Z Rolović

2017 AHA/ACC Focused Update of the 2014 AHA/ACC Guideline for the Management of Patients With Valvular Heart Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines

The ABC transporter Bcrp1/ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the side-population phenotype

Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities

CD39 activity correlates with stage and inhibits platelet reactivity in chronic lymphocytic leukemia

The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis

Tricuspid valve replacement: Fifteen years of experience with mechanical prostheses and bioprostheses

Thrombotic and Bleeding Complications of Prosthetic Heart Valves

The Role of Blood Component Removal in Essential and Reactive Thrombocytosis

GSK3 Deficiencies in Hematopoietic Stem Cells Initiate Pre-neoplastic State that Is Predictive of Clinical Outcomes of Human Acute Leukemia

Dysplasia Has A Differential Diagnosis: Distinguishing Genuine Myelodysplastic Syndromes (MDS) From Mimics, Imitators, Copycats and Impostors

Molecular pathogenesis of Philadelphia chromosome negative myeloproliferative disorders

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

CD39 and CD73 in immunity and inflammation

Evaluation of dysplasia through detailed cytomorphology in 3156 patients from the Düsseldorf Registry on myelodysplastic syndromes

Splenectomy for Primary and Recurrent Immune Thrombocytopenic Purpura (ITP)

Endocrine Disruption in Wildlife: A Critical Review of the Evidence

Myeloproliferative Disorders with Translocations of Chromosome 5q31–35: Role of the Platelet-Derived Growth Factor Receptor Beta

Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue

Evaluation and Management of Tricuspid Valve Disease

Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology [see comments]

The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes

Phthalate esters: Occurrence and biological effects

Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia.

Diagnosis of essential thrombocythemia at platelet counts between 400 and 600x10(9)/L. Gruppo Italiano Malattie Mieloproliferative Croniche(GIMMC).

ACC/AHA 2006 Guidelines for the Management of Patients With Valvular Heart Disease

P-glycoprotein plays a drug-efflux–independent role in augmenting cell survival in acute myeloblastic leukemia and is associated with modulation of a sphingomyelin-ceramide apoptotic pathway

2020 ACC/AHA Guideline for the Management of Patients With Valvular Heart Disease: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines

2017 AHA/ACC Focused Update of the 2014 AHA/ACC Guideline for the Management of Patients With Valvular Heart Disease

Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes

2008 Focused Update Incorporated Into the ACC/AHA 2006 Guidelines for the Management of Patients With Valvular Heart Disease

The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia

Autoimmune thrombocytopenic purpura

HIGH-DOSE INTRAVENOUS GAMMAGLOBULIN FOR IDIOPATHIC THROMBOCYTOPENIC PURPURA IN CHILDHOOD

Late thrombosis of the Björk-Shiley tilting disc valve in the tricuspid position

In vitro drug sensitivity of leukemic progenitors and P‐glycoprotein expression in adult acute myeloid leukemia: correlation with induction treatment outcome

Recurrent venous thrombosis in a patient with chronic lymphocytic leukemia and acquired protein S deficiency

Myelofibrosis in Primary Myelodysplastic Syndromes: Clinical and Biological Significance

Immunologic Abnormalities in Myelodysplastic Syndromes: Clinical Features and Characteristics of the Lymphoid Population

Spontaneous Remission in Adults with Primary Myelodysplastic Syndromes: Incidence and Characteristics of Patients

The determination of spontaneous megakaryocyte colony formation is an unequivocal test for discrimination between essential thrombocythaemia and reactive thrombocytosis

[A case of thalassemia minor].

A case of chronic myeloid leukemia without Ph1 translocation

Comparative Studies of the Viability of Human Platelets Stored at 4 C in Plastic and Glass Containers

Megakaryocytopoiesis in Experimentally Induced Immune Thrombocytopenia