Works matching DE "DYSFIBRINOGENEMIA"

Results: 30

Erythrocyte hyperaggregation and thrombogenic dysfibrinogenemia.

Published in:

Clinical Hemorheology & Microcirculation, 1998, v. 18, n. 4, p. 235

By:

Nguyen;
Drouet;
Boisseau;
Léger;
Juchet;
Bierme;
Cambus

Publication type:

Article

Dysfibrinogenemia and multiple sclerosis: spuriously associated or causally linked?

Published in:

Hippokratia, 2018, v. 21, n. 1, p. 49

By:

V. K., Kimiskidis;
E., Papadakis;
V., Papaliagkas;
S., Papagiannopoulos;
D. K., Galanakis

Publication type:

Article

LABORATORY INVESTIGATION OF THROMBOPHILIA.

Published in:

Journal of Medical Biochemistry, 2014, v. 33, n. 1, p. 28, doi. 10.2478/jomb-2013-0041

By:

Margetić, Sandra

Publication type:

Article

Genetic Thrombophilias and Pregnancy Loss.

Published in:

2006

By:

Kujovich, Jody L.

Publication type:

Editorial

Hypodysfibrinogenemia with a Heterozygous Mutation of γCys326Ser by the Novel Transversion of TGT to TCT in a Patient with Pulmonary Thromboembolism and Right Ventricular Thrombus.

Published in:

2017

By:

Ushijima, akiko;
Komai, Taichi;
Masukawa, atsuko;
Oikawa, Keiko;
Morita, Norishige;
asai, Satomi;
Mukai, Saki;
Okumura, Nobuo;
Kobayashi, Yoshinori;
Miyachi, Hayato

Publication type:

Case Study

Structural Changes in the Fibrin Network of a Pretoria Family with Dysfibrinogenemia: A Scanning Electron Microscopical Study.

Published in:

Ultrastructural Pathology, 2006, v. 30, n. 3, p. 167, doi. 10.1080/01913120600689772

By:

Pretorius, E.;
Briedenhann, S.;
Marx, J.;
Franz, R. C.

Publication type:

Article

Use of Chromogenic Assay of Factor X to Accept or Reject INR Results in Warfarin Treated Patients.

Published in:

2009

By:

Sanfelippo, Michael J.;
Zinsmaster, Wendy;
Scherr, Doris L.;
Shaw, Gene R.

Publication type:

Case Study

Ventricular Tachycardia in Acute Fulminant Myocarditis: Medical Management and Follow-up.

Published in:

Pediatric Cardiology, 2008, v. 29, n. 2, p. 416, doi. 10.1007/s00246-007-9044-8

By:

Sharma, J.R.;
Sathanandam, S.;
Rao, S.P.;
Acharya, S.;
Flood, V.

Publication type:

Article

Disseminated intravascular coagulation after isolated mild head injury.

Published in:

Acta Neurochirurgica, 2009, v. 151, n. 11, p. 1521, doi. 10.1007/s00701-009-0258-9

By:

Pereira, Erlick A. C.;
Green, Alexander L.;
Chandran, Hari;
Joshi, Shabin M.;
Shlugman, David;
Cudlip, Simon A.

Publication type:

Article

Diagnosis and Prognosis.

Published in:: Current Medical Literature: Pulmonary Hypertension, 2010, v. 1, n. 2, p. 52
Publication type:: Article

Hypercoagulability in a Patient with Hypodysfibrinogenemia:Implic ations for Clinical Management.

Published in:

Acta Haematologica, 1999, v. 101, n. 4, p. 209, doi. 10.1159/000040956

By:

Wulf;
Unterhalt;
Buchwald;
Zenker;
Kreuzer;
Hiddemann

Publication type:

Article

Presence of Idiopathic Thrombocytopenic Purpura and Autoimmune Hemolytic Anemia in the Patients with Common Variable Immunodeficiency.

Published in:

Iranian Journal of Allergy, Asthma & Immunology, 2008, v. 7, n. 3, p. 169

By:

Ramyar, Asghar;
Aghamohammadi, Asghar;
Moazzami, Kasra;
Rezaei, Nima;
Yeganeh, Mehdi;
Cheraghi, Taher;
Pouladi, Nima;
Heydari, Golnaz;
Abolhassani, Hassan;
Amirzargar, Ali Akbar;
Parvaneh, Nima;
Moin, Mostafa

Publication type:

Article

Management of inherited dysfibrinogenemia during pregnancy: a description of four consecutive cases.

Published in:

2007

By:

Franchini, Massimo;
Raffaelli, Ricciarda;
Musola, Mariella;
Memmo, Alessia;
Poli, Giovanni;
Franchi, Massimo;
Pizzolo, Giovanni;
Veneri, Dino

Publication type:

Letter

Thromboelastography predicts risks of obstetric complication occurrence in (hypo)dysfibrinogenemia patients under non-pregnant state.

Published in:

Clinical & Experimental Pharmacology & Physiology, 2016, v. 43, n. 2, p. 149, doi. 10.1111/1440-1681.12509

By:

Zhou, Jingyi;
Xin, Yu;
Ding, Qiulan;
Jiang, Linlin;
Chen, Yaopeng;
Dai, Jing;
Lu, Yeling;
Wu, Xi;
Liang, Qian;
Wang, Hongli;
Wang, Xuefeng

Publication type:

Article

Disfibrinojenemi ve Homosisteinemili Genç Bir Olguda Nonarteritik Anterior İskemik Optik Nöropati.

