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Items: 1 to 50 of 72

1.

Identification of Clinical and Laboratory Parameters Associated with the Development of Acute Chest Syndrome during Vaso-Occlusive Episodes in Children with Sickle Cell Disease: A Preliminary Step before Assessing Specific and Early Treatment Strategies.

Madhi F, Kamdem A, Jung C, Carlier-Gonod A, Biscardi S, Busca J, Arnaud C, Hau I, Narbey D, Epaud R, Pondarre C.

J Clin Med. 2019 Nov 1;8(11). pii: E1839. doi: 10.3390/jcm8111839.

2.

Serum Immunoglobulin Levels in Children with Sickle Cell Disease: A Large Prospective Study.

Cherif-Alami S, Hau I, Arnaud C, Kamdem A, Coulon B, Idoux E, Bechet S, Creidy R, Bernaudin F, Epaud R, Pondarré C.

J Clin Med. 2019 Oct 15;8(10). pii: E1688. doi: 10.3390/jcm8101688.

3.

Evaluation of Outcomes and Quality of Care in Children with Sickle Cell Disease Diagnosed by Newborn Screening: A Real-World Nation-Wide Study in France.

Brousse V, Arnaud C, Lesprit E, Quinet B, Odièvre MH, Etienne-Julan M, Guillaumat C, Elana G, Belloy M, Garnier N, Chamouine A, Dumesnil C, Montalembert M, Pondarre C, Bernaudin F, Couque N, Boutin E, Bardakjian J, Djennaoui F, Ithier G, Benkerrou M, Thuret I.

J Clin Med. 2019 Oct 2;8(10). pii: E1594. doi: 10.3390/jcm8101594.

4.

Extensive multilineage analysis in patients with mixed chimerism after allogeneic transplantation for sickle cell disease: insight into hematopoiesis and engraftment thresholds for gene therapy.

Magnani A, Pondarré C, Bouazza N, Magalon J, Miccio A, Six E, Roudaut C, Arnaud C, Kamdem A, Touzot F, Gabrion A, Magrin E, Couzin C, Fusaro M, André I, Vernant JP, Gluckman E, Bernaudin F, Bories D, Cavazzana M.

Haematologica. 2019 Sep 19. pii: haematol.2019.227561. doi: 10.3324/haematol.2019.227561. [Epub ahead of print]

5.

Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France.

Bernaudin F, Dalle JH, Bories D, Peffault de Latour R, Robin M, Bertrand Y, Pondarre C, Vannier JP, Neven B, Kuentz M, Maury S, Lutz P, Paillard C, Yakouben K, Thuret I, Galambrun C, Dhedin N, Jubert C, Rohrlich P, Bay JO, Suarez F, Raus N, Vernant JP, Gluckman E, Poirot C, Socié G; Société Française de Greffe de Moelle et de Thérapie Cellulaire.

Haematologica. 2019 May 16. pii: haematol.2018.213207. doi: 10.3324/haematol.2018.213207. [Epub ahead of print]

6.

Risk factors and outcomes according to age at transplantation with an HLA-identical sibling for sickle cell disease.

Cappelli B, Volt F, Tozatto-Maio K, Scigliuolo GM, Ferster A, Dupont S, Simões BP, Al-Seraihy A, Aljurf MD, Almohareb F, Belendez C, Matthes S, Dhedin N, Pondarre C, Dalle JH, Bertrand Y, Vannier JP, Kuentz M, Lutz P, Michel G, Rafii H, Neven B, Zecca M, Bader P, Cavazzana M, Labopin M, Locatelli F, Magnani A, Ruggeri A, Rocha V, Bernaudin F, de La Fuente J, Corbacioglu S, Gluckman E; Eurocord, the Cellular Therapy and Immunobiology Working Party (CTIWP) and the Paediatric Diseases Working Party (PDWP) of the EBMT.

Haematologica. 2019 Dec;104(12):e543-e546. doi: 10.3324/haematol.2019.216788. Epub 2019 Apr 24. No abstract available.

7.

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.

