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Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry.
Published in:
Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 102, doi. 10.1186/s13023-014-0183-8
By:
- Desplantes, Claire;
- Fremond, Marie Louis;
- Beaupain, Blandine;
- Luc Harousseau, Jean;
- Buzyn, Agnès;
- Pellier, Isabelle;
- Roques, Gaelle;
- Morville, Pierre;
- Paillard, Catherine;
- Bruneau, Julie;
- Pinson, Lucile;
- Jeziorski, Eric;
- Vannier, Jean Pierre;
- Picard, Capucine;
- Bellanger, Florence;
- Romero, Norma;
- de Pontual, Loïc;
- Lapillonne, Hélène;
- Lutz, Patrick;
- Bellanné Chantelot, Christine
Publication type:
Article
Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry.
Published in:
2014
By:
- Desplantes, Claire;
- Fremond, Marie Louise;
- Beaupain, Blandine;
- Harousseau, Jean Luc;
- Buzyn, Agnès;
- Pellier, Isabelle;
- Roques, Gaelle;
- Morville, Pierre;
- Paillard, Catherine;
- Bruneau, Julie;
- Pinson, Lucile;
- Jeziorski, Eric;
- Vannier, Jean Pierre;
- Picard, Capucine;
- Bellanger, Florence;
- Romero, Norma;
- de Pontual, Loïc;
- Lapillonne, Hélène;
- Lutz, Patrick;
- Chantelot, Christine Bellanné
Publication type:
Journal Article
Ex vivo generation of fully mature human red blood cells from hematopoietic stem cells.
Published in:
Nature Biotechnology, 2005, v. 23, n. 1, p. 69, doi. 10.1038/nbt1047
By:
- Giarratana, Marie-Catherine;
- Kobari, Ladan;
- Lapillonne, Hélène;
- Chalmers, David;
- Kiger, Laurent;
- Cynober, Thérèse;
- Marden, Michael C.;
- Wajcman, Henri;
- Douay, Luc
Publication type:
Article
Les leucémies aiguës myéloïdes pédiatriques.
Published in:
Médecine Thérapeutique: Pédiatrie, 2019, v. 22, n. 2, p. 85, doi. 10.1684/mtp.2019.0724
By:
- Leverger, Guy;
- Petit, Arnaud;
- Lapillonne, Hélène
Publication type:
Article
Molecular signature of erythroblast enucleation in human embryonic stem cells.
Published in:
Stem Cells, 2015, v. 33, n. 8, p. 2431, doi. 10.1002/stem.2027
By:
- Rouzbeh, Shaghayegh;
- Kobari, Ladan;
- Durand, Charles;
- Hebert, Nicolas;
- Mazurier, Christelle;
- Douay, Luc;
- Cambot, Marie;
- Faussat, Anne-Marie;
- Lapillonne, Hélène
Publication type:
Article
Treatment outcomes of childhood PICALM::MLLT10 acute leukaemias.
Published in:
British Journal of Haematology, 2024, v. 204, n. 2, p. 576, doi. 10.1111/bjh.19067
By:
- Mark, Catherine;
- Meshinchi, Soheil;
- Joyce, Brooklyn;
- Gibson, Brenda;
- Harrison, Christine;
- Bergmann, Anke K.;
- Goemans, Bianca F.;
- Pronk, Cornelis Jan H.;
- Lapillonne, Helene;
- Leverger, Guy;
- Antoniou, Evangelia;
- Schneider, Markus;
- Attarbaschi, Andishe;
- Dworzak, Michael;
- Stary, Jan;
- Tomizawa, Daisuke;
- Ebert, Sabine;
- Lejman, Monika;
- Kolb, E. Anders;
- Schmiegelow, Kjeld
Publication type:
Article
A circulating subset of BRAF<sup>V600E</sup>‐positive cells in infants with high‐risk Langerhans cell histiocytosis treated with BRAF inhibitors.
Published in:
British Journal of Haematology, 2021, v. 194, n. 4, p. 745, doi. 10.1111/bjh.17721
By:
- Poch, Rita;
- Le Louet, Solenne;
- Hélias‐Rodzewicz, Zofia;
- Hachem, Nawa;
- Plat, Geneviève;
- Barkaoui, Mohamed‐Aziz;
- Lapillonne, Hélène;
- Delhommeau, François;
- Emile, Jean‐François;
- Donadieu, Jean;
- Héritier, Sébastien
Publication type:
Article
Assessing bleeding risk in 18 children with Osteogenesis imperfecta.
Published in:
British Journal of Haematology, 2021, v. 192, n. 4, p. 785, doi. 10.1111/bjh.17303
By:
- Léguillier, Teddy;
- Favier, Rémi;
- Harroche, Annie;
- Lasne, Dominique;
- Bachelot‐Loza, Christilla;
- Borgel, Delphine;
- Boussaroque, Agathe;
- Pascreau, Tiffany;
- Lallemant‐Dudek, Pauline;
- Gkalea, Vasiliki;
- Haguet, Marie‐Clotilde;
- Cormier‐Daire, Valérie;
- Beaudeux, Jean‐Louis;
- Monnot, Sophie;
- Lapillonne, Hélène;
- Baujat, Geneviève;
- Forin, Véronique;
- Nivet‐Antoine, Valérie
Publication type:
Article
Circulating cell-free BRAF<sup>V600E</sup> as a biomarker in children with Langerhans cell histiocytosis.
