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Journal Articles

Plasma-derived VWF/FVIII prophylaxis in children under 6 with VWD: First results from wil-33

Akshat Jain, Cindy Leissinger, Vladimir Vdovin, Pavel Zharkov, Leonid Dubey, Valentin Ţurea, Zorica Antevska, Ester Zapotocka, Bohumir Blazek, Susan Halimeh, Amanda Rodriguez, Tarja-Elina Weisz, Cristina Solomon, Robert Sidonio, Jr.

Blood (2025) 146 (Supplement 1): 4855.

https://doi.org/10.1182/blood-2025-4855

Published: 2025

Journal Articles

Red-lilly app: A digital tool for the evaluation of menstrual bleeding patterns to support the early detection of bleeding disorders in women

Susan Halimeh, Ayman Daoud, Evangelia Antoniou

Blood (2025) 146 (Supplement 1): 4862.

https://doi.org/10.1182/blood-2025-4862

Published: 2025

Journal Articles

Development of an Early and Complete Examination Protocol for Women and Girls with Inherited Bleeding Disorders (WGBD)

Susan Halimeh, Mohamad Ayman Daoud, Derya Schmitz, Bjoern Habermann

Blood (2024) 144 (Supplement 1): 3970.

https://doi.org/10.1182/blood-2024-211072

Published: 2024

Journal Articles

Interim Results of a New Examination Protocol for Women and Girls with Inherited Bleeding Disorders (WGBD)

Susan Halimeh, Mohamad Ayman Daoud, Derya Schmitz, Bjoern Habermann

Blood (2024) 144 (Supplement 1): 3974.

https://doi.org/10.1182/blood-2024-211155

Published: 2024

Journal Articles

Changes in Health-Related Quality of Life, Pain and Functional Parameters in People with Hemophilia and People with Osteoarthritis - a Comparative Follow-up of Physiotherapeutic Training (Physio-FUN Study)

Susan Halimeh, Manuela Siebert, Marc Rosenthal, Ralf Kalinowski, Sylvia von Mackensen

Blood (2023) 142 (Supplement 1): 7301.

https://doi.org/10.1182/blood-2023-177553

Published: 2023

Journal Articles

Earliest Possible Detection and Intervention for Synovitis in Hemophilia- Results from a Single Center Retrospective Cohort Study

Susan Halimeh, Mohamad Ayman Daoud, Manuela Siebert, Jennifer Zappek, Marc Rosenthal

Blood (2023) 142 (Supplement 1): 7236.

https://doi.org/10.1182/blood-2023-179309

Published: 2023

Journal Articles

Assessment of Haemophilia Patients' and Other Bleeding Disorders Needs of Psychosocial Support and Health Care Needs and Their Utilization in Haemophilia Treatment Centres (ILLUSTRATE Study)

Sylvia von Mackensen, Louis Gallmann, Manuela Siebert, Susan Halimeh

Blood (2023) 142 (Supplement 1): 5065.

https://doi.org/10.1182/blood-2023-187236

Published: 2023

Journal Articles

A Comparison of Health-Related Quality of Life, Pain and Functional Parameters between People with Hemophilia and People with Osteoarthritis - Preliminary Results of the Physio-FUN Study

Sylvia von Mackensen, Manuela Siebert, Marc Rosenthal, Ralf Kalinowski, Susan Halimeh

Blood (2023) 142 (Supplement 1): 7232.

https://doi.org/10.1182/blood-2023-179396

Published: 2023

Journal Articles

Longitudinal Patient Analysis Suggests a Positive Correlation of IL-10/IL-6 and FVIII Inhibitor Amount

Susan Halimeh, Manuela Siebert, Ann-Catrin Omlor, Clivia Lisowski, Janine Becker-Gotot

Blood (2023) 142 (Supplement 1): 5374.

https://doi.org/10.1182/blood-2023-182178

Published: 2023

Journal Articles

Monitoring of Patient-Reported Outcomes in Patients with Bleeding Disorders to Assure Quality of Care: Results from a Single Outpatient Haemophilia Treatment Centre in Germany

Sylvia Von Mackensen, Susan Halimeh

Blood (2022) 140 (Supplement 1): 13065.

https://doi.org/10.1182/blood-2022-170160

Published: 2022

Journal Articles

Guiding Pups with Severe Hemophilia a and Their Parents from Diagnosis to a Full Prophylactic Schedule Mitigating the Risk of Bleed and the Risk for Inhibitor Formation - a Single Centre Approach

Susan Halimeh, Hannelore Rott, Manuela Siebert, Günther Kappert, Dirk Reinhardt

Blood (2022) 140 (Supplement 1): 8472–8473.

https://doi.org/10.1182/blood-2022-168988

Published: 2022

Journal Articles

Genotype-Phenotype Relationship Among 1200 Unrelated White Patients with Inherited FVII Deficiency: A Three-Center Database Study

Susan Halimeh, Gili Kenet, Piotr Kuta, Maria Shneyder, Tido Bajorat, Ulrike Nowak-Göttl

Blood (2021) 138 (Supplement 1): 589.

https://doi.org/10.1182/blood-2021-153580

Published: 2021

Journal Articles

An Individualized Approach to Treating Pups with Severe Hemophilia a: Which Factors Correlate with the Low Rate of Inhibitor Development?