Hadjadj J, Aladjidi N, Fernandes H, Leverger G, Magérus-Chatinet A, Mazerolles F, Stolzenberg MC, Jacques S, Picard C, Rosain J, Fourrage C, Hanein S, Zarhrate M, Pasquet M, Abou Chahla W, Barlogis V, Bertrand Y, Pellier I, Colomb Bottollier E, Fouyssac F, Blouin P, Thomas C, Cheikh N, Dore E, Pondarre C, Plantaz D, Jeziorski E, Millot F, Garcelon N, Ducassou S, Perel Y, Leblanc T, Neven B, Fischer A, Rieux-Laucat F; members of the French Reference Center for Pediatric Autoimmune Cytopenia (CEREVANCE).

Blood. 2019 Jul 4;134(1):9-21. doi: 10.1182/blood-2018-11-887141. Epub 2019 Apr 2.

PMID:
30940614
8.

Ovarian tissue cryopreservation for fertility preservation in 418 girls and adolescents up to 15 years of age facing highly gonadotoxic treatment. Twenty years of experience at a single center.

Poirot C, Brugieres L, Yakouben K, Prades-Borio M, Marzouk F, de Lambert G, Pacquement H, Bernaudin F, Neven B, Paye-Jaouen A, Pondarre C, Dhedin N, Drouineaud V, Chalas C, Martelli H, Michon J, Minard V, Lezeau H, Doz F, Sarnacki S, Philippe-Chomette P, Dufour C, Laurence V, Baruchel A, Wolf JP, Boissel N, Valteau-Couanet D, Dalle JH.

Acta Obstet Gynecol Scand. 2019 May;98(5):630-637. doi: 10.1111/aogs.13616. Epub 2019 Apr 14.

PMID:
30919447
9.

Association of Matched Sibling Donor Hematopoietic Stem Cell Transplantation With Transcranial Doppler Velocities in Children With Sickle Cell Anemia.

Bernaudin F, Verlhac S, Peffault de Latour R, Dalle JH, Brousse V, Petras E, Thuret I, Paillard C, Neven B, Galambrun C, Divialle-Doumdo L, Pondarré C, Guitton C, Missud F, Runel C, Jubert C, Elana G, Ducros-Miralles E, Drain E, Taïeb O, Arnaud C, Kamdem A, Malric A, Elmaleh-Bergès M, Vasile M, Leveillé E, Socié G, Chevret S; DREPAGREFFE Trial Investigators.

JAMA. 2019 Jan 22;321(3):266-276. doi: 10.1001/jama.2018.20059.

10.

Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice.

Hofmann I, Geer MJ, Vögtle T, Crispin A, Campagna DR, Barr A, Calicchio ML, Heising S, van Geffen JP, Kuijpers MJE, Heemskerk JWM, Eble JA, Schmitz-Abe K, Obeng EA, Douglas M, Freson K, Pondarré C, Favier R, Jarvis GE, Markianos K, Turro E, Ouwehand WH, Mazharian A, Fleming MD, Senis YA.

Blood. 2018 Sep 27;132(13):1399-1412. doi: 10.1182/blood-2017-08-802769. Epub 2018 Jun 13.

11.

High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients.

Floch A, Gien D, Tournamille C, Chami B, Habibi A, Galactéros F, Bierling P, Djoudi R, Pondarré C, Peyrard T, Pirenne F.

Transfusion. 2018 Jun;58(6):1527-1535. doi: 10.1111/trf.14633. Epub 2018 Apr 29.

PMID:
29707783
12.

Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia.

Thompson AA, Walters MC, Kwiatkowski J, Rasko JEJ, Ribeil JA, Hongeng S, Magrin E, Schiller GJ, Payen E, Semeraro M, Moshous D, Lefrere F, Puy H, Bourget P, Magnani A, Caccavelli L, Diana JS, Suarez F, Monpoux F, Brousse V, Poirot C, Brouzes C, Meritet JF, Pondarré C, Beuzard Y, Chrétien S, Lefebvre T, Teachey DT, Anurathapan U, Ho PJ, von Kalle C, Kletzel M, Vichinsky E, Soni S, Veres G, Negre O, Ross RW, Davidson D, Petrusich A, Sandler L, Asmal M, Hermine O, De Montalembert M, Hacein-Bey-Abina S, Blanche S, Leboulch P, Cavazzana M.

N Engl J Med. 2018 Apr 19;378(16):1479-1493. doi: 10.1056/NEJMoa1705342.

