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Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest study.
J Thromb Haemost. 2023 Aug;21(8):2126-2136. doi: 10.1016/j.jtha.2023.04.035. Epub 2023 May 11.
J Thromb Haemost. 2023.
PMID: 37172732
Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
Casini A, Brungs T, Lavenu-Bombled C, Vilar R, Neerman-Arbez M, de Moerloose P.
Casini A, et al. Among authors: brungs t.
J Thromb Haemost. 2017 May;15(5):876-888. doi: 10.1111/jth.13655. Epub 2017 Mar 6.
J Thromb Haemost. 2017.
PMID: 28211264
Free article.
Review.
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Amniotic Fluid Embolism Coagulopathy Guided by the Point-of-Care Quantra QStat® Hemostasis System: A Case Report.
Fradin E, Belin O, Bonnet D, Caron I, Brungs T.
Fradin E, et al. Among authors: brungs t.
Cureus. 2024 Mar 2;16(3):e55387. doi: 10.7759/cureus.55387. eCollection 2024 Mar.
Cureus. 2024.
PMID: 38562331
Free PMC article.
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Case Report: Co-infection with SARS-CoV-2 and influenza H1N1 in a patient with acute respiratory distress syndrome and a pulmonary sarcoidosis.
Baala L, Benzekri-Lefevre D, Bret L, Guillaume C, Courtellemont L, El Khalil A, Guery T, Iquel S, Perche O, Khadre K, Brungs T, Decker J, Francia T, Bois J, Delamare B, Guinard J, Got L, Briault S, Boulain T, Legac E.
Baala L, et al. Among authors: brungs t.
F1000Res. 2020 Dec 18;9:1482. doi: 10.12688/f1000research.26924.2. eCollection 2020.
F1000Res. 2020.
PMID: 35528205
Free PMC article.
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Management of congenital quantitative fibrinogen disorders: a Delphi consensus.
Casini A, de Moerloose P; Congenital Fibrinogen Disorders Group.
Casini A, et al.
Haemophilia. 2016 Nov;22(6):898-905. doi: 10.1111/hae.13061. Epub 2016 Sep 19.
Haemophilia. 2016.
PMID: 27640400
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