Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 32 Records) |
| Query Trace: Disease and ADAMTS13[original query] |
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| Lower levels of ADAMTS13 are associated with cardiovascular disease in young patients. Atherosclerosis 2009 Nov 207 (1): 250-4. Bongers T N, de Bruijne E L E, Dippel D W J, de Jong A J, Deckers J W, Poldermans D, de Maat M P M, Leebeek F W |
| Association between ADAMTS13 polymorphisms and risk of cardiovascular events in chronic coronary disease. Thrombosis research 2010 Jan 125 (1): 61-6. Schettert Isolmar T, Pereira Alexandre C, Lopes Neuza H, Hueb Whady A, Krieger Jose |
| The role of human leukocyte antigens as predisposing and/or protective factors in patients with idiopathic thrombotic thrombocytopenic purpura. Annals of hematology 2012 Apr 91 (4): 507-10. John Marie-Luise, Hitzler Walter, Scharrer In |
A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.
Blood 2012 Sep . Arning A, Hiersche M, Witten A, Kurlemann G, Kurnik K, Manner D, Stoll M, Nowak-Göttl U |
| ADAMTS13 gene variants and function in women with preeclampsia: a population- based nested case- control study from the HUNT Study. Thrombosis research 2015 Aug 136 (2): 282-8. von Krogh Anne-Sophie, Kremer Hovinga Johanna A, Romundstad Pål R, Roten Linda T, Lämmle Bernhard, Waage Anders, Quist-Paulsen Pett |
| Protective effect of a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 haplotype on coronary artery disease. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2017 Jun 28 (4): 286-294. Lasom Supakanya, Komanasin Nantarat, Settasatian Nongnuch, Settasatian Chatri, Kukongviriyapan Upa, Intharapetch Pongsak, Senthong Vich |
| Epidemiology and pathophysiology of adulthood-onset thrombotic microangiopathy with severe ADAMTS13 deficiency (thrombotic thrombocytopenic purpura): a cross-sectional analysis of the French national registry for thrombotic microangiopathy. The Lancet. Haematology 2016 May 3 (5): e237-45. Mariotte Eric, Azoulay Elie, Galicier Lionel, Rondeau Eric, Zouiti Fouzia, Boisseau Pierre, Poullin Pascale, de Maistre Emmanuel, Provôt François, Delmas Yahsou, Perez Pierre, Benhamou Ygal, Stepanian Alain, Coppo Paul, Veyradier Agnès, |
| The role of human leukocyte antigen DRB1-DQB1 haplotypes in the susceptibility to acquired idiopathic thrombotic thrombocytopenic purpura. Human immunology 2016 Nov . Sinkovits György, Szilágyi Ágnes, Farkas Péter, Inotai Dóra, Szilvási Anikó, Tordai Attila, Rázsó Katalin, Réti Marienn, Prohászka Zolt |
| Association of a disintegrin and metalloproteinase with a thrombospondin type 1 motif member 13 polymorphisms with severity of coronary stenosis in type 2 diabetes mellitus. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2018 23 59. Lasom Supakanya, Komanasin Nantarat, Settasatian Nongnuch, Settasatian Chatri, Kukongviriyapan Upa, Intharapetch Pongs |
| Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next-generation sequencing. Research and practice in thrombosis and haemostasis 2018 7 1 (1): 69-80. Fidalgo Teresa, Martinho Patrícia, Pinto Catarina S, Oliveira Ana C, Salvado Ramon, Borràs Nina, Coucelo Margarida, Manco Licínio, Maia Tabita, Mendes M João, Del Orbe Barreto Rafael, Corrales Irene, Vidal Francisco, Ribeiro M Letíc |
| ADAMTS13 Gene Mutations Influence ADAMTS13 Conformation and Disease Age-Onset in the French Cohort of Upshaw-Schulman Syndrome. Thrombosis and haemostasis 2018 10 118 (11): 1902-1917. Joly Bérangère S, Boisseau Pierre, Roose Elien, Stepanian Alain, Biebuyck Nathalie, Hogan Julien, Provot François, Delmas Yahsou, Garrec Céline, Vanhoorelbeke Karen, Coppo Paul, Veyradier Agnès, |