13.

Neonatal Alloimmune Thrombocytopenia With Amegakaryocytosis, B Lymphopenia, and Villitis.

Dony A, Buenerd A, Pondarre C.

Pediatrics. 2018 Apr;141(Suppl 5):S506-S509. doi: 10.1542/peds.2016-1340.

14.

Late effects after hematopoietic stem cell transplantation for β-thalassemia major: the French national experience.

Rahal I, Galambrun C, Bertrand Y, Garnier N, Paillard C, Frange P, Pondarré C, Dalle JH, de Latour RP, Michallet M, Steschenko D, Moshous D, Lutz P, Stephan JL, Rohrlich PS, Yakoub-Agha I, Bernaudin F, Piguet C, Aladjidi N, Badens C, Berger C, Socié G, Dumesnil C, Castex MP, Poirée M, Lambilliotte A, Thomas C, Simon P, Auquier P, Michel G, Loundou A, Agouti I, Thuret I.

Haematologica. 2018 Jul;103(7):1143-1149. doi: 10.3324/haematol.2017.183467. Epub 2018 Mar 29.

15.

Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea.

Bernaudin F, Arnaud C, Kamdem A, Hau I, Lelong F, Epaud R, Pondarré C, Pissard S.

Blood Adv. 2018 Mar 27;2(6):626-637. doi: 10.1182/bloodadvances.2017014555.

16.

[Cerebral vasculopathy in children with sickle cell disease: Key issues and the latest data].

Corvest V, Blais S, Dahmani B, De Tersant M, Etienney AC, Maroni A, Ormières C, Roussel A, Pondarré C.

Arch Pediatr. 2018 Jan;25(1):63-71. doi: 10.1016/j.arcped.2017.11.015. Epub 2017 Dec 16. Review. French.

PMID:
29254735
17.

Allogeneic/Matched Related Transplantation for β-Thalassemia and Sickle Cell Anemia.

Bernaudin F, Pondarré C, Galambrun C, Thuret I.

Adv Exp Med Biol. 2017;1013:89-122. doi: 10.1007/978-1-4939-7299-9_4.

PMID:
29127678
18.

Design of the DREPAGREFFE trial: A prospective controlled multicenter study evaluating the benefit of genoidentical hematopoietic stem cell transplantation over chronic transfusion in sickle cell anemia children detected to be at risk of stroke by transcranial Doppler (NCT 01340404).

Chevret S, Verlhac S, Ducros-Miralles E, Dalle JH, de Latour RP, de Montalembert M, Benkerrou M, Pondarré C, Thuret I, Guitton C, Lesprit E, Etienne-Julan M, Elana G, Vannier JP, Lutz P, Neven B, Galambrun C, Paillard C, Runel C, Jubert C, Arnaud C, Kamdem A, Brousse V, Missud F, Petras M, Doumdo-Divialle L, Berger C, Fréard F, Taieb O, Drain E, Elmaleh M, Vasile M, Khelif Y, Bernaudin M, Chadebech P, Pirenne F, Socié G, Bernaudin F.

Contemp Clin Trials. 2017 Nov;62:91-104. doi: 10.1016/j.cct.2017.08.008. Epub 2017 Aug 15.

PMID:
28821470
19.

Childhood immune thrombocytopenia: A nationwide cohort study on condition management and outcomes.

Grimaldi-Bensouda L, Nordon C, Leblanc T, Abenhaim L, Allali S, Armari-Alla C, Berger C, Courcoux MF, Fouyssac F, Guillaumat C, Guitton C, Le Moine P, Mazingue F, Pondarré C, Thomas C, Pasquet M, Perel Y, Leverger G, Aladjidi N.

Pediatr Blood Cancer. 2017 Jul;64(7). doi: 10.1002/pbc.26389. Epub 2016 Dec 1.

PMID:
27905681
20.

A nonsense mutation in the DNA repair factor Hebo causes mild bone marrow failure and microcephaly.

Zhang S, Pondarre C, Pennarun G, Labussiere-Wallet H, Vera G, France B, Chansel M, Rouvet I, Revy P, Lopez B, Soulier J, Bertrand P, Callebaut I, de Villartay JP.

