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Managing the Unusual Causes of Fetal Anemia.
Published in:
2020
By:
- Maisonneuve, Emeline;
- Ben M'Barek, Imane;
- Leblanc, Thierry;
- Da Costa, Lydie;
- Friszer, Stéphanie;
- Pernot, Françoise;
- Thomas, Pauline;
- Castaigne, Vanina;
- Toly N'Dour, Cécile;
- Mailloux, Agnès;
- Cortey, Anne;
- Jouannic, Jean-Marie;
- Ben M'Barek, Imane;
- Da Costa, Lydie;
- Toly N'Dour, Cécile
Publication type:
journal article
Mechanical Signature of Red Blood Cells Flowing Out of a Microfluidic Constriction Is Impacted by Membrane Elasticity, Cell Surface-to-Volume Ratio and Diseases.
Published in:
Frontiers in Physiology, 2020, v. 11, p. 1, doi. 10.3389/fphys.2020.00576
By:
- Faivre, Magalie;
- Renoux, Céline;
- Bessaa, Amel;
- Da Costa, Lydie;
- Joly, Philippe;
- Gauthier, Alexandra;
- Connes, Philippe
Publication type:
Article
One-Fifth of Children with Sickle Cell Anemia Show Exercise-Induced Hemoglobin Desaturation: Rate of Perceived Exertion and Role of Blood Rheology.
Published in:
Journal of Clinical Medicine, 2020, v. 9, n. 1, p. 133, doi. 10.3390/jcm9010133
By:
- Brousse, Valentine;
- Pondarre, Corinne;
- Arnaud, Cecile;
- Kamden, Annie;
- de Montalembert, Mariane;
- Boutonnat-Faucher, Benedicte;
- Bourdeau, Hélène;
- Charlot, Keyne;
- Grévent, David;
- Verlhac, Suzanne;
- da Costa, Lydie;
- Connes, Philippe
Publication type:
Article
Agranulocytosis in patients with Diamond‐Blackfan anaemia (DBA) treated with deferiprone for post‐transfusion iron overload: A retrospective study of the French DBA cohort.
Published in:
British Journal of Haematology, 2022, v. 199, n. 2, p. 285, doi. 10.1111/bjh.18366
By:
- Lecornec, Nicolas;
- Castex, Marie‐Pierre;
- Réguerre, Yves;
- Moreau, Philippe;
- Marie, Isabelle;
- Garçon, Loïc;
- Da Costa, Lydie;
- Leblanc, Thierry
Publication type:
Article
The use of next‐generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper*.
Published in:
British Journal of Haematology, 2022, v. 198, n. 3, p. 459, doi. 10.1111/bjh.18191
By:
- Roy, Noémi B. A.;
- Da Costa, Lydie;
- Russo, Roberta;
- Bianchi, Paola;
- Mañú‐Pereira, Maria del Mar;
- Fermo, Elisa;
- Andolfo, Immacolata;
- Clark, Barnaby;
- Proven, Melanie;
- Sanchez, Mayka;
- van Wijk, Richard;
- van der Zwaag, Bert;
- Layton, Mark;
- Rees, David;
- Iolascon, Achille
Publication type:
Article
Unexplained iron overload with haemolytic anaemia should prompt looking for morphological changes in erythroid precursors.
Published in:
British Journal of Haematology, 2022, v. 197, n. 2, p. 132, doi. 10.1111/bjh.18030
By:
- Rieu, Jean‐Baptiste;
- Largeaud, Laetitia;
- Da Costa, Lydie;
- Cougoul, Pierre
Publication type:
Article
Relevance of Howell‐Jolly body counts for measuring spleen function in sickle cell disease.