| The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: key findings at enrollment until 2017. Haematologica 2019 2 104 (10): 2107-2115. van Dorland Hendrika A, Taleghani Magnus Mansouri, Sakai Kazuya, Friedman Kenneth D, George James N, Hrachovinova Ingrid, Knöbl Paul N, von Krogh Anne Sophie, Schneppenheim Reinhard, Aebi-Huber Isabella, Bütikofer Lukas, Largiadèr Carlo R, Cermakova Zuzana, Kokame Koichi, Miyata Toshiyuki, Yagi Hideo, Terrell Deirdra R, Vesely Sara K, Matsumoto Masanori, Lämmle Bernhard, Fujimura Yoshihiro, Kremer Hovinga Johanna A, |
| The ADAMTS13-VWF axis is dysregulated in chronic thromboembolic pulmonary hypertension. The European respiratory journal 2019 1 53 (3): . Newnham Michael, South Kieron, Bleda Marta, Auger William R, Barberà Joan A, Bogaard Harm, Bunclark Katherine, Cannon John E, Delcroix Marion, Hadinnapola Charaka, Howard Luke S, Jenkins David, Mayer Eckhard, Ng Choo, Rhodes Christopher J, Screaton Nicholas, Sheares Karen, Simpson Michael A, Southwood Mark, Su Li, Taboada Dolores, Traylor Matthew, Trembath Richard C, Villar Sofia S, Wilkins Martin R, Wharton John, Gräf Stefan, Pepke-Zaba Joanna, Laffan Michael, Lane David A, Morrell Nicholas W, Toshner Ma |
| Recipient ADAMTS13 Single-Nucleotide Polymorphism Predicts Relapse after Unrelated Bone Marrow Transplantation for Hematologic Malignancy. International journal of molecular sciences 2019 1 20 (1): . Nomoto Haruka, Takami Akiyoshi, Espinoza J Luis, Onizuka Makoto, Kashiwase Koichi, Morishima Yasuo, Fukuda Takahiro, Kodera Yoshihisa, Doki Noriko, Miyamura Koichi, Mori Takehiko, Nakao Shinji, Morishita Eri |
| COVID-19-Related Coagulopathy-Is Transferrin a Missing Link? Diagnostics (Basel, Switzerland) 2020 8 10 (8): . McLaughlin Katie-May, Bechtel Marco, Bojkova Denisa, Münch Christian, Ciesek Sandra, Wass Mark N, Michaelis Martin, Cinatl Jindri |
| ADAMTS12, a new candidate gene for pediatric stroke. PloS one 2020 8 15 (8): e0237928. Witten Anika, Rühle Frank, de Witt Marlous, Barysenka Andrei, Stach Michael, Junker Ralf, Nowak-Göttl Ulrike, Stoll Moni |
| In silico features of ADAMTS13 contributing to plasmatic ADAMTS13 levels in neonates with congenital heart disease. Thrombosis research 2020 6 193 66-76. Katneni Upendra K, Holcomb David D, Hernandez Nancy E, Hamasaki-Katagiri Nobuko, Hunt Ryan C, Bar Haim, Ibla Juan C, Kimchi-Sarfaty Cha |
| Susceptible gene polymorphism in patients with three-vessel coronary artery disease. BMC cardiovascular disorders 2020 Apr 20 (1): 172. Liu Ru, Song Lei, Jiang Lin, Tang Xiaofang, Xu Lianjun, Gao Zhan, Zhao Xueyan, Xu Jingjing, Gao Runlin, Yuan Jinqi |
| The HLA Variant rs6903608 Is Associated with Disease Onset and Relapse of Immune-Mediated Thrombotic Thrombocytopenic Purpura in Caucasians. Journal of clinical medicine 2020 10 9 (10): . Mancini Ilaria, Giacomini Elisa, Pontiggia Silvia, Artoni Andrea, Ferrari Barbara, Pappalardo Emanuela, Gualtierotti Roberta, Trisolini Silvia Maria, Capria Saveria, Facchini Luca, Codeluppi Katia, Rinaldi Erminia, Pastore Domenico, Campus Simona, Caria Cinzia, Caddori Aldo, Nicolosi Daniela, Giuffrida Gaetano, Agostini Vanessa, Roncarati Umberto, Mannarella Clara, Fragasso Alberto, Podda Gian Marco, Birocchi Simone, Cerbone Anna Maria, Tufano Antonella, Menna Giuseppe, Pizzuti Michele, Ronchi Michela, De Fanti Alessandro, Amarri Sergio, Defina Marzia, Bocchia Monica, Cerù Silvia, Gattillo Salvatore, Rosendaal Frits R, Peyvandi Flo |
| Clinical Features and Gene Mutation Analysis of Congenital Thrombotic Thrombocytopenic Purpura in Neonates. Frontiers in pediatrics 2020 10 8 546248. Wang Jiali, Zhao |
| Current prophylactic plasma infusion protocols do not adequately prevent long-term cumulative organ damage in the Japanese congenital thrombotic thrombocytopenic purpura cohort. British journal of haematology 2021 May . Sakai Kazuya, Fujimura Yoshihiro, Miyata Toshiyuki, Isonishi Ayami, Kokame Koichi, Matsumoto Masano |
