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Sarret, Catherine
231  results:
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1

Robot-assisted gait training improves walking and cerebral ..:

Julien, Laura ; Moreau-Pernet, Guillemette ; Rochette, Emmanuelle...
Pediatric Research.  , 2024
Link: https://doi.org/10.1038/..
 
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2

Characterization of novel CACNA1A splice variants by RNA‐se..:

Riant, Florence ; Burglen, Lydie ; Corpechot, Michaelle...
Clinical Genetics.  104 (2023)  3 - p. 365-370 , 2023
Link: https://doi.org/10.1111/..
 
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3

Establishing Patient-Centered Outcomes for MCT8 Deficiency:..:

Wilpert, Nina-Maria ; Tonduti, Davide ; Vaia, Ylenia...
Neuropsychiatric Disease and Treatment.  19 (2023)  - p. 2195-2216 , 2023
Link: https://doi.org/10.2147/..
 
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4

Prospective Multicenter Validation of a Simple Blood Test f..:

Mochel, Fanny ; Gras, Domitille ; Luton, Marie-Pierre...
Neurology.  100 (2023)  23 - p. , 2023
Link: https://doi.org/10.1212/..
 
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5

Correction to: Use of MFM-20 to monitor SMA types 1 and 2 p..:

Le Goff, Laure ; Seferian, Andreea ; Phelep, Aurelie...
Neurological Sciences.  44 (2022)  3 - p. 1139-1139 , 2022
Link: https://doi.org/10.1007/..
 
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6

Use of MFM-20 to monitor SMA types 1 and 2 patients treated..:

Le Goff, Laure ; Seferian, Andreea ; Phelep, Aurelie...
Neurological Sciences.  44 (2022)  1 - p. 329-337 , 2022
Link: https://doi.org/10.1007/..
 
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7

Efficacy of Caffeine in ADCY5‐Related Dyskinesia: A Retrosp..:

Méneret, Aurélie ; Mohammad, Shekeeb S. ; Cif, Laura...
Movement Disorders.  37 (2022)  6 - p. 1294-1298 , 2022
Link: https://doi.org/10.1002/..
 
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8

Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley ..:

Masnada, Silvia ; Sarret, Catherine ; Antonello, Clara Eleonora...
Molecular Genetics and Metabolism.  135 (2022)  1 - p. 109-113 , 2022
Link: https://doi.org/10.1016/..
 
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9

Neural correlates of rehabilitation program with robot-assi..:

Pontier, Bénédicte ; Sontheimer, Anna ; Coste, Jérôme...
Annals of Physical and Rehabilitation Medicine.  64 (2021)  4 - p. 101411 , 2021
Link: https://doi.org/10.1016/..
 
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10

High rate of hypomorphic variants as the cause of inherited..:

Benkirane, Mehdi ; Marelli, Cecilia ; Guissart, Claire...
Genetics in Medicine.  23 (2021)  11 - p. 2160-2170 , 2021
Link: https://doi.org/10.1038/..
 
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11

KCNT1-related epilepsies and epileptic encephalopathies: ph..:

Bonardi, Claudia M ; Heyne, Henrike O ; Fiannacca, Martina...
Brain.  144 (2021)  12 - p. 3635-3650 , 2021
Link: https://doi.org/10.1093/..
 
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12

Clinical features of homozygous FIG4‐p.Ile41Thr Charcot‐Mar..:

Lafontaine, Maxime ; Lia, Anne‐Sophie ; Bourthoumieu, Sylvie...
Annals of Clinical and Translational Neurology.  8 (2021)  2 - p. 471-476 , 2021
Link: https://doi.org/10.1002/..
 
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13

Normal intellectual skills in patients with Rhombencephalos..:

Bonnetain, Marie-France ; Rougeot-Jung, Christelle ; Sarret, Catherine...
European Journal of Paediatric Neurology.  29 (2020)  - p. 92-100 , 2020
Link: https://doi.org/10.1016/..
 
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14

Neuropsychological study in 19 French patients with White‐S..:

Garde, Aurore ; Cornaton, Jenny ; Sorlin, Arthur...
Clinical Genetics.  99 (2020)  3 - p. 407-417 , 2020
Link: https://doi.org/10.1111/..
 
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15

Palliative Care in SMA Type 1: A Prospective Multicenter Fr..:

Hully, Marie ; Barnerias, Christine ; Chabalier, Delphine...
Frontiers in Pediatrics.  8 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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