Doris Boeckelmann

Freiburg, BW, Germany

Last Updated: 09/26/2026

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Found 26 publications

Platelet Type Von Willebrand Disease - Diagnostic and Therapeutic Challenges.

Platelet Type Von Willebrand Disease - Diagnostic and Therapeutic Challenges.

Journal: Hamostaseologie
Published: August 28, 2026

Navigating the Diagnostic and Clinical Spectrum of Thrombocytopenia and Thrombocytopathy: Lessons from a Case Series.

Navigating the Diagnostic and Clinical Spectrum of Thrombocytopenia and Thrombocytopathy: Lessons from a Case Series.

Journal: Hamostaseologie
Published: May 04, 2026

Late Diagnosis of NBEAL2-related Gray Platelet Syndrome in Finnish Siblings with Lifelong Thrombocytopenia.

Late Diagnosis of NBEAL2-related Gray Platelet Syndrome in Finnish Siblings with Lifelong Thrombocytopenia.

Journal: Hamostaseologie
Published: October 15, 2025

Impact of prophylaxis, inhibitors, and genetics on joint outcomes according to the IPSG-MRI score in hemophilia A, B and vWD type 3.

Impact of prophylaxis, inhibitors, and genetics on joint outcomes according to the IPSG-MRI score in hemophilia A, B and vWD type 3.

Journal: Frontiers in medicine
Published: July 17, 2025

RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series.

RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series.

Journal: Frontiers in medicine
Published: June 30, 2025

The Diagnostic Assessment of Inherited Platelet Function Defects - Part 1: An Overview of the Diagnostic Approach and Laboratory Methods.

The Diagnostic Assessment of Inherited Platelet Function Defects - Part 1: An Overview of the Diagnostic Approach and Laboratory Methods.

Journal: Hamostaseologie
Published: January 27, 2025

The Diagnostic Assessment of Platelet Function Defects - Part 2: Update on Platelet Disorders.

The Diagnostic Assessment of Platelet Function Defects - Part 2: Update on Platelet Disorders.

Journal: Hamostaseologie
Published: January 27, 2025

Catheter Intervention in a Patient with Intracranial Aneurysms and Glanzmann Thrombasthenia Caused by a Novel Homozygous Likely Pathogenic Variant in the ITGA2B Gene.

Catheter Intervention in a Patient with Intracranial Aneurysms and Glanzmann Thrombasthenia Caused by a Novel Homozygous Likely Pathogenic Variant in the ITGA2B Gene.

Journal: Diseases (Basel, Switzerland)
Published: May 14, 2024

Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopenia.

Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopenia.

Journal: Journal of thrombosis and haemostasis : JTH
Published: September 11, 2023

Inherited Platelet Disorders: A Short Introduction.

Inherited Platelet Disorders: A Short Introduction.

Journal: Hamostaseologie
Published: February 22, 2023

High-throughput microfluidic blood testing to phenotype genetically linked platelet disorders: an aid to diagnosis.

High-throughput microfluidic blood testing to phenotype genetically linked platelet disorders: an aid to diagnosis.

Journal: Blood advances
Published: January 27, 2023

Glanzmann Thrombasthenia in Pakistani Patients: Identification of 7 Novel Pathogenic Variants in the Fibrinogen Receptor αIIbβ3.

Glanzmann Thrombasthenia in Pakistani Patients: Identification of 7 Novel Pathogenic Variants in the Fibrinogen Receptor αIIbβ3.

Journal: Cells
Published: November 15, 2022
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Last Updated: 09/26/2026