Hasil Pencarian - Sara Al‐Khawaga

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  1. 1
    A Systematic Review of Childhood Diabetes Research in the Middle East Region

    A Systematic Review of Childhood Diabetes Research in the Middle East Region oleh Saras Saraswathi, Sara Al-Khawaga, Sara Al-Khawaga, Naser Elkum, Khalid Hussain

    Diterbitkan 2019-11-01
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  2. 2
    Potential application of mesenchymal stem cells and their exosomes in lung injury: an emerging therapeutic option for COVID-19 patients

    Potential application of mesenchymal stem cells and their exosomes in lung injury: an emerging therapeutic option for COVID-19 patients oleh Sara Al-Khawaga, Essam M. Abdelalim

    Diterbitkan 2020-10-01
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  3. 3
    A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency

    A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency oleh Sara Al-Khawaga, Sara Al-Khawaga, Sara Al-Khawaga, Jehan AlRayahi, Faiyaz Khan, Saras Saraswathi, Reem Hasnah, Basma Haris, Idris Mohammed, Idris Mohammed, Essam M. Abdelalim, Essam M. Abdelalim, Khalid Hussain

    Diterbitkan 2019-07-01
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  4. 4
    The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism

    The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism oleh Sonya Galcheva, Hüseyin Demirbilek, Sara Al-Khawaga, Khalid Hussain

    Diterbitkan 2019-02-01
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  5. 5
    Correction to: Enhanced differentiation of human pluripotent stem cells into pancreatic progenitors co-expressing PDX1 and NKX6.1

    Correction to: Enhanced differentiation of human pluripotent stem cells into pancreatic progenitors co-expressing PDX1 and NKX6.1 oleh Bushra Memon, Manale Karam, Sara Al-Khawaga, Essam M. Abdelalim

    Diterbitkan 2018-10-01
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  6. 6
    Enhanced differentiation of human pluripotent stem cells into pancreatic progenitors co-expressing PDX1 and NKX6.1

    Enhanced differentiation of human pluripotent stem cells into pancreatic progenitors co-expressing PDX1 and NKX6.1 oleh Bushra Memon, Manale Karam, Sara Al-Khawaga, Essam M. Abdelalim

    Diterbitkan 2018-01-01
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  7. 7
    Diabetes Mellitus in a Patient With Lafora Disease: Possible Links With Pancreatic β-Cell Dysfunction and Insulin Resistance

    Diabetes Mellitus in a Patient With Lafora Disease: Possible Links With Pancreatic β-Cell Dysfunction and Insulin Resistance oleh Ramona C. Nicolescu, Sara Al-Khawaga, Berge A. Minassian, Khalid Hussain

    Diterbitkan 2019-01-01
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  8. 8
    Ion Transporters, Channelopathies, and Glucose Disorders

    Ion Transporters, Channelopathies, and Glucose Disorders oleh Huseyin Demirbilek, Sonya Galcheva, Dogus Vuralli, Sara Al-Khawaga, Khalid Hussain

    Diterbitkan 2019-05-01
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  9. 9
    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 oleh Ahmed K. Elsayed, Sara Al-Khawaga, Khalid Hussain, Essam M. Abdelalim

    Diterbitkan 2021-07-01
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  10. 10
    Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c.613-7T>G) in the SLC2A2 gene

    Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c.613-7T>G) in the SLC2A2 gene oleh Ahmed K. Elsayed, Maryam Aghadi, Sara Al-Khawaga, Khalid Hussain, Essam M. Abdelalim

    Diterbitkan 2020-04-01
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  11. 11
    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 oleh Ahmed K. Elsayed, Maryam Aghadi, Gowher Ali, Sara Al-Khawaga, Khalid Hussain, Essam M. Abdelalim

    Diterbitkan 2020-01-01
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  12. 12
    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 oleh Yasmin W. Abu Aqel, Gowher Ali, Ahmed K. Elsayed, Sara Al-Khawaga, Khalid Hussain, Essam M. Abdelalim

    Diterbitkan 2020-10-01
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  13. 13
    Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype

    Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype oleh Idris Mohammed, Sara Al‐Khawaga, David Bohanna, Abdusamea Shabani, Faiyaz Khan, Donald R. Love, Zafar Nawaz, Khalid Hussain

    Diterbitkan 2020-06-01
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  14. 14
    Treatment and molecular profiling of acrodermatitis continua of Hallopeau during pregnancy using targeted therapy

    Treatment and molecular profiling of acrodermatitis continua of Hallopeau during pregnancy using targeted therapy oleh Sara Al-Khawaga, MD, Roopesh Krishnankutty, PhD, Gulab Sher, PhD, Khairunnisa Hussain, MD, Joerg Buddenkotte, MD, PhD, Martin Steinhoff, MD, PhD

    Diterbitkan 2021-10-01
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  15. 15
    The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar

    The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar oleh Sara Al‐Khawaga, Idris Mohammed, Saras Saraswathi, Basma Haris, Reem Hasnah, Amira Saeed, Hakeem Almabrazi, Najeeb Syed, Puthen Jithesh, Ahmed El Awwa, Amal Khalifa, Fawziya AlKhalaf, Goran Petrovski, Essam M. Abdelalim, Khalid Hussain

    Diterbitkan 2019-10-01
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  16. 16
    Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar

    Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar oleh Basma Haris, Saras Saraswathi, Sara Al‐Khawaga, Reem Hasnah, Amira Saeed, Shihab Mundekkadan, Noor Hamed, Houda Afyouni, Tasneem Abdel‐Karim, Shayma Mohammed, Amel Khalifa, Maryam Al‐Maadheed, Mahmoud Al‐Zyoud, Ahmed Shamekh, Ahmed Elawwa, Fawziya Al‐Khalaf, Sabri Boughorbel, Goran Petrovski, Khalid Hussain

    Diterbitkan 2021-12-01
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  17. 17
    Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar

    Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar oleh Basma Haris, Ikhlak Ahmed, Najeeb Syed, Hakeem Almabrazi, Saras Saraswathi, Sara Al-Khawaga, Amira Saeed, Shihab Mundekkadan, Idris Mohammed, Sanaa Sharari, Iman Hawari, Noor Hamed, Houda Afyouni, Tasneem Abdel-Karim, Shayma Mohammed, Amel Khalifa, Maryam Al-Maadheed, Mahmoud Zyoud, Ahmed Shamekh, Ahmed Elawwa, Mohammed Y. Karim, Fawziya Al-Khalaf, Zohreh Tatari-Calderone, Goran Petrovski, Khalid Hussain

    Diterbitkan 2021-09-01
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