Christoph Male

ORCID: 0000-0002-4989-6421
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About
Contact & Profiles
Research Areas
  • Blood Coagulation and Thrombosis Mechanisms
  • Hemophilia Treatment and Research
  • Venous Thromboembolism Diagnosis and Management
  • Platelet Disorders and Treatments
  • Pharmaceutical studies and practices
  • Central Venous Catheters and Hemodialysis
  • Cancer-related gene regulation
  • Atrial Fibrillation Management and Outcomes
  • Chronic Myeloid Leukemia Treatments
  • Heart Failure Treatment and Management
  • Vascular anomalies and interventions
  • Cardiac Arrhythmias and Treatments
  • Systemic Lupus Erythematosus Research
  • Blood groups and transfusion
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Congenital Heart Disease Studies
  • Cardiac pacing and defibrillation studies
  • Diet and metabolism studies
  • Metabolism and Genetic Disorders
  • Pharmaceutical Economics and Policy
  • Child and Adolescent Health
  • Epilepsy research and treatment
  • Hemoglobinopathies and Related Disorders
  • Iron Metabolism and Disorders
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema

Medical University of Vienna
2016-2025

Universitätsklinik für Kinder und Jugendpsychiatrie
2013-2024

University of Vienna
1993-2023

Vienna General Hospital
2001-2023

Medizinische Hochschule Hannover
2023

Spanish National Centre for Cardiovascular Research
2023

University of Bamberg
2023

Building Bridges
2023

Artificial Intelligence in Medicine (Canada)
2023

Guy's and St Thomas' NHS Foundation Trust
2023

Christoph Male Anthonie W.A. Lensing Joseph S. Palumbo Riten Kumar Ildar Nurmeev and 95 more Kerry Hege Damien Bonnet Philip Connor Hélène L. Hooimeijer Marcela Torres Anthony K.C. Chan Gili Kenet Susanne Holzhauer Amparo Santamaría Pascal Amédro Elizabeth Chalmers Paolo Simioni Rukhmi Bhat Donald L. Yee O. Lvova Jan Beyer‐Westendorf Tina Biss Ida Martinelli Paola Saracco Marjolein Peters Krisztián Kállay Cynthia Gauger M. Patricia Massicotte Guy Young Ákos F. Pap Madhurima Majumder William T. Smith Jürgen F. Heubach Scott D. Berkowitz Kirstin Thelen Dagmar Kubitza Mark Crowther Martin H. Prins Paul Monagle Angelo Claudio Molinari Ulrike Nowak- Gottl Juan José Chain Jeremy Robertson Katharina Thom Werner Streif Rudolf Schwarz Klaus Schmitt Gernot Grangl An Van Damme Philip Maes Veerle Labarque Antônio Sérgio Petrilli Sandra Loggeto Estela Azeka Leonardo R. Brandão Doan Le Christine Sabapathy Paola Giordano Runhui Wu Jie Ding Wenyan Huang Jianhua Mao Päivi M. Lähteenmäki Pascal Amédro Stéphane Decramer Toralf Bernig Martin Chada Gcf Chan Krisztian Kally B. Nolan Shoshana Revel‐Vilk Hannah Tamary Carina Levin Daniela Tormene Maria Abbattista Andrea Artoni Takanari Ikeyama Ryo Inuzuka Satoshi Yasukochi Michelle Morales Soto Karina Anastacia Solís‐Labastida Monique H. Suijker Marike Bartels R. Y. J. Tamminga C Heleen Van Ommen D. Maroeska W. M. te Loo Rui Anjos Lyudmila Zubarovskaya Н.М. Попова Elena Samochatova М. Б. Белогурова Pavel Svirin Tatiana Shutova В. В. Лебедев О. Л. Барбараш Pei Lin Koh J. Mei Ľudmila Podracká Rubén Berrueco María Florencia Fernández

