Publications by authors named "Odile Fenneteau"

54Publications

Brandalise syndrome: a rare inclusion cell disease.

Blood 2020 Sep;136(11):1373

Hôpital R. Debré.

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http://dx.doi.org/10.1182/blood.2019001167DOI Listing
September 2020

Systemic chloroquine intoxication: a hint from the peripheral blood smear.

Am J Hematol 2020 07 3;95(7):873-875. Epub 2020 Apr 3.

Sorbonne Université, Assistance Publique-Hôpitaux de Paris (APHP), Institut E3M, Hôpital La Pitié-Salpêtrière, service de médecine interne 2, Paris, France.

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http://dx.doi.org/10.1002/ajh.25788DOI Listing
July 2020

Maintenance Therapy With Interleukin-2 for Childhood AML: Results of ELAM02 Phase III Randomized Trial.

Hemasphere 2018 Dec 29;2(6):e159. Epub 2018 Nov 29.

Department of Pediatric Hematology and Oncology, Assistance Publique-Hôpitaux de Paris, GH HUEP, Armand Trousseau Hospital, Paris, France; Sorbonne Université, UMRS_938, Paris, France.

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http://dx.doi.org/10.1097/HS9.0000000000000159DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745961PMC
December 2018

Shwachman-Diamond syndrome: a case report.

Ann Biol Clin (Paris) 2018 Aug;76(4):435-438

Laboratoire d'hématologie, Centre hospitalier Le Mans, Le Mans, France.

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http://www.john-libbey-eurotext.fr/medline.md?doi=10.1684/ab
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http://dx.doi.org/10.1684/abc.2018.1358DOI Listing
August 2018

Down syndrome-like acute megakaryoblastic leukemia in a patient with Cornelia de Lange syndrome.

Haematologica 2018 06 7;103(6):e274-e276. Epub 2017 Dec 7.

Assistance Publique des Hôpitaux de Paris (AP-HP), Hôpital Robert Debré, Département de Génétique, France

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http://dx.doi.org/10.3324/haematol.2017.178590DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058797PMC
June 2018

Diagnostic difficulty of beta-thalassemia syndrome in a multi-transfused patient: contribution of myelogram and studying parents.

Ann Biol Clin (Paris) 2017 Oct;75(5):562-568

Laboratoire de génétique moléculaire, Hôpital Robert Debré, AP-HP, Paris, France.

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http://dx.doi.org/10.1684/abc.2017.1284DOI Listing
October 2017

Congenital neutropenia in the era of genomics: classification, diagnosis, and natural history.

Br J Haematol 2017 11 6;179(4):557-574. Epub 2017 Sep 6.

Département de Génétique, AP-HP Hôpital Pitié-Salpêtrière, UPMC Univ Paris 06, Paris, France.

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http://dx.doi.org/10.1111/bjh.14887DOI Listing
November 2017

Recommendations for cerebrospinal fluid examination in acute leukemia.

Ann Biol Clin (Paris) 2017 Oct;75(5):503-512

Service d'hématologie biologique, CHU de Nancy, Vandoeuvre-lès-Nancy, France.

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http://dx.doi.org/10.1684/abc.2017.1250DOI Listing
October 2017

Limited benefits of presymptomatic cord blood transplantation in neurovisceral acid sphingomyelinase deficiency (ASMD) intermediate type.

Eur J Paediatr Neurol 2017 Nov 29;21(6):907-911. Epub 2017 Jul 29.

Reference Centre for Inborn Errors of Metabolism, Robert Debré University Hospital, APHP, Paris, France; UMR1141, PROTECT, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2017.07.015DOI Listing
November 2017

ANKRD26 normocytic thrombocytopenia: a family report.

Ann Biol Clin (Paris) 2016 Jun;74(3):317-22

Centre de référence des pathologies plaquettaires (CRPP), Service d'hématologie biologique, CHU Robert Debré, AP-HP, Paris, France.

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http://dx.doi.org/10.1684/abc.2016.1142DOI Listing
June 2016

Glucose-6-phosphate dehydrogenase deficiency: the added value of cytology.

Ann Biol Clin (Paris) 2016 Jun;74(3):299-305

Service d'hématologie biologique, Hôpital Robert Debré, AP-HP, Paris, France, Université Paris 7-Denis Diderot, Sorbonne Paris Cité, Paris, France, Inserm U1149, CRI, Faculté de médecine Bichat Claude Bernard, Paris, France, Laboratoire d'Excellence, GR-Ex, Paris, France.

