Testosterone-and cortisol-secreting oncocytic adrenocortical adenoma in the pediatric age-group

MK Al Badi, I Al-Alwan, M Al-Dubayee… - Pediatric and …, 2018 - journals.sagepub.com
Oncocytic tumors are epithelial neoplasms that occur in various organs, including adrenal
glands. Oncocytic adrenocortical adenomas and carcinomas are uncommon but well-known …

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

…, A Toygar, V Mudryi, M Al Badi… - Proceedings of the …, 2017 - National Acad Sciences
… (K) The OH group in the L251S mutation makes a hydrogen bond with R361 from the adjacent
subunit, thus enhancing the interaction at the dimer interface. (L) The … Maryam Al Badi

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

MK Al-Badi, HS Al-Azkawi, MS Al-Yahyaei… - 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 …

Genetic mutations associated with neonatal diabetes mellitus in Omani patients

…, M Al Kharusi, N Al Sukaiti, M Al Badi… - 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 …

A unique genotype of pseudohypoaldosteronism type 1b in a highly consanguineous population

…, A Al Shidhani, A Al Sinani, M Al Badi… - Journal of the …, 2021 - academic.oup.com
Maryam Al Badi , Maryam Al Badi … Renin-aldosterone response, urinary Na/K ratio and
growth in pseudohypoaldosteronism patients with mutations in epithelial sodium channel (ENaC) …

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 …

[HTML][HTML] Case report: investigation and molecular genetic diagnosis of familial hypomagnesaemia

J Willows, M Al Badi, C Richardson, A Al Sinani… - …, 2019 - ncbi.nlm.nih.gov
Genetic mutations causing familial hypomagnesaemia syndromes are well-recognised.
Affected patients can present with severe symptoms of hypomagnesaemia, such as seizures or …

Higher serum alkaline phosphatase activity in infants born to vitamin D–deficient mothers

I Al Alwan, M Al Badi, M Badri, W Tamimi… - Archives of …, 2019 - Springer
Our research shows that the newborns of vitamin D–deficient mothers have higher serum
alkaline phosphatase (ALP) activity compared with those of vitamin D–non-deficient mothers, …

[PDF][PDF] Smartphone applications for improved pharmaceutical care

MH Al Badi, HR Chitme - International Journal of Pharmaceutical …, 2015 - academia.edu
SMARTPHONE APPLICATIONS FOR IMPROVED PHARMACEUTICAL CARE Maryam Hamdan
Al Badi and Havagiray R. Chitme … Maryam Hamdan Al Badi and Havagiray R. Chitme …

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

…, AH Al Rawahi, O Ahmed, K Al Musalhi, M Al Badi - 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 …