Lina G. Elzubair

Khamis Mushait, Saudi Arabia

Last Updated: 09/26/2026

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Found 14 publications

Retraction: The Association Between Janus Kinase 2 and Factor V Leiden Mutations and Thrombotic Complications in Patients With Myeloproliferative Disorders: A Study From Saudi Arabia.

Retraction: The Association Between Janus Kinase 2 and Factor V Leiden Mutations and Thrombotic Complications in Patients With Myeloproliferative Disorders: A Study From Saudi Arabia.

Journal: Cureus
Published: July 03, 2026

A Novel Homozygous ITGA2B Variant Associated With Recurrent Epistaxis in a Four-Year-Old Girl: A Case Report.

A Novel Homozygous ITGA2B Variant Associated With Recurrent Epistaxis in a Four-Year-Old Girl: A Case Report.

Journal: Cureus
Published: February 03, 2026

A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.

A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.

Journal: Cureus
Published: November 25, 2025

First Reported Case of Glucose-6-Phosphate Isomerase Deficiency in a Saudi Child With Hemolytic Anemia.

First Reported Case of Glucose-6-Phosphate Isomerase Deficiency in a Saudi Child With Hemolytic Anemia.

Journal: Cureus
Published: October 17, 2025

Dehydrated Hereditary Stomatocytosis (DHS): A Rare Inherited Hemolytic Disorder With Unusual Hypochromic Microcytic Anemia.

Dehydrated Hereditary Stomatocytosis (DHS): A Rare Inherited Hemolytic Disorder With Unusual Hypochromic Microcytic Anemia.

Journal: Cureus
Published: March 27, 2025

A Novel Variant of GP9 Gene Resulting in Bernard-Soulier Syndrome: A Case Report.

A Novel Variant of GP9 Gene Resulting in Bernard-Soulier Syndrome: A Case Report.

Journal: Cureus
Published: December 25, 2024

The Association Between Janus Kinase 2 and Factor V Leiden Mutations and Thrombotic Complications in Patients With Myeloproliferative Disorders: A Study From Saudi Arabia.

The Association Between Janus Kinase 2 and Factor V Leiden Mutations and Thrombotic Complications in Patients With Myeloproliferative Disorders: A Study From Saudi Arabia.

Journal: Cureus
Published: November 24, 2024

A Rare THPO Gene Mutation in a Saudi Female Child: A Case Report and Literature Review.

A Rare THPO Gene Mutation in a Saudi Female Child: A Case Report and Literature Review.

Journal: Cureus
Published: September 30, 2024

Hermansky-Pudlak Syndrome Type 2: A Case Report on an Ultra-Rare Disorder.

Hermansky-Pudlak Syndrome Type 2: A Case Report on an Ultra-Rare Disorder.

Journal: Cureus
Published: July 22, 2024

A Novel Variant in the DIAPH1 Gene Causing Macrothrombocytopenia and Non-syndromic Hearing Loss in a Pediatric Saudi Girl.

A Novel Variant in the DIAPH1 Gene Causing Macrothrombocytopenia and Non-syndromic Hearing Loss in a Pediatric Saudi Girl.

Journal: Cureus
Published: May 25, 2024

Familial Hemophagocytic Lymphohistiocytosis (FHLH) Perforin Deficiency: A Case Study and Literature Review.

Familial Hemophagocytic Lymphohistiocytosis (FHLH) Perforin Deficiency: A Case Study and Literature Review.

Journal: Cureus
Published: March 08, 2024

A Rare MPIG6B Gene Mutation in a Saudi Adolescent Male With Thrombocytopenia, Anemia, and Myelofibrosis: A Case Report.

A Rare MPIG6B Gene Mutation in a Saudi Adolescent Male With Thrombocytopenia, Anemia, and Myelofibrosis: A Case Report.

Journal: Cureus
Published: February 11, 2024
Showing 1-12 of 14

Last Updated: 09/26/2026