Published in:
American Journal of Hematology, 2023, v. 98, n. 5, p. E110, doi. 10.1002/ajh.26879
By:
- Pourdieu, Charlotte;
- El Hoss, Sara;
- Le Roux, Enora;
- Pages, Justine;
- Koehl, Bérengère;
- Missud, Florence;
- Holvoet, Laurent;
- Ithier, Ghislaine;
- Benkerrou, Malika;
- Haouari, Zinedine;
- Da Costa, Lydie;
- El Nemer, Wassim;
- Laurance, Sandrine;
- Aronovicz, Yves Colin;
- Le Van Kim, Caroline;
- Fenneteau, Odile;
- Lainey, Elodie;
- Brousse, Valentine
Publication type:
Article
High Resolution Genome-Wide Analysis of Chromosomal Alterations in Burkitt's Lymphoma.
Published in:
PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0007089
By:
- Toujani, Saloua;
- Dessen, Philippe;
- Ithzar, Nathalie;
- Danglot, Gisèle;
- Richon, Catherine;
- Vassetzky, Yegor;
- Robert, Thomas;
- Lazar, Vladimir;
- Bosq, Jacques;
- Da Costa, Lydie;
- Pèrot, Christine;
- Ribrag, Vincent;
- Patte, Catherine;
- Wiels, Jöelle;
- Bernheim, Alain
Publication type:
Article
Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study.
Published in:
Annals of Hematology, 2011, v. 90, n. 7, p. 759, doi. 10.1007/s00277-010-1138-3
By:
- Mullier, François;
- Lainey, Elodie;
- Fenneteau, Odile;
- Costa, Lydie Da;
- Schillinger, Françoise;
- Bailly, Nicolas;
- Cornet, Yvan;
- Chatelain, Christian;
- Dogne, Jean-Michel;
- Chatelain, Bernard
Publication type:
Article
Impact of surface-area-to-volume ratio, internal viscosity and membrane viscoelasticity on red blood cell deformability measured in isotonic condition.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-43200-y
By:
- Renoux, Céline;
- Faivre, Magalie;
- Bessaa, Amel;
- Da Costa, Lydie;
- Joly, Philippe;
- Gauthier, Alexandra;
- Connes, Philippe
Publication type:
Article
Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis.
Published in:
European Journal of Haematology, 2018, v. 101, n. 4, p. 566, doi. 10.1111/ejh.13135
By:
- Orvain, Corentin;
- Da Costa, Lydie;
- Van Wijk, Richard;
- Pissard, Serge;
- Picard, Véronique;
- Mansour‐Hendili, Lamisse;
- Cunat, Séverine;
- Giansily‐Blaizot, Muriel;
- Cartron, Guillaume;
- Schved, Jean‐François;
- Aguilar‐Martinez, Patricia
Publication type:
Article
Steroid resistance in Diamond Blackfan anemia associates with p57Kip2 dysregulation in erythroid progenitors.
Published in:
2020
By:
- Ashley, Ryan J.;
- Hongxia Yan;
- Nan Wang;
- Hale, John;
- Dulmovits, Brian M.;
- Papoin, Julien;
- Olive, Meagan E.;
- Udeshi, Namrata D.;
- Carr, Steven A.;
- Vlachos, Adrianna;
- Lipton, Jeffrey M.;
- Da Costa, Lydie;
- Hillyer, Christopher;
- Kinet, Sandrina;
- Taylor, Naomi;
- Mohandas, Narla;
- Narla, Anupama;
- Blanc, Lionel;
- Yan, Hongxia;
- Wang, Nan
Publication type:
journal article
A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome.
Published in:
2017
By:
- Gras, Domitille;
- Cousin, Christelle;
- Kappeler, Caroline;
- Fung, Cheuk‐Wing;
- Auvin, Stéphane;
- Essid, Nouha;
- Chung, Brian Hy;
- Da Costa, Lydie;
- Hainque, Elodie;
- Luton, Marie‐Pierre;
- Petit, Vincent;
- Vuillaumier‐Barrot, Sandrine;
- Boespflug‐Tanguy, Odile;
- Roze, Emmanuel;
- Mochel, Fanny
Publication type:
journal article
Hereditary spherocytosis associated with Noonan syndrome mimicking a dyserythropoietic anaemia.
