E-LIB Suche - Ergebnisse für: Cestèle, Sandrine

1

Brainstem depolarization–induced lethal apnea associated wi..:

Jansen, Nico A. ; Cestèle, Sandrine ; Marco, Silvia Sanchez...
Proceedings of the National Academy of Sciences. 121 (2024) 14 - p. , 2024

Link: https://doi.org/10.1073/..

2

Gain of function SCN1A disease‐causing variants: Expanding ..:

Matricardi, Sara ; Cestèle, Sandrine ; Trivisano, Marina...
Epilepsia. 64 (2023) 5 - p. 1331-1347 , 2023

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

3

Voltage‐gated sodium channels in genetic epilepsy: up and d..:

Rusina, Evgeniia ; Simonti, Martina ; Duprat, Fabrice..
Journal of Neurochemistry. , 2023

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

4

Structure-function relationship of new peptides activating ..:

Lopez, Ludivine ; De Waard, Stephan ; Meudal, Hervé...
Biomedicine & Pharmacotherapy. 165 (2023) - p. 115173 , 2023

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

5

Predictive precision medicine efforts for voltage-gated sod..:

Mantegazza, Massimo ; Cestèle, Sandrine
Brain. 145 (2022) 12 - p. 4148-4150 , 2022

Link: https://doi.org/10.1093/..

6

Initiation of migraine-related cortical spreading depolariz..:

Chever, Oana ; Zerimech, Sarah ; Scalmani, Paolo...
Journal of Clinical Investigation. 131 (2021) 21 - p. , 2021

Link: https://doi.org/10.1172/..

7

Pathophysiological mechanisms of migraine and epilepsy: Sim..:

Mantegazza, Massimo ; Cestèle, Sandrine
Neuroscience Letters. 667 (2018) - p. 92-102 , 2018

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

8

Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Resp..:

Dhifallah, Sandra ; Lancaster, Eric ; Merrill, Shana...
Frontiers in Molecular Neuroscience. 11 (2018) - p. , 2018

Link: https://doi.org/10.3389/..

9

Post-translational dysfunctions in channelopathies of the n..:

Terragni, Benedetta ; Scalmani, Paolo ; Franceschetti, Silvana..
Neuropharmacology. 132 (2018) - p. 31-42 , 2018

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

10

Depletion of the Fragile X Mental Retardation Protein in Em..:

Khalfallah, Olfa ; Jarjat, Marielle ; Davidovic, Laetitia...
Stem Cells. 35 (2016) 2 - p. 374-385 , 2016

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

11

Rescuable folding defective NaV1.1 (SCN1A) mutants in epile..:

Bechi, Giulia ; Rusconi, Raffaella ; Cestèle, Sandrine...
Neurobiology of Disease. 75 (2015) - p. 100-114 , 2015

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

12

Nonfunctional Nav1.1 familial hemiplegic migraine mutanttra..:

Cestèle, Sandrine ; Schiavon, Emanuele ; Rusconi, Raffaella..
Proceedings of the National Academy of Sciences of the United States of America. 110 (2013) 43 - p. 17546-17551 , 2013

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

13

Loss‐of‐function KCNH2 mutation in a family with long QT sy..:

Partemi, Sara ; Cestèle, Sandrine ; Pezzella, Marianna...
Epilepsia. 54 (2013) 8 - p. , 2013

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

14

Nonfunctional NaV1.1 familial hemiplegic migraine mutant tr..:

Cestèle, Sandrine ; Schiavon, Emanuele ; Rusconi, Raffaella..
Proceedings of the National Academy of Sciences. 110 (2013) 43 - p. 17546-17551 , 2013

Link: https://doi.org/10.1073/..

15

Divergent effects of the T1174S SCN1A mutation associated w..:

Cestèle, Sandrine ; Labate, Angelo ; Rusconi, Raffaella...
Epilepsia. 54 (2013) 5 - p. 927-935 , 2013

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