Michael Geylis
Beersheba, D, Israel
Last Updated: 09/26/2026
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Found 10 publications
Alternative Pathway Complement Dysregulation in Atypical HUS: A Case Communication.
Journal: The Israel Medical Association journal : IMAJ
Published: August 06, 2026
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure.
Journal: Kidney international reports
Published: May 14, 2023
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome.
Journal: European journal of human genetics : EJHG
Published: October 13, 2022
Risk factors for childhood chronic kidney disease: a population-based study.
Journal: Pediatric nephrology (Berlin, Germany)
Published: March 11, 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
Hodgkin's lymphoma, nephrotic syndrome, and echinococcosis cysts: an unusual association and literature review.
Journal: Pediatric hematology and oncology
Published: February 21, 2019
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I.
Journal: Annals of human genetics
Published: October 11, 2018
Severe neutropenia in children after renal transplantation: incidence, course, and treatment with granulocyte colony-stimulating factor.
Journal: Pediatric nephrology (Berlin, Germany)
Published: January 08, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026