J Exp Med. 2016 May 30;213(6):1011-28. doi: 10.1084/jem.20151183. Epub 2016 May 16.

21.

Long-term treatment follow-up of children with sickle cell disease monitored with abnormal transcranial Doppler velocities.

Bernaudin F, Verlhac S, Arnaud C, Kamdem A, Hau I, Leveillé E, Vasile M, Kasbi F, Madhi F, Fourmaux C, Biscardi S, Gluckman E, Socié G, Dalle JH, Epaud R, Pondarré C.

Blood. 2016 Apr 7;127(14):1814-22. doi: 10.1182/blood-2015-10-675231. Epub 2016 Feb 5.

PMID:
26851292
22.

Platelet and not erythrocyte microparticles are procoagulant in transfused thalassaemia major patients.

Agouti I, Cointe S, Robert S, Judicone C, Loundou A, Driss F, Brisson A, Steschenko D, Rose C, Pondarré C, Bernit E, Badens C, Dignat-George F, Lacroix R, Thuret I.

Br J Haematol. 2015 Nov;171(4):615-24. doi: 10.1111/bjh.13609. Epub 2015 Jul 24.

PMID:
26205481
23.

G6PD deficiency and absence of α-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia.

Joly P, Garnier N, Kebaili K, Renoux C, Dony A, Cheikh N, Renard C, Ceraulo A, Cuzzubbo D, Pondarré C, Martin C, Pialoux V, Francina A, Bertrand Y, Connes P.

Eur J Haematol. 2016 Apr;96(4):404-8. doi: 10.1111/ejh.12607. Epub 2015 Jun 30.

PMID:
26072930
24.

[Information for parents of children with sickle cell trait detected by neonatal screening: A 10-year experience].

Joly P, Badens C, Fekih S, Philippe N, Merono F, Thuret I, Pondarré C.

Arch Pediatr. 2015 May;22(5):562-3. doi: 10.1016/j.arcped.2015.02.020. Epub 2015 Apr 1. French. No abstract available.

PMID:
25842198
25.

Chronic and acute anemia and extracranial internal carotid stenosis are risk factors for silent cerebral infarcts in sickle cell anemia.

Bernaudin F, Verlhac S, Arnaud C, Kamdem A, Vasile M, Kasbi F, Hau I, Madhi F, Fourmaux C, Biscardi S, Epaud R, Pondarré C.

Blood. 2015 Mar 5;125(10):1653-61. doi: 10.1182/blood-2014-09-599852. Epub 2014 Dec 22.

PMID:
25533032
26.

[Thalassemia alpha].

Pondarré C.

Rev Prat. 2014 Oct;64(8):1138-9. French. No abstract available.

PMID:
25510145
27.

[Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects].

Joly P, Pondarre C, Badens C.

Ann Biol Clin (Paris). 2014 Nov-Dec;72(6):639-68. doi: 10.1684/abc.2014.1015. Review. French.

28.

Newly diagnosed immune thrombocytopenic purpura in childhood: successful implementation of a limited intervention strategy in the setting of pediatric emergency care.

Rohmer B, Valla FV, Baleydier F, Launay V, Dommange-Romero F, Pondarré C.

J Pediatr. 2015 Feb;166(2):480-2. doi: 10.1016/j.jpeds.2014.10.001. Epub 2014 Nov 18.

PMID:
25454932
29.

ERCC6L2 mutations link a distinct bone-marrow-failure syndrome to DNA repair and mitochondrial function.

Tummala H, Kirwan M, Walne AJ, Hossain U, Jackson N, Pondarre C, Plagnol V, Vulliamy T, Dokal I.

Am J Hum Genet. 2014 Feb 6;94(2):246-56. doi: 10.1016/j.ajhg.2014.01.007.

30.

Autoimmune disorders and quadrivalent human papillomavirus vaccination of young female subjects.

Grimaldi-Bensouda L, Guillemot D, Godeau B, Bénichou J, Lebrun-Frenay C, Papeix C, Labauge P, Berquin P, Penfornis A, Benhamou PY, Nicolino M, Simon A, Viallard JF, Costedoat-Chalumeau N, Courcoux MF, Pondarré C, Hilliquin P, Chatelus E, Foltz V, Guillaume S, Rossignol M, Abenhaim L; PGRx-AID Study Group.

