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Are gated communities indispensable for residents?

Urbani izziv, 2016-06, Vol.27 (1), p.149-161

2016

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An unusual cause of multiple organ dysfunction syndrome in the pediatric intensive care unit: hemophagocytic lymphohistiocytosis

Pediatric critical care medicine, 2009-05, Vol.10 (3), p.285-290

2009

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Feasibility of Using Thrombin Generation Assay (TGA) for Monitoring Bypassing Agent Therapy in Patients With Hemophilia Having Inhibitors

Clinical and applied thrombosis/hemostasis, 2013-07, Vol.19 (4), p.389-394

2013

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Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome

The journal of pediatric research, 2019-09, Vol.6 (3), p.252-255

2019

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An Evaluation of the DDAVP Infusion Test With PFA-100 and vWF Activity Assays to Distinguish vWD Types in Children

Clinical and applied thrombosis/hemostasis, 2011-10, Vol.17 (5), p.441-448

2011

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Hemophagocytic lymphohistiocytosis associated with H1N1 virus infection and visceral leishmaniasis in a 4.5-month-old infant

Revista da Sociedade Brasileira de Medicina Tropical, 2012-06, Vol.45 (3), p.407-406

2012

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Varicella-Zoster Virus Infections in Pediatric Malignancy Patients: A Seven-Year Analysis

Turkish journal of haematology, 2016-12, Vol.33 (4), p.346-348

2016

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Resemblance to vWD Types and Laboratory Diagnosis of Obligatory Carriers of Type 3 von Willebrand Disease

Clinical and applied thrombosis/hemostasis, 2011-11, Vol.17 (6), p.E21-E24

2011

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A Systematic Overview of Adolescents’ Smartphone Habits and Internet Addiction During the COVID-19 Era

Psikiyatride güncel yaklaşimlar, 2022-12, Vol.14 (4), p.510-517

2022

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Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia

Annals of nuclear medicine, 2012, Vol.26 (1), p.41-46

2012

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The Evaluation of Taking Iron Supplements in Children Aged 6 Months-2 Years

The journal of pediatric research, 2017-09, Vol.4 (3), p.156-159

2017

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Evaluation of children with macrocytosis: clinical study

The Pan African medical journal, 2018, Vol.31 (54)

2018

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Which tests can most effectively indicate the clinical phenotype of paediatric haemophilia patients with prophylaxis?

Blood coagulation & fibrinolysis, 2021-06, Vol.32 (4), p.259-265

2021

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Supply Chain Risk Management: Cases and Industry Insights

1, 2022

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Imatinib Treatment Alone in Philadelphia-Positive Acute Lymphoblastic Leukemia: Is It Enough

Case reports in oncology, 2011-06, Vol.4 (2), p.323-326

2011

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Evaluation of Bleeding Phenotype of Inherited Factor VII Deficiency in Children With a Bleeding Assessment Tool and Global Assays

Journal of pediatric hematology/oncology, 2020-08, Vol.42 (6), p.e527-e530

2020

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Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis

European journal of haematology, 2024-07, Vol.113 (1), p.82-89

2024

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So ograjene skupnosti za stanovalce nepogrešljive?

Urbani izziv, 2016-06, Vol.27 (1), p.63-75

2016

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Thrombin Generation Assay and by-Passing Therapies in Patients with Inhibitors

Blood, 2011-11, Vol.118 (21), p.3322-3322

2011

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Ali so ograjene skupnosti za stanovalce nepogrešljive?

Urbani izziv, 2016-06, Vol.27 (1), p.63-75

2016

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A New Homozygous Mutation (c.393-394del TA/c.393-394del TA) in the NT5C3 Gene Associated With Pyrimidine-5'-Nucleotidase Deficiency: A Case Report

Journal of pediatric hematology/oncology, 2019-11, Vol.41 (8), p.e484-e486

2019

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Relation between NT-proBNP Levels, Iron Overload, and Early Stage of Myocardial Dysfunction in β-Thalassemia Major Patients

Echocardiography (Mount Kisco, N.Y.), 2012-03, Vol.29 (3), p.318-325

2012

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Successful immune tolerance induction with low-dose coagulation factor VIII in a patient with hemophilia A from a developing country

Blood coagulation & fibrinolysis, 2016-09, Vol.27 (6), p.729-731

2016

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Aplastic Anemia as an Immune-mediated Complication of Thymoma: A Case Report

Journal of pediatric hematology/oncology, 2018-10, Vol.40 (7), p.e464-e466

2018

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Successful Hematopoietic Stem Cell Transplantation In a Child With Paroxysmal Nocturnal Hemoglobinuria

Blood, 2013-11, Vol.122 (21), p.5469-5469

2013

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Are gated communities indispensable for residents?

An unusual cause of multiple organ dysfunction syndrome in the pediatric intensive care unit: hemophagocytic lymphohistiocytosis

Feasibility of Using Thrombin Generation Assay (TGA) for Monitoring Bypassing Agent Therapy in Patients With Hemophilia Having Inhibitors

Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome

An Evaluation of the DDAVP Infusion Test With PFA-100 and vWF Activity Assays to Distinguish vWD Types in Children

Hemophagocytic lymphohistiocytosis associated with H1N1 virus infection and visceral leishmaniasis in a 4.5-month-old infant

Varicella-Zoster Virus Infections in Pediatric Malignancy Patients: A Seven-Year Analysis

Resemblance to vWD Types and Laboratory Diagnosis of Obligatory Carriers of Type 3 von Willebrand Disease

A Systematic Overview of Adolescents’ Smartphone Habits and Internet Addiction During the COVID-19 Era

Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia

The Evaluation of Taking Iron Supplements in Children Aged 6 Months-2 Years

Evaluation of children with macrocytosis: clinical study

Which tests can most effectively indicate the clinical phenotype of paediatric haemophilia patients with prophylaxis?

Supply Chain Risk Management: Cases and Industry Insights

Imatinib Treatment Alone in Philadelphia-Positive Acute Lymphoblastic Leukemia: Is It Enough

Evaluation of Bleeding Phenotype of Inherited Factor VII Deficiency in Children With a Bleeding Assessment Tool and Global Assays

Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis

So ograjene skupnosti za stanovalce nepogrešljive?

Thrombin Generation Assay and by-Passing Therapies in Patients with Inhibitors

Ali so ograjene skupnosti za stanovalce nepogrešljive?

A New Homozygous Mutation (c.393-394del TA/c.393-394del TA) in the NT5C3 Gene Associated With Pyrimidine-5'-Nucleotidase Deficiency: A Case Report

Relation between NT-proBNP Levels, Iron Overload, and Early Stage of Myocardial Dysfunction in β-Thalassemia Major Patients

Successful immune tolerance induction with low-dose coagulation factor VIII in a patient with hemophilia A from a developing country

Aplastic Anemia as an Immune-mediated Complication of Thymoma: A Case Report

Successful Hematopoietic Stem Cell Transplantation In a Child With Paroxysmal Nocturnal Hemoglobinuria

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