Efficacy of Semaglutide in Pediatric Patients With Bardet-Biedl Syndrome and Alström Syndrome حسب Hajar Dauleh (18002500)

مؤلفون آخرون:

A Novel Homozygous <i>MC2R</i> Variant Leading to Type-1 Familial Glucocorticoid Deficiency حسب Idris Mohammed (751020)

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The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism حسب Sonya Galcheva (14172121)

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A Systematic Review of Childhood Diabetes Research in the Middle East Region حسب Saras Saraswathi (612858)

مؤلفون آخرون:

Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly حسب Umm-Kulthum Ismail Umlai (12040352)

مؤلفون آخرون:

An induced pluripotent stem cell line derived from a patient with neonatal diabetes and Fanconi-Bickel syndrome caused by a homozygous mutation in the SLC2A2 gene حسب Ahmed K. Elsayed (13275302)

مؤلفون آخرون:

Genetic epidemiology of Woodhouse-Sakati Syndrome in the Greater Middle East region and beyond: a systematic review حسب Amira Kohil (15257285)

مؤلفون آخرون:

Fanconi–Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia حسب Sanaa Sharari (12561952)

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Challenges in child and adolescent health across the Arab Gulf countries—Focus on metabolic health حسب Basma Haris (12040355)

مؤلفون آخرون:

Alpelisib Therapy in 2 Patients With Congenital Hyperinsulinism حسب Khalid Alburshad (22467244)

مؤلفون آخرون:

Aberrant development of pancreatic beta cells derived from human iPSCs with FOXA2 deficiency حسب Ahmed K. Elsayed (13275302)

مؤلفون آخرون:

Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 Gene حسب Basma Haris (12040355)

مؤلفون آخرون:

Ion Transporters, Channelopathies, and Glucose Disorders حسب Huseyin Demirbilek (566044)

مؤلفون آخرون:

Infancy onset diabetes mellitus in a patient with a novel homozygous LRBA mutation حسب Iman Hawari (12561958)

مؤلفون آخرون:

Glucose control during Ramadan fasting in a teenager with type 1 diabetes on MiniMed 670G hybrid closed-loop system حسب Goran Petrovski (129836)

مؤلفون آخرون:

10-Day structured initiation protocol from multiple daily injection to hybrid closed-loop system in children and adolescents with type 1 diabetes حسب Goran Petrovski (129836)

مؤلفون آخرون:

Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2 حسب Ahmed K. Elsayed (13275302)

مؤلفون آخرون:

Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene حسب Yasmin W. Abu Aqel (17100289)

مؤلفون آخرون:

One-year experience of hybrid closed-loop system in children and adolescents with type 1 diabetes previously treated with multiple daily injections: drivers to successful outcomes حسب Goran Petrovski (129836)

مؤلفون آخرون:

Haploinsufficiency of the <i>FOXA2</i> associated with a complex clinical phenotype حسب Idris Mohammed (751020)

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