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The Journal of Biological Chemistry
|
November 23, 2000
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V
F Tagliavini, P M Lievens, C Tranchant, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
May 26, 2023
Royal jelly mediates fibrotic signaling, collagen cross-linking and cell proliferation in cardiac fibroblasts
Doa'a G F Al-U'datt, Muhammad H Alu'datt, Carole C Tranchant, et al.
Journal of Medical Genetics
|
April 10, 2009
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease
S Lesage, C Condroyer, A Lannuzel, et al.
Revue Neurologique
|
September 21, 2023
French validation of the Quality of life in Essential Tremor Questionnaire (QUEST) and the Essential Tremor Embarrassment Assessment (ETEA)
A Marques, I Rieu, B Pereira, et al.
NPJ Parkinson'S Disease
|
December 15, 2020
A randomized controlled double-blind study of rotigotine on neuropsychiatric symptoms in de novo PD
A Castrioto, S Thobois, M Anheim, et al.
BMJ Open
|
April 1, 2022
Protocol for SYNchronising Exercises, Remedies in GaIt and Cognition at Home (SYNERGIC@Home): feasibility of a home-based double-blind randomised controlled trial to improve gait and cognition in individuals at risk for dementia
Chris McGibbon, Pam Jarrett, Grant Handrigan, et al.
Revue Neurologique
|
September 27, 2021
Validation of a non-motor fluctuations questionnaire in Parkinson's disease
F Faggianelli, A Loundou, K Baumstarck, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 16, 2015
New insights into orthostatic hypotension in multiple system atrophy: a European multicentre cohort study
A Pavy-Le Traon, A Piedvache, S Perez-Lloret, et al.
Journal of Medical Genetics
|
October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes
S Tezenas du Montcel, F Clot, M Vidailhet, et al.
Revue Neurologique
|
April 22, 2014
[Cerebrotendinous xanthomatosis: a multicentric retrospective study of 15 adults, clinical and paraclinical typical and atypical aspects]
C Lionnet, C Carra, X Ayrignac, et al.
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of 20
Search research articles
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Showing results (181-190 of 197) with videos related to
Sort By:
Page
of 20
The Journal of Biological Chemistry
|
November 23, 2000
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V
F Tagliavini, P M Lievens, C Tranchant, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
May 26, 2023
Royal jelly mediates fibrotic signaling, collagen cross-linking and cell proliferation in cardiac fibroblasts
Doa'a G F Al-U'datt, Muhammad H Alu'datt, Carole C Tranchant, et al.
Journal of Medical Genetics
|
April 10, 2009
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease
S Lesage, C Condroyer, A Lannuzel, et al.
Revue Neurologique
|
September 21, 2023
French validation of the Quality of life in Essential Tremor Questionnaire (QUEST) and the Essential Tremor Embarrassment Assessment (ETEA)
A Marques, I Rieu, B Pereira, et al.
NPJ Parkinson'S Disease
|
December 15, 2020
A randomized controlled double-blind study of rotigotine on neuropsychiatric symptoms in de novo PD
A Castrioto, S Thobois, M Anheim, et al.
BMJ Open
|
April 1, 2022
Protocol for SYNchronising Exercises, Remedies in GaIt and Cognition at Home (SYNERGIC@Home): feasibility of a home-based double-blind randomised controlled trial to improve gait and cognition in individuals at risk for dementia
Chris McGibbon, Pam Jarrett, Grant Handrigan, et al.
Revue Neurologique
|
September 27, 2021
Validation of a non-motor fluctuations questionnaire in Parkinson's disease
F Faggianelli, A Loundou, K Baumstarck, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 16, 2015
New insights into orthostatic hypotension in multiple system atrophy: a European multicentre cohort study
A Pavy-Le Traon, A Piedvache, S Perez-Lloret, et al.
Journal of Medical Genetics
|
October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes
S Tezenas du Montcel, F Clot, M Vidailhet, et al.
Revue Neurologique
|
April 22, 2014
[Cerebrotendinous xanthomatosis: a multicentric retrospective study of 15 adults, clinical and paraclinical typical and atypical aspects]
C Lionnet, C Carra, X Ayrignac, et al.
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of 20