Published in:
Pediatric Blood & Cancer, 2023, v. 70, n. 4, p. 1, doi. 10.1002/pbc.30121
By:
- Faggetter, Sarah;
- Ferster, Alina;
- Dedeken, Laurence;
- Demulder, Anne;
- David‐Nguyen, Ludvine;
- Fenneteau, Odile;
- Parisot, Melanie;
- Nitschke, Patrick;
- Vial, Yoann;
- Da Costa, Lydie
Publication type:
Article
MYH9‐related disease mutations cause abnormal red blood cell morphology through increased myosin‐actin binding at the membrane.
Published in:
American Journal of Hematology, 2019, v. 94, n. 6, p. 667, doi. 10.1002/ajh.25472
By:
- Smith, Alyson S.;
- Pal, Kasturi;
- Nowak, Roberta B.;
- Demenko, Anastasiya;
- Zaninetti, Carlo;
- Da Costa, Lydie;
- Favier, Remi;
- Pecci, Alessandro;
- Fowler, Velia M.
Publication type:
Article
Subtotal and total splenectomy for hereditary pyropoikilocytosis: Benefits and outcomes.
Published in:
American Journal of Hematology, 2018, v. 93, n. 10, p. E340, doi. 10.1002/ajh.25223
By:
- Pincez, Thomas;
- Guitton, Corinne;
- Landman‐Parker, Judith;
- Brousse, Valentine;
- Gauthier, Frédéric;
- Da Costa, Lydie;
- Ghazal, Kaldoun;
- Dufillot, Denis;
- Tchernia, Gil;
- Picard, Véronique;
- Garçon, Loïc
Publication type:
Article
A biomimetic microfluidic chip to study the circulation and mechanical retention of red blood cells in the spleen.
Published in:
American Journal of Hematology, 2015, v. 90, n. 4, p. 339, doi. 10.1002/ajh.23941
By:
- Picot, Julien;
- Ndour, Papa Alioune;
- Lefevre, Sophie D.;
- El Nemer, Wassim;
- Tawfik, Harvey;
- Galimand, Julie;
- Da Costa, Lydie;
- Ribeil, Jean-Antoine;
- de Montalembert, Mariane;
- Brousse, Valentine;
- Le Pioufle, Bruno;
- Buffet, Pierre;
- Le Van Kim, Caroline;
- Français, Olivier
Publication type:
Article
Genetic variants in the noncoding region of RPS19 gene in Diamond-Blackfan anemia: Potential implications for phenotypic heterogeneity.
Published in:
American Journal of Hematology, 2010, v. 85, n. 2, p. 111, doi. 10.1002/ajh.21601
By:
- Crétien, Aurore;
- Proust, Alexis;
- Delaunay, Jean;
- Rincé, Patricia;
- Leblanc, Thierry;
- Ducrocq, Rolande;
- Simansour, Maud;
- Marie, Isabelle;
- Tamary, Hannah;
- Meerpohl, Jörg;
- Niemeyer, Charlotte;
- Gazda, Hanna;
- Sieff, Colin;
- Ball, Sarah;
- Tchernia, Gil;
- Mohandas, Narla;
- Da Costa, Lydie
Publication type:
Article
Retinal atrophy and markers of systemic and cerebrovascular severity in homozygous sickle cell disease.
Published in:
European Journal of Ophthalmology, 2022, v. 32, n. 6, p. 3258, doi. 10.1177/11206721221090794
By:
- Martin, Gilles C.;
- Brousse, Valentine;
- Connes, Philippe;
- Grevent, David;
- Kossorotoff, Manoelle;
- Da Costa, Lydie;
- Bourdeau, Hélène;
- Charlot, Keyne;
- Boutonnat-Faucher, Bénédicte;
- Allali, Slimane;
- De Montalembert, Mariane;
- Bremond-Gignac, Dominique;
- Vidal, Pierre-Paul;
- Robert, Matthieu P.
Publication type:
Article
New variant of unclassified congenital dyserythropoietic anaemia: the concept of the erythroid regulator?
