Abeer M. Miqdad
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 14 publications
Saudi Initiative of Bronchiolitis Diagnosis, Management, and Prevention 2024 updated consensus on the prevention of respiratory syncytial virus.
Journal: Annals of thoracic medicine
Published: March 27, 2024
GABA transaminase deficiency. Case report and literature review.
Journal: Clinical case reports
Published: July 23, 2020
Confirming the involvement of PIEZO2 in the etiology of Marden-Walker syndrome.
Journal: American journal of medical genetics. Part A
Published: July 02, 2020
Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans.
Journal: Human genetics
Published: November 04, 2019
Bronchiolitis in children: The Saudi initiative of bronchiolitis diagnosis, management, and prevention (SIBRO).
Journal: Annals of thoracic medicine
Published: August 21, 2018
The most frequent ABCA3 nonsense mutation -p.Tyr1515* (Y1515X) causing lethal neonatal respiratory failure in a term neonate.
Journal: Annals of thoracic medicine
Published: August 16, 2017
Gonadal mosaicism for ACTA1 gene masquerading as autosomal recessive nemaline myopathy.
Journal: American journal of medical genetics. Part A
Published: February 25, 2016
Report of a case of Raine syndrome and literature review.
Journal: American journal of medical genetics. Part A
Published: January 07, 2015
Sirenomelia and severe caudal regression syndrome.
Journal: Saudi medical journal
Published: January 01, 2015
Genetic, chromosomal, and syndromic causes of neural tube defects.
Journal: Saudi medical journal
Published: January 01, 2015
Last Updated: 09/26/2026