Showing 1 - 8 results of 8 for search 'Omar I. Saadah', query time: 0.07s Refine Results
  1. 1
    Extraintestinal Manifestations of Inflammatory Bowel Disease in Middle Eastern Patients

    Extraintestinal Manifestations of Inflammatory Bowel Disease in Middle Eastern Patients by Heba Adam, Maryam Alqassas, Omar I. Saadah, Mahmoud Mosli

    Published 2020
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  2. 2
    Granulomatous hepatitis in a Saudi child with defect: a case report and literature review

    Granulomatous hepatitis in a Saudi child with defect: a case report and literature review by Meshari A. Alaifan, Ohood Abusharifah, Rana Yagoub Bokhary, Babajan Banaganapalli, Noor Ahmad Shaik, Naglaa M. Kamal, Omar I. Saadah

    Published 2022
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  3. 3
    Oral and dental manifestations of celiac disease in children: a case-control study

    Oral and dental manifestations of celiac disease in children: a case-control study by Farah A. Alsadat, Najlaa M. Alamoudi, Azza A. El-Housseiny, Osama M. Felemban, Faisal M. Dardeer, Omar I. Saadah

    Published 2021
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  4. 4
    Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study

    Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study by Naglaa M. Kamal, Omar I. Saadah, Shahad S. Alheraiti, Ruwayd Attar, Asmaa D. Alsufyani, Moratda H.F. El-Shabrawi, Laila M. Sherief

    Published 2022
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  5. 5
    Dental maturity in children with celiac disease: a case-control study

    Dental maturity in children with celiac disease: a case-control study by Najlaa M. Alamoudi, Farah A. Alsadat, Azza A. El-Housseiny, Osama M. Felemban, Amani A. Al Tuwirqi, Rana H. Mosli, Omar I. Saadah

    Published 2020
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  6. 6
    Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families

    Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families by Omar I. Saadah, Omar I. Saadah, Babajan Banaganapalli, Babajan Banaganapalli, Naglaa M. Kamal, Naglaa M. Kamal, Ahmed N. Sahly, Ahmed N. Sahly, Hadeel A. Alsufyani, Arif Mohammed, Aftab Ahmad, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Noor Ahmad Shaik, Noor Ahmad Shaik, Ramu Elango, Ramu Elango

    Published 2021
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  7. 7
    Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients

    Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients by Huda Husain Al-Numan, Huda Husain Al-Numan, Rana Mohammed Jan, Rana Mohammed Jan, Najla bint Saud Al-Saud, Omran M. Rashidi, Nuha Mohammad Alrayes, Hadeel A. Alsufyani, Abdulrahman Mujalli, Abdulrahman Mujalli, Noor Ahmad Shaik, Noor Ahmad Shaik, Mahmoud Hisham Mosli, Mahmoud Hisham Mosli, Ramu Elango, Ramu Elango, Omar I. Saadah, Omar I. Saadah, Babajan Banaganapalli, Babajan Banaganapalli

    Published 2022
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  8. 8
    Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease

    Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease by Arwa Mastoor Alharthi, Arwa Mastoor Alharthi, Babajan Banaganapalli, Babajan Banaganapalli, Sabah M. Hassan, Sabah M. Hassan, Omran Rashidi, Bandar Ali Al-Shehri, Meshari A. Alaifan, Meshari A. Alaifan, Bakr H. Alhussaini, Bakr H. Alhussaini, Hadeel A. Alsufyani, Kawthar Saad Alghamdi, Khalda Khalid Nasser, Khalda Khalid Nasser, Khalda Khalid Nasser, Yagoub Bin-Taleb, Ramu Elango, Ramu Elango, Noor Ahmad Shaik, Noor Ahmad Shaik, Omar I. Saadah, Omar I. Saadah

    Published 2022
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