E-LIB Suche - Ergebnisse für: Mignot, Sandra

1

Unique inflammatory signature in haemophilic arthropathy: m..:

Mignot, Sandra ; Cagnard, Nicolas ; Albaud, Benoit...
Journal of Cellular and Molecular Medicine. 24 (2020) 24 - p. 14453-14466 , 2020

Link: https://doi.org/10.1111/..

2

Mechanisms of control of the inflammation in haemophilic ar..:

Mignot, Sandra
NNT: 2020UNIP5182. , 2020

Link: https://theses.hal.scien..

3

Mechanisms of control of the inflammation in haemophilic ar..:

Mignot, Sandra
NNT: 2020UNIP5182. , 2020

Link: https://theses.hal.scien..

4

Mécanismes de contrôle de l'inflammation dans l'arthropathi..:

Mignot, Sandra
http://www.theses.fr/2020UNIP5182/document. , 2020

Link: http://www.theses.fr/202..

5

Unique inflammatory signature in haemophilic arthropathy: m..:

Mignot, Sandra ; Cagnard, Nicolas ; Albaud, Benoit...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753994/. , 2020

Link: http://www.ncbi.nlm.nih...

6

Musical education: school subject' status and value ; L'édu..:

Mignot, Sandra
dumas-01174695. , 2014

Link: https://dumas.ccsd.cnrs...

7

Musical education: school subject' status and value ; L'édu..:

Mignot, Sandra
dumas-01174695. , 2014

Link: https://dumas.ccsd.cnrs...

8

Growth charts in DYRK1A syndrome:

Lanvin, Pierre‐Louis ; Goronflot, Thomas ; Isidor, Bertrand...
American Journal of Medical Genetics Part A. 194 (2023) 1 - p. 9-16 , 2023

Link: https://doi.org/10.1002/..

9

Neurodevelopmental phenotype in 36 new patients with 8p inv..:

Vibert, Roseline ; Mignot, Cyril ; Keren, Boris...
Clinical Genetics. 101 (2021) 3 - p. 307-316 , 2021

Link: https://doi.org/10.1111/..

10

Further delineation of BCAP31-linked intellectual disabilit..:

Whalen, Sandra ; Shaw, Marie ; Mignot, Cyril...
European Journal of Human Genetics. 29 (2021) 9 - p. 1405-1417 , 2021

Link: https://doi.org/10.1038/..

11

The complete loss of function of the SMS gene results in a ..:

Larcher, Lise ; Norris, Joy W. ; Lejeune, Elodie...
European Journal of Medical Genetics. 63 (2020) 4 - p. 103777 , 2020

Link: https://doi.org/10.1016/..

12

Prenatal exome sequencing in 65 fetuses with abnormality of..:

Heide, Solveig ; Spentchian, Myrtille ; Valence, Stéphanie...
Genetics in Medicine. 22 (2020) 11 - p. 1887-1891 , 2020

Link: https://doi.org/10.1038/..

13

Author Correction: A framework to identify contributing gen..:

Tabet, Anne-Claude ; Rolland, Thomas ; Ducloy, Marie...
npj Genomic Medicine. 4 (2019) 1 - p. , 2019

Link: https://doi.org/10.1038/..

14

Early-onset encephalopathy with paroxysmal movement disorde..:

Marzin, Pauline ; Mignot, Cyril ; Dorison, Nathalie...
Brain and Development. 40 (2018) 9 - p. 768-774 , 2018

Link: https://doi.org/10.1016/..

15

Loss of tubulin deglutamylaseCCP1 causes infantile‐onset ne..:

Shashi, Vandana ; Magiera, Maria M ; Klein, Dennis...
The EMBO Journal. 37 (2018) 23 - p. , 2018

Link: https://doi.org/10.15252..