Ruth Schreiber
Beersheba, D, Israel
Last Updated: 09/26/2026
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Found 16 publications
Alternative Pathway Complement Dysregulation in Atypical HUS: A Case Communication.
Journal: The Israel Medical Association journal : IMAJ
Published: August 06, 2026
Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula Ancestry.
Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation
Published: December 31, 2024
Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney Failure.
Journal: Kidney international reports
Published: October 09, 2024
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure.
Journal: Kidney international reports
Published: May 14, 2023
RAAS-deficient organoids indicate delayed angiogenesis as a possible cause for autosomal recessive renal tubular dysgenesis.
Journal: Nature communications
Published: April 26, 2023
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome.
Journal: European journal of human genetics : EJHG
Published: October 13, 2022
Hypoparathyroidism-retardation-dysmorphism syndrome-Clinical insights from a large longitudinal cohort in a single medical center.
Journal: Frontiers in pediatrics
Published: April 09, 2022
RENAL TUBULAR DYSGENESIS SECONDARY TO MUTATIONS IN GENES ENCODING THE RENIN-ANGIOTENSIN SYSTEM
Journal: Harefuah
Published: December 27, 2021
Glomerular involvement in children with H syndrome.
Journal: Pediatric nephrology (Berlin, Germany)
Published: August 06, 2020
Listeria Meningitis in an Immunocompetent Adolescent.
Journal: The Israel Medical Association journal : IMAJ
Published: March 10, 2020
Hodgkin's lymphoma, nephrotic syndrome, and echinococcosis cysts: an unusual association and literature review.
Journal: Pediatric hematology and oncology
Published: February 21, 2019
Last Updated: 09/26/2026