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Items: 1 to 50 of 75

1.

Leukemia Cutis in Childhood Acute Myeloid Leukemia: Epidemiological, Clinical, Biological, and Prognostic Characteristics of Patients Included in the ELAM02 Study.

Gouache E, Greze V, Strullu M, Saultier P, Fenneteau O, Gandemer V, Ragu C, Auvrignon A, Boutroux H, Lapillonne H, Pasquet M, Leverger G.

Hemasphere. 2018 Oct;2(5):e141. doi: 10.1097/HS9.0000000000000141. Epub 2018 Oct 2. No abstract available.

2.

Shwachman-Diamond syndrome: a case report.

Kaabar M, Lemaire P, Cussac V, Besancon A, Martin-Coignard D, Fenneteau O, Laribi K, Pineau-Vincent F.

Ann Biol Clin (Paris). 2018 Aug 1;76(4):435-438. doi: 10.1684/abc.2018.1358.

PMID:
30078780
3.

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome.

Bellanné-Chantelot C, Schmaltz-Panneau B, Marty C, Fenneteau O, Callebaut I, Clauin S, Docet A, Damaj GL, Leblanc T, Pellier I, Stoven C, Souquere S, Antony-Debré I, Beaupain B, Aladjidi N, Barlogis V, Bauduer F, Bensaid P, Boespflug-Tanguy O, Berger C, Bertrand Y, Carausu L, Fieschi C, Galambrun C, Schmidt A, Journel H, Mazingue F, Nelken B, Quah TC, Oksenhendler E, Ouachée M, Pasquet M, Saada V, Suarez F, Pierron G, Vainchenker W, Plo I, Donadieu J.

Blood. 2018 Sep 20;132(12):1318-1331. doi: 10.1182/blood-2017-12-820308. Epub 2018 Jun 18.

PMID:
29914977
4.

SNP-array lesions in core binding factor acute myeloid leukemia.

Duployez N, Boudry-Labis E, Roumier C, Boissel N, Petit A, Geffroy S, Helevaut N, Celli-Lebras K, Terré C, Fenneteau O, Cuccuini W, Luquet I, Lapillonne H, Lacombe C, Cornillet P, Ifrah N, Dombret H, Leverger G, Jourdan E, Preudhomme C.

Oncotarget. 2018 Jan 8;9(5):6478-6489. doi: 10.18632/oncotarget.24031. eCollection 2018 Jan 19.

5.

Acute megakaryoblastic leukemia (excluding Down syndrome) remains an acute myeloid subgroup with inferior outcome in the French ELAM02 trial.

Teyssier AC, Lapillonne H, Pasquet M, Ballerini P, Baruchel A, Ducassou S, Fenneteau O, Petit A, Cuccuini W, Ragu C, Preudhomme C, Mercher T, Sirvent N, Leverger G.

Pediatr Hematol Oncol. 2017 Nov;34(8):425-427. doi: 10.1080/08880018.2017.1414905. Epub 2018 Jan 5.

PMID:
29303660
6.

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

Vial Y, Lachenaud J, Verloes A, Besnard M, Fenneteau O, Lainey E, Marceau-Renaut A, Preudhomme C, Baruchel A, Cavé H, Drunat S.

Haematologica. 2018 Jun;103(6):e274-e276. doi: 10.3324/haematol.2017.178590. Epub 2017 Dec 7. No abstract available.

7.

Acute Myeloid Leukemia With Central Nervous System Involvement in Children: Experience From the French Protocol Analysis ELAM02.

Felix A, Leblanc T, Petit A, Nelkem B, Bertrand Y, Gandemer V, Sirvent A, Paillard C, Schmitt C, Rohrlich PS, Fenneteau O, Ragu C, Michel G, Auvrignon A, Baruchel A, Leverger G.

J Pediatr Hematol Oncol. 2018 Jan;40(1):43-47. doi: 10.1097/MPH.0000000000001034.

PMID:
29189507
8.

