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Journal Articles

Thrombotic Thrombocytopenic Purpura: 100 Years of Research on Moschcowitz's Syndrome

Spero R. Cataland, Paul Coppo, Marie Scully, MBE, Bernhard Lämmle

Blood blood.2023022277.

https://doi.org/10.1182/blood.2023022277

Published: 2024

Includes: Supplemental data

Journal Articles

ADAMTS13 recovery in caplacizumab-treated TTP

Bernhard Lämmle

Blood (2024) 143 (18): 1785–1786.

https://doi.org/10.1182/blood.2024023862

Published: 2024

Journal Articles

Value of Prophylactic Plasma Treatment and Incidence of Acute Episodes in Patients Enrolled in the International Hereditary Thrombotic Thrombocytopenic Purpura Registry

Blood (2023) 142 (Supplement 1): 691.

https://doi.org/10.1182/blood-2023-184580

Published: 2023

Journal Articles

Insight into the Natural History of Hereditary Thrombotic Thrombocytopenic Purpura: Short- and Long-Term Outcomes in a Longitudinally Followed Large Patient Cohort of the International Hereditary TTP Registry

Blood (2023) 142 (Supplement 1): 4003.

https://doi.org/10.1182/blood-2023-185053

Published: 2023

Journal Articles

Caplacizumab Frontline Added to Therapeutic Plasma Exchange and Immunosuppression Prevents Unfavorable Outcomes in Immune-Mediated TTP: An International Real-World Study of the TTP-IWG (The Capla 500 Project)

Blood (2023) 142 (Supplement 1): 2636.

https://doi.org/10.1182/blood-2023-179316

Published: 2023

Journal Articles

Mechanisms of ADAMTS13 inhibition in iTTP

Bernhard Lämmle

Blood (2023) 141 (24): 2919–2920.

https://doi.org/10.1182/blood.2023020512

Published: 2023

Journal Articles

Neonatal Exchange Transfusion: When Should We Think about Hereditary Thrombotic Thrombocytopenic Purpura (hTTP)?

Erika Tarasco, Kenneth D. Friedman, James N. George, Paul Knöbl, Ingrid Hrachovinova, Masanori Matsumoto, Reinhard Schneppenheim, Anne Sophie Von Krogh, Bernhard Lammle, Johanna A. Kremer Hovinga Strebel

Blood (2022) 140 (Supplement 1): 336–337.

https://doi.org/10.1182/blood-2022-168612

Published: 2022

Journal Articles

Severe High Molecular Weight Kininogen (HK) Deficiency: Clinical Characteristics, Deficiency-Causing KNG1 Variants in Reported and New Cases, and Estimated Prevalence

Anke Adenaeuer, Stefano Barco, Alice Trinchero, Hanan Nazir, Sarah Krutmann, Chiara Ambaglio, Vincenzo Rocco, Ylenia Pancione, Luigi Tomao, Arlette Ruiz de Saez, Marion Echenagucia, Friederike Häuser, Karl J. Lackner, Heidi Rossmann, Bernhard Lämmle

Blood (2021) 138 (Supplement 1): 3200.

https://doi.org/10.1182/blood-2021-152959

Published: 2021

Journal Articles

Chronically Elevated Interleukin-6 Disturbs the Coagulation Cascade in Mice

Tanja Knopp, Jeremy Lagrange, Rebecca Jung, Johannes Wild, Heidi Rossmann, Henri M.H. Spronk, Thomas Wunderlich, Nadine Hoevelmeyer, Thomas Münzel, Bernhard Lämmle, Wolfram Ruf, Philip Wenzel, Ari Waisman, Susanne Helena Karbach

Blood (2021) 138 (Supplement 1): 2065.

https://doi.org/10.1182/blood-2021-149628

Published: 2021

Journal Articles

Long-Term Renal Outcomes in Hereditary TTP Patients: Data from the International Hereditary TTP Registry

Erika Tarasco, Ralph Wendt, Anne Sophie von Krogh, Sibylle Tschumi, James N. George, Masanori Matsumoto, Paul Knöbl, Reinhard Schneppenheim, Bernhard Lämmle, other members of Hereditary TTP Registry Steering Committee, Johanna A. Kremer Hovinga Strebel

Blood (2021) 138 (Supplement 1): 770.

https://doi.org/10.1182/blood-2021-146128

Published: 2021

Journal Articles

Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura

Erika Tarasco, Lukas Bütikofer, Kenneth D. Friedman, James N. George, Ingrid Hrachovinova, Paul N. Knöbl, Masanori Matsumoto, Anne Sophie von Krogh, Isabella Aebi-Huber, Zuzana Cermakova, Magdalena Górska-Kosicka, Katarzyna A. Jalowiec, Carlo R. Largiadèr, Zoltán Prohászka, György Sinkovits, Jerzy Windyga, Bernhard Lämmle, Johanna A. Kremer Hovinga

Blood (2021) 137 (25): 3563–3575.

https://doi.org/10.1182/blood.2020009801

Published: 2021

Includes: Supplemental data

Journal Articles

Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura

Blood (2020) 136 (3): 353–361.

https://doi.org/10.1182/blood.2019004221

Published: 2020

Includes: Supplemental data

Journal Articles

Genotype-Phenotype Correlation in Congenital TTP: New Insights from a Multicentre Study with 121 Patients