Published in:
British Journal of Haematology, 2017, v. 178, n. 3, p. 457, doi. 10.1111/bjh.14695
By:
- Héritier, Sébastien;
- Hélias ‐ Rodzewicz, Zofia;
- Lapillonne, Hélène;
- Terrones, Nathalie;
- Garrigou, Sonia;
- Normand, Corinne;
- Barkaoui, Mohamed ‐ Aziz;
- Miron, Jean;
- Plat, Geneviève;
- Aladjidi, Nathalie;
- Pagnier, Anne;
- Deville, Anne;
- Gillibert ‐ Yvert, Marion;
- Moshous, Despina;
- Lefèvre ‐ Utile, Alain;
- Lutun, Anne;
- Paillard, Catherine;
- Thomas, Caroline;
- Jeziorski, Eric;
- Nizard, Philippe
Publication type:
Article
VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesis.
Published in:
American Journal of Hematology, 2021, v. 96, n. 4, p. E121, doi. 10.1002/ajh.26099
By:
- Lunati, Ariane;
- Petit, Arnaud;
- Lapillonne, Hélène;
- Gameiro, Christine;
- Saillour, Virginie;
- Garel, Catherine;
- Doummar, Diane;
- Qebibo, Leila;
- Aissat, Abdelrazak;
- Fanen, Pascale;
- Bartolucci, Pablo;
- Galactéros, Fréderic;
- Funalot, Benoit;
- Burglen, Lydie;
- Mansour‐Hendili, Lamisse
Publication type:
Article
Influence of dietary cholesterol on vitamin d metabolism in formula-fed preterm neonates.
Published in:
2002
By:
- Picaud, Jean-Charles;
- Boucher, Philippe;
- Lapillonne, Alexandre;
- Berthouze, Magali;
- Delvin, Edgar;
- Boehm, Günther;
- Claris, Oliver;
- Laborie, Sophie;
- Reygrobellet, Bernadette;
- Lapillonne, Helene;
- Glorieux, Francis H.;
- Salle, Bernard L.
Publication type:
journal article
Stem cell mobilization in idiopathic steroid-sensitive nephrotic syndrome.
Published in:
Pediatric Nephrology, 2008, v. 23, n. 8, p. 1251, doi. 10.1007/s00467-008-0793-2
By:
- Lapillonne, Hélène;
- Leclerc, Annelaure;
- Ulinski, Tim;
- Balu, Laurent;
- Garnier, Arnaud;
- Dereuddre-Bosquet, Nathalie;
- Watier, Hervé;
- Schlageter, Marie-Hélène;
- Deschênes, Georges
Publication type:
Article
Ex vivo drug sensitivity profiling‐guided treatment of a relapsed pediatric mixed‐phenotype acute leukemia with venetoclax and azacitidine.
Published in:
Pediatric Blood & Cancer, 2022, v. 69, n. 10, p. 1, doi. 10.1002/pbc.29678
By:
- Gonzales, Fanny;
- Guilmatre, Audrey;
- Barthélémy, Adeline;
- Lapillonne, Hélène;
- Pottier, Nicolas;
- Leverger, Guy;
- Petit, Arnaud;
- Cheok, Meyling H.
Publication type:
Article
CFFM4: a new member of the CD20/FcεRIβ family.
Published in:
Immunogenetics, 2001, v. 53, n. 6, p. 468, doi. 10.1007/s002510100345
By:
- Gingras, Marie-Claude;
- Lapillonne, Hélène;
- Margolin, Judith F.
Publication type:
Article
Rituximab in steroid-dependent idiopathic nephrotic syndrome in childhood—follow-up after CD19 recovery.
Published in:
Nephrology Dialysis Transplantation, 2012, v. 27, n. 3, p. 1083, doi. 10.1093/ndt/gfr405
By:
- Sellier-Leclerc, Anne-Laure;
- Baudouin, Véronique;
- Kwon, Thérésa;
- Macher, Marie-Alice;
- Guérin, Valérie;
- Lapillonne, Hélène;
- Deschênes, Georges;
- Ulinski, Tim
Publication type:
Article
Bone Marrow Clonogenic Myeloid Progenitors from NPM1-Mutated AML Patients Do Not Harbor the NPM1 Mutation: Implication for the Cell-Of-Origin of NPM1+ AML.
Published in:
Genes, 2020, v. 11, n. 1, p. 73, doi. 10.3390/genes11010073
By:
- Diaz de la Guardia, Rafael;
- González-Silva, Laura;
- López-Millán, Belén;
- Rodríguez-Sevilla, Juan José;
- Baroni, Matteo L.;
- Bueno, Clara;
- Anguita, Eduardo;
- Vives, Susana;
- Palomo, Laura;
- Lapillonne, Helene;
- Varela, Ignacio;
- Menendez, Pablo
Publication type:
Article
Germline RUNX1 variants in paediatric patients in a French specialised centre.
Published in:
EJHaem, 2023, v. 4, n. 1, p. 145, doi. 10.1002/jha2.594
By:
- Liu, Cécile;
- Ballerini, Paola;
- Nguyen, Guillaume;
- Mincheva, Zoia;
- Copin, Bruno;
- Bouslama, Boutheina;
- Leverger, Guy;
- Petit, Arnaud;
- Favier, Rémi;
- Lapillonne, Hélène;
- Boutroux, Hélène
Publication type:
Article

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