Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 8 (of 8 Records) |
Query Trace: Afibrinogenemia[original query] |
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Diagnosis of congenital fibrinogen disorders. Annales de biologie clinique 2016 Aug 74 (4): 405-412. Lebreton Aurélien, Casini Alessand |
Mutational Epidemiology of Congenital Fibrinogen Disorders. Thrombosis and haemostasis 2018 10 118 (11): 1867-1874. Casini Alessandro, Blondon Marc, Tintillier Veronique, Goodyer Matthew, Sezgin Melike E, Gunes Adalet M, Hanss Michel, de Moerloose Philippe, Neerman-Arbez Margueri |
Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations. Thrombosis research 2019 9 182 133-140. Wypasek Ewa, Klukowska Anna, Zdziarska Joanna, Zawilska Krystyna, Treli?ski Jacek, Iwaniec Teresa, Mital Andrzej, Pietrys Danuta, Sydor Wojciech, Neerman-Arbez Marguerite, Undas Anet |
Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population. Thrombosis journal 2019 4 17 5. Naz Arshi, Biswas Arijit, Khan Tehmina Nafees, Goodeve Anne, Ahmed Nisar, Saqlain Nazish, Ahmed Shariq, Ujjan Ikram Din, Shamsi Tahir S, Oldenburg Johann |
Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations. International journal of laboratory hematology 2020 7 42 (5): 619-627. Tavasoli Behnaz, Safa Majid, Dorgalaleh Akbar, Ghasemi Jahan B, Rezaei Makhouri Farahnaz, Rezvani Mohammad R, Ahmadi Abbas, Tabibian Shadi, Jazebi Mohammad, Baghaipour Mohammad R, Zaker Farh |
Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population. Haemophilia : the official journal of the World Federation of Hemophilia 2021 8 27 (6): 1022-1027. Shen Ming-Ching, Wang Jiaan-Der, Tsai Woei, Lin Ching-Yeh, Lin Jen-Shiou, Kuo Su-Feng, Lin Po-Te, Huang Ying-Chih, Hung Mei-H |
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2021 7 60 (6): 103203. Mohsenian Samin, Seidizadeh Omid, Mirakhorli Mojgan, Jazebi Mohammad, Azarkeivan Azi |
Risk and Management of Intracerebral Hemorrhage in Patients with Bleeding Disorders. Seminars in thrombosis and hemostasis 2022 1 48 (3): 344-355. Dorgalaleh Akbar, Farshi Yadolah, Haeri Kamand, Ghanbari Omid Baradarian, Ahmadi Abb |
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- Page last updated:Apr 22, 2024
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