10.1016/s2352-3026(19)30219-4 article EN The Lancet Haematology 2019-11-05
Ming‐Chih Lin Leonardo R. Brandão Matteo Luciani Lisa Bomgaars Elizabeth Chalmers and 88 more Lesley Mitchell Ildar Nurmeev Anjali Sharathkumar Pavel Svirin Kirill Gorbatikov Igor Tartakovsky Monika Simetzberger Fenglei Huang Zhichao Sun Jörg Kreuzer Savion Gropper Paul A. Reilly Martina Brueckmann Manuela Albisetti Ildar Nurmeev А. И. Сафина Ondřej Zapletal Leonardo R. Brandão Tomáš Kuhn Tomáš Votava Judy Felgenhauer Anjali Sharathkumar Pavel Svirin Ali Amid Ming‐Chih Lin Kirill Gorbatikov Paola Saracco Csongor Kiss Susan Halimeh Madlen Reschke Beate Wulff Michèle David Zbyněk Novák I.I. Trunina Manuela Albisetti Tony Frisk Heidi Glosli Andreas H. Groll O. Lvova İlgen Şaşmaz Darintr Sosothikul Virginija Žilinskaitė Erin Cockrell V. A. Digtyar I Hadacová Sauli Palmu Anjali Pawar Joyce Maria Annichino Bizzacchi Ümran Çalışkan Tıraje Celkan Dmytro Dmytrіiev Colleen Druzgal Graciela Elena Antonis Kattamis Ramazan Kavakli Christoph Male Nihal Özdemir An Van Damme T. N. Zvereva Aanen Aarli Rogelio Alejandro Paredes Aguilera Selin Aytaç Jorge David Aivazoglou Carneiro Antonio Chistolini M.G. Mazzucconi Fernando F. Corrales‐Medina Françis Couturaud Stacey E Croteau Cameron C. Trenor Michael Damgaard Natalia Dixon A.N. Galustyan Jiří Hák Marianne Hoffmann Alphan Küpesiz Veerle Labarque Chris Van Geet Ming‐Chih Lin Yun‐Ching Fu Sandra Regina Loggetto Veerle Mondelaers Irena Odri-Komazec Shoshana Revel‐Vilk Julián Sevilla Luciano Fuzzato Silva José Kerr Saraiva Fernando Montes‐Tapia Wendy Woods‐Swafford

10.1016/s2352-3026(20)30368-9 article EN The Lancet Haematology 2020-12-05

Summary Objective To compare the efficacy and safety of ketogenic diet ( KD ) with standard adrenocorticotropic hormone ACTH treatment in infants West syndrome. Methods In this parallel‐cohort (PC) randomized controlled trial RCT ), were randomly allocated to or high‐dose . Those who could not be followed a PC Primary end point was electroclinical remission at day 28. Secondary points time remission, relapse after initial response, seizure freedom last follow‐up, adverse effects,...

10.1111/epi.14679 article EN Epilepsia 2019-02-23

The incidence of FIX inhibitors in severe hemophilia B (SHB) is not well defined. Frequencies 3-5% have been reported but most studies to date were small, including patients with different severities, and without prospective follow-up for inhibitor incidence. Study objective was investigate SHB followed up 500 exposure days (ED), the frequency allergic reactions, relationship genotypes. Consecutive previously untreated (PUPs) enrolled into PedNet cohort included. Detailed data collected...

10.3324/haematol.2019.239160 article EN cc-by-nc Haematologica 2020-01-09

Anticoagulant treatment of pediatric cerebral venous thrombosis has not been evaluated in randomized trials. We the safety and efficacy rivaroxaban standard anticoagulants predefined subgroup children with (CVT) who participated EINSTEIN-Jr trial. Children CVT were (2:1), after initial heparinization, to or (continued on heparin switched vitamin K antagonist). The main period was 3 months. primary outcome, symptomatic recurrent thromboembolism (VTE), principal major clinically relevant...

