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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 10, 2026
Phenotypic Diversity in Autosomal Recessive Hypophosphatemic Rickets Type 2
Maimoona Al Qanoobi, Maryam Al Badi, Aisha Al Sinani, et al.
Oman Medical Journal
|
August 29, 2025
Hyperthyroidism Presenting as Jaundice in a Child
Tawfiq Taki Al Lawati, Aisha Al Sinani, Fatma Ali Ramadhan Al Lawati
F1000Research
|
December 11, 2019
Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia
Jamie Willows, Maryam Al Badi, Chloe Richardson, et al.
Oman Medical Journal
|
May 12, 2015
A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature
Aisha Al-Sinani, Waad-Allah S Mula-Abed, Manal Al-Kindi, et al.
Paediatrics and International Child Health
|
July 25, 2012
A novel leprechaunism mutation, Cys807Arg, in an Arab infant: a rare cause of hypoglycaemia
Zaineb S Baqir, Tawfiq T Al-Lawati, Saniya O Al Hussaini, et al.
Clinical & Translational Immunology
|
July 11, 2017
Agammaglobulinaemia despite terminal B-cell differentiation in a patient with a novel <i>LRBA</i> mutation
Nashat Al Sukaiti, Khwater AbdelRahman, Jalila AlShekaili, et al.
Diabetes Research and Clinical Practice
|
January 25, 2021
Use of ambulatory glucose monitoring and analysis of ambulatory glucose profile in clinical practice for diabetes management; a position statement of the Arab Society of Paediatric Endocrinology and diabetes
Asma Deeb, Tawfik Muammar, Hussain Alsaffar, et al.
Journal of Autism and Developmental Disorders
|
February 28, 2025
Could a National Screening Program Reduce the Age of Diagnosis of Autism Spectrum Disorder?
Watfa Al-Mamari, Ahmed B Idris, Hafsa Al Aamri, 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.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 10, 2026
Phenotypic Diversity in Autosomal Recessive Hypophosphatemic Rickets Type 2
Maimoona Al Qanoobi, Maryam Al Badi, Aisha Al Sinani, et al.
Oman Medical Journal
|
August 29, 2025
Hyperthyroidism Presenting as Jaundice in a Child
Tawfiq Taki Al Lawati, Aisha Al Sinani, Fatma Ali Ramadhan Al Lawati
F1000Research
|
December 11, 2019
Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia
Jamie Willows, Maryam Al Badi, Chloe Richardson, et al.
Oman Medical Journal
|
May 12, 2015
A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature
Aisha Al-Sinani, Waad-Allah S Mula-Abed, Manal Al-Kindi, et al.
Paediatrics and International Child Health
|
July 25, 2012
A novel leprechaunism mutation, Cys807Arg, in an Arab infant: a rare cause of hypoglycaemia
Zaineb S Baqir, Tawfiq T Al-Lawati, Saniya O Al Hussaini, et al.
Clinical & Translational Immunology
|
July 11, 2017
Agammaglobulinaemia despite terminal B-cell differentiation in a patient with a novel <i>LRBA</i> mutation
Nashat Al Sukaiti, Khwater AbdelRahman, Jalila AlShekaili, et al.
Diabetes Research and Clinical Practice
|
January 25, 2021
Use of ambulatory glucose monitoring and analysis of ambulatory glucose profile in clinical practice for diabetes management; a position statement of the Arab Society of Paediatric Endocrinology and diabetes
Asma Deeb, Tawfik Muammar, Hussain Alsaffar, et al.
Journal of Autism and Developmental Disorders
|
February 28, 2025
Could a National Screening Program Reduce the Age of Diagnosis of Autism Spectrum Disorder?
Watfa Al-Mamari, Ahmed B Idris, Hafsa Al Aamri, 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.
Page
of 1