Susan Halimeh, Hannelore Rott, Günther Kappert, Manuela Siebert, Dirk Reinhardt

Blood (2021) 138 (Supplement 1): 2106.

https://doi.org/10.1182/blood-2021-153255

Published: 2021

Journal Articles

Treatment of Women with Heavy Menstrual Bleeding with a Combination Therapy of Agnus Castus and Tranexamic Acid - Experiences of a German Single Centre

Susan Halimeh, Sylvia Von Mackensen, Lina Lourak, June Schwarzbach, Manuela Siebert

Blood (2021) 138 (Supplement 1): 1043.

https://doi.org/10.1182/blood-2021-153644

Published: 2021

Journal Articles

How Caring for Toddlers and Young Children with Severe Haemophilia Impacts on Caregiver's Burden

Susan Halimeh, MD, Manuela Siebert, Sylvia Von Mackensen

Blood (2019) 134 (Supplement_1): 3461.

https://doi.org/10.1182/blood-2019-131185

Published: 2019

Journal Articles

Practical Utilisation of Octapharma FVIII Concentrates in Previously Untreated and Minimally Treated Haemophilia a Patients Entering Routine Clinical Treatment with Nuwiq ® , Octanate ® or Wilate ® — the Protect-NOW Study

Johannes Oldenburg, MD PhD, Anna Pavlova, MD PhD, Susan Halimeh, MD, Robert Klamroth, Joris Versteden, Martina Jansen, Larisa Belyanskaya, PhD

Blood (2018) 132 (Supplement 1): 5034.

https://doi.org/10.1182/blood-2018-99-116577

Published: 2018

Journal Articles

Detection of Early Deterioration of Joints in Children with Haemophilia — Results of the German Energy Study

Susan Halimeh, MD, Günther Kappert, Hannelore Rott, Manuela Siebert, Randy Moore, Sylvia Von Mackensen

Blood (2018) 132 (Supplement 1): 828.

https://doi.org/10.1182/blood-2018-99-113309

Published: 2018

Journal Articles

Do We Really Need Plasma-Derived FVIII Concentrates in Every PUP to Minimize the Risk of Inhibitor Development?

Susan Halimeh, MD, Hannelore Rott, PhD, Manuela Siebert, Günther Kappert

Blood (2018) 132 (Supplement 1): 3522.

https://doi.org/10.1182/blood-2018-99-114756

Published: 2018

Journal Articles

Managment of Deliveries in Carriers for Hemophila A and Low FVIII Levels with Recombinant FVIII Fc Fusion Protein

Susan Halimeh, MD, Hannelore Rott, Manuela Siebert, Günther Kappert

Blood (2017) 130 (Supplement 1): 4897.

https://doi.org/10.1182/blood.V130.Suppl_1.4897.4897

Published: 2017

Journal Articles

Prospective Evaluation of Bleeding Incidence in Fibrinogen Deficiency (PRO-RBDD Study)

Blood (2016) 128 (22): 207.

https://doi.org/10.1182/blood.V128.22.207.207

Published: 2016

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Plasma-derived VWF/FVIII prophylaxis in children under 6 with VWD: First results from wil-33

Red-lilly app: A digital tool for the evaluation of menstrual bleeding patterns to support the early detection of bleeding disorders in women

Development of an Early and Complete Examination Protocol for Women and Girls with Inherited Bleeding Disorders (WGBD)

Interim Results of a New Examination Protocol for Women and Girls with Inherited Bleeding Disorders (WGBD)

Changes in Health-Related Quality of Life, Pain and Functional Parameters in People with Hemophilia and People with Osteoarthritis - a Comparative Follow-up of Physiotherapeutic Training (Physio-FUN Study)

Earliest Possible Detection and Intervention for Synovitis in Hemophilia- Results from a Single Center Retrospective Cohort Study

Assessment of Haemophilia Patients' and Other Bleeding Disorders Needs of Psychosocial Support and Health Care Needs and Their Utilization in Haemophilia Treatment Centres (ILLUSTRATE Study)

A Comparison of Health-Related Quality of Life, Pain and Functional Parameters between People with Hemophilia and People with Osteoarthritis - Preliminary Results of the Physio-FUN Study

Longitudinal Patient Analysis Suggests a Positive Correlation of IL-10/IL-6 and FVIII Inhibitor Amount

Monitoring of Patient-Reported Outcomes in Patients with Bleeding Disorders to Assure Quality of Care: Results from a Single Outpatient Haemophilia Treatment Centre in Germany

Guiding Pups with Severe Hemophilia a and Their Parents from Diagnosis to a Full Prophylactic Schedule Mitigating the Risk of Bleed and the Risk for Inhibitor Formation - a Single Centre Approach

Genotype-Phenotype Relationship Among 1200 Unrelated White Patients with Inherited FVII Deficiency: A Three-Center Database Study

An Individualized Approach to Treating Pups with Severe Hemophilia a: Which Factors Correlate with the Low Rate of Inhibitor Development?

Treatment of Women with Heavy Menstrual Bleeding with a Combination Therapy of Agnus Castus and Tranexamic Acid - Experiences of a German Single Centre

How Caring for Toddlers and Young Children with Severe Haemophilia Impacts on Caregiver's Burden

Practical Utilisation of Octapharma FVIII Concentrates in Previously Untreated and Minimally Treated Haemophilia a Patients Entering Routine Clinical Treatment with Nuwiq ® , Octanate ® or Wilate ® — the Protect-NOW Study

Detection of Early Deterioration of Joints in Children with Haemophilia — Results of the German Energy Study

Do We Really Need Plasma-Derived FVIII Concentrates in Every PUP to Minimize the Risk of Inhibitor Development?

Managment of Deliveries in Carriers for Hemophila A and Low FVIII Levels with Recombinant FVIII Fc Fusion Protein

Prospective Evaluation of Bleeding Incidence in Fibrinogen Deficiency (PRO-RBDD Study)

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American Society of Hematology

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