Human Genome Epidemiology Literature Finder
|
Records 1 - 13 (of 13 Records) |
| Query Trace: Syndrome and ADAMTS13[original query] |
|---|
| Is factor V Leiden a risk factor for thrombotic microangiopathies without severe ADAMTS 13 deficiency? Thrombosis and haemostasis 2005 Dec 94 (6): 1186-9. Krieg Soraya, Studt Jan-Dirk, Sulzer Irmela, Lämmle Bernhard, Kremer Hovinga Johanna |
| A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan. PloS one 2015 10 (5): e0124655. Yoshida Yoko, Miyata Toshiyuki, Matsumoto Masanori, Shirotani-Ikejima Hiroko, Uchida Yumiko, Ohyama Yoshifumi, Kokubo Tetsuro, Fujimura Yoshihi |
| 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, |
| Targeted exome sequencing in anti-factor H antibody negative HUS reveals multiple variations. Clinical and experimental nephrology 2017 9 22 (3): 653-660. Thergaonkar R W, Narang Ankita, Gurjar Bahadur Singh, Tiwari Pradeep, Puraswani Mamta, Saini Himanshi, Sinha Aditi, Varma Binuja, Mukerji Mitali, Hari Pankaj, Bagga Arvi |
| 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, |
| [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 |
| 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 |
| 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 |
| 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 |
| A single-center experience of post-transplant atypical hemolytic uremic syndrome. Clinical nephrology 2023 6 . Bassam G Abu Jawdeh, Muhammad A Kh |
| Increased Complement Activation and Decreased ADAMTS13 Activity Are Associated with Genetic Susceptibility in Patients with Preeclampsia/HELLP Syndrome Compared to Healthy Pregnancies: An Observational Case-Controlled Study. Journal of personalized medicine 2024 4 14 (4): . Theodora-Maria Venou, Evangelia Vetsiou, Christos Varelas, Angelos Daniilidis, Kyriakos Psarras, Evaggelia-Evdoxia Koravou, Maria Koutra, Tasoula Touloumenidou, Vasilis Tsolakidis, Apostolia Papalexandri, Fani Minti, Evdokia Mandala, Konstantinos Dinas, Efthymia Vlachaki, Eleni Gavriila |
- Page last reviewed:Feb 1, 2024
- Content source: