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Mathilde Renaud

Showing results (1-10 of 79) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|March 22, 2021
Reply to: "Autosomal-Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common Biomarker"Mathilde Renaud, Christine Tranchant, Michel Koenig, et al.
Annales D'Endocrinologie|September 22, 2024
Recurrent primary hyperparathyroidism: A well-hidden genetic predispositionGabriel Berkebile, Jérome Chatelin, Mathilde Renaud, et al.
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.
BMJ Case Reports|September 14, 2017
Dilation of epidural space and posterior soft tissue veins in Hirayama diseaseJean-Baptiste Chanson, Mathilde Renaud, Andoni Echaniz-Laguna, 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.
Pageof 8

Showing results (1-10 of 79) with videos related to

Sort By:
Pageof 8
Movement Disorders : Official Journal of the Movement Disorder Society|March 22, 2021
Reply to: "Autosomal-Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common Biomarker"Mathilde Renaud, Christine Tranchant, Michel Koenig, et al.
Annales D'Endocrinologie|September 22, 2024
Recurrent primary hyperparathyroidism: A well-hidden genetic predispositionGabriel Berkebile, Jérome Chatelin, Mathilde Renaud, et al.
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.
BMJ Case Reports|September 14, 2017
Dilation of epidural space and posterior soft tissue veins in Hirayama diseaseJean-Baptiste Chanson, Mathilde Renaud, Andoni Echaniz-Laguna, 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.
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