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http://dx.doi.org/10.1684/abc.2016.1136DOI Listing
June 2016

Juvenile myelomonocytic leukaemia and Noonan syndrome.

J Med Genet 2014 Oct 5;51(10):689-97. Epub 2014 Aug 5.

INSERM UMR_S1131, Institut Universitaire d'Hématologie, Université Paris Diderot, Paris-Sorbonne-Cité, Paris, France Département de Génétique, Assistance Publique des Hôpitaux de Paris (AP-HP), Hôpital Robert Debré, Paris, France.

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http://jmg.bmj.com/content/early/2014/08/05/jmedgenet-2014-1
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http://jmg.bmj.com/cgi/doi/10.1136/jmedgenet-2014-102611
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http://dx.doi.org/10.1136/jmedgenet-2014-102611DOI Listing
October 2014

Mutation spectrum and genotype-phenotype correlations in a large French cohort of MYH9-Related Disorders.

Mol Genet Genomic Med 2014 Jul 7;2(4):297-312. Epub 2014 Feb 7.

Service d'Hématologie Biologique and National Reference Center on Inherited Platelet Disorders, Hôpital Robert-Debré 48 Boulevard Sérurier, 75019, Paris, France.

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http://doi.wiley.com/10.1002/mgg3.68
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http://dx.doi.org/10.1002/mgg3.68DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113270PMC
July 2014

Schistocytes.

Transfusion 2014 Jun;54(6):1459

Laboratory of Hematology, University Hospital, Nancy, France.

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http://dx.doi.org/10.1111/trf.12523DOI Listing
June 2014

Performance of rapid diagnostic tests for imported malaria in clinical practice: results of a national multicenter study.

PLoS One 2013 30;8(9):e75486. Epub 2013 Sep 30.

AP-HP (Assistance Publique des Hôpitaux de Paris), Hôpital Bichat, Laboratoire de Parasitologie-Centre National de Référence du Paludisme, Paris, France ; Université Paris Descartes, UMR 216, Paris, France ; Institut de Recherche pour le Développement, UMR 216, Paris, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0075486PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787089PMC
May 2014

Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.

Blood Rev 2013 Jul 9;27(4):167-78. Epub 2013 May 9.

AP-HP, Service d'Hématologie Biologique, Hôpital R. Debré, Paris, F-75019, France.

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http://dx.doi.org/10.1016/j.blre.2013.04.003DOI Listing
July 2013

Platelet morphology analysis.

Methods Mol Biol 2013 ;992:207-25

Hematology Department and Grand East Competence Center on Inherited Platelet Disorders, CHU Nancy, Nancy, France.

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http://dx.doi.org/10.1007/978-1-62703-339-8_16DOI Listing
September 2013

Longitudinal study assessing the return of chloroquine susceptibility of Plasmodium falciparum in isolates from travellers returning from West and Central Africa, 2000-2011.

Authors:
Myriam Gharbi Jennifer A Flegg Véronique Hubert Eric Kendjo Jessica E Metcalf Lionel Bertaux Philippe J Guérin Jacques Le Bras Ahmed Aboubaca Patrice Agnamey Adela Angoulvant Patricia Barbut Didier Basset Ghania Belkadi Anne Pauline Bellanger Dieudonné Bemba Françoise Benoit-Vica Antoine Berry Marie-Laure Bigel Julie Bonhomme Françoise Botterel Olivier Bouchaud Marie-Elisabeth Bougnoux Patrice Bourée Nathalie Bourgeois Catherine Branger Laurent Bret Bernadette Buret Enrique Casalino Sylviane Chevrier Frédérique Conquere de Monbrison Bernadette Cuisenier Martin Danis Marie-Laure Darde Ludovic De Gentile Jean-Marie Delarbre Pascal Delaunay Anne Delaval Guillaume Desoubeaux Michel Develoux Jean Dunand Rémy Durand Odile Eloy Nathalie Fauchet Bernard Faugere Alber Faye Odile Fenneteau Pierre Flori Madeleine Fontrouge Chantal Garabedian Françoise Gayandrieu Nadine Godineau Pascal Houzé Sandrine Houzé Jean-Pierre Hurst Houria Ichou Laurence Lachaud Agathe Lebuisson Magalie Lefevre Anne-Sophie LeGuern Gwenaë Le Moal Daniel Lusina Marie-Claude Machouart Denis Malvy Sophie Matheron Danièle Maubon Denis Mechali Bruno Megarbane Guillaume Menard Laurence Millon Muriel Mimoun Aiach Philippe Minodier Christelle Morelle Gilles Nevez Philippe Parola Daniel Parzy Olivier Patey Pierre Patoz Pascale Penn Alice Perignon Stéphane Picot Jean-Etienne Pilo Isabelle Poilane Denis Pons Marie Poupart Bruno Pradines Didier Raffenot Christophe Rapp Marie-Catherine Receveur Claudine Sarfati Yaye Senghor Fabrice Simon Jean-Yves Siriez Nicolas Taudon Marc Thellier Maxime Thouvenin Dominique Toubas

