[HTML][HTML] Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy: A one-decade single-center …

…, WA Mula-Abed, AM Al-Senani - Saudi Medical …, 2019 - ncbi.nlm.nih.gov
Objectives: To report the genotype-phenotype characteristics, demographic features and
clinical outcome of Omani patients with congenital hyperinsulinism (CHI). Methods: We …

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency

…, JW Funder, A Al Senani… - Proceedings of the …, 2017 - National Acad Sciences
Mutations in 11β-hydroxysteroid dehydrogenase type 2 gene (HSD11B2) cause an extraordinarily
rare autosomal recessive disorder, apparent mineralocorticoid excess (AME). AME is …

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

…, A Al Senani, N Elbarbary, Z Siklar, M Berberoglu… - Diabetes, 2017 - Am Diabetes Assoc
Aisha Al Senani; Aisha Al Senani … Johnson, Elisa De Franco, Hana Lango Allen, Aisha
Al Senani, Nancy Elbarbary, Zeynep Siklar, Merih Berberoglu, Zineb Imane, Alireza Haghighi, …

Genetic mutations associated with neonatal diabetes mellitus in Omani patients

A Al Senani, N Hamza, H Al Azkawi… - Journal of Pediatric …, 2018 - degruyter.com
Background: Neonatal diabetes mellitus (NDM) is a rare disorder worldwide where diabetes
is diagnosed in the first 6 months of life. However, Oman has a relatively high incidence of …

Metabolic and other morbid complications in congenital generalized lipodystrophy type 4

…, N Gagne, F Babalola, A Al Senani… - American Journal of …, 2024 - Wiley Online Library
Morbidity and mortality rates in patients with autosomal recessive, congenital generalized
lipodystrophy type 4 (CGL4), an ultra‐rare disorder, remain unclear. We report on 30 females …

[HTML][HTML] Demographic features and etiology of congenital hypothyroidism at the national diabetes and endocrine center in Oman from 2004 to 2016

M Al Jafari, S Jose, A Al Senani - Oman Medical Journal, 2020 - ncbi.nlm.nih.gov
Objectives Congenital hypothyroidism (CH) is the most common endocrine disorder in
neonates as well as one of the few preventable causes of severe learning difficulties. Early …

[PDF][PDF] Efficacy of a high initial dose of L-thyroxine in the treatment of congenital hypothyroidism

NAM Al-Jurayyan, RNA Al-Jurayyan, AMS Al Senani - development, 2010 - academia.edu
Results of a treatment strategy using an initial dosage of 10–15 μg/kg/day of L-thyroxine
was evaluated in a prospective longitudinal study in King Khalid University Hospital, Riyadh, …

A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred

M Yau, HSA Azkawi, S Haider, A Khattab… - Annals of the New …, 2016 - Wiley Online Library
Apparent mineralocorticoid excess (AME) is a rare autosomal recessive genetic disorder
causing severe hypertension in childhood due to a deficiency of 11β‐hydroxysteroid …

[PDF][PDF] The Effect of Vitamin D Status of Type 1 Diabetic Children on their Glycemic Control

A Al Senani, AH Al Rawahi, O Ahmed, K Al Musalhi… - teikyomedicaljournal.com
The knowledge of the important role of vitamin D in bone health is well-established. It has a
direct effect on calcium and phosphate metabolism. Vitamin D deficiency is generally …

2nd Genetics Conference: Genetics in developing countries, unique challenges and opportunities: Sultan Qaboos University, 9–11 March 2014

…, B Hassan, Y Tamimi, A Al-Senani… - Sultan Qaboos …, 2014 - europepmc.org
The global disease pattern has shifted, with a more dominant prevalence of chronic disease
such as type 2 diabetes, metabolic syndrome, cancer and cardiovascular diseases. The inter…