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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 21, 2020
The odyssey of complex neurogenetic disorders: From undetermined to positive
Valeria Salinas, Patricia Vega, Luca Marsili, et al.
Neurology. Clinical Practice
|
June 30, 2025
Community Disadvantage Is Associated With More Severe Motor Symptoms in Parkinson Disease
Emily J Hill, Samuel Blaise Marcucci, Kelly DeLano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 9, 2020
Appropriateness, safety, and effectiveness of "drip and ship" teleconsultation model in Southeastern Tuscany: a feasibility study
Simone Gallerini, Luca Marsili, Vincenzo Groccia, et al.
Research Square
|
October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European population
Lara M Lange, Kristin Levine, Susan H Fox, et al.
NPJ Parkinson'S Disease
|
March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European population
Lara M Lange, Kristin Levine, Susan H Fox, et al.
Frontiers in Aging Neuroscience
|
November 2, 2020
Phenotype-Agnostic Molecular Subtyping of Neurodegenerative Disorders: The Cincinnati Cohort Biomarker Program (CCBP)
Andrea Sturchio, Luca Marsili, Joaquin A Vizcarra, et al.
Archives of Neurology
|
February 16, 2011
Excessive daytime sleepiness in multiple system atrophy (SLEEMSA study)
Claudia Moreno-López, Joan Santamaría, Manuel Salamero, et al.
Neurology
|
February 13, 2019
Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseases
Alberto J Espay, Joaquin A Vizcarra, Luca Marsili, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 23, 2019
The Parkinson's disease e-diary: Developing a clinical and research tool for the digital age
Joaquin A Vizcarra, Álvaro Sánchez-Ferro, Walter Maetzler, et al.
American Journal of Human Genetics
|
June 10, 2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias
Paulina Cunha, Emilien Petit, Marie Coutelier, et al.
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Showing results (111-120 of 120) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 120 results.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
October 21, 2020
The odyssey of complex neurogenetic disorders: From undetermined to positive
Valeria Salinas, Patricia Vega, Luca Marsili, et al.
Neurology. Clinical Practice
|
June 30, 2025
Community Disadvantage Is Associated With More Severe Motor Symptoms in Parkinson Disease
Emily J Hill, Samuel Blaise Marcucci, Kelly DeLano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 9, 2020
Appropriateness, safety, and effectiveness of "drip and ship" teleconsultation model in Southeastern Tuscany: a feasibility study
Simone Gallerini, Luca Marsili, Vincenzo Groccia, et al.
Research Square
|
October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European population
Lara M Lange, Kristin Levine, Susan H Fox, et al.
NPJ Parkinson'S Disease
|
March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European population
Lara M Lange, Kristin Levine, Susan H Fox, et al.
Frontiers in Aging Neuroscience
|
November 2, 2020
Phenotype-Agnostic Molecular Subtyping of Neurodegenerative Disorders: The Cincinnati Cohort Biomarker Program (CCBP)
Andrea Sturchio, Luca Marsili, Joaquin A Vizcarra, et al.
Archives of Neurology
|
February 16, 2011
Excessive daytime sleepiness in multiple system atrophy (SLEEMSA study)
Claudia Moreno-López, Joan Santamaría, Manuel Salamero, et al.
Neurology
|
February 13, 2019
Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseases
Alberto J Espay, Joaquin A Vizcarra, Luca Marsili, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 23, 2019
The Parkinson's disease e-diary: Developing a clinical and research tool for the digital age
Joaquin A Vizcarra, Álvaro Sánchez-Ferro, Walter Maetzler, et al.
American Journal of Human Genetics
|
June 10, 2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias
Paulina Cunha, Emilien Petit, Marie Coutelier, et al.
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of 12