E-LIB Suche - Ergebnisse für: Millat, G.

1

NEXN-mediated cardiomyopathies: Prevalence, phenotypic expr..:

Hermida, A. ; Ader, F. ; Millat, G....
Archives of Cardiovascular Diseases Supplements. 15 (2023) 1 - p. 43 , 2023

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

2

ALPK3 gene in cardiomyopathies: Which phenotypes? Which mod..:

Ader, F. ; Bensalah, M. ; Millat, G....
Archives of Cardiovascular Diseases Supplements. 15 (2023) 1 - p. 38 , 2023

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

3

Atrial structural remodeling gene variants in patients with..:

Puertas, R. Doñate ; Millat, G. ; Ernens, I....
Archives of Cardiovascular Diseases Supplements. 10 (2018) 2 - p. 237 , 2018

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

4

Single, short in‐del, and copy number variations detection ..:

Marmontel, O. ; Charrière, S. ; Simonet, T....
Clinical Genetics. 94 (2018) 1 - p. 132-140 , 2018

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

5

TRPM4 variants associated with long QT syndrome:

Thomas, H. ; Liu, H. ; Salle, L....
Archives of Cardiovascular Diseases Supplements. 9 (2017) 2 - p. 200-201 , 2017

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

6

Reducing body myopathy as a new phenotype of Filamin C muta..:

Janin, A. ; Manel, V. ; Millat, G..
Neuromuscular Disorders. 27 (2017) - p. S120 , 2017

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

7

Truncating mutations on myofibrillar myopathies causing gen..:

Janin, A. ; N'Guyen, K. ; Habib, G....
Clinical Genetics. 92 (2017) 6 - p. 616-623 , 2017

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

8

Characterization of oseltamivir-resistant population dynami..:

Pichon, M. ; Gaymard, A. ; Josset, L....
Journal of Clinical Virology. 82 (2016) - p. S42-S43 , 2016

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

9

Small-scale benthos distribution modelling in a North Sea t..:

Singer, A. ; Schückel, U. ; Beck, M....
Marine Ecology Progress Series. 551 (2016) - p. 13-30 , 2016

Link: https://www.jstor.org/st..

10

Assessing resilience in long-term ecological data sets:

Müller, F. ; Bergmann, M. ; Dannowski, R....
Ecological Indicators. 65 (2016) - p. 10-43 , 2016

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

11

Homozygous PKP2 deletion associated with neonatal left vent..:

Ramond, F. ; Janin, A. ; Di Filippo, S....
Clinical Genetics. 91 (2016) 1 - p. 126-130 , 2016

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

12

Nouvelle mutation du gène KCNH2 chez une patiente diagnosti..:

Chanséaume, A. ; Millat, G. ; Roux, A.
Revue Neurologique. 170 (2014) 4 - p. 304-305 , 2014

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

13

Une dysfonction sinusale en rapport avec une nouvelle mutat..:

Selly, J.-B. ; Boumahni, B. ; Edmar, A....
Archives de Pédiatrie. 19 (2012) 8 - p. 837-841 , 2012

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

14

Molecular characterization of a large MYBPC3 rearrangement ..:

Chanavat, V. ; Seronde, M.F. ; Bouvagnet, P....
European Journal of Medical Genetics. 55 (2012) 3 - p. 163-166 , 2012

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

15

Place de la maladie de Fabry au sein des cardiomyopathies h..:

Bouvagnet, P. ; Millat, G. ; Rousson, R...
La Revue de Médecine Interne. 31 (2010) - p. S233-S237 , 2010

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