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Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.
Published in:
Human Genetics, 2001, v. 108, n. 3, p. 237, doi. 10.1007/s004390100469
By:
- Neerman-Arbez, M.;
- de Moerloose, P.;
- Honsberger, A.;
- Parlier, G.;
- Arnuti, B.;
- Biron, C.;
- Borg, J.-Y.;
- Eber, S.;
- Meili, E.;
- Peter-Salonen, K.;
- Ripoll, L.;
- Vervel, C.;
- d'Oiron, R.;
- Staeger, P.;
- Antonarakis, S. E.;
- Morris, M. A.
Publication type:
Article
Prevalence of anticardiolipin and antinuclear antibodies in an elderly hospitalized population and mortality after a 6-year follow-up.
Published in:
1997
By:
- de Moerloose, P.;
- Boehlen, F.;
- Reber, G.;
- Dechevrens, O.;
- Herrmann, F.;
- Michel, J.-R
Publication type:
Letter
Potentiation of delayed-type hypersensitivity by pertussigen or cyclophosphamide with release of different lymphokines.
Published in:
Immunology, 1987, v. 61, n. 4, p. 483
By:
- Sewell, W. A.;
- de Moerloose, P. A.;
- Hamilton, J. A.;
- Schrader, J. W.;
- Mackay, I. R.;
- Vadas, M. A.
Publication type:
Article
Le polytraumatisé et les anomalies de l'hémostase.
Published in:
1998
By:
- Guay, J;
- Ozier, Y;
- de Moerloose, P;
- Samana, C M;
- Bélisle, S;
- Hardy, J F
Publication type:
journal article
Orthotopic liver transplantation in hemophilia B: a case report.
Published in:
Transplant International, 1995, v. 8, n. 6, p. 485, doi. 10.1111/j.1432-2277.1995.tb01560.x
By:
- Kadry, Z.;
- Moerloose, P.;
- Giostra, E.;
- Morel, P.;
- Huber, O.;
- Meili, E.;
- Blum, H.E.;
- Mentha, G.
Publication type:
Article
Anti-apolipoprotein A-1 IgG in patients with myocardial infarction promotes inflammation through TLR2/CD14 complex.
Published in:
Journal of Internal Medicine, 2012, v. 272, n. 4, p. 344, doi. 10.1111/j.1365-2796.2012.02530.x
By:
- Pagano, S.;
- Satta, N.;
- Werling, D.;
- Offord, V.;
- de Moerloose, P.;
- Charbonney, E.;
- Hochstrasser, D.;
- Roux-Lombard, P.;
- Vuilleumier, N.
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
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
Published in:
Haemophilia, 2017, v. 23, n. 4, p. 583, doi. 10.1111/hae.13190
By:
- Casini, A.;
- Vilar, R.;
- Beauverd, Y.;
- Aslan, D.;
- Devreese, K.;
- Mondelaers, V.;
- Alberio, L.;
- Gubert, C.;
- Moerloose, P.;
- Neerman-Arbez, M.
Publication type:
Article
Outcome measures in European patients with haemophilia.
Published in:
Haemophilia, 2017, v. 23, n. 2, p. 222, doi. 10.1111/hae.13085
By:
- Hermans, C.;
- Klamroth, R.;
- Richards, M.;
- Moerloose, P.;
- Garrido, R. P.;
- Altisent, C.;
- Astermark, J.;
- Batorova, A.;
- Carvalho, M.;
- Dolan, G.;
- Fijnvandraat, K.;
- Holme, P.A.;
- Holstein, K.;
- Jimenez‐Yuste, V.;
- Katsarou, O.;
- Kavakli, K.;
- Lambert, T.;
- Lopéz, F.;
- Pérez, R.;
- Rocino, A.
Publication type:
Article
Management of congenital quantitative fibrinogen disorders: a Delphi consensus.
