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Molecular and Cellular Endocrinology
|
September 6, 2017
Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population
Meshael M Alswailem, Ohoud S Alzahrani, Doha S Alhomaidah, et al.
Frontiers in Genetics
|
January 29, 2026
Phenotype and genotype of hypophosphatasia cases in Saudi Arabia: multi-center case cohort
Afaf Alsagheir, Ali Mcrabi, Meshari Alquayt, et al.
Frontiers in Endocrinology
|
October 31, 2025
The role of digital health in growth hormone therapy: perspectives from Gulf Cooperation Council pediatric endocrinologists
Walid Kaplan, Abdullah Alherbish, Abdullah Aljnaibi, et al.
Journal of Clinical Lipidology
|
December 29, 2023
Modern approaches to the management of homozygous familial hypercholesterolemia in the Middle East and North Africa
Abdullah Al-Ashwal, Afaf Alsagheir, Mohammed Al Dubayee, et al.
Diabetes & Metabolic Syndrome
|
March 14, 2026
Impact of early life exposure to active play and movement on health and wellbeing across the lifespan: A narrative review of RCTs from 2020-2025
Andrew P Hills, Fadiah Alkhattabi, Reem Alahmed, et al.
Journal of the Endocrine Society
|
July 14, 2021
A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population
Ali S Alzahrani, Meshael Alswailem, Bassam Bin Abbas, et al.
Frontiers in Endocrinology
|
June 22, 2023
The clinical characteristics and quality of life of 248 pediatric and adult patients with Congenital Adrenal Hyperplasia
Edi A Shafaay, Mohammed A Aldriweesh, Ghadeer L Aljahdali, et al.
Journal of Clinical Lipidology
|
June 19, 2025
Homozygous familial hypercholesterolemia in a high-consanguinity population: Insights from a Saudi cohort
Afaf Alsagheir, Ismail A Abdullah, Mohammed Albitar, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 17, 2018
Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis
Minjing Zou, Ali S Alzahrani, Ali Al-Odaib, et al.
Journal of the Endocrine Society
|
February 2, 2026
Molecular Genetics of 1α-Hydroxylase Deficiency in the Saudi Population
Bassam Bin-Abbas, Afaf Alsagheir, Balgees Alghamdi, et al.
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of 6
Search research articles
Search
Showing results (31-40 of 51) with videos related to
Sort By:
Page
of 6
Molecular and Cellular Endocrinology
|
September 6, 2017
Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population
Meshael M Alswailem, Ohoud S Alzahrani, Doha S Alhomaidah, et al.
Frontiers in Genetics
|
January 29, 2026
Phenotype and genotype of hypophosphatasia cases in Saudi Arabia: multi-center case cohort
Afaf Alsagheir, Ali Mcrabi, Meshari Alquayt, et al.
Frontiers in Endocrinology
|
October 31, 2025
The role of digital health in growth hormone therapy: perspectives from Gulf Cooperation Council pediatric endocrinologists
Walid Kaplan, Abdullah Alherbish, Abdullah Aljnaibi, et al.
Journal of Clinical Lipidology
|
December 29, 2023
Modern approaches to the management of homozygous familial hypercholesterolemia in the Middle East and North Africa
Abdullah Al-Ashwal, Afaf Alsagheir, Mohammed Al Dubayee, et al.
Diabetes & Metabolic Syndrome
|
March 14, 2026
Impact of early life exposure to active play and movement on health and wellbeing across the lifespan: A narrative review of RCTs from 2020-2025
Andrew P Hills, Fadiah Alkhattabi, Reem Alahmed, et al.
Journal of the Endocrine Society
|
July 14, 2021
A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population
Ali S Alzahrani, Meshael Alswailem, Bassam Bin Abbas, et al.
Frontiers in Endocrinology
|
June 22, 2023
The clinical characteristics and quality of life of 248 pediatric and adult patients with Congenital Adrenal Hyperplasia
Edi A Shafaay, Mohammed A Aldriweesh, Ghadeer L Aljahdali, et al.
Journal of Clinical Lipidology
|
June 19, 2025
Homozygous familial hypercholesterolemia in a high-consanguinity population: Insights from a Saudi cohort
Afaf Alsagheir, Ismail A Abdullah, Mohammed Albitar, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 17, 2018
Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis
Minjing Zou, Ali S Alzahrani, Ali Al-Odaib, et al.
Journal of the Endocrine Society
|
February 2, 2026
Molecular Genetics of 1α-Hydroxylase Deficiency in the Saudi Population
Bassam Bin-Abbas, Afaf Alsagheir, Balgees Alghamdi, et al.
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of 6