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Rachel Becker

Showing results (41-50 of 47) with videos related to

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American Journal of Nephrology|June 18, 2005
Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in IsraelYaacov Frishberg, Choni Rinat, Adel Shalata, et al.
Clinical Chemistry|November 11, 2025
Emerging Threat of XylazineKyla M Jorgenson, Robert A Middleberg, Brandy L Young, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 30, 2006
Hyperostosis-hyperphosphatemia syndrome: a congenital disorder of O-glycosylation associated with augmented processing of fibroblast growth factor 23Yaacov Frishberg, Nobuaki Ito, Choni Rinat, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in DHDPSL are responsible for primary hyperoxaluria type IIIRuth Belostotsky, Eric Seboun, Gregory H Idelson, et al.
Kidney International|September 2, 2019
Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndromeAshish K Solanki, Eugen Widmeier, Ehtesham Arif, et al.
Kidney International Reports|October 18, 2023
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney FailureYishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, et al.
Pediatric Nephrology (Berlin, Germany)|January 7, 2022
A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insightsBen Pode-Shakked, Yishay Ben-Moshe, Ortal Barel, et al.
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Showing results (41-50 of 47) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 47 results.
American Journal of Nephrology|June 18, 2005
Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in IsraelYaacov Frishberg, Choni Rinat, Adel Shalata, et al.
Clinical Chemistry|November 11, 2025
Emerging Threat of XylazineKyla M Jorgenson, Robert A Middleberg, Brandy L Young, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 30, 2006
Hyperostosis-hyperphosphatemia syndrome: a congenital disorder of O-glycosylation associated with augmented processing of fibroblast growth factor 23Yaacov Frishberg, Nobuaki Ito, Choni Rinat, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in DHDPSL are responsible for primary hyperoxaluria type IIIRuth Belostotsky, Eric Seboun, Gregory H Idelson, et al.
Kidney International|September 2, 2019
Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndromeAshish K Solanki, Eugen Widmeier, Ehtesham Arif, et al.
Kidney International Reports|October 18, 2023
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney FailureYishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, et al.
Pediatric Nephrology (Berlin, Germany)|January 7, 2022
A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insightsBen Pode-Shakked, Yishay Ben-Moshe, Ortal Barel, et al.
Pageof 5