Talal M. Almaghamsi
Jeddah, Saudi Arabia
Last Updated: 09/26/2026
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Found 9 publications
Identification of cystic fibrosis transmembrane conductance regulator gene (CFTR) variants: A retrospective study on the western and southern regions of Saudi Arabia.
Journal: Saudi medical journal
Published: July 31, 2023
Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients.
Journal: Journal of human genetics
Published: September 22, 2021
Severe asthma in children: An official statement from Saudi Pediatric Pulmonology Association.
Journal: Saudi medical journal
Published: September 20, 2021
A single-centre study of genetic mutations, audiology, echocardiogram and pulmonary function in Saudi children with osteogenesis imperfecta.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: September 12, 2021
Unusual Prominent Pulmonary Involvement in a Homozygous PRF1 Gene Variant in a Female Patient.
Journal: Journal of clinical immunology
Published: August 28, 2020
Cystic fibrosis gene mutations and polymorphisms in Saudi men with infertility.
Journal: Annals of Saudi medicine
Published: August 08, 2020
Childhood Asthma Awareness in Saudi Arabia: Five-Year Follow-Up Study.
Journal: Journal of asthma and allergy
Published: July 21, 2020
Genotype patterns for mutations of the cystic fibrosis transmembrane conductance regulator gene: a retrospective descriptive study from Saudi Arabia.
Journal: Annals of Saudi medicine
Published: February 07, 2020
Geographic distribution of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Saudi Arabia.
Journal: International journal of pediatrics & adolescent medicine
Published: August 01, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026