Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review

por Habeb, Abdelhadi M.
Publicado 2013

Response to oral gliclazide in a pre-pubertal child with hepatic nuclear factor-1 alpha maturity onset diabetes of the young

por Habeb, Abdelhadi M., George, Elizabeth T., Mathew, Verghese, Hattersley, Andrew L.
Publicado 2011

The spectrum of congenital heart diseases in down syndrome: A retrospective study from Northwest Saudi Arabia

por Morsy, Mohamed M., Algrigri, Osama O., Salem, Sherif S., Abosedera, Mostafa M., Abutaleb, Ashraf R., Al-Harbi, Khaled M., Al-Mozainy, Ibrahim S., Alnajjar, Abdulhameed A., Habeb, Abdelhadi M., Abo-Haded, Hany M.
Publicado en Saudi Med J (2016)

Liver Disease and Other Comorbidities in Wolcott-Rallison Syndrome: Different Phenotype and Variable Associations in a Large Cohort

por Habeb, Abdelhadi M., Deeb, Asma, Johnson, Matthew, Abdullah, Mohammed, Abdulrasoul, Majidah, Al-Awneh, Hussain, Al-Maghamsi, Mohammed S.F., Al-Murshedi, Fathiya, Al-Saif, Ramlah, Al-Sinani, Siham, Ramadan, Dina, Tfayli, Hala, Flanagan, Sarah E., Ellard, Sian
Publicado en Horm Res Paediatr (2015)

Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome

por Habeb, Abdelhadi M., Flanagan, Sarah E., Zulali, Mohamed A., Abdullah, Mohamed A., Pomahačová, Renata, Boyadzhiev, Veselin, Colindres, Lesby E., Godoy, Guillermo V., Vasanthi, Thiruvengadam, Al Saif, Ramlah, Setoodeh, Aria, Haghighi, Amirreza, Haghighi, Alireza, Shaalan, Yomna, Hattersley, Andrew T., Ellard, Sian, De Franco, Elisa
Publicado en Diabetologia (2018)

Homozygous Resistance to Thyroid Hormone β: Can Combined Antithyroid Drug and Triiodothyroacetic Acid Treatment Prevent Cardiac Failure?

por Moran, Carla, Habeb, Abdelhadi M., Kahaly, George J., Kampmann, Christoph, Hughes, Marina, Marek, Jan, Rajanayagam, Odelia, Kuczynski, Adam, Vargha-Khadem, Faraneh, Morsy, Mofeed, Offiah, Amaka C., Poole, Ken, Ward, Kate, Lyons, Greta, Halsall, David, Berman, Lol, Watson, Laura, Baguley, David, Mollon, John, Moore, Anthony T., Holder, Graham E., Dattani, Mehul, Chatterjee, Krishna
Publicado en J Endocr Soc (2017)

Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ

por Nicholas, Adeline K., Serra, Eva G., Cangul, Hakan, Alyaarubi, Saif, Ullah, Irfan, Schoenmakers, Erik, Deeb, Asma, Habeb, Abdelhadi M., Almaghamsi, Mohammad, Peters, Catherine, Nathwani, Nisha, Aycan, Zehra, Saglam, Halil, Bober, Ece, Dattani, Mehul, Shenoy, Savitha, Murray, Philip G., Babiker, Amir, Willemsen, Ruben, Thankamony, Ajay, Lyons, Greta, Irwin, Rachael, Padidela, Raja, Tharian, Kavitha, Davies, Justin H., Puthi, Vijith, Park, Soo-Mi, Massoud, Ahmed F., Gregory, John W., Albanese, Assunta, Pease-Gevers, Evelien, Martin, Howard, Brugger, Kim, Maher, Eamonn R., Chatterjee, V. Krishna K., Anderson, Carl A., Schoenmakers, Nadia
Publicado en J Clin Endocrinol Metab (2016)