H. Nazir

发表

Sickle cell disease in Oman and HBS Oman: a brief review

Y. Wali, H. Albalushi, H. Nazir, 2017 .

Incorporation of Evidence-based Guidelines on Bleeding Risk Assessment Prior to Surgery into Practice: Real-time Experience

R. Al-Abri, Y. Wali, A. Al-Rawas, 2022, Oman medical journal.

Hematopoietic Stem Cell Transplantation For Patients With Autosomal Recessive Complete Interferon Gamma Receptor 2 Deficiency: Experience In Oman.

R. Handgretinger, I. Elnour, D. Dennison, 2021, Transplantation and cellular therapy.

Fresh-Frozen Plasma Transfusion for Replacement Therapy in a Child with Hypoplasminogenemia and Ligneous Conjunctivitis: An Alternative Option to Delay Recurrence

A. Pathare, H. Nazir, Maha Mameesh, 2018 .

Effect of Hydroxyurea Therapy on Growth Parameters in Older Children with Sickle Cell Disease

Y. Wali, Saif Al-Yaarubi, Doaa Khater, 2016 .

Neutropenia and Life-threatening Agranulocytosis Among Children With β-Thalassemia Treated With Oral Iron Chelators in a Community With Background of Ethnic Neutropenia

H. Nazir, Maryam Alshizawi, 2019, Journal of pediatric hematology/oncology.

c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans

B. Lämmle, P. Wild, K. Lackner, 2020, Journal of thrombosis and haemostasis : JTH.

T-cell depleted haploidentical hematopoietic stem cell transplantation for patients with familial hemophagocytic lymphohistiocytosis who do not have matched family donors: Experience in Oman.

D. Dennison, H. Nazir, F. Ba Alawi, 2020, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Preoperative transfusion versus no transfusion policy in sickle cell disease patients: a randomized trial

Y. Wali, A. Al-Rawas, R. Al Abri, 2020, Transfusion.

Y. Wali, Doaa Khater, H. Nazir, 2020, Transfusion.

Congenital Langerhans Cell Histiocytosis Presenting with a Hemorrhagic Papulovesicular Eruption: A Case Report

H. Nazir, I. Al-Hadabi, Buthaina Al-Musalhi, 2021 .

Brucellosis masquerading as ITP in an Omani child with thrombocytopenia

H. Nazir, 2018, Hematology & Transfusion International Journal.

Human Parvovirus B19 in Children with Sickle Cell Disease; Poking the Spleen.

Y. Wali, A. Al-Rawas, M. Zachariah, 2017, Oman medical journal.

Cardio-protective effect of regular transfusion in children with non-transfusion dependent thalassemia (NTDT): A cohort study

Y. Wali, Islam Elghamry, Doaa Khater, 2022, Acta bio-medica : Atenei Parmensis.

Methotrexate induced encephalopathy in acute lymphoblastic leukemia in Omani children

Y. Wali, M. Zachariah, H. Nazir, 2017 .

Vincristine‐induced neuropathy in pediatric patients with acute lymphoblastic leukemia in Oman: Frequent autonomic and more severe cranial nerve involvement

D. Jaju, Y. Wali, M. Zacharia, 2017, Pediatric blood & cancer.

Impact of Dietary Pattern Application on the Nutritional Status of Adolescents with Leukemia Undergoing Chemotherapy

H. Nazir, G. Mansy, Y. Jaafar, 2015, Alexandria Scientific Nursing Journal.

Anti-D-induced severe hemolytic disease of the newborn in an Omani newborn born a rhesus-positive mother

N. Fawaz, H. Nazir, S. Al Hosni, 2018 .

Efficacy and Safety of Dapsone Versus Trimethoprim/Sulfamethoxazol for Pneumocystis Jiroveci Prophylaxis in Children With Acute Lymphoblastic Leukemia With a Background of Ethnic Neutropenia

Y. Wali, Doaa Khater, H. Nazir, 2017, Journal of pediatric hematology/oncology.

Liver Enzymes Changes and Safety Profile of Deferasirox Iron Chelator in Omani Children with Thalassemia Major

Y. Wali, A. Al-Rawas, M. Al-Khabori, 2014 .

Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence.

B. Lämmle, K. Lackner, H. Rossmann, 2022, Journal of thrombosis and haemostasis : JTH.