Results
|
1.
|
|
|
2.
|
|
|
3.
|
|
|
4.
|
|
|
5.
|
|
|
6.
|
[Factor IX assays in treated hemophilia B patients]. [electronic resource] by
- Pouplard, Claire
- Jeanpierre, Emmanuelle
- Lasne, Dominique
- Le Cam Duchez, Véronique
- Eschwege, Valérie
- Flaujac, Claire
- Galinat, Hubert
- Harzallah, Ines
- Proulle, Valérie
- Smahi, Motalib
- Sobas, Frédéric
- Ternisien, Catherine
- Toulon, Pierre
- Voisin, Sophie
- Nougier, Christophe
Producer: 20190624
In:
Annales de biologie clinique vol. 77
Availability: No items available.
|
|
7.
|
[Factor VIII assays in treated hemophilia A patients]. [electronic resource] by
- Lasne, Dominique
- Pouplard, Claire
- Nougier, Christophe
- Eschwege, Valérie
- Le Cam Duchez, Véronique
- Proulle, Valérie
- Smahi, Motalib
- Harzallah, Ines
- Voisin, Sophie
- Toulon, Pierre
- Sobas, Frédéric
- Galinat, Hubert
- Flaujac, Claire
- Ternisien, Catherine
- Jeanpierre, Emmanuelle
Producer: 20190624
In:
Annales de biologie clinique vol. 77
Availability: No items available.
|
|
8.
|
Factor VIII and IX assays for post-infusion monitoring in hemophilia patients: Guidelines from the French BIMHO group (GFHT). [electronic resource] by
- Jeanpierre, Emmanuelle
- Pouplard, Claire
- Lasne, Dominique
- Le Cam Duchez, Véronique
- Eschwege, Valérie
- Flaujac, Claire
- Galinat, Hubert
- Harzallah, Ines
- Proulle, Valérie
- Smahi, Motalib
- Sobas, Frédéric
- Stepina, Nataliia
- Toulon, Pierre
- Voisin, Sophie
- Ternisien, Catherine
- Nougier, Christophe
Producer: 20210601
In:
European journal of haematology vol. 105
Availability: No items available.
|
|
9.
|
A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity. [electronic resource] by
- Jeandidier, Eric
- Gervais, Carine
- Radford-Weiss, Isabelle
- Zink, Estelle
- Gangneux, Catherine
- Eischen, Alice
- Galoisy, Anne Cécile
- Helias, Catherine
- Dano, Laurent
- Cammarata, Ornella
- Jung, Georges
- Harzallah, Inès
- Guérin, Eric
- Martzolff, Lionel
- Drénou, Bernard
- Lioure, Bruno
- Tancrédi, Céline
- Rimelen, Valérie
- Mauvieux, Laurent
Producer: 20121009
In:
Cancer genetics vol. 205
Availability: No items available.
|
|
10.
|
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non-homologous Robertsonian translocation. Should we still perform prenatal diagnosis? [electronic resource] by
- Moradkhani, Kamran
- Cuisset, Laurence
- Boisseau, Pierre
- Pichon, Olivier
- Lebrun, Marine
- Hamdi-Rozé, Houda
- Maurin, Marie-Laure
- Gruchy, Nicolas
- Manca-Pellissier, Marie-Christine
- Malzac, Perrine
- Bilan, Frédéric
- Audrezet, Marie-Pierre
- Saugier-Veber, Pascale
- Fauret-Amsellem, Anne-Laure
- Missirian, Chantal
- Kuentz, Paul
- Egea, Gregory
- Guichet, Agnès
- Creveaux, Isabelle
- Janel, Caroline
- Harzallah, Ines
- Touraine, Renaud
- Goumy, Carole
- Joyé, Nicole
- Puechberty, Jacques
- Haquet, Emmanuelle
- Chantot-Bastaraud, Sandra
- Schmitt, Sébastien
- Gosset, Philippe
- Duban-Bedu, Bénédicte
- Delobel, Bruno
- Vago, Philippe
- Vialard, François
- Gomes, Denise Molina
- Siffroi, Jean-Pierre
- Bonnefont, Jean-Paul
- Dupont, Jean-Michel
- Jonveaux, Philippe
- Doco-Fenzy, Martine
- Sanlaville, Damien
- Le Caignec, Cédric
Producer: 20200706
In:
Prenatal diagnosis vol. 39
Availability: No items available.
|