Search Results - "ALHENC-GELAS, Martine" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Heparin‐induced thrombocytopenia: Construction of a pretest diagnostic score derived from the analysis of a prospective multinational database, with internal validation

Heparin‐induced thrombocytopenia: Construction of a pretest diagnostic score derived from the analysis of a prospective multinational database, with internal validation

by Tardy‐Poncet, Brigitte, Maistre, Emmanuel, Pouplard, Claire, Presles, Emilie, Alhenc‐Gelas, Martine, Lasne, Dominique, Horellou, Marie‐Hélène, Mouton, Christine, Serre‐Sapin, Anne, Bauters, Anne, Nguyen, Philippe, Mullier, François, Perrin, Julien, Le Gal, Grégoire, Morange, Pierre‐Emmanuel, Grunebaum, Lélia, Lillo‐Le Louet, Agnès, Elalamy, Ismail, Gruel, Yves, Greinacher, Andreas, Lecompte, Thomas, Tardy, Bernard
Published in Journal of thrombosis and haemostasis (01.08.2021)

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Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

by Picard, Véronique, Nowak-Göttl, Ulrike, Biron-Andreani, Christine, Fouassier, Marc, Frere, Corinne, Goualt-Heilman, Michèle, de Maistre, Emmanuel, Regina, Sandra, Rugeri, Lucia, Ternisien, Catherine, Trichet, Catherine, Vergnes, Christine, Aiach, Martine, Alhenc-Gelas, Martine
Published in Human mutation (01.06.2006)

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Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement

Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement

by Alhenc Gelas, Martine, Juin, Fabrice, de Raucourt, Emmanuelle, Gandrille, Sophie, Borgel, Delphine, Aiach, Martine
Published in Thrombosis and haemostasis (01.04.2007)

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Novel Splice Site Mutation in the PROS1 Gene in a Polish Patient with Venous Thromboembolism: c.602-2delA, Splice Acceptor Site of Exon 7

Novel Splice Site Mutation in the PROS1 Gene in a Polish Patient with Venous Thromboembolism: c.602-2delA, Splice Acceptor Site of Exon 7

by Mrożek, Magdalena, Wypasek, Ewa, Alhenc-Gelas, Martine, Potaczek, Daniel P, Undas, Anetta
Published in Medicina (Kaunas, Lithuania) (22.09.2020)

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Role of protein S deficiency in children with venous thromboembolism. An observational international cohort study

Role of protein S deficiency in children with venous thromboembolism. An observational international cohort study

by Klostermeier, Ulrich C, Limperger, Verena, Kenet, Gili, Kurnik, Karin, Alhenc Gelas, Martine, Finckh, Ulrich, Junker, Ralf, Heller, Christine, Zieger, Barbara, Knöfler, Ralf, Holzhauer, Susanne, Mesters, Rolf, Krümpel, Anne, Nowak-Göttl, Ulrike
Published in Thrombosis and haemostasis (01.02.2015)

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Clinical and laboratory characteristics of children with venous thromboembolism and protein C‐deficiency: an observational Israeli‐German cohort study

Clinical and laboratory characteristics of children with venous thromboembolism and protein C‐deficiency: an observational Israeli‐German cohort study

by Limperger, Verena, Klostermeier, Ulrich C., Kenet, Gili, Holzhauer, Susanne, Alhenc Gelas, Martine, Finckh, Ulrich, Junker, Ralf, Heller, Christine, Zieger, Barbara, Kurnik, Karin, Knöfler, Ralf, Mesters, Rolf, Halimeh, Susan, Nowak‐Göttl, Ulrike
Published in British journal of haematology (01.11.2014)

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Heparin-induced Thrombocytopenia Diagnosis: A Retrospective Study Comparing Heparin-induced Platelet Activation Test to 14C-serotonin Release Assay

Heparin-induced Thrombocytopenia Diagnosis: A Retrospective Study Comparing Heparin-induced Platelet Activation Test to 14C-serotonin Release Assay

by Gonthier, Marie-Caroline, Gendron, Nicolas, Eloy, Philippine, Bourrienne, Marie-Charlotte, Alhenc-Gelas, Martine, Pouplard, Claire, Tardy, Bernard, Szymezak, Jean, Burdet, Charles, Gkalea, Vasiliki, Faille, Dorothée, Ajzenberg, Nadine
Published in TH open : companion journal to thrombosis and haemostasis (01.10.2021)

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Functional Flow Cytometric Assay for Reliable and Convenient Heparin-Induced Thrombocytopenia Diagnosis in Daily Practice

