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Ayman Bakkar
Observed names:
Ayman A Bakkar,
Ayman A. Bakkar,
Ayman A. Bakkar A.
Institution:
Armed Forces Hospital
Observed institution:
Armed Forces Hospital
ORCID:
0000-0003-0266-8728
Observed ORCID:
0000-0003-0266-8728
OpenAlex ID:
A5029771679
The Impact of COVID-19 Pandemic Lockdown on the Incidence of New-Onset Type 1 Diabetes and Ketoacidosis Among Saudi Children
2021
·
Aqeel Alaqeel
, Fahad Aljuraibah
, et al.
·
Frontiers in Endocrinology
·
60
PDF
Vici syndrome with pathogenic homozygous EPG5 gene mutation: A case report and literature review
2020
·
Kamal T. Abidi
, Naglaa M. Kamal
, et al.
·
Medicine
·
14
Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation
2023
·
Ayman A Bakkar
, Abdulaziz Alsaedi
, et al.
·
Clinical Medicine Insights Endocrinology and Diabetes
·
11
PDF
Late presentation of necrotizing enterocolitis associated with rotavirus infection in a term infant with hyperinsulinism on octreotide therapy: A case report
2017
·
Abdulaziz A. Alsaedi
, Ayman A. Bakkar
, et al.
·
Medicine
·
7
Sotos syndrome: A case report of 1st genetically proven case from Saudi Arabia with a novel mutation in NSD1 gene
2018
·
Naglaa M. Kamal
, Jwaher M. Althobiti
, et al.
·
Medicine
·
4
Idiopathic hypoparathyroidism with extensive intracranial calcification in children: First report from Saudi Arabia
2017
·
Naglaa M. Kamal
, Hamed A. Alghamdi
, et al.
·
Medicine
·
4
Sjogren–Larsson Syndrome: A case series of five members from an extended family with a novel mutation
2020
·
Kamel T. Abidi
, Naglaa M. Kamal
, et al.
·
Molecular Genetics & Genomic Medicine
·
3
PDF
Short- and long-term complications of insulin pump therapy in children and adolescents with type 1 diabetes: a multicenter cross-sectional study from Saudi Arabia
2025
·
Ayman Bakkar
, Enad Althobaiti
, et al.
·
Therapeutic Advances in Chronic Disease
·
2
Comprehensive analysis of disease spectrum and mortality in Sanjad–Sakati syndrome: an international rare disease registry study
2026
·
Angham Almutair
, Katharina Karas
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
1
Novel Melano-Cortin-2-Receptor Gene Mutation Presenting With Infantile Cholestasis: A Case Report
2022
·
Abdulaziz Alsaedi
, Naglaa M Kamal
, et al.
·
Clinical Medicine Insights Case Reports
·
1
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Works count:
10
Citation count:
107
H-index:
4
I10-index:
3
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