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

Trawinski É, Fenneteau O, Le Mouel L, Ithier G, Couque N.

Ann Biol Clin (Paris). 2017 Oct 1;75(5):562-568. doi: 10.1684/abc.2017.1284.

PMID:
28958966
9.

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

Donadieu J, Beaupain B, Fenneteau O, Bellanné-Chantelot C.

Br J Haematol. 2017 Nov;179(4):557-574. doi: 10.1111/bjh.14887. Epub 2017 Sep 6. Review.

PMID:
28875503
10.

Recommendations for cerebrospinal fluid examination in acute leukemia.

Girard S, Fenneteau O, Mestrallet F, Troussard X, Lesesve JF.

Ann Biol Clin (Paris). 2017 Oct 1;75(5):503-512. doi: 10.1684/abc.2017.1250. Review.

PMID:
28853417
11.

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

Mercati O, Pichard S, Ouachée M, Froissart R, Fenneteau O, Roche B, Elmaleh-Bergès M, Bertrand Y, Ogier de Baulny H, Vanier MT, Schiff M.

Eur J Paediatr Neurol. 2017 Nov;21(6):907-911. doi: 10.1016/j.ejpn.2017.07.015. Epub 2017 Jul 29.

PMID:
28801223
12.

ANKRD26 normocytic thrombocytopenia: a family report.

Vincenot A, Hurtaud-Roux MF, René O, Binard S, Fenneteau O, Schlegel N.

Ann Biol Clin (Paris). 2016 Jun 1;74(3):317-22. doi: 10.1684/abc.2016.1142.

PMID:
27108925
13.

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

Roelens M, Dossier C, Fenneteau O, Couque N, Da Costa L.

Ann Biol Clin (Paris). 2016 Jun 1;74(3):299-305. doi: 10.1684/abc.2016.1136.

PMID:
27101632
14.

Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia.

Cavé H, Caye A, Ghedira N, Capri Y, Pouvreau N, Fillot N, Trimouille A, Vignal C, Fenneteau O, Alembik Y, Alessandri JL, Blanchet P, Boute O, Bouvagnet P, David A, Dieux Coeslier A, Doray B, Dulac O, Drouin-Garraud V, Gérard M, Héron D, Isidor B, Lacombe D, Lyonnet S, Perrin L, Rio M, Roume J, Sauvion S, Toutain A, Vincent-Delorme C, Willems M, Baumann C, Verloes A.

Eur J Hum Genet. 2016 Aug;24(8):1124-31. doi: 10.1038/ejhg.2015.273. Epub 2016 Jan 13.

15.

Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer.

Da Costa L, Suner L, Galimand J, Bonnel A, Pascreau T, Couque N, Fenneteau O, Mohandas N; Society of Hematology and Pediatric Immunology (SHIP) group; French Society of Hematology (SFH).

Blood Cells Mol Dis. 2016 Jan;56(1):9-22. doi: 10.1016/j.bcmd.2015.09.001. Epub 2015 Sep 16.

16.

Pyrimidine 5'-nucleotidase deficiency associated to a polymalformative syndrome.

Altounian L, Perrin J, Fouyssac F, Fenneteau O, Da Costa L, Bahuau M, Leheup B, Jonveaux P, Lesesve JF.

Ann Biol Clin (Paris). 2015 Sep-Oct;73(5):587-90. doi: 10.1684/abc.2015.1078.

17.

Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network.

Caye A, Strullu M, Guidez F, Cassinat B, Gazal S, Fenneteau O, Lainey E, Nouri K, Nakhaei-Rad S, Dvorsky R, Lachenaud J, Pereira S, Vivent J, Verger E, Vidaud D, Galambrun C, Picard C, Petit A, Contet A, Poirée M, Sirvent N, Méchinaud F, Adjaoud D, Paillard C, Nelken B, Reguerre Y, Bertrand Y, Häussinger D, Dalle JH, Ahmadian MR, Baruchel A, Chomienne C, Cavé H.