Published in:
Haemophilia, 2016, v. 22, n. 6, p. 898, doi. 10.1111/hae.13061
By:
- Casini, A.;
- Moerloose, P.;
- Barbay, Virginie;
- Barro, Claire;
- Biron, Christine;
- Boehlen, Françoise;
- Brand, Brigit;
- Brungs, Thomas;
- Chamouni, Pierre;
- Claeyssens, Ségolène;
- Colin, Véronique;
- Maistre, Emmanuel;
- Desconclois, Céline;
- Devalet, Bérangère;
- D'Oiron, Roseline;
- Fontana, Pierre;
- Hanss, Michel;
- Hermans, Cédric;
- Lavenu‐Bombled, Cécile;
- Lebreton, Aurélien
Publication type:
Article
Can the phenotype of inherited fibrinogen disorders be predicted?
Published in:
Haemophilia, 2016, v. 22, n. 5, p. 667, doi. 10.1111/hae.12967
By:
- Casini, A.;
- Moerloose, P.
Publication type:
Article
Rare coagulation disorders: fibrinogen, factor VII and factor XIII.
Published in:
Haemophilia, 2016, v. 22, p. 61, doi. 10.1111/hae.12965
By:
- Moerloose, P.;
- Schved, J.‐F.;
- Nugent, D.
Publication type:
Article
Hypertension, haematuria and renal functioning in haemophilia - a cross-sectional study in Europe.
Published in:
Haemophilia, 2016, v. 22, n. 2, p. 248, doi. 10.1111/hae.12847
By:
- Holme, P. A.;
- Combescure, C.;
- Tait, R.C.;
- Berntorp, E.;
- Rauchensteiner, S.;
- Moerloose, P.;
- Pabinger‐Fasching, Ingrid;
- Hermans, Cedric;
- d'Oiron, Roseline;
- Negrier, Claude;
- Klamroth, Robert;
- Marquardt, Natascha;
- Staritz, Peter;
- Martinowitz, Uri;
- Kenet, Gili;
- Lubetsky, Aharon;
- Cannavò, Nino;
- Tagliaferri, Annarita;
- Schutgens, Roger;
- Windyga, Jerzy
Publication type:
Article
Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature.
Published in:
Haemophilia, 2015, v. 21, n. 6, p. 820, doi. 10.1111/hae.12719
By:
- Casini, A.;
- Sokollik, C.;
- Lukowski, S. W.;
- Lurz, E.;
- Rieubland, C.;
- Moerloose, P.;
- Neerman‐Arbez, M.
Publication type:
Article
Congenital combined deficiency of coagulation factors VII and X - different genetic mechanisms.
Published in:
Haemophilia, 2015, v. 21, n. 3, p. 386, doi. 10.1111/hae.12604
By:
- Pavlova, A.;
- Preisler, B.;
- Driesen, J.;
- Moerloose, P.;
- Zieger, B.;
- Hütker, S.;
- Dengler, K.;
- Harbrecht, U.;
- Oldenburg, J.
Publication type:
Article
Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis.
Published in:
Haemophilia, 2015, v. 21, n. 1, p. e108, doi. 10.1111/hae.12584
By:
- Lebreton, A.;
- Casini, A.;
- Alhayek, R.;
- Kouteich, K. L.;
- Neerman‐Arbez, M.;
- Moerloose, P.
Publication type:
Article
FXI concentrate use and risk of thrombosis.
Published in:
Haemophilia, 2014, v. 20, n. 4, p. e349, doi. 10.1111/hae.12457
By:
- Bolton‐Maggs, P.;
- Goudemand, J.;
- Hermans, C.;
- Makris, M.;
- Moerloose, P.
Publication type:
Article
Novel products for haemostasis.
Published in:
Haemophilia, 2014, v. 20, p. 29, doi. 10.1111/hae.12413
By:
- SHIMA, M.;
- HERMANS, C.;
- DE MOERLOOSE, P.
Publication type:
Article
Novel products for haemostasis.
Published in:
Haemophilia, 2014, v. 20, p. 29, doi. 10.1111/hae.12413
By:
- Shima, M.;
- Hermans, C.;
- Moerloose, P.
Publication type:
Article
Cancer detection and management in patients with haemophilia: a retrospective European multicentre study.
Published in:
Haemophilia, 2014, v. 20, n. 1, p. 78, doi. 10.1111/hae.12250
By:
- Biron‐Andreani, C.;
- Moerloose, P.;
- D'oiron, R.;
- Chambost, H.;
- Schved, J.‐F.;
- Hermans, C.
