Renin–Angiotensin System Implications to COVID-19 Comorbidities

por Alsufyani, Hadeel A., Alrefaie, Zienab
Publicado 2020

Involvement of α(1B)-adrenoceptors and Rho kinase in contractions of rat aorta and mouse spleen

por Alsufyani, Hadeel A., Docherty, James R.
Publicado 2023

The renin angiotensin aldosterone system and COVID-19

por Alsufyani, Hadeel A., Docherty, James R.
Publicado 2020

Roles for α(1)-adrenoceptors during contractions by electrical field stimulation in mouse vas deferens

por Alsufyani, Hadeel A., Docherty, James R.
Publicado 2021

Prevalence of Celiac Disease in Children and Adolescents With Inflammatory Bowel Disease

por Eskander, Ayman, Saadah, Omar I, Abdelrazek, Abdelrahman A, Mosli, Mahmoud, Alsufyani, Hadeel A., Meshaal, Safa, Hasnoon, Amera M, Tarek, Sara, Abdelgalil, Abobakr
Publicado 2020

Transition Readiness Into Adult Health Care in Children With Inflammatory Bowel Disease

por Alsufyani, Hadeel A., Jar, Sondos, Jambi, Wehad S, Meer, Nuha, Bajunaid, Weam, Albaradei, Hadeel A, Alharbi, Nadin A, Aziz, Haneen, Mosli, Mahmoud, Saadah, Omar I
Publicado 2023

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

por Saadah, Omar I., Banaganapalli, Babajan, Kamal, Naglaa M., Sahly, Ahmed N., Alsufyani, Hadeel A., Mohammed, Arif, Ahmad, Aftab, Nasser, Khalidah Khalid, Al-Aama, Jumana Y., Shaik, Noor Ahmad, Elango, Ramu
Publicado 2021

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

por Al-Numan, Huda Husain, Jan, Rana Mohammed, Al-Saud, Najla bint Saud, Rashidi, Omran M., Alrayes, Nuha Mohammad, Alsufyani, Hadeel A., Mujalli, Abdulrahman, Shaik, Noor Ahmad, Mosli, Mahmoud Hisham, Elango, Ramu, Saadah, Omar I., Banaganapalli, Babajan
Publicado 2022

Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis

por Jan, Rana Mohammed, Al-Numan, Huda Husain, Al-Twaty, Nada Hassan, Alrayes, Nuha, Alsufyani, Hadeel A., Alaifan, Meshari A., Alhussaini, Bakr H., Shaik, Noor Ahmad, Awan, Zuhier, Qari, Yousef, Saadah, Omar I., Banaganapalli, Babajan, Mosli, Mahmoud Hisham, Elango, Ramu
Publicado 2023

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

por Alharthi, Arwa Mastoor, Banaganapalli, Babajan, Hassan, Sabah M., Rashidi, Omran, Al-Shehri, Bandar Ali, Alaifan, Meshari A., Alhussaini, Bakr H., Alsufyani, Hadeel A., Alghamdi, Kawthar Saad, Nasser, Khalda Khalid, Bin-Taleb, Yagoub, Elango, Ramu, Shaik, Noor Ahmad, Saadah, Omar I.
Publicado 2022