Nat Genet. 2015 Nov;47(11):1334-40. doi: 10.1038/ng.3420. Epub 2015 Oct 12.

PMID:
26457648
18.

Performance evaluation of the Sysmex XN-1000 hematology analyzer in assessment of the white blood cell count differential in pediatric specimens.

Becker PH, Fenneteau O, Da Costa L.

Int J Lab Hematol. 2016 Feb;38(1):54-63. doi: 10.1111/ijlh.12436. Epub 2015 Sep 26.

PMID:
26407903
19.

Juvenile myelomonocytic leukaemia and Noonan syndrome.

Strullu M, Caye A, Lachenaud J, Cassinat B, Gazal S, Fenneteau O, Pouvreau N, Pereira S, Baumann C, Contet A, Sirvent N, Méchinaud F, Guellec I, Adjaoud D, Paillard C, Alberti C, Zenker M, Chomienne C, Bertrand Y, Baruchel A, Verloes A, Cavé H.

J Med Genet. 2014 Oct;51(10):689-97. doi: 10.1136/jmedgenet-2014-102611. Epub 2014 Aug 5.

PMID:
25097206
20.

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

Saposnik B, Binard S, Fenneteau O, Nurden A, Nurden P, Hurtaud-Roux MF, Schlegel N; French MYH9 networka.

Mol Genet Genomic Med. 2014 Jul;2(4):297-312. doi: 10.1002/mgg3.68. Epub 2014 Feb 7.

21.

Schistocytes.

Lesesve JF, Fenneteau O, Zini G.

Transfusion. 2014 Jun;54(6):1459. doi: 10.1111/trf.12523. No abstract available.

PMID:
24911907
22.

Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis.

Flex E, Jaiswal M, Pantaleoni F, Martinelli S, Strullu M, Fansa EK, Caye A, De Luca A, Lepri F, Dvorsky R, Pannone L, Paolacci S, Zhang SC, Fodale V, Bocchinfuso G, Rossi C, Burkitt-Wright EM, Farrotti A, Stellacci E, Cecchetti S, Ferese R, Bottero L, Castro S, Fenneteau O, Brethon B, Sanchez M, Roberts AE, Yntema HG, Van Der Burgt I, Cianci P, Bondeson ML, Cristina Digilio M, Zampino G, Kerr B, Aoki Y, Loh ML, Palleschi A, Di Schiavi E, Carè A, Selicorni A, Dallapiccola B, Cirstea IC, Stella L, Zenker M, Gelb BD, Cavé H, Ahmadian MR, Tartaglia M.

Hum Mol Genet. 2014 Aug 15;23(16):4315-27. doi: 10.1093/hmg/ddu148. Epub 2014 Apr 4.

23.

[Epidemiology and prognosis of childhood cancers at Gabriel-Touré Teaching Hospital (Bamako, Mali)].

Togo B, Traoré F, Togo AP, Togo P, Diakité AA, Traoré B, Touré A, Coulibaly Y, Traoré CB, Fenneteau O, Sylla F, Dumke H, Diallo M, Diallo G, Sidibé T.

Med Sante Trop. 2014 Jan-Mar;24(1):68-72. doi: 10.1684/mst.2014.0291. French.

24.

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

Houzé S, Boutron I, Marmorat A, Dalichampt M, Choquet C, Poilane I, Godineau N, Le Guern AS, Thellier M, Broutier H, Fenneteau O, Millet P, Dulucq S, Hubert V, Houzé P, Tubach F, Le Bras J, Matheron S.

PLoS One. 2013 Sep 30;8(9):e75486. doi: 10.1371/journal.pone.0075486. eCollection 2013.

25.

An intragenic ERG deletion is a marker of an oncogenic subtype of B-cell precursor acute lymphoblastic leukemia with a favorable outcome despite frequent IKZF1 deletions.

