I agree that this site is using cookies. You can find further informations here.
X
Fretigny, M.
~ 100  results:
Search for persons X
?
1

PB0210 Heterozygous Structural Variation Mimicking Homozygo..:

Jourdy, Y. ; Chamouni, P. ; Fretigny, M....
Research and Practice in Thrombosis and Haemostasis.  7 (2023)  - p. 101282 , 2023
Link: https://doi.org/10.1016/..
 
?
2

Prednisolone treatment induced temporary factor IX normaliz..:

Carrette, M. ; Feugray, G. ; Chamouni, P....
Transfusion and Apheresis Science.  58 (2019)  4 - p. 512-514 , 2019
Link: https://doi.org/10.1016/..
 
?
3

Recurrent F8 and F9 gene variants result from a founder eff..:

Lassalle, F. ; Marmontel, O. ; Zawadzki, C....
Haemophilia.  24 (2018)  4 - p. , 2018
Link: https://doi.org/10.1111/..
 
?
4

Molecular cytogenetic characterization of five F8 complex r..:

Jourdy, Y. ; Chatron, N. ; Fretigny, M....
Haemophilia.  23 (2017)  4 - p. , 2017
Link: https://doi.org/10.1111/..
 
?
5

Study of six patients with completeF9deletion characterized..:

Jourdy, Y. ; Chatron, N. ; Carage, M.-L....
Journal of Thrombosis and Haemostasis.  14 (2016)  10 - p. 1988-1993 , 2016
Link: https://doi.org/10.1111/..
 
?
6

Five int22h homologous copies at the Xq28 locus identified ..:

Lannoy, N. ; Ravoet, M. ; Grisart, B....
Thrombosis Research.  137 (2016)  - p. 224-227 , 2016
Link: https://doi.org/10.1016/..
 
?
7

Genotyping might help therapeutic decision‐making in patien..:

Rugeri, L. ; Fretigny, M. ; Dargaud, Y...
Haemophilia.  22 (2016)  5 - p. , 2016
Link: https://doi.org/10.1111/..
 
?
8

Characterization of five associations of F8 missense mutati..:

Jourdy, Y. ; Nougier, C. ; Roualdes, O....
Haemophilia.  22 (2016)  4 - p. 583-589 , 2016
Link: https://doi.org/10.1111/..
 
?
9

Usefulness of an in vitro cellular expression model for hae..:

Roualdes, O. ; Nougier, C. ; Fretigny, M....
Haemophilia.  21 (2015)  3 - p. , 2015
Link: https://doi.org/10.1111/..
 
?
10

Diagnosis and management challenges in patients with mild h..:

Trossaert, M. ; Lienhart, A. ; Nougier, C....
Haemophilia.  20 (2014)  4 - p. 550-558 , 2014
Link: https://doi.org/10.1111/..
 
?
11

Management of bleeding in severe factor V deficiency with a..:

Ardillon, L. ; Lefrançois, A. ; Graveleau, J....
Vox Sanguinis.  107 (2014)  1 - p. 97-99 , 2014
Link: https://doi.org/10.1111/..
 
?
12

Characterization of four novel molecular changes in the pro..:

Nougier, C. ; Roualdes, O. ; Fretigny, M....
Haemophilia.  20 (2013)  2 - p. , 2013
Link: https://doi.org/10.1111/..
 
?
13

Apports de la génétique dans la prise en charge de l'hémoph..:

Vinciguerra, C. ; Frétigny, M. ; Négrier, C.
Archives de Pédiatrie.  17 (2010)  6 - p. 620-621 , 2010
Link: https://doi.org/10.1016/..
 
?
14

Contribution of genetical analysis for diagnosis of von Wil..:

VICTOR, M. ; RUGERI, L. ; NOUGIER, C....
Haemophilia.  15 (2009)  2 - p. 610-612 , 2009
Link: https://doi.org/10.1111/..
 
?
15

Evaluation of the coulter LH 750 haematology analyzer compa..:

Igout, J. ; Fretigny, M. ; Vasse, M....
Clinical and Laboratory Haematology.  26 (2004)  1 - p. 1-7 , 2004
Link: https://doi.org/10.1111/..
 
1-15