Published in:

Retina-Vitreus/Journal of Retina-Vitreous, 2012, v. 20, n. 4, p. 311

By:

YUSUFOĞLU, Elif;
ALTIPARMAK, Uğur Emrah;
FEN, Turgay;
ÜNEY, Güner;
ACAR, Mehmet Akif;
ÖRNEK, Firdevs

Publication type:

Article

Syndromes of Thrombosis and Hypercoagulability: Congenital and Acquired Thrombophilias.

Published in:

Clinical & Applied Thrombosis/Hemostasis, 1998, v. 4, n. 1, p. 25, doi. 10.1177/107602969800400106

By:

Bick, Rodger L.;
Kaplan, Harold

Publication type:

Article

Liver Cirrhosis Manifested by Dysfibrinogenemia.

Published in:

Clinical & Applied Thrombosis/Hemostasis, 1997, v. 3, n. 2, p. 102, doi. 10.1177/107602969700300206

By:

Wajima, Takeshi

Publication type:

Article

Familial Thrombophilia: A Review Analysis.

Published in:

Clinical & Applied Thrombosis/Hemostasis, 1996, v. 2, n. 4, p. 227, doi. 10.1177/107602969600200402

By:

Van den Belt, Angelique G. M.;
Prins, Martin H.;
Huisman, Menno V.;
Hirsh, Jack

Publication type:

Article

Sneddon Syndrome revealing dysfibrinogenemia.

Published in:

International Journal of Dermatology, 2003, v. 42, n. 7, p. 561, doi. 10.1046/j.1365-4362.2003.01723_1.x

By:

Khosrotehrani, Kiarash;
Leroy-Matheron, Catherine;
Mourier, Claude;
Revuz, Jean;
Bagot, Martine

Publication type:

Article

A novel fibrinogen variant – Liberec: dysfibrinogenaemia associated with γ Tyr262Cys substitution.

Published in:

European Journal of Haematology, 2008, v. 81, n. 2, p. 123, doi. 10.1111/j.1600-0609.2008.01094.x

By:

Kotlín, Roman;
Sobotková, Alžběta;
Suttnar, Jiří;
Salaj, Peter;
Walterová, Lenka;
Riedel, Tomáš;
Reicheltová, Zuzana;
Dyr, Jan Evangelista

Publication type:

Article

Dysfibrinogenemia during pregnancy treated successfully with fibrinogen.

Published in:

2003

By:

Yamanaka, Yoshihiko;
Takeuchi, Kyousuke;
Sugimoto, Makoto;
Sato, Asomi;
Nakago, Satoshi;
Maruo, Takeshi

Publication type:

journal article

Can Mutations Identified in Congenital Fibrinogen Disorders Explain the Clinical Manifestations?

Published in:

Journal of Coagulation Disorders, 2010, v. 2, n. 2, p. 1

By:

Neerman-Arbez, Marguerite;
Tirefort, Yordanka;
de Moerloose, Philippe

Publication type:

Article

Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization.

Published in:

Haemophilia, 2017, v. 23, n. 4, p. e340, doi. 10.1111/hae.13268

By:

Amri, Y.;
Jouini, H.;
Becheur, M.;
Dabboubi, R.;
Mahjoub, B.;
Messaoud, T.;
Sfar, M. T.;
Casini, A.;
Moerloose, P.;
Toumi, N. E. H.

Publication type:

Article

Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.

Published in:

Haemophilia, 2015, v. 21, n. 6, p. 846, doi. 10.1111/hae.12712

By:

Hua, B.;
Li, K.;
Lee, A.;
Poon, M.‐C.;
Zhao, Y.

Publication type:

Article

Participation and risk-taking behaviour in sports in children with haemophilia.

Published in:

Haemophilia, 2009, v. 15, n. 3, p. 686, doi. 10.1111/j.1365-2516.2009.02006.x

By:

KÖITER, J.;
VAN GENDEREN, F. R.;
BRONS, P. P. T.;
NIJHUIS-VAN DER SANDEN, M. W. G.

Publication type:

Article

Factor XIII deficiency in south-east Iran.

Published in:

2004

By:

Eshghi, P.;
Abolghasemi, H.;
Sanei-Moghaddam, E.;
Anwar, R.;
Jazebi, M.;
Amid, A.;
Alatt, F. A.

Publication type:

Letter

The dysfibrinogenaemias.

Published in:

British Journal of Haematology, 2001, v. 114, n. 2, p. 249, doi. 10.1046/j.1365-2141.2001.02892.x

By:

Roberts, Harold R.;
Stinchcombe, Thomas E.;
Gabriel, Don A.

Publication type:

Article

Electrospray ionization mass spectrometry identification of fibrinogen Banks Peninsula (γ280Tyr→Cys): a new variant with defective polymerization.

Published in:

British Journal of Haematology, 1998, v. 101, n. 1, p. 24, doi. 10.1046/j.1365-2141.1998.00663.x

By:

Fellowes, Andrew P.;
Brennan, Stephen O.;
Ridgway, Hayley J.;
Heaton, David C.;
George, Peter M.

Publication type:

Article

A Chinese family with congenital Dysfibrinogenemia carries a heterozygous missense mutation in FGA: Concerning the genetic abnormality and clinical treatment.

Published in:

Pakistan Journal of Medical Sciences, 2017, v. 33, n. 4, p. 1, doi. 10.12669/pjms.334.12828

By:

Jihao Zhou;
Peng Zhu;
Xinyou Zhang

Publication type:

Article

Building an immune-mediated coagulopathy consensus: early recognition and evaluation to enhance post-surgical patient safety.

Published in:

Patient Safety in Surgery, 2009, v. 3, p. 1, doi. 10.1186/1754-9493-3-8

By:

Ness, Paul;
Creer, Michael;
Rodgers, George M.;
Naoum, Joseph J.;
Renkens, Kenneth;
Voils, Stacy A.;
Alexander, W. Allan

Publication type:

Article