Showing 1 - 20 results of 30 for search 'Khalid Hussain (110443)', query time: 0.02s Refine Results
  1. 1
    Efficacy of Semaglutide in Pediatric Patients With Bardet-Biedl Syndrome and Alström Syndrome

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

    Published 2025
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  2. 2
    A Novel Homozygous <i>MC2R</i> Variant Leading to Type-1 Familial Glucocorticoid Deficiency

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

    Published 2022
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  3. 3
    The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism

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

    Published 2019
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  4. 4
    A Systematic Review of Childhood Diabetes Research in the Middle East Region

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

    Published 2019
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  5. 5
    Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly

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

    Published 2022
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  6. 6
    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

    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 by Ahmed K. Elsayed (13275302)

    Published 2021
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  7. 7
    Genetic epidemiology of Woodhouse-Sakati Syndrome in the Greater Middle East region and beyond: a systematic review

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

    Published 2023
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  8. 8
    Fanconi–Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia

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

    Published 2020
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  9. 9
    Challenges in child and adolescent health across the Arab Gulf countries—Focus on metabolic health

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

    Published 2025
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  10. 10
    Alpelisib Therapy in 2 Patients With Congenital Hyperinsulinism

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

    Published 2025
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  11. 11
    Aberrant development of pancreatic beta cells derived from human iPSCs with FOXA2 deficiency

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

    Published 2022
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  12. 12
    Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 Gene

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

    Published 2024
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  13. 13
    Ion Transporters, Channelopathies, and Glucose Disorders

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

    Published 2019
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  14. 14
    Infancy onset diabetes mellitus in a patient with a novel homozygous LRBA mutation

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

    Published 2022
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  15. 15
    Glucose control during Ramadan fasting in a teenager with type 1 diabetes on MiniMed 670G hybrid closed-loop system

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

    Published 2019
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  16. 16
    10-Day structured initiation protocol from multiple daily injection to hybrid closed-loop system in children and adolescents with type 1 diabetes

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

    Published 2020
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  17. 17
    Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2

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

    Published 2020
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  18. 18
    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

    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 by Yasmin W. Abu Aqel (17100289)

    Published 2020
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  19. 19
    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

    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 by Goran Petrovski (129836)

    Published 2022
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  20. 20
    Haploinsufficiency of the <i>FOXA2</i> associated with a complex clinical phenotype

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

    Published 2020
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