Clappier E, Auclerc MF, Rapion J, Bakkus M, Caye A, Khemiri A, Giroux C, Hernandez L, Kabongo E, Savola S, Leblanc T, Yakouben K, Plat G, Costa V, Ferster A, Girard S, Fenneteau O, Cayuela JM, Sigaux F, Dastugue N, Suciu S, Benoit Y, Bertrand Y, Soulier J, Cavé H.

Leukemia. 2014 Jan;28(1):70-7. doi: 10.1038/leu.2013.277. Epub 2013 Sep 25.

PMID:
24064621
26.

In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia.

Strullu M, Caye A, Cassinat B, Fenneteau O, Touzot F, Blauwblomme T, Rodriguez R, Latour S, Petit A, Barlogis V, Galambrun C, Leblanc T, Baruchel A, Chomienne C, Cavé H.

Leukemia. 2013 Dec;27(12):2404-7. doi: 10.1038/leu.2013.203. Epub 2013 Jul 4. No abstract available.

PMID:
23823657
27.

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

Da Costa L, Galimand J, Fenneteau O, Mohandas N.

Blood Rev. 2013 Jul;27(4):167-78. doi: 10.1016/j.blre.2013.04.003. Epub 2013 May 9. Review.

PMID:
23664421
28.

Platelet morphology analysis.

Latger-Cannard V, Fenneteau O, Salignac S, Lecompte TP, Schlegel N.

Methods Mol Biol. 2013;992:207-25. doi: 10.1007/978-1-62703-339-8_16.

PMID:
23546716
29.

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

Gharbi M, Flegg JA, Hubert V, Kendjo E, Metcalf JE, Bertaux L, Guérin PJ, Le Bras J; Members of the French National Reference Centre for Imported Malaria Study, Aboubaca A, Agnamey P, Angoulvant A, Barbut P, Basset D, Belkadi G, Bellanger AP, Bemba D, Benoit-Vica F, Berry A, Bigel ML, Bonhomme J, Botterel F, Bouchaud O, Bougnoux ME, Bourée P, Bourgeois N, Branger C, Bret L, Buret B, Casalino E, Chevrier S, Conquere de Monbrison F, Cuisenier B, Danis M, Darde ML, De Gentile L, Delarbre JM, Delaunay P, Delaval A, Desoubeaux G, Develoux M, Dunand J, Durand R, Eloy O, Fauchet N, Faugere B, Faye A, Fenneteau O, Flori P, Fontrouge M, Garabedian C, Gayandrieu F, Godineau N, Houzé P, Houzé S, Hurst JP, Ichou H, Lachaud L, Lebuisson A, Lefevre M, LeGuern AS, Le Moal G, Lusina D, Machouart MC, Malvy D, Matheron S, Maubon D, Mechali D, Megarbane B, Menard G, Millon L, Aiach MM, Minodier P, Morelle C, Nevez G, Parola P, Parzy D, Patey O, Patoz P, Penn P, Perignon A, Picot S, Pilo JE, Poilane I, Pons D, Poupart M, Pradines B, Raffenot D, Rapp C, Receveur MC, Sarfati C, Senghor Y, Simon F, Siriez JY, Taudon N, Thellier M, Thouvenin M, Toubas D.

Malar J. 2013 Jan 25;12:35. doi: 10.1186/1475-2875-12-35.

30.

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

Beaussant Cohen S, Fenneteau O, Plouvier E, Rohrlich PS, Daltroff G, Plantier I, Dupuy A, Kerob D, Beaupain B, Bordigoni P, Fouyssac F, Delezoide AL, Devouassoux G, Nicolas JF, Bensaid P, Bertrand Y, Balabanian K, Chantelot CB, Bachelerie F, Donadieu J.

Orphanet J Rare Dis. 2012 Sep 25;7:71. doi: 10.1186/1750-1172-7-71.

31.

How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B(12) absorption?

Boina Abdallah A, Ogier de Baulny H, Kozyraki R, Passemard S, Fenneteau O, Lebon S, Rigal O, Mesples B, Yacouben K, Giraudier S, Benoist JF, Schiff M.

