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Villard, Alexandra
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1

Accuracy of reverse shoulder arthroplasty angle according t..:

Werthel, Jean-David ; Villard, Alexandra ; Kazum, Efi..
Journal of Shoulder and Elbow Surgery.  32 (2023)  2 - p. 310-317 , 2023
Link: https://doi.org/10.1016/..
 
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2

Femoral condyle bone mineral density in osteoarthritis diff..:

Rougereau, Grégoire ; Villard, Alexandra ; Langlais, Tristan...
Orthopaedics & Traumatology: Surgery & Research.  109 (2023)  5 - p. 103584 , 2023
Link: https://doi.org/10.1016/..
 
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3

KERNIS, A.J.: Simple Songs / Valentines / 2 Songs (Trevigne.. 

Naxos Music Library
Hildegard of Bingen ; Kernis, Aaron Jay ; Bible - Old Testament... , 2017
Link: http://suub.naxosmusicli..
 
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4

The different clinical facets of SYN1-related neurodevelopm..:

Parenti, Ilaria ; Leitão, Elsa ; Kuechler, Alma...
Frontiers in Cell and Developmental Biology.  10 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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5

DEF6 deficiency, a mendelian susceptibility to EBV infectio..:

Fournier, Benjamin ; Tusseau, Maud ; Villard, Marine...
Journal of Allergy and Clinical Immunology.  147 (2021)  2 - p. 740-743.e9 , 2021
Link: https://doi.org/10.1016/..
 
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6

Exome sequencing in congenital ataxia identifies two new ca..:

Valence, Stéphanie ; Cochet, Emmanuelle ; Rougeot, Christelle...
Genetics in Medicine.  21 (2019)  3 - p. 553-563 , 2019
Link: https://doi.org/10.1038/..
 
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7

Clinical study of 19 patients with SCN8A‐related epilepsy: ..:

Denis, Julien ; Villeneuve, Nathalie ; Cacciagli, Pierre...
Epilepsia.  60 (2019)  5 - p. 845-856 , 2019
Link: https://doi.org/10.1111/..
 
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8

Genetic and phenotypic heterogeneity suggest therapeutic im..:

Wolff, Markus ; Johannesen, Katrine M. ; Hedrich, Ulrike B. S....
Brain.  140 (2017)  5 - p. 1316-1336 , 2017
Link: https://doi.org/10.1093/..
 
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9

Is SCN8A-related epilepsy recognizable ? Description of 15 ..:

Denis, Julien ; Caccciagli, Pierre ; Lacoste, Caroline...
European Journal of Paediatric Neurology.  21 (2017)  - p. e168 , 2017
Link: https://doi.org/10.1016/..
 
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10

Whole exome sequencing in non progressive congenital ataxia..:

Valence, Stéphanie ; Garel, Catherine ; Chantot Bastaraud, Sandra...
European Journal of Paediatric Neurology.  21 (2017)  - p. e10-e11 , 2017
Link: https://doi.org/10.1016/..
 
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11

Phylogeography of a migratory songbird across its Canadian ..:

Haché, Samuel ; Bayne, Erin M. ; Villard, Marc‐André...
Ecology and Evolution.  7 (2017)  16 - p. 6078-6088 , 2017
Link: https://doi.org/10.1002/..
 
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12

Variable clinical expression in patients with mosaicism for..:

Milh, Mathieu ; Lacoste, Caroline ; Cacciagli, Pierre...
American Journal of Medical Genetics Part A.  167 (2015)  10 - p. 2314-2318 , 2015
Link: https://doi.org/10.1002/..
 
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13

A recurrent KCNQ2 pore mutation causing early onset epilept..:

Abidi, Affef ; Devaux, Jérôme J. ; Molinari, Florence...
Neurobiology of Disease.  80 (2015)  - p. 80-92 , 2015
Link: https://doi.org/10.1016/..
 
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14

Epileptic patients with de novo STXBP1 mutations: Key clini..:

Di Meglio, Chloé ; Lesca, Gaetan ; Villeneuve, Nathalie...
Epilepsia.  56 (2015)  12 - p. 1931-1940 , 2015
Link: https://doi.org/10.1111/..
 
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15

E-learning et never events : à propos des erreurs de progra..:

Villard, Florine ; Lecoq, Anne-Lise ; Rehosevo, Zafitiana...
Le Pharmacien Hospitalier et Clinicien.  49 (2014)  4 - p. 323 , 2014
Link: https://doi.org/10.1016/..
 
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