E Levrat, I Aboukhamis, P de Moerloose… - Blood Coagulation & …, 2011 - journals.lww.com ... Case Reports. A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family. ... Most reported mutations leading to congenital afibrinogenemia are located in FGA encoding the fibrinogen A α-chain. ... Related articles - All 5 versions
Y Chevalier, Y Dargaud, L Argaud, J Ninet… - Thrombosis …, 2011 - ncbi.nlm.nih.gov ... 2011 Apr 13. [Epub ahead of print] Successive bleeding and thrombotic complications in a patient with afibrinogenemia: A case report. Chevalier Y, Dargaud Y, Argaud L, Ninet J, Jouanneau E, Négrier C. Unité d'Hémostase Clinique, Hopital Edouard Herriot, Lyon, France. ... Related articles - All 2 versions
[HTML] from jisppd.comGD Chandan, AG Annaji, S Bhatnagar… - Journal of Indian …, 2011 - Medknow ... Cellulitis on face in a patient with congenital afibrinogenemia GD Chandan 1 , AG Annaji 2 , S Bhatnagar 3 , U Mohandas 1 , P Dave 1 1 Department of Pedodontics and Preventive Dentistry, VS Dental College and Hospital, Bangalore, India 2 Department of Oral Medicine and ... Related articles - All 3 versions
[PDF] from banglajol.infoT Nazrin, P Attawar, M Moniruzzaman… - Pulse, 2011 - banglajol.info Page 1. Afibrinogenemia 1 2 3 4 ... Abstract 1,2 Afibrinogenemia is a rare bleeding disorder with an estimated prevalence of 1: 10,00,000. It is an autosomal recessive disease resulting from mutations in any of the 3 genes that encodes the 3 polypeptide chains of fibrinogen 3 ... Related articles - View as HTML - All 2 versions
A Pathengay, S Ambatipudi… - Retinal Cases and Brief …, 2011 - journals.lww.com ... Congenital afibrinogenemia and hypofibrinogenemia are rare disorders. Unlike congenital ... affected families. Congenital hypofibrinogenemia occurs commonly in the heterozygous genotype and afibrinogenemia in the homozygous genotype. ... Related articles - All 3 versions
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