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Récidive d'un syndrome de Willebrand acquis chez une patiente en rupture de traitement d'une maladie de Crohn.
Published in:
Annales de Biologie Clinique, 2022, v. 80, n. 1, p. 69, doi. 10.1684/abc.2021.1692
By:
- Hormi, Myriam;
- Le Méné, Melchior;
- Comparon, Céline;
- El Kout, Imededdine;
- Baran-Marszak, Fanny;
- Itzhar-Baikian, Nathalie;
- Siguret, Virginie;
- Dhote, Robin
Publication type:
Article
TP53 mutations at codon 234 are associated with chlorambucil treatment in chronic lymphocytic leukemia.
Published in:
American Journal of Hematology, 2022, v. 97, n. 4, p. E159, doi. 10.1002/ajh.26479
By:
- Lazarian, Grégory;
- Theves, Floriane;
- Hormi, Myriam;
- Letestu, Rémi;
- Eclache, Virginie;
- Bidet, Audrey;
- Cornillet‐Lefebvre, Pascale;
- Davi, Frédéric;
- Delabesse, Eric;
- Estienne, Marie‐Hélène;
- Etancelin, Pascaline;
- Kosmider, Olivier;
- Laibe, Sophy;
- Lode, Laurence;
- Muller, Marc;
- Nadal, Nathalie;
- Naguib, Dina;
- Pastoret, Cédric;
- Poulain, Stéphanie;
- Sujobert, Pierre
Publication type:
Article
Pairing MCL‐1 inhibition with venetoclax improves therapeutic efficiency of BH3‐mimetics in AML.
Published in:
European Journal of Haematology, 2020, v. 105, n. 5, p. 588, doi. 10.1111/ejh.13492
By:
- Hormi, Myriam;
- Birsen, Rudy;
- Belhadj, Maya;
- Huynh, Tony;
- Cantero Aguilar, Lilia;
- Grignano, Eric;
- Haddaoui, Lamya;
- Guillonneau, Francois;
- Mayeux, Patrick;
- Hunault, Mathilde;
- Tamburini, Jérôme;
- Kosmider, Olivier;
- Fontenay, Michaela;
- Bouscary, Didier;
- Chapuis, Nicolas
Publication type:
Article
Diversity of TP53 Mutations in CLL: Retrospective Analysis of 450 Mutations from the French Innovative Leukemia Organization (FILO) Group.
Published in:
Clinical Lymphoma, Myeloma & Leukemia, 2017, v. 17, p. S301, doi. 10.1016/j.clml.2017.07.096
By:
- Hormi, Myriam;
- Baran-Marszak, Fanny;
- Véronèse, Lauren;
- Sujobert, Pierre;
- Davi, Frederic;
- Poulain, Stéphanie;
- Estienne, Marie-Hélène;
- Bidet, Audrey;
- Delabesse, Eric;
- Giraudier, Stéphane;
- Pastoret, Cédric;
- Cornillet-Lefebvre, Pascale;
- Laibe, Sophy;
- Lode, Laurence;
- Naguib, Dina;
- Nguyen-Khac, Florence;
- Kosmider, Olivier;
- Muller, Marc;
- Souci, Thierry;
- Cymbalista, Florence
Publication type:
Article
The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots.
Published in:
Human Mutation, 2023, p. 1, doi. 10.1155/2023/4880113
By:
- Lazarian, Grégory;
- Leroy, Bernard;
- Theves, Floriane;
- Hormi, Myriam;
- Letestu, Rémi;
- Eclache, Virginie;
- Tueur, Giulia;
- Ameur, Adam;
- Bidet, Audrey;
- Cornillet-Lefebvre, Pascale;
- Davi, Frédéric;
- Delabesse, Eric;
- Estienne, Marie-Hélène;
- Etancelin, Pascaline;
- Kosmider, Olivier;
- Laibe, Sophy;
- Muller, Marc;
- Nadal, Nathalie;
- Naguib, Dina;
- Pastoret, Cédric
Publication type:
Article
Absence of Missense Variant Detection in Inherited Dysfibrinogenemia May Result from a Poor Raw Data Analysis Algorithm or Mosaicism.
Published in:
2023
By:
- De Mazancourt, Philippe;
- Mazoyer, Elisabeth;
- Hormi, Myriam;
- Hanss, Michel
Publication type:
Case Study

Found: 6

Récidive d'un syndrome de Willebrand acquis chez une patiente en rupture de traitement d'une maladie de Crohn.

TP53 mutations at codon 234 are associated with chlorambucil treatment in chronic lymphocytic leukemia.

Pairing MCL‐1 inhibition with venetoclax improves therapeutic efficiency of BH3‐mimetics in AML.

Diversity of TP53 Mutations in CLL: Retrospective Analysis of 450 Mutations from the French Innovative Leukemia Organization (FILO) Group.

The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots.

Absence of Missense Variant Detection in Inherited Dysfibrinogenemia May Result from a Poor Raw Data Analysis Algorithm or Mosaicism.