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Viorica Chelban

Showing results (1-10 of 47) with videos related to

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Handbook of Clinical Neurology|September 25, 2024
White matter disorders with cerebral calcification in adulthoodViorica Chelban, Henry Houlden
Movement Disorders : Official Journal of the Movement Disorder Society|March 7, 2018
Autonomic dysfunction in genetic forms of synucleinopathiesViorica Chelban, Ekawat Vichayanrat, Lucia Schottlaende, et al.
Journal of Neurology|November 22, 2018
An update on advances in magnetic resonance imaging of multiple system atrophyViorica Chelban, Martina Bocchetta, Sara Hassanein, et al.
Annals of Clinical and Translational Neurology|February 23, 2018
<i>GLS</i> loss of function causes autosomal recessive spastic ataxia and optic atrophyDavid S Lynch, Viorica Chelban, Jana Vandrovcova, et al.
Practical Neurology|March 17, 2023
Multiple system atrophyYee Yen Goh, Emma Saunders, Samantha Pavey, et al.
Journal of Neurology|May 22, 2020
An update on MSA: premotor and non-motor features open a window of opportunities for early diagnosis and interventionViorica Chelban, Daniela Catereniuc, Daniela Aftene, et al.
Journal of Neurology|August 22, 2016
Severe axonal neuropathy is a late manifestation of SPG11Andreea Manole, Viorica Chelban, Nourelhoda A Haridy, et al.
Movement Disorders Clinical Practice|August 27, 2024
Clinical Practices and Opinions toward Gastrostomy Use in Patients with Atypical Parkinsonian Syndromes: A National Survey in the UKChristopher Kobylecki, Yee Yen Goh, Rahema Mohammad, et al.
Neurobiology of Aging|October 30, 2016
Analysis of the prion protein gene in multiple system atrophyViorica Chelban, Andreea Manole, Lasse Pihlstrøm, et al.
Journal of Neurology|May 24, 2020
A novel frameshift deletion in autosomal recessive SBF1-related syndromic neuropathy with necklace fibresQiang Gang, Conceição Bettencourt, Janice Holton, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Handbook of Clinical Neurology|September 25, 2024
White matter disorders with cerebral calcification in adulthoodViorica Chelban, Henry Houlden
Movement Disorders : Official Journal of the Movement Disorder Society|March 7, 2018
Autonomic dysfunction in genetic forms of synucleinopathiesViorica Chelban, Ekawat Vichayanrat, Lucia Schottlaende, et al.
Journal of Neurology|November 22, 2018
An update on advances in magnetic resonance imaging of multiple system atrophyViorica Chelban, Martina Bocchetta, Sara Hassanein, et al.
Annals of Clinical and Translational Neurology|February 23, 2018
<i>GLS</i> loss of function causes autosomal recessive spastic ataxia and optic atrophyDavid S Lynch, Viorica Chelban, Jana Vandrovcova, et al.
Practical Neurology|March 17, 2023
Multiple system atrophyYee Yen Goh, Emma Saunders, Samantha Pavey, et al.
Journal of Neurology|May 22, 2020
An update on MSA: premotor and non-motor features open a window of opportunities for early diagnosis and interventionViorica Chelban, Daniela Catereniuc, Daniela Aftene, et al.
Journal of Neurology|August 22, 2016
Severe axonal neuropathy is a late manifestation of SPG11Andreea Manole, Viorica Chelban, Nourelhoda A Haridy, et al.
Movement Disorders Clinical Practice|August 27, 2024
Clinical Practices and Opinions toward Gastrostomy Use in Patients with Atypical Parkinsonian Syndromes: A National Survey in the UKChristopher Kobylecki, Yee Yen Goh, Rahema Mohammad, et al.
Neurobiology of Aging|October 30, 2016
Analysis of the prion protein gene in multiple system atrophyViorica Chelban, Andreea Manole, Lasse Pihlstrøm, et al.
Journal of Neurology|May 24, 2020
A novel frameshift deletion in autosomal recessive SBF1-related syndromic neuropathy with necklace fibresQiang Gang, Conceição Bettencourt, Janice Holton, et al.
Pageof 5