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Year Number of Results
1986 1
1988 1
1996 1
1997 1
1998 2
1999 1
2000 2
2001 2
2002 2
2003 1
2004 2
2005 2
2008 1
2009 1
2010 2
2011 3
2012 3
2013 1
2014 1
2015 1
2016 4
2017 2
2018 2
2019 1
2020 7
2021 1
2022 3
2023 3
2024 3

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55 results

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Page 1
Rituximab for High-Risk, Mature B-Cell Non-Hodgkin's Lymphoma in Children.
Minard-Colin V, Aupérin A, Pillon M, Burke GAA, Barkauskas DA, Wheatley K, Delgado RF, Alexander S, Uyttebroeck A, Bollard CM, Zsiros J, Csoka M, Kazanowska B, Chiang AK, Miles RR, Wotherspoon A, Adamson PC, Vassal G, Patte C, Gross TG; European Intergroup for Childhood Non-Hodgkin Lymphoma; Children’s Oncology Group. Minard-Colin V, et al. N Engl J Med. 2020 Jun 4;382(23):2207-2219. doi: 10.1056/NEJMoa1915315. N Engl J Med. 2020. PMID: 32492302 Free PMC article. Clinical Trial.
Molecular and clinicopathologic characterization of pediatric histiocytoses.
Hélias-Rodzewicz Z, Donadieu J, Terrones N, Barkaoui MA, Lambilliotte A, Moshous D, Thomas C, Azarnoush S, Pasquet M, Mansuy L, Aladjidi N, Jeziorski E, Marec-Berard P, Gilibert-Yvert M, Spiegel A, Saultier P, Pellier I, Pagnier A, Pertuisel S, Poiree M, Bodet D, Millot F, Isfan F, Stephan JL, Leruste A, Rigaud C, Filhon B, Carausu L, Reguerre Y, Kieffer I, Brichard B, Ben Jannet R, Bakari M, Idbaih A, Bodemer C, Cohen-Aubart F, Haroche J, Tazi A, Boudjemaa S, Fraitag S, Emile JF, Heritier S; French Histiocytosis Study Group. Hélias-Rodzewicz Z, et al. Among authors: lambilliotte a. Am J Hematol. 2023 Jul;98(7):1058-1069. doi: 10.1002/ajh.26938. Epub 2023 Apr 28. Am J Hematol. 2023. PMID: 37115038
Childhood Langerhans cell histiocytosis with severe lung involvement: a nationwide cohort study.
Le Louet S, Barkaoui MA, Miron J, Galambrun C, Aladjidi N, Chastagner P, Kebaili K, Armari-Alla C, Lambilliotte A, Lejeune J, Moshous D, Della Valle V, Sileo C, Ducou Le Pointe H, Chateil JF, Renolleau S, Piloquet JE, Portefaix A, Epaud R, Chiron R, Bugnet E, Lorillon G, Tazi A, Emile JF, Donadieu J, Héritier S. Le Louet S, et al. Among authors: lambilliotte a. Orphanet J Rare Dis. 2020 Sep 9;15(1):241. doi: 10.1186/s13023-020-01495-5. Orphanet J Rare Dis. 2020. PMID: 32907615 Free PMC article.
Epstein-Barr Virus in Childhood and Adolescent Classic Hodgkin Lymphoma in a French Cohort of 301 Patients.
Pereira V, Boudjemaa S, Besson C, Leblanc T, Rigaud C, Leruste A, Garnier N, Lambilliotte A, Simonin M, Curtillet C, Bonneau-Lagacherie J, Coulomb A, Landman-Parker J. Pereira V, et al. Among authors: lambilliotte a. J Pediatr Hematol Oncol. 2022 Nov 1;44(8):e1033-e1038. doi: 10.1097/MPH.0000000000002403. Epub 2022 Jan 28. J Pediatr Hematol Oncol. 2022. PMID: 35091521
Incidence and risk factors for clinical neurodegenerative Langerhans cell histiocytosis: a longitudinal cohort study.
Héritier S, Barkaoui MA, Miron J, Thomas C, Moshous D, Lambilliotte A, Mazingue F, Kebaili K, Jeziorski E, Plat G, Aladjidi N, Pacquement H, Galambrun C, Brugières L, Leverger G, Mansuy L, Paillard C, Deville A, Pagnier A, Lutun A, Gillibert-Yvert M, Stephan JL, Cohen-Aubart F, Haroche J, Pellier I, Millot F, Gandemer V, Martin-Duverneuil N, Taly V, Hélias-Rodzewicz Z, Emile JF, Hoang-Xuan K, Idbaih A, Donadieu J. Héritier S, et al. Among authors: lambilliotte a. Br J Haematol. 2018 Nov;183(4):608-617. doi: 10.1111/bjh.15577. Epub 2018 Nov 12. Br J Haematol. 2018. PMID: 30421536 Free article. Clinical Trial.
Autoimmune cytopenia and Kabuki syndrome in paediatrics: Insights in 11 patients.
Bianchi C, Margot H, Fernandes H, Pasquet M, Priqueler L, Roy-Peaud F, Bauduer F, Bayart S, Garnier N, Fain O, Van Gils J, Joly SB, Rialland F, Paillard C, Deparis M, Lambilliotte A, Leblanc T, Fahd M, Leverger G, Héritier S, Geneviève D, Rieux-Laucat F, Picard C, Neyraud C, Aladjidi N. Bianchi C, et al. Among authors: lambilliotte a. Br J Haematol. 2024 May;204(5):1899-1907. doi: 10.1111/bjh.19387. Epub 2024 Mar 3. Br J Haematol. 2024. PMID: 38432067
Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1.
Allegrini B, NGuyen LD, Mignotet M, Etchebest C, Fenneteau O, Platon J, Lambilliotte A, Guizouarn H, Da Costa L. Allegrini B, et al. Among authors: lambilliotte a. Blood Cells Mol Dis. 2023 Nov;103:102780. doi: 10.1016/j.bcmd.2023.102780. Epub 2023 Jul 20. Blood Cells Mol Dis. 2023. PMID: 37516005
Childhood pulmonary Langerhans cell histiocytosis: a comprehensive clinical-histopathological and BRAFV600E mutation study from the French national cohort.
Kambouchner M, Emile JF, Copin MC, Coulomb-Lherminé A, Sabourin JC, Della Valle V, Sileo C, Ducou Le Pointe H, Bégueret H, Galmiche L, Lambilliotte A, Paraf F, Piche M, Piguet C, Rullier A, Secq V, Serre I, Bernaudin JF, Donadieu J. Kambouchner M, et al. Among authors: lambilliotte a. Hum Pathol. 2019 Jul;89:51-61. doi: 10.1016/j.humpath.2019.04.005. Epub 2019 May 3. Hum Pathol. 2019. PMID: 31054893
[Neonatal screening of sickle cell anemia in metropolitan France].
Bardakjian J, Benkerrou M, Bernaudin F, Briard ML, Ducrocq R, Lambilliotte A, Léna-Russo D, de Montalembert M, Thuret I, Bégué P, Elion J, Galactéros F; Travail du Groupe sur le dépistage néonatal de la drépanocytose. Bardakjian J, et al. Among authors: lambilliotte a. Arch Pediatr. 2000 Dec;7(12):1261-3. doi: 10.1016/s0929-693x(00)00140-8. Arch Pediatr. 2000. PMID: 11147058 French. No abstract available.
55 results