J Intern Med. 2014 Apr;275(4):398-408. doi: 10.1111/joim.12155. Epub 2013 Nov 22.

31.

Short-term femoral catheter insertion: a promising alternative to consistently allow long-term erythrocytapheresis therapy in children with sickle cell anemia.

Billard M, Combet S, Hequet O, Kébaïli K, Lorthois S, Pondarre C.

J Pediatr. 2013 Feb;162(2):423-6. doi: 10.1016/j.jpeds.2012.09.009. Epub 2012 Oct 23.

PMID:
23092526
32.

French multicenter 22-year experience in stem cell transplantation for beta-thalassemia major: lessons and future directions.

Galambrun C, Pondarré C, Bertrand Y, Loundou A, Bordigoni P, Frange P, Lutz P, Mialou V, Rubie H, Socié G, Schneider P, Bernaudin F, Paillard C, Michel G, Badens C, Thuret I; French Rare Disease Center for Thalassemia; French Society of Bone Marrow Transplantation.

Biol Blood Marrow Transplant. 2013 Jan;19(1):62-8. doi: 10.1016/j.bbmt.2012.08.005. Epub 2012 Aug 11.

33.

Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells.

Ceccaldi R, Parmar K, Mouly E, Delord M, Kim JM, Regairaz M, Pla M, Vasquez N, Zhang QS, Pondarre C, Peffault de Latour R, Gluckman E, Cavazzana-Calvo M, Leblanc T, Larghero J, Grompe M, Socié G, D'Andrea AD, Soulier J.

Cell Stem Cell. 2012 Jul 6;11(1):36-49. doi: 10.1016/j.stem.2012.05.013. Epub 2012 Jun 7.

34.

Deferasirox-induced renal impairment in children: an increasing concern for pediatricians.

Dubourg L, Laurain C, Ranchin B, Pondarré C, Hadj-Aïssa A, Sigaudo-Roussel D, Cochat P.

Pediatr Nephrol. 2012 Nov;27(11):2115-2122. doi: 10.1007/s00467-012-2170-4. Epub 2012 Apr 24.

PMID:
22527533
35.

Genotypic screening of the main opiate-related polymorphisms in a cohort of 139 sickle cell disease patients.

Joly P, Gagnieu MC, Bardel C, Francina A, Pondarre C, Martin C.

Am J Hematol. 2012 May;87(5):534-6. doi: 10.1002/ajh.23137. Epub 2012 Mar 19.

36.

The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score.

Joly P, Pondarré C, Bardel C, Francina A, Martin C.

Eur J Haematol. 2012 Jan;88(1):61-7. doi: 10.1111/j.1600-0609.2011.01705.x. Epub 2011 Nov 15.

PMID:
21910753
37.

A novel deletion/insertion caused by a replication error in the β-globin gene locus control region.

Joly P, Lacan P, Garcia C, Meley R, Pondarré C, Francina A.

Hemoglobin. 2011;35(4):316-22. doi: 10.3109/03630269.2011.571331.

PMID:
21797698
38.

Hemophagocytic lymphohistiocytosis with Munc13-4 mutation: a cause of recurrent fatal hydrops fetalis.

Bechara E, Dijoud F, de Saint Basile G, Bertrand Y, Pondarré C.

Pediatrics. 2011 Jul;128(1):e251-4. doi: 10.1542/peds.2010-0764. Epub 2011 Jun 6.

PMID:
21646258
39.

Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia.

Kannengiesser C, Sanchez M, Sweeney M, Hetet G, Kerr B, Moran E, Fuster Soler JL, Maloum K, Matthes T, Oudot C, Lascaux A, Pondarré C, Sevilla Navarro J, Vidyatilake S, Beaumont C, Grandchamp B, May A.

Haematologica. 2011 Jun;96(6):808-13. doi: 10.3324/haematol.2010.039164. Epub 2011 Mar 10.

40.

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions.

Quentin S, Cuccuini W, Ceccaldi R, Nibourel O, Pondarre C, Pagès MP, Vasquez N, Dubois d'Enghien C, Larghero J, Peffault de Latour R, Rocha V, Dalle JH, Schneider P, Michallet M, Michel G, Baruchel A, Sigaux F, Gluckman E, Leblanc T, Stoppa-Lyonnet D, Preudhomme C, Socié G, Soulier J.

