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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

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

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

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

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

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

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

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

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

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

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

Journal Articles

Impact of SERPINC1, PROC and PROS1 Mutations on the Thrombotic Phenotype in Children with Venous Thromboembolism: An Observational Multicenter Cohort Study

Verena Limperger, Gili Kenet, MD, Christine Heller, MD, Karin Kurnik, Ralf Knoefler, Rolf M Mesters, MD, Susan Halimeh, MD, Ulrike Nowak-Göttl

Blood (2014) 124 (21): 583.

https://doi.org/10.1182/blood.V124.21.583.583

Published: 2014

Journal Articles

Characterization of Patients with Glanzmann Thrombasthenia and Identification of 17 Novel Mutations

Kirstin Sandrock-Lang, PhD, Johannes Oldenburg, MD PhD, Verena Wiegering, MD, Susan Halimeh, MD, Sentot Santoso, Karin Kurnik, Lars Fischer, Dimitrios Tsakiris, MD, Michael Sigl-Kraetzig, Brigit Brand, MD, Katharina Kraetzer, Niklas Deeg, Eileen Busse, Zieger Barbara

Blood (2014) 124 (21): 1460.

https://doi.org/10.1182/blood.V124.21.1460.1460

Published: 2014

Journal Articles

Reference Ranges of Coagulation Parameters in Pregnancies of Healthy Women and Women with Mild Bleeding Disorders

Susan Halimeh, MD, Hannelore Rott, MD, Ihsan Osseiran, MD, Guenther Kappert, MD, Manuela Siebert

Blood (2014) 124 (21): 5068.

https://doi.org/10.1182/blood.V124.21.5068.5068

Published: 2014

Journal Articles

Do Sexual Hormones Influence the Coagulation Parameters during the Normal Menstrual Cycle

Susan Halimeh, MD, Hannelore Rott, MD, Ihsan Osseiran, MD, Guenther Kappert, Manuela Siebert

Blood (2014) 124 (21): 5047.

https://doi.org/10.1182/blood.V124.21.5047.5047

Published: 2014

NARROW

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

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)

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

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)

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

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

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?

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

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

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

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)

Impact of SERPINC1, PROC and PROS1 Mutations on the Thrombotic Phenotype in Children with Venous Thromboembolism: An Observational Multicenter Cohort Study

Characterization of Patients with Glanzmann Thrombasthenia and Identification of 17 Novel Mutations

Reference Ranges of Coagulation Parameters in Pregnancies of Healthy Women and Women with Mild Bleeding Disorders

Do Sexual Hormones Influence the Coagulation Parameters during the Normal Menstrual Cycle

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American Society of Hematology

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ASH Publications

American Society of Hematology

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