The Epidemiology and Genetic Analysis of Children With Idiopathic Type 1 Diabetes in the State of Qatar

por Abdel-Karim, Tasneem, Haris, Basma, Afyouni, Houda, Mohammed, Shayma, Khalifa, Amel, Al-Maadheed, Maryam, Zyoud, Mahmoud, Elawwa, Ahmed, Al-Khalaf, Fawziya, Petrovski, Goran, Hussain, Khalid
Publicado 2021

Sib-pair subgroup familial type 1 diabetes mellitus in children in the state of Qatar

por Afyouni, Houda, Haris, Basma, Syed, Najeeb, Ahmed, Ikhlak, Hamed, Noor, Abdel-Karim, Tasneem, Mohammed, Shayma, Khalifa, Amel, Al-Maadheed, Maryam, Zyoud, Mahmoud, Elawwa, Ahmed, Al-Khalaf, Fawziya, Petrovski, Goran, Hussain, Khalid
Publicado 2022

Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar

por Haris, Basma, Saraswathi, Saras, Al‐Khawaga, Sara, Hasnah, Reem, Saeed, Amira, Mundekkadan, Shihab, Hamed, Noor, Afyouni, Houda, Abdel‐Karim, Tasneem, Mohammed, Shayma, Khalifa, Amel, Al‐Maadheed, Maryam, Al‐Zyoud, Mahmoud, Shamekh, Ahmed, Elawwa, Ahmed, Al‐Khalaf, Fawziya, Boughorbel, Sabri, Petrovski, Goran, Hussain, Khalid
Publicado 2021

Corneal nerve loss in children with type 1 diabetes mellitus without retinopathy or microalbuminuria

por Gad, Hoda, Al‐Jarrah, Bara, Saraswathi, Saras, Petropoulos, Ioannis N, Ponirakis, Georgios, Khan, Adnan, Singh, Parul, Al Khodor, Souhaila, Elawad, Mamoun, Almasri, Wesam, Abdelrahman, Hatim, Elawwa, Ahmed, Khalifa, Amel, Shamekh, Ahmed, Al‐Khalaf, Fawziya, Petrovski, Goran, Al Zyoud, Mahmoud, Al Maadheed, Maryam, Hendaus, Mohamed A, Hussain, Khalid, Akobeng, Anthony K, Malik, Rayaz A
Publicado 2020

Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar

por Haris, Basma, Ahmed, Ikhlak, Syed, Najeeb, Almabrazi, Hakeem, Saraswathi, Saras, Al-Khawaga, Sara, Saeed, Amira, Mundekkadan, Shihab, Mohammed, Idris, Sharari, Sanaa, Hawari, Iman, Hamed, Noor, Afyouni, Houda, Abdel-Karim, Tasneem, Mohammed, Shayma, Khalifa, Amel, Al-Maadheed, Maryam, Zyoud, Mahmoud, Shamekh, Ahmed, Elawwa, Ahmed, Karim, Mohammed Y., Al-Khalaf, Fawziya, Tatari-Calderone, Zohreh, Petrovski, Goran, Hussain, Khalid
Publicado 2021

Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

por Raimondo, Anne, Chakera, Ali J., Thomsen, Soren K., Colclough, Kevin, Barrett, Amy, De Franco, Elisa, Chatelas, Alisson, Demirbilek, Huseyin, Akcay, Teoman, Alawneh, Hussein, Flanagan, Sarah E., Van De Bunt, Martijn, Hattersley, Andrew T., Gloyn, Anna L., Ellard, Sian, Abduljabbar, Mohammad A., Al-Zyoud, Mahmoud, Aman, Syed, Bath, Louise, De, Parijat, Deshpande, Neeta, Durmaz, Erdem, Eickmeier, Frank, Elbarbary, Nancy Samir, Fillion, Marc, Jagadeesh, Sujatha M., Kershaw, Melanie, Khan, Waqas I., Mlynarski, Wojciech, Noyes, Kathryn, Peters, Catherine J., Shaw, Nick, Tiron, Irina, Turkkahraman, Doga, Turner, Lesley, Eltonbary, Khadiga Y., Yuksel, Bilgin
Publicado 2014