10.1182/bloodadvances.2020003244 article EN cc-by-nc-nd Blood Advances 2020-12-17
Neil A. Goldenberg John M. Kittelson Thomas C. Abshire Marc P. Bonaca James F. Casella and 85 more Rita Dale Jonathan L. Halperin Frances Hamblin Craig M. Kessler Marilyn J. Manco‐Johnson Robert F. Sidonio Alex C. Spyropoulos Philippe Gabríel Steg Alexander G.G. Turpie Sam Schulman James A. French John H. Fargo Shelley E. Crary Riten Kumar Rachel F. Grace Cameron C. Trenor Hope P. Wilson Lee Hilliard Gary M. Woods Kavita Patel Neil A. Goldenberg Eric Lowe Julie Jaffray Guy Young Madhvi Rajpurkar Jennifer Davila Arash Mahajerin James Cooper Sriya Gunawardena Ayesha Zia Janna M. Journeycake Shannon L. Carpenter Michael M Guerrera Yaser Diab Cristina Tarango Ralph A. Gruppo Suchitra S. Acharya Marcella D Torres Linda Shaffer Robert C. Mignacca Kristina M. Haley Michael Recht Courtney D. Thornburg Nirmish Shah Craig A. Mullen Deanna Mitchell Charles Nakar Marisol Betensky Courtney E. Lawrence Clifford M. Takemoto Clara Lo Ajovi B. Scott‐Emuakpor Roshni Kulkarni Alexandra J. Borst Sarah H. O’Brien Fernando F Corales-Medina Shalu Narang Nicole Kucine Michael Wang Arun Panigrahi Kerry McGowan Stuart L. Cramer Smita C. Dandekar Frederico Xavier Kristina M Knoll Anupam Verma A. Geddes Sanjay Ahuja Kerry Hege Deepti Raybagkar Anjali Sharathkumar Lakshmi V Srivath Osman Khan Colleen Druzgal Mihir D. Bhatt Anthony K.C. Chan Leonardo R. Brandão Patricia Massicotte C. Heleen van Ommen Christoph Male Paul Monagle Taizo A. Nakano William B. Mitchell William R. Hiatt Jeffrey I. Weitz

Among patients younger than 21 years of age, the optimal duration anticoagulant therapy for venous thromboembolism is unknown. To test hypothesis that a 6-week provoked noninferior to conventional 3-month in age. Randomized clinical trial involving 417 age with acute, enrolled at 42 centers 5 countries from 2008-2021. The main exclusions were severe deficiencies or prior thromboembolism. Patients without persistent antiphospholipid antibodies and whose thrombi resolved not completely...

10.1001/jama.2021.23182 article EN JAMA 2022-01-11

A prospective longitudinal cohort study was performed to assess the prevalence of iron deficiency in European infants at 12 mo age, and influence socio-economic status, dietary factors, growth morbidity on status. The consisted 488 normal term from primary healthcare centres 11 areas. Assessed were variables, intake, anthropometry regular intervals birth mo, haemoglobin, serum ferritin, mean corpuscular volume, transferrin saturation receptor concentrations age mo. anaemia 9.4%, 7.2%, 2.3%....

10.1080/080352501750197601 article EN Acta Paediatrica 2001-05-01

Summary Deep vein thrombosis (DVT) in children occurs primarily the upper body venous system. This prospective diagnostic study compared bilateral venography and ultrasound for detection of DVT system 66 with acute lymphoblastic leukemia. Results were interpreted by central blinded adjudication. occurred 29% (19/66) patients. While 15/19 detected (sensitivity 79%), only 7/19 37%). The 12 but not located subclavian or more veins. Three 4 jugular vein. We conclude that is insensitive may be...

10.1055/s-0037-1613054 article EN Thrombosis and Haemostasis 2002-01-01

To investigate if the factor V Leiden mutation (F-V-LM) and/or prothrombin gene G 20210 A variant (P-G20210A-V) are risk factors for acute stroke in Austrian children.33 children with ischemic documented by computer tomography magnetic resonance imaging of brain were enrolled an open multicenter survey.6/33 had F-V-LM (5 heterozygous, 1 homozygous). This represents 18% (95% CI: 6.7-39.9%) our pediatric population and thus exceeds expected prevalence 4,6% (Fischer's exact test, p = 0.01). was...

10.1055/s-0037-1615355 article EN Thrombosis and Haemostasis 1998-01-01

The goals were to assess the frequency of spontaneous closure isolated secundum atrial septal defect in children and identify predictors closure.A retrospective cohort study was performed a tertiary care pediatric cardiology center. Consecutive patients (n = 200) diagnosed as having defects (no multiple or fenestrated defects, no additional congenital heart disease, syndromes) monitored for > 6 months with serial 2-dimensional echocardiography, according standardized protocol.The median age...

10.1542/peds.2005-3037 article EN PEDIATRICS 2006-10-01

The life expectancy of non-severe hemophilia A (HA) patients equals the non-hemophilic population. However, data on effect inhibitor development mortality and hemophilia-related causes death are scarce. neutralizing factor VIII antibodies in HA may dramatically change their clinical outcome due to severe bleeding complications.We assessed association between occurrence inhibitors with HA.In this retrospective cohort study, vital status were collected for 2709 (107 inhibitors) who treated...

10.1111/jth.12990 article EN publisher-specific-oa Journal of Thrombosis and Haemostasis 2015-04-25
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