Malar J 2013 Jan 25;12:35. Epub 2013 Jan 25.

Mère et enfant face aux infections tropicales, IRD unité mixte de recherche 216, Université Paris Descartes-Paris V, 4 avenue de l'Observatoire, Paris Cedex 06 75270, France.

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http://dx.doi.org/10.1186/1475-2875-12-35DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583707PMC
January 2013

Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry.

Orphanet J Rare Dis 2012 Sep 25;7:71. Epub 2012 Sep 25.

AP-HP, Registre Français des Neutropénies Chroniques Sévères, Centre de Référence des Déficits Immunitaires Héréditaires, Service d'Hémato-Oncologie Pédiatrique Hôpital Trousseau, 26 avenue du Dr Netter, 75012 Paris, France.

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http://dx.doi.org/10.1186/1750-1172-7-71DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585856PMC
September 2012

Proper desensitization of CXCR4 is required for lymphocyte development and peripheral compartmentalization in mice.

Blood 2012 Jun 20;119(24):5722-30. Epub 2012 Mar 20.

Inserm Unité Mixte de Recherche (UMR) S996, Université Paris-Sud, Laboratory of Excellence in Research on Medication and Innovative Therapeutics, Clamart, France.

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http://dx.doi.org/10.1182/blood-2012-01-403378DOI Listing
June 2012

Congenital neutropenia: diagnosis, molecular bases and patient management.

Orphanet J Rare Dis 2011 May 19;6:26. Epub 2011 May 19.

Service d'Hémato-Oncologie Pédiatrique Registre des neutropénies congénitales, AP-HP Hopital Trousseau, 26 avenue du Dr Netter, Paris, France.

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http://dx.doi.org/10.1186/1750-1172-6-26DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127744PMC
May 2011

Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study.

Ann Hematol 2011 Jul 22;90(7):759-68. Epub 2010 Dec 22.

Hematology Laboratory - Namur Thrombosis and Hemostasis Center (NTHC), UCL Mont-Godinne, 1, avenue Gaston Therasse, 5530, Yvoir, Belgium.

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http://dx.doi.org/10.1007/s00277-010-1138-3DOI Listing
July 2011

[Usefulness of gray platelets observation in ARC syndrome].

Ann Biol Clin (Paris) 2010 Jul-Aug;68(4):485-9

Service d'immuno-hématologie, Hôpital Bichat, Paris.

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http://www.john-libbey-eurotext.fr/medline.md?doi=10.1684/ab
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http://dx.doi.org/10.1684/abc.2010.0453DOI Listing
September 2010

Vacuolation of neutrophils and acanthocytosis in child with medium chain acyl-CoA dehydrogenase deficiency.

Br J Haematol 2008 Mar 19;140(6):595. Epub 2008 Jan 19.

Service d'Hématologie Biologie, Hôpital Robert Debré, AP-HP, Paris, France.

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http://doi.wiley.com/10.1111/j.1365-2141.2007.06849.x
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http://dx.doi.org/10.1111/j.1365-2141.2007.06849.xDOI Listing
March 2008

Phenotype and genotype for thiopurine methyltransferase activity in the French Caucasian population: impact of age.

Eur J Clin Pharmacol 2004 Apr 12;60(2):89-96. Epub 2004 Mar 12.

Laboratoire de Pharmacologie, Hôtel-Dieu, 9 Quai Moncousu, 44093 Nantes cedex 1, France.

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http://dx.doi.org/10.1007/s00228-004-0732-5DOI Listing
April 2004