Ralf Knöfler

University Hospital Carl Gustav Carus — Germany

Medicine · Health Sciences

19h-index1.7kcitations143works1.52yr avg
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Research Topics

Platelet Disorders and Treatments(46), Blood Coagulation and Thrombosis Mechanisms(31), Hemophilia Treatment and Research(18), Venous Thromboembolism Diagnosis and Management(17), Myeloproliferative Neoplasms: Diagnosis and Treatment(17)

Publications131 total

RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series
Frontiers in Medicine·2025Open Access
Erratum: “Diagnosis of Inherited Platelet Disorders”: Update of the Interdisciplinary S2k-Guideline [*] of the Permanent Pediatric Commission of the Society of Thrombosis and Haemostasis Research (GTH e.V.)
Hämostaseologie·2025Open Access
“Diagnosis of Inherited Platelet Disorders”: Update of the Interdisciplinary S2k-Guideline [] of the Permanent Pediatric Commission of the Society of Thrombosis and Haemostasis Research (GTH e.V.)
Hämostaseologie·2025· 2 citedOpen Access
Landscape and Spectrum of VWF Variants in Type 2 Von Willebrand Disease: Insights from a German Patient Cohort
Thrombosis and Haemostasis·2025· 3 citedOpen Access
Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor
Genome Medicine·2025· 5 citedOpen Access
Compassionate Use of Osocimab in Preventing Thrombotic Complications Without Incremental Bleeding: A Case Report
TH Open·2025Open Access
Changes in Hemophilia Treatment in the Eastern Part of Germany between 2015 and 2021—Data from the Kompetenznetz Hämorrhagische Diathese Ost (KHDO)
Hämostaseologie·2025· 1 citedOpen Access
Evaluation of platelet parameters in pediatric oncology patients undergoing myelotoxic chemotherapy.
Hämostaseologie·2025
Compassionate use of osocimab in preventing thrombotic complications without incremental bleeding: a case report
Hämostaseologie·2025· 1 cited
The Diagnostic Assessment of Inherited Platelet Function Defects - Part 1: An Overview of the Diagnostic Approach and Laboratory Methods
Hämostaseologie·2025· 2 citedOpen Access
Misshandlung oder Gerinnungsstörung?
hautnah dermatologie·2024
Misshandlung oder Gerinnungsstörung?
Pädiatrie·2024· 1 cited
Unravelling the spectrum of von Willebrand factor variants in quantitative von Willebrand disease: results from a German cohort study
Journal of Thrombosis and Haemostasis·2024· 6 citedOpen Access
Efficacy of emicizumab in patients with severe haemophilia A without factor VIII inhibitors in Germany: evaluation of real-life data documented by the smart medication eDiary
Therapeutic Advances in Hematology·2024Open Access
Quantitativer Ultraschall bei Kindern und Jugendlichen mit Hämophilie
RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren·2023
Treatment of Inherited Platelet Disorders: Current Status and Future Options
Hämostaseologie·2023· 11 citedOpen Access
Gerinnungsdiagnostik bei Kindeswohlgefährdung
Monatsschrift Kinderheilkunde·2023· 5 citedOpen Access
Immune tolerance achievement by low dose factor VIII in PUPs and MTPs under prophylaxis with emicizumab: two case reports
Hämostaseologie·2023
Impact of Tyrosine Kinase Inhibitors Applied for First-Line Chronic Myeloid Leukemia Treatment on Platelet Function in Whole Blood of Healthy Volunteers In Vitro
Hämostaseologie·2023· 4 citedOpen Access
Influencing Factors and Differences in Born Aggregometry in Specialized Hemostaseological Centers: Results of a Multicenter Laboratory Comparison
TH Open·2022· 5 citedOpen Access
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Frequent Co-authors

Werner Streif(11), Susan Halimeh(8), S. Gehrisch(7), Martin Olivieri(7), Barbara Zieger(6), Susanne Holzhauer(6), Eberhard Kuhlisch(6), Ulrike Nowak‐Göttl(5), Tetsumei Urano(5), Akikazu Takada(5), Judith Lohse(5), Christine Heller(4), Christoph Bidlingmaier(4), Gili Kenet(4), Jolanta Małyszko(4), Gabriele Siegert(4), G Weissbach(4), Gabriele Strauß(4), W. Eberl(4), Michael Krause(4)