Celine Falaise - System, Marseille Public University Hospital

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论文共 33 篇作者统计合作学者相似作者

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Thrombomodulin (p.cys537stop) is Released from Cells by an Unusual Membrane Insertion/leakage Mechanism

Clara Bernard, Andréa Pin,Nathalie Hezard,Vincent Ernest,Céline Falaise, Camille Roze,Stéphanie Simoncini,Romaric Lacroix, Pierre-Emmanuel Morange,Franck Peiretti

Blood Advances (2024)

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Thrombopénies Constitutionnelles

Cécile Lavenu-Bombled,Céline Falaise,Adeline Blandinieres,Paquita Nurden, Marie-Christine Alessi,Paul Saultier

Perfectionnement en Pédiatrie (2024)

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Relationship Between Plasma Tissue Factor Pathway Inhibitor (TFPI) Levels, Thrombin Generation and Clinical Risk of Bleeding in Patients with Severe Haemophilia A or B

Brigitte Tardy-Poncet,Aurelie Montmartin,Herve Chambost,Anne Lienhart,Birgit Frotscher,Pierre-Emmanuel Morange,Celine Falaise,Fanny Collange,Yesim Dargaud, Marie Toussaint-Hacquard,Laurent Ardillon,Benedicte Wibaut,Emmanuelle Jeanpierre,Philippe Nguyen,Fabienne Volot,Bernard Tardy

HAEMOPHILIA（2024）

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Association of Laboratory Test Results with the Bleeding History in Patients with Inherited Platelet Function Disorders (the Bleeding Assesment Tool - LABoratory Tests Substudy): Communication from the Platelet Physiology ISTH-SSC

Paolo Gresele,Emanuela Falcinelli,Loredana Bury,Marie-Christine Alessi,Giuseppe Guglielmini,Celine Falaise,Gianmarco Podda,Mathieu Fiore,Francesco Mazziotta,Teresa Sevivas,Nuria Bermejo,Erica De Candia,Meera Chitlur,Michele P. Lambert, Luca Barcella,Ana C. Glembotsky,Marie Lordkipanidze

Research and practice in thrombosis and haemostasisno. 1 (2023): 102305-102305

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Emergency Management of Patients with Glanzmann Thrombasthenia: Consensus Recommendations from the French Reference Center for Inherited Platelet Disorders

Mathieu Fiore, Janine-Sophie Giraudet,Marie-Christine Alessi,Céline Falaise,Dominique Desprez,Roseline d’Oiron,Sophie Voisin,Marie-Françoise Hurtaud,Hélène Boutroux,Paul Saultier,Cécile Lavenu-Bombled,Gilles Bagou,Xavier Dubucs,Anthony Chauvin,Christophe Leroy, Francine Meckert, François Kerbaul,Nicolas Giraud,Ambra Pühler,Ana Rath

ORPHANET JOURNAL OF RARE DISEASESno. 1 (2023)

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P1672: OCCUPATIONAL INTEGRATION OF ADULTS WITH SEVERE HAEMOPHILIA (INTHEMO): A STUDY BASED ON THE FRANCECOAG REGISTRY

Ngọc Ánh Nguyễn,Pascal Auquier,Any Beltran Anzola, Roseline d’Oiron,Thierry Lambert,Céline Falaise,Christine Biron‐Andréani,Anne Lienhart,Jenny Goudemand,Antoine Rauch,B. Wibaut,Sabine Castet,Dominique Desprez,Annie Harroche,Natalie Stieltjes,Annie Borel‐Derlon,Marc Trossaërt, Amandine Celli,Benoît Guillet,Sophie Bayart,Marie‐Anne Bertrand,Alexandra Fournel,Guillaume Mourey,Valérie Gay,Pierre Chamouni,Emmanuelle de Raucourt,Birgit Frotscher, Michele N. Martin, Mathieu Puyade,B. Tardy,Stéphane Vanderbecken,Fabienne Genre-Volot,Philippe Nguyên,Benoı̂t Polack,Caroline Oudot‐Challard,Stéphane Girault, Annelise Voyer,Aurélien Lebreton,Abel Hassoun, Philippe Moreau,Pierre‐Simon Rohrlich,Karine Baumstarck,Mohamed Boucékine,Vanessa Milien, Natacha Rosso,Clémence Tabelé,M Viprey,Nicolas Giraud,Thomas Sannié,Hérvè Chambost,Noémie Resseguier

HemaSphereno. S3 (2023): e623777c-e623777c

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Early changes in bleeding perception and quality of life in children and adolescents receiving emicizumab prophylaxis for severe haemophilia A without inhibitor

Celine Falaise,Martine Roche,Sophie Gensollen,Nathalie Hezard,Mohamed Boucekine,Pascal Auquier,Herve Chambost,Paul Saultier

HAEMOPHILIA（2022）

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Reinvestigation of Unidentified Causative Variants in FXI‐deficient Patients: Focus on Gene Segment Deletions

Philippe De Mazancourt,Annie Harroche, Katia Pouymayou,Marianne Sigaud,Celine Falaise,Natalie Stieltjes,Sabine-Marie Castet,Brigitte Tardy,Christophe Zawadzki,Jenny Goudemand,Yesim Dargaud

Haemophilia（2022）

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Early Changes in Bleeding Perception and Quality of Life in Children and Adolescents Receiving Emicizumab Prophylaxis for Severe Haemophilia A Without Inhibitor

Marion Marro, Audrey Françoise Petit,Céline Falaise,Martine Roche, S. Gensollen,Nathalie Hézard,Mohamed Boucékine,Pascal Auquier,Hérvè Chambost,Paul Saultier

Haemophiliano. 1 (2022): 397-400

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