Fanconi–Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia

por Sharari, Sanaa, Abou-Alloul, Mohamad, Hussain, Khalid, Ahmad Khan, Faiyaz
Publicado 2020

Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype

por Mohammed, Idris, Al‐Khawaga, Sara, Bohanna, David, Shabani, Abdusamea, Khan, Faiyaz, Love, Donald R., Nawaz, Zafar, Hussain, Khalid
Publicado 2020

A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency

por Al-Khawaga, Sara, AlRayahi, Jehan, Khan, Faiyaz, Saraswathi, Saras, Hasnah, Reem, Haris, Basma, Mohammed, Idris, Abdelalim, Essam M., Hussain, Khalid
Publicado 2019

Understanding the Mechanism of Diabetes Mellitus in a LRBA-Deficient Patient

por Hawari, Iman, Ericsson, Johan, Kabeer, Basirudeen Syed Ahamed, Chaussabel, Damien, Alsulaiti, Asma, Sharari, Sanaa A., Maccalli, Cristina, Khan, Faiyaz Ahmad, Hussain, Khalid
Publicado 2022