Published in:
British Journal of Haematology, 2012, v. 157, n. 1, p. 148, doi. 10.1111/j.1365-2141.2011.08932.x
By:
- Gay, Julie;
- Fournier, Martine;
- Pierre-Eugène, Cécile;
- Fontenay, Michaela;
- Charpentier, Agnès;
- Mayeux, Patrick;
- Pissard, Serge;
- Costa, Lydie Da;
- Beaumont, Carole;
- Rose, Christian
Publication type:
Article
Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT Pathway.
Published in:
PLoS Genetics, 2015, v. 11, n. 7, p. 1, doi. 10.1371/journal.pgen.1005326
By:
- Antunes, Ana T.;
- Goos, Yvonne J.;
- Pereboom, Tamara C.;
- Hermkens, Dorien;
- Wlodarski, Marcin W.;
- Da Costa, Lydie;
- MacInnes, Alyson W.
Publication type:
Article
Ribosomal Protein Mutations Induce Autophagy through S6 Kinase Inhibition of the Insulin Pathway.
Published in:
PLoS Genetics, 2014, v. 10, n. 5, p. 1, doi. 10.1371/journal.pgen.1004371
By:
- Heijnen, Harry F.;
- van Wijk, Richard;
- Pereboom, Tamara C.;
- Goos, Yvonne J.;
- Seinen, Cor W.;
- van Oirschot, Brigitte A.;
- van Dooren, Rowie;
- Gastou, Marc;
- Giles, Rachel H.;
- van Solinge, Wouter;
- Kuijpers, Taco W.;
- Gazda, Hanna T.;
- Bierings, Marc B.;
- Da Costa, Lydie;
- MacInnes, Alyson W.
Publication type:
Article
Fetal cerebral hemorrhage due to X-linked GATA1 gene mutation.
Published in:
2018
By:
- Bouchghoul, Hanane;
- Quelin, Chloé;
- Loget, Philippe;
- Encha‐Razavi, Féréchté;
- Senat, Marie‐Victoire;
- Maheut, Lorraine;
- Galimand, Julie;
- Collardeau‐Frachon, Sophie;
- Da Costa, Lydie;
- Martinovic, Jelena;
- Encha-Razavi, Féréchté;
- Senat, Marie-Victoire;
- Collardeau-Frachon, Sophie
Publication type:
journal article
The ribosomal basis of diamond-blackfan anemia: mutation and database update.
Published in:
2010
By:
- Boria, Ilenia;
- Garelli, Emanuela;
- Gazda, Hanna T.;
- Aspesi, Anna;
- Quarello, Paola;
- Pavesi, Elisa;
- Ferrante, Daniela;
- Meerpohl, Joerg J.;
- Kartal, Mutlu;
- Da Costa, Lydie;
- Proust, Alexis;
- Leblanc, Thierry;
- Simansour, Maud;
- Dahl, Niklas;
- Fröjmark, Anne-Sophie;
- Pospisilova, Dagmar;
- Cmejla, Radek;
- Beggs, Alan H.;
- Sheen, Mee R.;
- Landowski, Michael
Publication type:
Other
The Glucocorticoid Receptor Polymorphism Landscape in Patients With Diamond Blackfan Anemia Reveals an Association Between Two Clinically Relevant Single Nucleotide Polymorphisms and Time to Diagnosis.
Published in:
Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.745032
By:
- Lonetti, Annalisa;
- Indio, Valentina;
- Dianzani, Irma;
- Ramenghi, Ugo;
- Da Costa, Lydie;
- Pospíšilová, Dagmar;
- Migliaccio, Anna Rita
Publication type:
Article
GATA-1 Defects in Diamond–Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease.
Published in:
Genes, 2022, v. 13, n. 3, p. 447, doi. 10.3390/genes13030447
By:
- van Dooijeweert, Birgit;
- Kia, Sima Kheradmand;
- Dahl, Niklas;
- Fenneteau, Odile;
- Leguit, Roos;
- Nieuwenhuis, Edward;
- van Solinge, Wouter;
- van Wijk, Richard;
- Da Costa, Lydie;
- Bartels, Marije
Publication type:
Article

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