Publication type:
Article
Applicability of the European Society of Cardiology guidelines on management of acute coronary syndromes to people with haemophilia - an assessment by the ADVANCE Working Group.
Published in:
Haemophilia, 2013, v. 19, n. 6, p. 833, doi. 10.1111/hae.12189
By:
- Staritz, P.;
- Moerloose, P.;
- Schutgens, R.;
- Dolan, G.
Publication type:
Article
Recommendations for assessment, monitoring and follow-up of patients with haemophilia.
Published in:
Haemophilia, 2012, v. 18, n. 3, p. 319, doi. 10.1111/j.1365-2516.2011.02671.x
By:
- DE MOERLOOSE, P.;
- FISCHER, K.;
- LAMBERT, T.;
- WINDYGA, J.;
- BATOROVA, A.;
- LAVIGNE-LISSALDE, G.;
- ROCINO, A.;
- ASTERMARK, J.;
- HERMANS, C.
Publication type:
Article
Management of acute haemarthrosis in haemophilia A without inhibitors: literature review, European survey and recommendations.
Published in:
Haemophilia, 2011, v. 17, n. 3, p. 383, doi. 10.1111/j.1365-2516.2010.02449.x
By:
- Hermans, C.;
- De Moerloose, P.;
- Fisher, K.;
- Holstein, K.;
- Klamroth, R.;
- Lambert, T.;
- Lavigne-Lissalde, G.;
- Perez, R.;
- Richards, M.;
- Dolan, G.
Publication type:
Article
The role of prophylaxis in bleeding disorders.
Published in:
Haemophilia, 2010, v. 16, p. 189, doi. 10.1111/j.1365-2516.2010.02319.x
By:
- BERNTORP, E.;
- de MOERLOOSE, P.;
- LJUNG, R. C. R.
Publication type:
Article
Replacement therapy for invasive procedures in patients with haemophilia: literature review, European survey and recommendations.
Published in:
Haemophilia, 2009, v. 15, n. 3, p. 639, doi. 10.1111/j.1365-2516.2008.01950.x
By:
- HERMANS, C.;
- ALTISENT, C.;
- BATOROVA, A.;
- CHAMBOST, H.;
- DE MOERLOOSE, P.;
- KARAFOULIDOU, A.;
- KLAMROTH, R.;
- RICHARDS, M.;
- WHITE, B.;
- DOLAN, G.
Publication type:
Article
European curriculum for thrombosis and haemostasis.
Published in:
Haemophilia, 2009, v. 15, n. 1, p. 337, doi. 10.1111/j.1365-2516.2008.01836.x
By:
- ASTERMARK, J.;
- NEGRIER, C.;
- HERMANS, C.;
- HOLME, P. A.;
- KLAMROTH, R.;
- KOTSI, P.;
- DE MOERLOOSE, P.;
- PASI, J.;
- ROCINO, A.;
- VON DEPKA, M.;
- WINDYGA, J.;
- LUDLAM, C. A.
Publication type:
Article
A survey of adherence to haemophilia therapy in six European countries: results and recommendations.
Published in:
Haemophilia, 2008, v. 14, n. 5, p. 931, doi. 10.1111/j.1365-2516.2008.01843.x
By:
- DE MOERLOOSE, P.;
- URBANCIK, W.;
- VAN DEN BERG, H. M.;
- RICHARDS, M.
Publication type:
Article
Rare bleeding disorders.
Published in:
Haemophilia, 2008, v. 14, p. 202, doi. 10.1111/j.1365-2516.2008.01751.x
By:
- PEYVANDI, F.;
- CATTANEO, M.;
- INBAL, A.;
- DE MOERLOOSE, P.;
- SPREAFICO, M.
Publication type:
Article
Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype–genotype correlation.
Published in:
Haemophilia, 2008, v. 14, n. 4, p. 709, doi. 10.1111/j.1365-2516.2008.01760.x
By:
- DJAMBAS KHAYAT, C.;
- SALEM, N.;
- CHOUERY, E.;
- CORBANI, S.;
- MOIX, I.;
- NICOLAS, E.;
- MORRIS, M.A.;
- DE MOERLOOSE, P.;
- MÉGARBANÉ, A.
