Naglaa A. Fawaz

Squ
Muscat, MA, Oman

Last Updated: 09/26/2026

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Found 10 publications

Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia - lessons learned for prophylaxis.

Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia - lessons learned for prophylaxis.

Journal: The Journal of international medical research

Published: December 02, 2021

Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred-PK deficiency masquerading as congenital dyserythropoietic anemia.

Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred-PK deficiency masquerading as congenital dyserythropoietic anemia.

Journal: Clinical case reports

Published: November 01, 2021

Clinicopathological Profile of Paroxysmal Nocturnal Hemoglobinuria among Omani Patients: A Case Series.

Clinicopathological Profile of Paroxysmal Nocturnal Hemoglobinuria among Omani Patients: A Case Series.

Journal: Oman medical journal

Published: August 17, 2020

Immunophenotypic Characteristics of T-Acute Lymphoblastic Leukemia in Omani Patients: A Correlation with Demographic Factors.

Immunophenotypic Characteristics of T-Acute Lymphoblastic Leukemia in Omani Patients: A Correlation with Demographic Factors.

Journal: Oman medical journal

Published: February 23, 2018

Impact of Aberrant Myeloid Antigen Expression on Outcomes of Patients with T-cell Acute Lymphoblastic Leukemia.

Impact of Aberrant Myeloid Antigen Expression on Outcomes of Patients with T-cell Acute Lymphoblastic Leukemia.

Journal: Oman medical journal

Published: June 07, 2017

Impact of Educational Activities in Reducing Pre-Analytical Laboratory Errors: A quality initiative.

Impact of Educational Activities in Reducing Pre-Analytical Laboratory Errors: A quality initiative.

Journal: Sultan Qaboos University medical journal

Published: January 09, 2017

Alloimmunization in Patients with Sickle Cell Disease and Thalassemia: Experience of a Single Centre in Oman.

Alloimmunization in Patients with Sickle Cell Disease and Thalassemia: Experience of a Single Centre in Oman.

Journal: Mediterranean journal of hematology and infectious diseases

Published: October 09, 2016

Coexistence of sickle cell disease and severe congenital neutropenia: first impressions can be deceiving.

Coexistence of sickle cell disease and severe congenital neutropenia: first impressions can be deceiving.

Journal: European journal of haematology

Published: July 05, 2012

Idiopathic thrombocytopenic purpura and hypokalaemic dRTA with compensated haemolysis and striking acanthocytosis in a band 3 (SLC4A1/AE1) A858D homozygote.

Idiopathic thrombocytopenic purpura and hypokalaemic dRTA with compensated haemolysis and striking acanthocytosis in a band 3 (SLC4A1/AE1) A858D homozygote.

Journal: Annals of hematology

Published: June 02, 2012

dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state.

dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state.

Journal: European journal of haematology

Published: December 01, 2011

Showing 1-10 of 10

Last Updated: 09/26/2026