Nishath Hamza
Muscat, MA, Oman
Last Updated: 09/26/2026
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Found 16 publications
A scoping review exploring the health impact and sustainability of collaborative paediatric heart disease treatment programmes in developing countries.
Journal: Frontiers in pediatrics
Published: June 27, 2026
Clinical Heterogeneity of a TP53 Variant in a Consanguineous Omani Family: A Case Report Featuring a Homozygous Pathogenic Variant.
Journal: Case reports in genetics
Published: December 11, 2025
First Report of a Derivative Chromosome 13 with a Duplicated 11p15 Locus Associated with Silver-Russell Syndrome.
Journal: Sultan Qaboos University medical journal
Published: November 25, 2021
A Novel SPINK5 Gene Mutation Associated with Netherton Syndrome in an Omani Patient.
Journal: Sultan Qaboos University medical journal
Published: September 01, 2020
Spondylo-ocular Syndrome Due to a Novel Variant in XYLT2 in an Omani Patient.
Journal: Journal of pediatric genetics
Published: April 30, 2020
A first case report of hypohidrotic ectodermal dysplasia from Oman.
Journal: Clinical case reports
Published: September 25, 2019
Hereditary Paraganglioma in an Omani Family.
Journal: Oman medical journal
Published: September 03, 2019
Rare NF1 microdeletion syndrome in an Omani patient.
Journal: Clinical case reports
Published: February 15, 2018
Acquiring new N-glycosylation sites in variable regions of immunoglobulin genes by somatic hypermutation is a common feature of autoimmune diseases.
Journal: Annals of the rheumatic diseases
Published: October 19, 2017
Genetic mutations associated with neonatal diabetes mellitus in Omani patients.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 20, 2017
Repository of mutations from Oman: The entry point to a national mutation database.
Journal: F1000Research
Published: September 11, 2015
Last Updated: 09/26/2026