Publication type:
Article
Should prophylaxis be used in adolescent and adult patients with severe haemophilia? An European survey of practice and outcome data.
Published in:
Haemophilia, 2007, v. 13, n. 5, p. 473, doi. 10.1111/j.1365-2516.2007.01478.x
By:
- RICHARDS, M.;
- ALTISENT, C.;
- BATOROVA, A.;
- CHAMBOST, H.;
- DOLAN, G.;
- DE MOERLOOSE, P.;
- FRAGA, M.;
- HERMANS, C.;
- KARAFOULIDOU, A.;
- KLAMROTH, R.;
- LASSILA, R.;
- ROTHSCHILD, C.
Publication type:
Article
Recommendations for postmarketing surveillance studies in haemophilia and other bleeding disorders.
Published in:
Haemophilia, 2005, v. 11, n. 4, p. 353, doi. 10.1111/j.1365-2516.2005.01114.x
By:
- Lassila, R.;
- Rothschild, C.;
- Moerloose, P.;
- Richards, M.;
- Perez, R.;
- Gajek, H.
Publication type:
Article
Antiphospholipid antibodies and risk for recurrent vascular events.
Published in:
2004
By:
- Cabral AR;
- Ruiz-Irastorza G;
- Khamashta MA;
- Hughes GRV;
- Wahl D;
- Regnault V;
- de Moerloose P;
- Lecompte T;
- Levine SR;
- Brey RL;
- Tilley BC;
- Triplett DA;
- Thompson JLP;
- Sacco RL;
- Mohr JP;
- Cabral, Antonio R
Publication type:
commentary
Cell-mediated immunity to hepatitis B virus antigens in mice: correlation of in vivo and in vitro assays.
Published in:
Clinical & Experimental Immunology, 1986, v. 64, n. 2, p. 285
By:
- De Moerloose, P. A.;
- Frazer, I. H.;
- Sewell, W. A.;
- Collins, Elizabeth J.;
- Mackay, I. R.
Publication type:
Article
Severe thrombocytopenic purpura due to rubella infection in a patient with systemic lupus erythematosus.
Published in:
Lupus, 2003, v. 12, n. 2, p. 144, doi. 10.1191/0961203303lu279cr
By:
- Boehlen, F;
- Balavoine, J-F;
- de Moerloose, P
Publication type:
Article
The coagulopathy of massive transfusion.
Published in:
Vox Sanguinis, 2005, v. 89, n. 3, p. 123, doi. 10.1111/j.1423-0410.2005.00678.x
By:
- Hardy, Jean-François;
- de Moerloose, P.;
- Samama, C. M.
Publication type:
Article
Severe Neonatal Alloimmune Thrombocytopenia due toAnti-HPA-3a.
Published in:
Vox Sanguinis, 1998, v. 74, n. 3, p. 201, doi. 10.1159/000030932
By:
- Boehlen, F.;
- Kaplan, C.;
- de Moerloose, P.
Publication type:
Article
Not all statins interfere with clopidogrel during antiplatelet therapy.
Published in:
European Journal of Clinical Investigation, 2005, v. 35, n. 8, p. 476, doi. 10.1111/j.1365-2362.2005.01522.x
By:
- Mach, F.;
- Senouf, D.;
- Fontana, P.;
- Boehlen, F.;
- Reber, G.;
- Daali, Y.;
- de Moerloose, P.;
- Sigwart, U.
Publication type:
Article
Congenital α<sub>2</sub>-plasmin inhibitor deficiencies: a review.
Published in:
British Journal of Haematology, 2001, v. 114, n. 1, p. 4, doi. 10.1046/j.1365-2141.2001.02845.x
By:
- Favier, R.;
- Aoki, N.;
- de Moerloose, P.
Publication type:
Article
Prevalence of factor V Leiden and prothrombin G20210A mutations in unselected patients with venous thromboembolism.
Published in:
British Journal of Haematology, 2000, v. 110, n. 1, p. 125, doi. 10.1046/j.1365-2141.2000.02039.x
By:
- de Moerloose, P.;
- Reber, G.;
- Perrier, A.;
- Perneger, T.;
- Bounameaux, H.
Publication type:
Article

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