landau, et al.
American Journal of Human Genetics|November 2, 2010
Hyperchlorhidrosis caused by homozygous mutation in CA12, encoding carbonic anhydrase XIIMaya Feldshtein, Suliman Elkrinawi, Baruch Yerushalmi, et al.
Harefuah|November 21, 2024
[A NEW TRANSITION PROGRAM FOR KIDNEY TRANSPLANTED YOUNG ADULTS FROM PEDIATRIC TO ADULT CARE SERVICES]Yael Borovitz, Neomi Zanhendler, Noga Katz, et al.
Nephron. Physiology|August 19, 2011
Familial autosomal recessive renal tubular acidosis: importance of early diagnosisAsaf Vivante, Danny Lotan, Naomi Pode-Shakked, et al.
The Journal of Clinical Investigation|October 23, 2019
Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenaseMax Drabkin, Yuval Yogev, Lior Zeller, et al.
Pageof 12