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Documents Congenital Fibrinogen Disorders: An Update

Congenital Fibrinogen Disorders: An Update Philippe de Moerloose, MD1 Alessandro Casini, MD2 Marguerite Neerman-Arbez, PhD3 1Division of Angiology and Haemostasis, University

Documents Congenital Fibrinogen Disorders, FGA, FGB, and FGG Genes, Next-Generation Sequencing, Varies

and FGG Genes, Next-Generation Sequencing, Varies ___________________________________________________ ___________________________________________________ Document generated

Documents Fibrinogen deficiency in a dog - a case report

Fibrinogen deficiency in a dog - a case reportCASE REPORT Open Access Fibrinogen deficiency in a dog - a case report Franck Jolivet1, Armelle Diquélou1,2, Catherine

Documents Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular...

Microsoft Word - Fibrinogen Martin III_RA_SC_SC_TS_RA2_SC2.docxin the globular C-terminal domain of the γ-chain (p.Glu275Stop) 1Tomas Simurda, 2Sonia Caccia, 3Rosanna

Documents Fibrinogen Philadelphia. A hereditary hypodysfibrinogenemia characterized by fibrinogen...

J Martinez, … , S S Shapiro, A J Erslev J Clin Invest. 1974;53(2):600-611. https://doi.org/10.1172/JCI107595. A new, autosomally inherited abnormal fibrinogen associated

Documents Clinical Policy: Fibrinogen Concentrate [Human] (Fibryga, RiaSTAP)

CNC Combined LOB PA TemplateCHC-MCO Policy Submission A separate copy of this form must accompany each policy submitted for review. Policies submitted without this form will

Documents Congenital Fibrinogen Deficiency in India and Role of Human Fibrinogen Concentrate

Congenital Fibrinogen Deficiency in India and Role of Human Fibrinogen ConcentrateCongenital Fibrinogen Deficiency in India and Role of Human Fibrinogen Concentrate M. Joseph

Documents Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding.....

Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging

Documents A novel fibrinogen γ-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia....

© Annals of Translational Medicine. All rights reserved. Ann Transl Med 2021;9(16):1308 | https://dx.doi.org/10.21037/atm-21-3207 A novel fibrinogen γ-chain frameshift

Documents Human Fibrinogen Concentrate (RiaSTAP): Comparative Cost-Effectiveness Evaluation

Human Fibrinogen Concentrate (RiaSTAP): Comparative Cost-Effectiveness Evaluationin Health Agence canadienne des médicaments et des technologies de la santé