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F Bally

Showing results (21-30 of 62) with videos related to

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Journal of Clinical Microbiology|February 1, 1993
Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysisA Telenti, F Marchesi, M Balz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 20, 2018
Systematic review of movement disorders and oculomotor abnormalities in Whipple's diseaseJulien F Bally, Aurélie Méneret, Emmanuel Roze, et al.
Revue Medicale Suisse|April 25, 2025
[Neurosurgical therapies for movement disorders in 2025]Camille Varescon, Eduardo Martin-Moraud, Laura Cif, et al.
Clinical Parkinsonism & Related Disorders|March 29, 2022
Recognizing myorhythmia 4 months after stroke - A teaching videoSebastian Finkener, Tobias Piroth, Magdalena Högg, et al.
Ageing Research Reviews|November 30, 2023
Exercise and gait/movement analyses in treatment and diagnosis of Parkinson's DiseaseJohannes Burtscher, Eduardo Martin Moraud, Davide Malatesta, et al.
Revue Medicale Suisse|April 25, 2025
[Emerging disease-modifying therapies for Parkinson's disease]Anne-Laure Mahul-Mellier, Cécile Hubsch, Mayté Castro, et al.
AIDS (London, England)|January 6, 1999
Changes in renal function associated with indinavirK Boubaker, P Sudre, F Bally, et al.
Neurobiology of Aging|January 22, 2022
Genomic study of a large family with complex neurological phenotype including hearing loss, imbalance and action tremorJulien F Bally, Ming Zhang, Emily Dwosh, et al.
Parkinsonism & Related Disorders|February 5, 2020
Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?Julien F Bally, David P Breen, Susen Schaake, et al.
Parkinsonism & Related Disorders|April 20, 2020
Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency? Response from the authorsAnthony E Lang, Julien F Bally, David P Breen, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
Journal of Clinical Microbiology|February 1, 1993
Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysisA Telenti, F Marchesi, M Balz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 20, 2018
Systematic review of movement disorders and oculomotor abnormalities in Whipple's diseaseJulien F Bally, Aurélie Méneret, Emmanuel Roze, et al.
Revue Medicale Suisse|April 25, 2025
[Neurosurgical therapies for movement disorders in 2025]Camille Varescon, Eduardo Martin-Moraud, Laura Cif, et al.
Clinical Parkinsonism & Related Disorders|March 29, 2022
Recognizing myorhythmia 4 months after stroke - A teaching videoSebastian Finkener, Tobias Piroth, Magdalena Högg, et al.
Ageing Research Reviews|November 30, 2023
Exercise and gait/movement analyses in treatment and diagnosis of Parkinson's DiseaseJohannes Burtscher, Eduardo Martin Moraud, Davide Malatesta, et al.
Revue Medicale Suisse|April 25, 2025
[Emerging disease-modifying therapies for Parkinson's disease]Anne-Laure Mahul-Mellier, Cécile Hubsch, Mayté Castro, et al.
AIDS (London, England)|January 6, 1999
Changes in renal function associated with indinavirK Boubaker, P Sudre, F Bally, et al.
Neurobiology of Aging|January 22, 2022
Genomic study of a large family with complex neurological phenotype including hearing loss, imbalance and action tremorJulien F Bally, Ming Zhang, Emily Dwosh, et al.
Parkinsonism & Related Disorders|February 5, 2020
Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?Julien F Bally, David P Breen, Susen Schaake, et al.
Parkinsonism & Related Disorders|April 20, 2020
Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency? Response from the authorsAnthony E Lang, Julien F Bally, David P Breen, et al.
Pageof 7