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Basma Haris
Basma Haris
Sidra Medicine
Bestätigte E-Mail-Adresse bei sidra.org
Titel
Zitiert von
Zitiert von
Jahr
The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar
S Al‐Khawaga, I Mohammed, S Saraswathi, B Haris, R Hasnah, A Saeed, ...
Molecular genetics & genomic medicine 7 (10), e00753, 2019
282019
Somatostatin analogues for the treatment of hyperinsulinaemic hypoglycaemia
B Haris, S Saraswathi, K Hussain
Therapeutic Advances in Endocrinology and Metabolism 11, 2042018820965068, 2020
172020
A SLC16A1 mutation in an infant with ketoacidosis and neuroimaging assessment: expanding the clinical spectrum of MCT1 deficiency
S Al-Khawaga, J AlRayahi, F Khan, S Saraswathi, R Hasnah, B Haris, ...
Frontiers in Pediatrics 7, 299, 2019
122019
Rare antagonistic leptin variants and severe, early-onset obesity
JB Funcke, B Moepps, J Roos, J von Schnurbein, K Verstraete, ...
New England Journal of Medicine 388 (24), 2253-2261, 2023
112023
Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar
B Haris, I Ahmed, N Syed, H Almabrazi, S Saraswathi, S Al-Khawaga, ...
Scientific reports 11 (1), 18887, 2021
112021
Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar
B Haris, S Saraswathi, S Al‐Khawaga, R Hasnah, A Saeed, ...
Journal of Diabetes Investigation 12 (12), 2141-2148, 2021
82021
Maturity‐onset diabetes of the young (MODY) due to PDX1 mutation in a sib‐pair diabetes family from Qatar
B Haris, I Mohammed, N Syed, K Fakhro, K Hussain
Clinical Case Reports 9 (12), e05141, 2021
62021
Managing severe hypoglycaemia in patients with diabetes: current challenges and emerging therapies
H Demirbilek, D Vuralli, B Haris, K Hussain
Diabetes, Metabolic Syndrome and Obesity, 259-273, 2023
52023
Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi–Bickel Syndrome
S Sharari, B Kabeer, I Mohammed, B Haris, I Pavlovski, I Hawari, AA Bhat, ...
Biomedicines 10 (9), 2114, 2022
52022
A Novel Homozygous MC2R Variant Leading to Type-1 Familial Glucocorticoid Deficiency
I Mohammed, B Haris, K Hussain
Journal of the Endocrine Society 6 (6), bvac058, 2022
52022
Case Report: Hepatic Adenomatosis in a Patient With Prader–Willi Syndrome
H Dauleh, A Soliman, B Haris, A Khalifa, N Al Khori, K Hussain
Frontiers in Endocrinology 13, 826772, 2022
32022
Infancy onset diabetes mellitus in a patient with a novel homozygous LRBA mutation
I Hawari, B Haris, I Mohammed, J Ericsson, A Khalifa, K Hussain
Journal of Clinical and Translational Endocrinology: Case Reports 23, 100108, 2022
32022
Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient
S Sharari, M Aouida, I Mohammed, B Haris, AA Bhat, I Hawari, S Nisar, ...
Frontiers in Endocrinology 13, 841788, 2022
22022
Type 2 Diabetes Mellitus in a 7 Year Old Girl
B Haris, S Stafrace, K Hussain
International Medical Case Reports Journal, 245-250, 2022
22022
The epidemiology, clinical, biochemical, immunological and radiological features of youth onset type 2 diabetes mellitus in the state of Qatar
SM Ahmed, B Haris, S Saraswathi, A Elawwa, A Khalifa, M AlMaadheed, ...
Diabetology international, 1-6, 2022
22022
Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly
UKI Umlai, B Haris, K Hussain, PV Jithesh
Frontiers in Endocrinology 12, 783235, 2022
22022
The epidemiology and genetic analysis of children with idiopathic type 1 diabetes in the state of Qatar
T Abdel-Karim, B Haris, H Afyouni, S Mohammed, A Khalifa, ...
Journal of the Endocrine Society 5 (10), bvab131, 2021
22021
Understanding the Genetics of Early-Onset Obesity in a Cohort of Children From Qatar
I Mohammed, B Haris, T Al-Barazenji, D Vasudeva, S Tomei, I Al Azwani, ...
The Journal of Clinical Endocrinology & Metabolism 108 (12), 3201-3213, 2023
12023
Homozygous Insulin Promotor Gene Mutation Causing Permanent Neonatal Diabetes Mellitus and Childhood Onset Autoantibody Negative Diabetes in the Same Family
B Haris, I Mohammed, S Al-Khawaga, K Hussain
International Medical Case Reports Journal, 35-41, 2022
12022
The prevalence, immune profile, and clinical characteristics of children with celiac disease and type 1 diabetes mellitus in the state of Qatar
B Haris, A Abdellatief, H Afyouni, T Abdel-Karim, S Mohammed, A Khalifa, ...
Journal of Pediatric Endocrinology and Metabolism 34 (11), 1457-1461, 2021
12021
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