Soliman Alkrinawi
Beersheba, D, Israel
Last Updated: 09/26/2026
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Found 8 publications
Pediatric thermal epiglottitis: insights from a tertiary center experience.
Journal: European journal of pediatrics
Published: February 24, 2024
Stepwise genetic approach for the diagnosis of primary ciliary dyskinesia in highly consanguineous populations.
Journal: Archives of disease in childhood
Published: June 05, 2023
Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screening.
Journal: Molecular genetics & genomic medicine
Published: November 10, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities.
Journal: F1000Research
Published: September 29, 2016
Primary ciliary dyskinesia in Israel: Prevalence, clinical features, current diagnosis and management practices.
Journal: Respiratory medicine
Published: January 30, 2016
Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3 (-) secretion revealed by disease causing human mutation.
Journal: The Journal of physiology
Published: July 28, 2015
The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screening.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: June 16, 2015
Natural history and clinical manifestations of hyponatremia and hyperchlorhidrosis due to carbonic anhydrase XII deficiency.
Journal: Hormone research in paediatrics
Published: October 03, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026