Afaf Alsagheir

10PUBLICATIONS
23CO-AUTHORS
NeonatologyInformation systems development methodologies and practiceGenetic immunologyEndocrinologyMedical devices
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Publications (10)

|Apr 27, 2026
Denys-Drash Syndrome by WT1 Gene: Clinical Variability and Management Challenges in Two Saudi Infants.

|Mar 04, 2026
Real-World Experience With Control-IQ Technology in Saudi Children With Insulin-Dependent Diabetes: A Single-Center Observational Study.

Afaf Alsagheir, Bassam Bin-Abbas, Razan Alsagheir

|Feb 02, 2026
Molecular Genetics of 1α-Hydroxylase Deficiency in the Saudi Population.

Bassam Bin-Abbas, Afaf Alsagheir, Balgees Alghamdi

|Jan 08, 2026
StAR Protein Deficiency in Clinical Practice: A Case Series From Saudi Arabia.

Abeer Alabduljabbar, Dania Farooq, Sara Abid

|Jul 12, 2025
Hyperinsulinism-hyperammonemia syndrome associated with GLUD1 gene mutation: a case series.

Miral M Abdulghfar, Afaf Alsagheir, Ismail A Abdullah

|Mar 22, 2025
ADAT3 variants disrupt the activity of the ADAT tRNA deaminase complex and impair neuronal migration.

Jordi Del-Pozo-Rodriguez, Peggy Tilly, Romain Lecat

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Frequent Collaborators

3 joint publications

Raghad Alhuthil

1 joint publications

Amir Babiker

1 joint publications

Mohamed H Al-Hamed

1 joint publications

Melanie O'Leary