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Mathilde Renaud

Showing results (1-10 of 66) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2020
Autosomal Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common BiomarkerMathilde Renaud, Christine Tranchant, Michel Koenig, et al.
Clinical Nuclear Medicine|January 10, 2022
Brain 18F-FDG PET in Cowden SyndromeJustine Grangeret, Solene Frismand, Marie Muller, et al.
Clinical Nuclear Medicine|September 17, 2019
Atypical Parkinson Syndrome Hiding a MeningiomaCaroline Bund, Eric Ouvrard, Mathilde Renaud, et al.
Neurology. Genetics|January 3, 2024
Paroxysmal Ataxia: A Characteristic Feature of FGF14 Repeat Expansion (SCA27B)Cendrine Foucard, Marie Belley, Aude Sangare, et al.
Clinical and Translational Medicine|January 27, 2024
Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxiaDavid Pellerin, Matt C Danzi, Mathilde Renaud, et al.
BMC Neurology|June 3, 2014
Chronic Bickerstaff's encephalitis with cognitive impairment, a reality?Mathilde Renaud, Jérôme Aupy, Guillaume Camuset, et al.
European Journal of Medical Genetics|July 28, 2025
Further delineation of LRSAM1-related Charcot-Marie-Tooth type 2P with parkinsonismPauline Ducatel, Antoine Verger, Marion Selton, et al.
Parkinsonism & Related Disorders|October 18, 2019
Multiple System Atrophy: Phenotypic spectrum approach coupled with brain 18-FDG PETStephan Grimaldi, Mohamed Boucekine, Tatiana Witjas, et al.
American Journal of Medical Genetics. Part A|May 25, 2026
Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith-Magenis SyndromeAlbin Blanc, Christophe Nemos, Céline Bonnet, et al.
Journal of Research on Adolescence : the Official Journal of the Society for Research on Adolescence|March 14, 2026
Longitudinal changes in sexual identity during adolescence and their associations with sexual well-beingAlice Girouard, Alexa Martin-Storey, Jacinthe Dion, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2020
Autosomal Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common BiomarkerMathilde Renaud, Christine Tranchant, Michel Koenig, et al.
Clinical Nuclear Medicine|January 10, 2022
Brain 18F-FDG PET in Cowden SyndromeJustine Grangeret, Solene Frismand, Marie Muller, et al.
Clinical Nuclear Medicine|September 17, 2019
Atypical Parkinson Syndrome Hiding a MeningiomaCaroline Bund, Eric Ouvrard, Mathilde Renaud, et al.
Neurology. Genetics|January 3, 2024
Paroxysmal Ataxia: A Characteristic Feature of FGF14 Repeat Expansion (SCA27B)Cendrine Foucard, Marie Belley, Aude Sangare, et al.
Clinical and Translational Medicine|January 27, 2024
Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxiaDavid Pellerin, Matt C Danzi, Mathilde Renaud, et al.
BMC Neurology|June 3, 2014
Chronic Bickerstaff's encephalitis with cognitive impairment, a reality?Mathilde Renaud, Jérôme Aupy, Guillaume Camuset, et al.
European Journal of Medical Genetics|July 28, 2025
Further delineation of LRSAM1-related Charcot-Marie-Tooth type 2P with parkinsonismPauline Ducatel, Antoine Verger, Marion Selton, et al.
Parkinsonism & Related Disorders|October 18, 2019
Multiple System Atrophy: Phenotypic spectrum approach coupled with brain 18-FDG PETStephan Grimaldi, Mohamed Boucekine, Tatiana Witjas, et al.
American Journal of Medical Genetics. Part A|May 25, 2026
Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith-Magenis SyndromeAlbin Blanc, Christophe Nemos, Céline Bonnet, et al.
Journal of Research on Adolescence : the Official Journal of the Society for Research on Adolescence|March 14, 2026
Longitudinal changes in sexual identity during adolescence and their associations with sexual well-beingAlice Girouard, Alexa Martin-Storey, Jacinthe Dion, et al.
Pageof 7