Blood. 2011 Apr 14;117(15):e161-70. doi: 10.1182/blood-2010-09-308726. Epub 2011 Feb 16.

PMID:
21325596
41.

Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients.

Ceccaldi R, Briot D, Larghero J, Vasquez N, Dubois d'Enghien C, Chamousset D, Noguera ME, Waisfisz Q, Hermine O, Pondarre C, Leblanc T, Gluckman E, Joenje H, Stoppa-Lyonnet D, Socié G, Soulier J.

J Clin Invest. 2011 Jan;121(1):184-94. doi: 10.1172/JCI43836. Epub 2010 Dec 22.

42.

Characterization of mitochondrial ferritin-deficient mice.

Bartnikas TB, Campagna DR, Antiochos B, Mulhern H, Pondarré C, Fleming MD.

Am J Hematol. 2010 Dec;85(12):958-60. doi: 10.1002/ajh.21872. No abstract available.

43.

Complications and treatment of patients with β-thalassemia in France: results of the National Registry.

Thuret I, Pondarré C, Loundou A, Steschenko D, Girot R, Bachir D, Rose C, Barlogis V, Donadieu J, de Montalembert M, Hagege I, Pegourie B, Berger C, Micheau M, Bernaudin F, Leblanc T, Lutz L, Galactéros F, Siméoni MC, Badens C.

Haematologica. 2010 May;95(5):724-9. doi: 10.3324/haematol.2009.018051. Epub 2009 Dec 8.

44.

[Imerslund-Gräsbeck syndrome].

Choquet P, Levrat V, Pondarre C, Vianney C, Guffon N.

Arch Pediatr. 2009 Dec;16(12):1559-61. doi: 10.1016/j.arcped.2009.09.010. Epub 2009 Oct 23. French.

PMID:
19854032
45.

Successful salvage chemotherapy for isolated central nervous system (CNS) relapse in Burkitt lymphoma: monocentric experience of 3 pediatric patients.

Baleydier F, Pondarre C, Pages MP, Mialou V, Kebaili K, Pracros JP, Bertrand Y.

J Pediatr Hematol Oncol. 2008 Dec;30(12):972-5. doi: 10.1097/MPH.0b013e31818b3584.

PMID:
19131795
46.

Severe neurologic complication after delayed hemolytic transfusion reaction in 2 children with sickle cell anemia: significant diagnosis and therapeutic challenges.

Elenga N, Mialou V, Kebaïli K, Galambrun C, Bertrand Y, Pondarre C.

J Pediatr Hematol Oncol. 2008 Dec;30(12):928-30. doi: 10.1097/MPH.0b013e31818c9172.

PMID:
19131783
47.

Invasive aspergillosis and allogeneic hematopoietic stem cell transplantation in children: a 15-year experience.

Crassard N, Hadden H, Pondarré C, Hadden R, Galambrun C, Piens MA, Pracros JP, Souillet G, Basset T, Berthier JC, Philippe N, Bertrand Y.

Transpl Infect Dis. 2008 Jun;10(3):177-83. doi: 10.1111/j.1399-3062.2008.00304.x. Epub 2008 Mar 4.

PMID:
18331389
48.

Invasive aspergillosis in a paediatric haematology department: a 15-year review.

Crassard N, Hadden H, Piens MA, Pondarré C, Hadden R, Galambrun C, Pracros JP, Souillet G, Basset T, Berthier JC, Philippe N, Bertrand Y.

Mycoses. 2008 Mar;51(2):109-16. doi: 10.1111/j.1439-0507.2007.01449.x.

PMID:
18254746
49.

[A diagnostic approach for inherited thrombocytopenia].

Pondarre C.

Arch Pediatr. 2007 Jun;14(6):676-8. Epub 2007 Apr 6. French. No abstract available.

PMID:
17419013
50.

Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.

Proust A, Guillet B, Picard C, de Saint Basile G, Pondarré C, Tamary H, Dreyfus M, Tchernia G, Fischer A, Delaunay J.

Blood Cells Mol Dis. 2007 Jul-Aug;39(1):102-6. Epub 2007 Apr 2.

PMID:
17400488

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