Abdulsalam I. Libdeh-Abu

Mount Of Olives
Jerusalem, JM, Israel

Last Updated: 09/26/2026

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Found 16 publications

A Case of Heterozygous INS Gene Missense Variant in Neonatal Diabetes with Beta-Cell Autoantibodies: Experience in Limited Resources Setting.

A Case of Heterozygous INS Gene Missense Variant in Neonatal Diabetes with Beta-Cell Autoantibodies: Experience in Limited Resources Setting.

Journal: Hormone research in paediatrics

Published: January 06, 2025

Global Learner Feedback on Continuing Medical Education-Accredited e-Learning Modules in Pediatric Endocrinology and Diabetes: Cross-Sectional Study.

Global Learner Feedback on Continuing Medical Education-Accredited e-Learning Modules in Pediatric Endocrinology and Diabetes: Cross-Sectional Study.

Journal: JMIR medical education

Published: October 12, 2024

A Novel Homozygous BMP15 Mutation Causes Ovarian Dysgenesis and Primary Amenorrhea.

A Novel Homozygous BMP15 Mutation Causes Ovarian Dysgenesis and Primary Amenorrhea.

Journal: Journal of the Endocrine Society

Published: September 04, 2024

Unbiased phenotype and genotype matching maximizes gene discovery and diagnostic yield.

Unbiased phenotype and genotype matching maximizes gene discovery and diagnostic yield.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 11, 2023

Lessons Learned From COVID-19 Lockdown: An ASPED/MENA Study on Lifestyle Changes and Quality of Life During Ramadan Fasting in Children and Adolescents Living With Type 1 Diabetes.

Lessons Learned From COVID-19 Lockdown: An ASPED/MENA Study on Lifestyle Changes and Quality of Life During Ramadan Fasting in Children and Adolescents Living With Type 1 Diabetes.

Journal: Clinical medicine insights. Endocrinology and diabetes

Published: April 05, 2023

Retraction Notice to "Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation".

Retraction Notice to "Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation".

Journal: Journal of dermatological science

Published: February 04, 2023

Wolfram Syndrome-2, a Cause of Severe Gastrointestinal Bleeding: A Case Series and a Literature Review.

Wolfram Syndrome-2, a Cause of Severe Gastrointestinal Bleeding: A Case Series and a Literature Review.

Journal: JPGN reports

Published: November 16, 2022

Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village….

Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village….

Journal: BMJ global health

Published: August 16, 2021

Eligibility for growth hormone therapy in children born small for gestational age is substantially lower than expected.

Eligibility for growth hormone therapy in children born small for gestational age is substantially lower than expected.

Journal: Clinical endocrinology

Published: February 06, 2021

RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1.

RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1.

Journal: The Journal of clinical investigation

Published: January 08, 2021

Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity.

Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity.

Journal: American journal of medical genetics. Part A

Published: September 16, 2020

Combined Gestational Age- and Birth Weight-Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia.

Combined Gestational Age- and Birth Weight-Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia.

Journal: The Journal of clinical endocrinology and metabolism

Published: November 15, 2018

Showing 1-12 of 16

Last Updated: 09/26/2026