Mol Genet Metab. 2012 Sep;107(1-2):66-71. doi: 10.1016/j.ymgme.2012.07.007. Epub 2012 Jul 20.

PMID:
22854512
32.

LHX2 deregulation by juxtaposition with the IGH locus in a pediatric case of chronic myeloid leukemia in B-cell lymphoid blast crisis.

Nadal N, Chapiro E, Flandrin-Gresta P, Thouvenin S, Vasselon C, Beldjord K, Fenneteau O, Bernard O, Campos L, Nguyen-Khac F.

Leuk Res. 2012 Sep;36(9):e195-8. doi: 10.1016/j.leukres.2012.05.013. Epub 2012 Jun 22. No abstract available.

PMID:
22727509
33.

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome.

Donadieu J, Fenneteau O, Beaupain B, Beaufils S, Bellanger F, Mahlaoui N, Lambilliotte A, Aladjidi N, Bertrand Y, Mialou V, Perot C, Michel G, Fouyssac F, Paillard C, Gandemer V, Boutard P, Schmitz J, Morali A, Leblanc T, Bellanné-Chantelot C; Associated investigators of the French Severe Chronic Neutropenia Registry*.

Haematologica. 2012 Sep;97(9):1312-9. Epub 2012 Apr 4.

34.

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

Balabanian K, Brotin E, Biajoux V, Bouchet-Delbos L, Lainey E, Fenneteau O, Bonnet D, Fiette L, Emilie D, Bachelerie F.

Blood. 2012 Jun 14;119(24):5722-30. doi: 10.1182/blood-2012-01-403378. Epub 2012 Mar 20.

35.

[Childhood acute lymphoblastic leukemia: 12 cases in Mali].

Togo B, Traoré F, Diakité AA, Diallo S, Traoré B, Fenneteau O, Touré A, Traoré-Dicko F, Sylla M, Sidibé T, Leverger G.

Med Trop (Mars). 2011 Dec;71(6):629-31. French.

PMID:
22393639
36.

A new lysosomal storage disorder resembling Morquio syndrome in sibs.

Perrin L, Fenneteau O, Ilharreborde B, Capri Y, Gérard M, Quoc EB, Passemard S, Ghoumid J, Caillaud C, Froissart R, Tabet AC, Lebon S, El Ghouzzi V, Mazda K, Verloes A.

Eur J Med Genet. 2012 Mar;55(3):157-62. doi: 10.1016/j.ejmg.2012.01.001. Epub 2012 Jan 25.

PMID:
22330346
37.

Congenital neutropenia: diagnosis, molecular bases and patient management.

Donadieu J, Fenneteau O, Beaupain B, Mahlaoui N, Chantelot CB.

Orphanet J Rare Dis. 2011 May 19;6:26. doi: 10.1186/1750-1172-6-26. Review.

38.

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

Mullier F, Lainey E, Fenneteau O, Da Costa L, Schillinger F, Bailly N, Cornet Y, Chatelain C, Dogne JM, Chatelain B.

Ann Hematol. 2011 Jul;90(7):759-68. doi: 10.1007/s00277-010-1138-3. Epub 2010 Dec 22.

PMID:
21181161
39.

Evaluation of peroxidase activity by alpha-naphthol/pyronine staining compared with benzidine staining in 101 acute leukemia cases.

Latger-Cannard V, Bardet V, Malet M, Lagrange M, Empereur F, Fenneteau O.

Lab Hematol. 2010 Dec;16(4):76-82. doi: 10.1532/LH96.10007.

PMID:
21097443
40.

A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chain.

Garçon L, Iolascon A, Pissard S, Esposito MR, Russo R, Fenneteau O, Fénéant-Thibault M, Heimpel H, Delaunay J.

Hemoglobin. 2010;34(6):576-81. doi: 10.3109/03630269.2010.526922.

PMID:
21077766
41.

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.

