Rienk J. Tamminga

Groningen, GR, Netherlands

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 29 publications

Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy).

Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy).

Journal: HemaSphere

Published: March 25, 2024

A boy with joint pain associated with emicizumab treatment: The importance of plasma level measurement.

A boy with joint pain associated with emicizumab treatment: The importance of plasma level measurement.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: February 07, 2020

Bleeding phenotype and diagnostic characterization of patients with congenital platelet defects.

Bleeding phenotype and diagnostic characterization of patients with congenital platelet defects.

Journal: American journal of hematology

Published: January 26, 2020

The limitation of genetic testing in diagnosing patients suspected for congenital platelet defects.

The limitation of genetic testing in diagnosing patients suspected for congenital platelet defects.

Journal: American journal of hematology

Published: October 17, 2019

Congenital platelet disorders and health status-related quality of life.

Congenital platelet disorders and health status-related quality of life.

Journal: Research and practice in thrombosis and haemostasis

Published: July 30, 2019

Flow cytometric mepacrine fluorescence can be used for the exclusion of platelet dense granule deficiency.

Flow cytometric mepacrine fluorescence can be used for the exclusion of platelet dense granule deficiency.

Journal: Journal of thrombosis and haemostasis : JTH

Published: July 13, 2019

Sickle cell disease: Clinical presentation and management of a global health challenge.

Sickle cell disease: Clinical presentation and management of a global health challenge.

Journal: Blood reviews

Published: November 15, 2018

The pediatric acenocoumarol dosing algorithm: the Children Anticoagulation and Pharmacogenetics Study.

The pediatric acenocoumarol dosing algorithm: the Children Anticoagulation and Pharmacogenetics Study.

Journal: Journal of thrombosis and haemostasis : JTH

Published: March 14, 2018

Familial macrothrombocytopenia due to a double mutation in cis in the alpha-actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura.

Familial macrothrombocytopenia due to a double mutation in cis in the alpha-actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura.

Journal: Pediatric blood & cancer

Published: February 21, 2018

Intravenous immunoglobulin vs observation in childhood immune thrombocytopenia: a randomized controlled trial.

Intravenous immunoglobulin vs observation in childhood immune thrombocytopenia: a randomized controlled trial.

Journal: Blood

Published: February 14, 2018

Pediatric Diamond-Blackfan anemia in the Netherlands: An overview of clinical characteristics and underlying molecular defects.

Pediatric Diamond-Blackfan anemia in the Netherlands: An overview of clinical characteristics and underlying molecular defects.

Journal: European journal of haematology

Published: October 24, 2017

The phenotypic spectrum of germline YARS2 variants: from isolated sideroblastic anemia to mitochondrial myopathy, lactic acidosis and sideroblastic anemia 2.

The phenotypic spectrum of germline YARS2 variants: from isolated sideroblastic anemia to mitochondrial myopathy, lactic acidosis and sideroblastic anemia 2.

Journal: Haematologica

Published: October 17, 2017

Showing 1-12 of 29

Last Updated: 09/26/2026