Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 69 Records) |
Query Trace: ADAMTS13[original query] |
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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 |
Reference range for ADAMTS13 antigen, activity and anti-ADAMTS13 antibody in the healthy adult Singapore population. Singapore medical journal 2020 6 63 (4): 214-218. Tso Allison Ching Yee, Sum Christina Lai Lin, Ong Kiat H |
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 |
[Clinical characteristics of 83 patients with thrombotic thrombocytopenic purpura]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2020 4 41 (3): 216-221. Wang X Y, Liu X F, Xue F, Liu W, Chen Y F, Huang Y T, Fu R F, Zhang L, Yang R |
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 |
Identification and replication of novel genetic variants of ABO gene to reduce the incidence of diseases and promote longevity by modulating lipid homeostasis. Aging 2021 Nov 13 (22): 24655-24674. Ni Xiaolin, Bai Chen, Nie Chao, Qi Liping, Liu Yifang, Yuan Huiping, Zhu Xiaoquan, Sun Liang, Zhou Qi, Li Yan, Zhen Hefu, Su Huabing, Li Rongqiao, Lan Rushu, Pang Guofang, Lv Yuan, Zhang Wei, Yang Fan, Yao Yao, Chen Chen, Wang Zhaoping, Gao Danni, Zhang Nan, Zhang Shenqi, Zhang Li, Wu Zhu, Hu Caiyou, Zeng Yi, Yang |
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 |
Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis. PloS one 2021 10 16 (10): e0258675. Pagliari Maria Teresa, Cairo Andrea, Boscarino Marco, Mancini Ilaria, Pappalardo Emanuela, Bucciarelli Paolo, Martinelli Ida, Rosendaal Frits R, Peyvandi Flo |
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 |
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19. Viruses 2022 May 14 (6): . Zguro Kristina, Baldassarri Margherita, Fava Francesca, Beligni Giada, Daga Sergio, Leoncini Roberto, Galasso Lucrezia, Cirianni Michele, Rusconi Stefano, Siano Matteo, Francisci Daniela, Schiaroli Elisabetta, Luchi Sauro, Morelli Giovanna, Martinelli Enrico, Girardis Massimo, Busani Stefano, Parisi Saverio Giuseppe, Panese Sandro, Piscopo Carmelo, Capasso Mario, Tacconi Danilo, Spertilli Raffaelli Chiara, Giliberti Annarita, Gori Giulia, Katsikis Peter D, Lorubbio Maria, Calzoni Paola, Ognibene Agostino, Bocchia Monica, Tozzi Monica, Bucalossi Alessandro, Marotta Giuseppe, Furini Simone, Gen-Covid Multicenter Study , Renieri Alessandra, Fallerini Chia |
Genetic and Functional Evidence of Complement Dysregulation in Multiple Myeloma Patients with Carfilzomib-Induced Thrombotic Microangiopathy Compared to Controls. Journal of clinical medicine 2022 Jun 11 (12): . Gavriilaki Eleni, Dalampira Dimitra, Theodorakakou Foteini, Liacos Christine-Ivy, Kanellias Nikolaos, Eleutherakis-Papaiakovou Evangelos, Terpos Evangelos, Gavriatopoulou Maria, Verrou Evgenia, Triantafyllou Theodora, Sevastoudi Aggeliki, Koravou Evaggelia-Evdoxia, Touloumenidou Tasoula, Varelas Christos, Papalexandri Apostolia, Sakellari Ioanna, Dimopoulos Meletios A, Kastritis Efstathios, Katodritou Eiri |
[Immune-mediated thrombotic thrombocytopenic purpura and susceptible HLA alleles]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2022 5 63 (4): 277-285. Sakai Kazu |
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 |
Markers of Hereditary Thrombophilia with Unclear Significance. Hamostaseologie 2022 12 42 (6): 370-380. Sachs Ulrich J, Kirsch-Altena Anette, Müller Je |
The polymorphisms of extracellular matrix-remodeling genes are associated with pelvic organ prolapse. International urogynecology journal 2022 1 33 (2): 267-274. Li Lei, Ma Yidi, Yang Hua, Sun Zhijing, Chen Juan, Zhu L |
A single-center experience of post-transplant atypical hemolytic uremic syndrome. Clinical nephrology 2023 6 . Bassam G Abu Jawdeh, Muhammad A Kh |
Prognostic value of von Willebrand factor levels in patients with metastatic melanoma treated by immune checkpoint inhibitors. Journal for immunotherapy of cancer 2023 5 11 (5): . Julia-Christina Stadler, Laura Keller, Christian Mess, Alexander T Bauer, Julian Koett, Glenn Geidel, Isabel Heidrich, Sabine Vidal-Y-Sy, Antje Andreas, Carlotta Stramaglia, Mark Sementsov, Wiebcke Haberstroh, Benjamin Deitert, Inka Lilott Hoehne, Robin Reschke, Thomas Haalck, Klaus Pantel, Christoffer Gebhardt, Stefan W Schneid |
An Exploratory Study Using Next-Generation Sequencing to Identify Prothrombotic Variants in Patients with Cerebral Vein Thrombosis. International journal of molecular sciences 2023 5 24 (9): . Robert Anton Kramer, Robert Zimmermann, Julian Strobel, Susanne Achenbach, Armin Michael Ströbel, Holger Hackstein, David Alexander Christian Messerer, Sabine Schneid |
Von-Willebrand factor antigen: a biomarker for severe pregnancy complications in women with hereditary TTP? Journal of thrombosis and haemostasis : JTH 2023 3 . Davidesko Sharon, Pikovsky Oleg, Al-Athamen Kayed, Hackmon Rinat, Erez Offer, Miodownik Shayna, Rabinovich An |
Pathway-driven rare germline variants associated with transplant-associated thrombotic microangiopathy (TA-TMA). Thrombosis research 2023 3 225 39-46. Zhang Zhihui, Hong Wei, Wu Qian, Tsavachidis Spiridon, Li Jian-Rong, Amos Christopher I, Cheng Chao, Sartain Sarah E, Afshar-Kharghan Vahid, Dong Jing-Fei, Bhatraju Pavan, Martin Paul J, Makar Robert S, Bendapudi Pavan K, Li A |
Predictive Values of ADAMTS13, TBIL, and D-D for Prognosis of Patients with Thrombotic Thrombocytopenic Purpura. Clinical laboratory 2023 2 69 (2): . Liu Bo, Zhang Xiaoran, Yu Xuezho |
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 |
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- Page last updated:Apr 22, 2024
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