Anette Anette Van Dorland, PhD, Magnus Mansouri Taleghani, MD, Kenneth Dale Friedman, MD, James George, MD, Ingrid Hrachovinova, PhD, Paul Knöbl, MD PhD, Bernhard Lammle, MD, Masanori Matsumoto, MD, Anne Sophie von Krogh, MD, Reinhard Schneppenheim, MDPhD, Isabella Aebi-Huber, Bütikofer Lukas, PhD, Zuzana Cermakova, PhD, Petter Quist-Paulsen, MD PhD, Deirdra Terrell, PhD, Sara K. Vesely, PhD MPH, Yoshihiro Fujimura, MD PhD, Johanna A. Kremer Hovinga Strebel, MD

Blood (2018) 132 (Supplement 1): 376.

https://doi.org/10.1182/blood-2018-99-112095

Published: 2018

Journal Articles

Detection and Differential Diagnosis of Prekallikrein Deficiency: Genetic Study of New Families and Systematic Review of the Literature

Stefano Barco, Stefanie Sollfrank, Alice Trinchero, Luigi Tomao, Barbara Zieger, Johanna A. Kremer Hovinga, MD Prof, Laura Conti, Anke Adenäuer, Erwin Miloni, Karl J. Lackner, Heidi Rossmann, Bernhard Lammle, MD

Blood (2018) 132 (Supplement 1): 2496.

https://doi.org/10.1182/blood-2018-99-116030

Published: 2018

Journal Articles

Hemophagocytic Lymphohistiocytosis in Early Infancy- Pitfall of Differentiation between Hereditary and Infectious Reasons

Alexandra Russo, MD, Francesca Alt, MD, Marie Astrid Neu, MD, Stefan Eder, MD, Arthur Wingerter, MD, Khalifa El Malki, MD, Bernhard Lammle, MD, Joerg Faber, MD PhD

Blood (2018) 132 (Supplement 1): 4961.

https://doi.org/10.1182/blood-2018-99-117519

Published: 2018

Journal Articles

Gut microbiota regulate hepatic von Willebrand factor synthesis and arterial thrombus formation via Toll-like receptor-2

Blood (2017) 130 (4): 542–553.

https://doi.org/10.1182/blood-2016-11-754416

Published: 2017

Includes: Multimedia, Supplemental data

Journal Articles

Opana ER–induced thrombotic microangiopathy

Bernhard Lämmle

Blood (2017) 129 (7): 808–809.

https://doi.org/10.1182/blood-2016-12-754507

Published: 2017

Journal Articles

VWF and complement

Bernhard Lämmle

Blood (2015) 125 (6): 896–898.

https://doi.org/10.1182/blood-2014-12-612556

Published: 2015

Journal Articles

The splenic autoimmune response to ADAMTS13 in thrombotic thrombocytopenic purpura contains recurrent antigen-binding CDR3 motifs

Monica Schaller, Monique Vogel, Karim Kentouche, Bernhard Lämmle, Johanna A. Kremer Hovinga

Blood (2014) 124 (23): 3469–3479.

https://doi.org/10.1182/blood-2014-04-561142

Published: 2014

Includes: Supplemental data

Journal Articles

Pregnancy outcomes following recovery from acquired thrombotic thrombocytopenic purpura

Yang Jiang, Jennifer J. McIntosh, Jessica A. Reese, Cassandra C. Deford, Johanna A. Kremer Hovinga, Bernhard Lämmle, Deirdra R. Terrell, Sara K. Vesely, Eric J. Knudtson, James N. George

Blood (2014) 123 (11): 1674–1680.

https://doi.org/10.1182/blood-2013-11-538900

Published: 2014

NARROW

Thrombotic Thrombocytopenic Purpura: 100 Years of Research on Moschcowitz's Syndrome

ADAMTS13 recovery in caplacizumab-treated TTP

Value of Prophylactic Plasma Treatment and Incidence of Acute Episodes in Patients Enrolled in the International Hereditary Thrombotic Thrombocytopenic Purpura Registry

Insight into the Natural History of Hereditary Thrombotic Thrombocytopenic Purpura: Short- and Long-Term Outcomes in a Longitudinally Followed Large Patient Cohort of the International Hereditary TTP Registry

Caplacizumab Frontline Added to Therapeutic Plasma Exchange and Immunosuppression Prevents Unfavorable Outcomes in Immune-Mediated TTP: An International Real-World Study of the TTP-IWG (The Capla 500 Project)

Mechanisms of ADAMTS13 inhibition in iTTP

Neonatal Exchange Transfusion: When Should We Think about Hereditary Thrombotic Thrombocytopenic Purpura (hTTP)?

Severe High Molecular Weight Kininogen (HK) Deficiency: Clinical Characteristics, Deficiency-Causing KNG1 Variants in Reported and New Cases, and Estimated Prevalence

Chronically Elevated Interleukin-6 Disturbs the Coagulation Cascade in Mice

Long-Term Renal Outcomes in Hereditary TTP Patients: Data from the International Hereditary TTP Registry

Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura

Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura

Genotype-Phenotype Correlation in Congenital TTP: New Insights from a Multicentre Study with 121 Patients

Detection and Differential Diagnosis of Prekallikrein Deficiency: Genetic Study of New Families and Systematic Review of the Literature

Hemophagocytic Lymphohistiocytosis in Early Infancy- Pitfall of Differentiation between Hereditary and Infectious Reasons

Gut microbiota regulate hepatic von Willebrand factor synthesis and arterial thrombus formation via Toll-like receptor-2

Opana ER–induced thrombotic microangiopathy

VWF and complement

The splenic autoimmune response to ADAMTS13 in thrombotic thrombocytopenic purpura contains recurrent antigen-binding CDR3 motifs

Pregnancy outcomes following recovery from acquired thrombotic thrombocytopenic purpura

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American Society of Hematology

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American Society of Hematology

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