Arnaud L, Saison C, Helias V, Lucien N, Steschenko D, Giarratana MC, Prehu C, Foliguet B, Montout L, de Brevern AG, Francina A, Ripoche P, Fenneteau O, Da Costa L, Peyrard T, Coghlan G, Illum N, Birgens H, Tamary H, Iolascon A, Delaunay J, Tchernia G, Cartron JP.

Am J Hum Genet. 2010 Nov 12;87(5):721-7. doi: 10.1016/j.ajhg.2010.10.010. Epub 2010 Nov 4.

42.

[Usefulness of gray platelets observation in ARC syndrome].

Benet B, Lainey E, Fenneteau O, Baudouin V, Hurtaud-Roux MF.

Ann Biol Clin (Paris). 2010 Jul-Aug;68(4):485-9. doi: 10.1684/abc.2010.0453. French.

43.

Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia.

Pérez B, Mechinaud F, Galambrun C, Ben Romdhane N, Isidor B, Philip N, Derain-Court J, Cassinat B, Lachenaud J, Kaltenbach S, Salmon A, Désirée C, Pereira S, Menot ML, Royer N, Fenneteau O, Baruchel A, Chomienne C, Verloes A, Cavé H.

J Med Genet. 2010 Oct;47(10):686-91. doi: 10.1136/jmg.2010.076836. Epub 2010 Jun 12.

44.

Evaluation of the CellaVision DM automated microscope in pediatrics.

Billard M, Lainey E, Armoogum P, Alberti C, Fenneteau O, Da Costa L.

Int J Lab Hematol. 2010 Oct;32(5):530-8. doi: 10.1111/j.1751-553X.2009.01219.x. Epub 2010 Feb 2.

PMID:
20132350
45.

[Tolerance and efficacy of atovaquone-proguanil for the treatment of paediatric imported Plasmodium falciparum malaria in France: clinical practice in a university hospital in Paris].

Blondé R, Naudin J, Bigirimana Z, Holvoet L, Fenneteau O, Vitoux C, Bourdon O, Angoulvant F, Lorrot M, D'Ortenzio E, Bourrillon A, Le Bras J, Matheron S, Faye A.

Arch Pediatr. 2008 Mar;15(3):245-52. doi: 10.1016/j.arcped.2007.10.018. Epub 2008 Mar 5. French.

PMID:
18321692
46.

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

Lainey E, Ogier H, Fenneteau O.

Br J Haematol. 2008 Mar;140(6):595. doi: 10.1111/j.1365-2141.2007.06849.x. Epub 2008 Jan 19. No abstract available.

PMID:
18215202
47.

[Bone marrow examination of inherited diseases in children].

Fenneteau O, Lainey E.

Ann Biol Clin (Paris). 2007 Sep-Oct;65(5):483-503. Review. French.

48.

[Normal and abnormal cytological aspects of peripheral blood cells in neonates and young children].

Fenneteau O, Hurtaud-Roux MF, Schlegel N.

Ann Biol Clin (Paris). 2006 Jan-Feb;64(1):17-36. Review. French.

49.

[Reproductibility of the morphological identification of schisocytes and evaluation of non observer-dependent methods].

Lesesve JF, Lecompte T, Alla F, Fenneteau O, Cynober T, Siest JP, Troussard X, Flandrin G; Groupe français d'hématologie cellulaire (GFHC).

Ann Biol Clin (Paris). 2005 May-Jun;63(3):279-89. French.

50.

Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group.

Donadieu J, Leblanc T, Bader Meunier B, Barkaoui M, Fenneteau O, Bertrand Y, Maier-Redelsperger M, Micheau M, Stephan JL, Phillipe N, Bordigoni P, Babin-Boilletot A, Bensaid P, Manel AM, Vilmer E, Thuret I, Blanche S, Gluckman E, Fischer A, Mechinaud F, Joly B, Lamy T, Hermine O, Cassinat B, Bellanné-Chantelot C, Chomienne C; French Severe Chronic Neutropenia Study Group.

Haematologica. 2005 Jan;90(1):45-53.

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