Functional Flow Cytometric Assay for Reliable and Convenient Heparin-Induced Thrombocytopenia Diagnosis in Daily Practice

by Tardy-Poncet, Brigitte, Montmartin, Aurélie, Piot, Michele, Alhenc-Gelas, Martine, Nguyen, Philippe, Elalamy, Ismail, Greinacher, Andreas, Maistre, Emmanuel De, Lasne, Dominique, Horellou, Marie-Hélène, Le Gal, Grégoire, Lecompte, Thomas, Tardy, Bernard, On Behalf Of The Gfht-Hit Study Group
Published in Biomedicines (25.03.2021)

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Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

by Wypasek, Ewa, Potaczek, Daniel P, Alhenc-Gelas, Martine, Undas, Anetta
Published in Polskie archiwum medycyny wewne̦trznej (01.01.2014)

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Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene

Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene

by Picard, Véronique, Bura, Alessandra, Emmerich, Joseph, Alhenc‐Gelas, Martine, Biron, Christine, Houbouyan‐Reveillard, Lucie L., Molho, Pascale, Labatide‐Alanore, Agnès, Sié, Pierre, Toulon, Pierre, Verdy, Elisabeth, Aiach, Martine
Published in British journal of haematology (01.09.2000)

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Fetal Intracerebral Hemorrhage in Familial Thrombophilia

Fetal Intracerebral Hemorrhage in Familial Thrombophilia

by Crespin, Malvina, PharmD, Alhenc-Gelas, Martine, MD, Grangé, Gilles, MD, Fallet-Bianco, Catherine, MD, Fontenay, Michaela, MD, PhD
Published in Pediatric neurology (01.10.2009)

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Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes

Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes

by Alhenc-Gelas, M, Arnaud, E, Nicaud, V, Aubry, M L, Fiessinger, J N, Aiach, M, Emmerich, J
Published in Thrombosis and haemostasis (01.04.1999)

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The factor V gene A4070G mutation and the risk of venous thrombosis

The factor V gene A4070G mutation and the risk of venous thrombosis

by Alhenc-Gelas, M, Nicaud, V, Gandrille, S, van Dreden, P, Amiral, J, Aubry, M L, Fiessinger, J N, Emmerich, J, Aiach, M
Published in Thrombosis and haemostasis (01.02.1999)

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Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

by Borensztajn, Keren, Chafa, Ouerdia, Alhenc‐Gelas, Martine, Salha, Siham, Reghis, Abderrezak, Fischer, Anne‐Marie, Tapon‐Bretaudière, Jacqueline
Published in British journal of haematology (01.04.2002)

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The -33T-->C polymorphism in intron 7 of the TFPI gene influences the risk of venous thromboembolism, independently of the factor V Leiden and prothrombin mutations

The -33T-->C polymorphism in intron 7 of the TFPI gene influences the risk of venous thromboembolism, independently of the factor V Leiden and prothrombin mutations

by Ameziane, Nejma, Seguin, Cendrine, Borgel, Delphine, Fumeron, Frédéric, Moatti, Didier, Alhenc-Gelas, Martine, Grandchamp, Bernard, Aiach, Martine, Emmerich, Joseph, de Prost, Dominique
Published in Thrombosis and haemostasis (01.08.2002)

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Mutations in Promoter Region of Thrombomodulin and Venous Thromboembolic Disease

Mutations in Promoter Region of Thrombomodulin and Venous Thromboembolic Disease

by Le Flem, Lena, Picard, Veronique, Emmerich, Joseph, Gandrille, Sophie, Fiessinger, Jean-Noel, Aiach, Martine, Alhenc-Gelas, Martine
Published in Arteriosclerosis, thrombosis, and vascular biology (01.04.1999)

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Erratum: Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

Erratum: Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

by Picard, Véronique, Nowak-Göttl, Ulrike, Biron-Andreani, Christine, Fouassier, Marc, Frere, Corinne, Goualt-Heilman, Michèle, de Maistre, Emmanuel, Regina, Sandra, Rugeri, Lucia, Ternisien, Catherine, Trichet, Catherine, Vergnes, Christine, Aiach, Martine, Alhenc-Gelas, Martine
Published in Human mutation (01.11.2006)

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Conformational Asn187Asp/Lys antithrombin variants and thrombosis. Clinical and biological features in 13 new heterozygotes

Conformational Asn187Asp/Lys antithrombin variants and thrombosis. Clinical and biological features in 13 new heterozygotes

by Picard, Véronique, Bauters, Anne, Khairy, Mahnouch, Ochat, Nadège, Jude, Brigitte, Aiach, Martine, Alhenc-Gelas, Martine
Published in Thrombosis and haemostasis (01.01.2005)

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PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency

PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency

by Alhenc-Gelas, Martine, Plu-Bureau, Genevieve, Horellou, Marie Hélène, Rauch, Antoine, Suchon, Pierre
Published in Thrombosis and haemostasis (01.03.2016)

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First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosis

First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosis

by Wypasek, Ewa, Alhenc-Gelas, Martine, Undas, Anetta
Published in Thrombosis research (01.07.2013)

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