| Complement Factor I Mutation May Contribute to Development of Thrombotic Microangiopathy in Lupus Nephritis. Frontiers in medicine 2021 2 7 621609. Tseng Min-Hua, Fan Wen-Lang, Liu Hsuan, Yang Chia-Yu, Ding Jhao-Jhuang, Lee Hwei-Jen, Huang Shih-Ming, Lin Shih-Hua, Huang Jing-Lo |
| Identification of a novel genetic locus associated with immune-mediated thrombotic thrombocytopenic purpura. Haematologica 2021 2 107 (3): 574-582. Stubbs Matthew J, Coppo Paul, Cheshire Chris, Veyradier Agnès, Dufek Stephanie, Levine Adam P, Thomas Mari, Patel Vaksha, Connolly John O, Hubank Michael, Benhamou Ygal, Galicier Lionel, Poullin Pascale, Kleta Robert, Gale Daniel P, Stanescu Horia, Scully Marie |
| MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity. Journal of personalized medicine 2021 Nov 11 (11): . Cappadona Claudio, Paraboschi Elvezia Maria, Ziliotto Nicole, Bottaro Sandro, Rimoldi Valeria, Gerussi Alessio, Azimonti Andrea, Brenna Daniele, Brunati Andrea, Cameroni Charlotte, Campanaro Giovanni, Carloni Francesca, Cavadini Giacomo, Ciravegna Martina, Composto Antonio, Converso Giuseppe, Corbella Pierluigi, D'Eugenio Davide, Dal Rì Giovanna, Di Giorgio Sofia Maria, Grondelli Maria Chiara, Guerrera Lorenza, Laffoucriere Georges, Lando Beatrice, Lopedote Leandro, Maizza Benedetta, Marconi Elettra, Mariola Carlotta, Matronola Guia Margherita, Menga Luca Maria, Montorsi Giulia, Papatolo Antonio, Patti Riccardo, Profeta Lorenzo, Rebasti Vera, Smidili Alice, Tarchi Sofia Maria, Tartaglia Francesco Carlo, Tettamanzi Gaia, Tinelli Elena, Stuani Riccardo, Bolchini Cristiana, Pattini Linda, Invernizzi Pietro, Degenhardt Frauke, Franke Andre, Duga Stefano, Asselta Rosan |
| The global carrier frequency and genetic prevalence of Upshaw-Schulman syndrome. BMC genomic data 2021 11 22 (1): 50. Zhao Ting, Fan Shanghua, Sun L |
| ADAMTS-13-VWF axis in sickle cell disease patients. Annals of hematology 2021 Jan . Ladeira Valéria Sutana, Barbosa Amanda Rodrigues, Oliveira Marina Mendes, Ferreira Letícia Gonçalves Resende, de Oliveira Júnior Wander Valadares, de Oliveira Renó Cristiane, Reis Edna Afonso, Chaves Daniel Gonçalves, Dusse Luci Maria Sant'Ana, Dos Santos Hérica Lima, de Barros Pinheiro Melina, Rios Danyelle Romana Alv |
| Genetic Variation in ADAMTS13 is Related to VWF Levels, Atrial Fibrillation and Cerebral Ischemic Events. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2022 28 10760296221141893. Warlo Ellen M K, Bratseth Vibeke, Pettersen Alf-Åge R, Holme Pål Andre, Arnesen Harald, Seljeflot Ingebjørg, Opstad Trine |
| Focused panel sequencing points to genetic predisposition in non-cirrhotic intrahepatic portal hypertension patients in India. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2023 10 . Rekha Aaron, Kalpana Premkumar, Aaron Chapla, B Vijayalekshmi, Uday Zachariah, Elwyn Elias, Thomas Alex Kodiatte, Dolly Daniel, John Jude, K A Balasubramanian, Sukesh C Nair, Nihal Thomas, Banumathi Ramakrishna, C E Eapen, Ashish Go |
| Identification of 8 Rare Deleterious Variants in ADAMTS13 by Next-generation Sequencing in a Chinese Population with Thrombotic Thrombocytopenic Purpura. Current medical science 2023 10 43 (5): 1043-1050. Xiao Wang, Xing-Jie Hao, Cheng-Guqiu Dai, Ya-Jie Ding, Lv Xiong, Jun Deng, Jing-Jing Jia |
| Carfilzomib-associated thrombotic microangiopathy: clinical features and outcomes. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2024 4 . Adrien Joseph, Stéphanie Harel, Laurent Mesnard, Cédric Rafat, Silène Knapp, Anne Rumpler, Carole Philipponnet, Christophe Barba, Jean-Michel Rebibou, David Buob, Alexandre Hertig, Jacques Vargaftig, Jean-Michel Halimi, Bertrand Arnulf, Anne-Sophie Bretaud, Bérangère Joly, Steven Grangé, Paul Cop |
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