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Andrew Singleton

Showing results (91-100 of 286) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2004
Exercise-induced dystonia as a preceding symptom of familial Parkinson's diseaseMichiko K Bruno, Bernard Ravina, Gaetan Garraux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 9, 2008
Novel progranulin mutation: screening for PGRN mutations in a Portuguese series of FTD/CBS casesRita Joao Guerreiro, Isabel Santana, Jose Miguel Bras, et al.
BMC Neurology|July 11, 2006
Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohortRita J Guerreiro, Jose M Bras, Isabel Santana, et al.
Human Molecular Genetics|September 13, 2015
A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's diseaseCelia Kun-Rodrigues, Christos Ganos, Rita Guerreiro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 3, 2002
Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and CaucasiansS H Subramony, Dena Hernandez, Amanda Adam, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2005
Taiwanese cases of SCA2 are derived from a single founderParastoo Momeni, Chin-Song Lu, Yah-Huei Wu Chou, et al.
Annals of Medicine|April 3, 2008
Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy studyMaarit Tanskanen, Terhi Peuralinna, Tuomo Polvikoski, et al.
Scientific Reports|March 19, 2021
Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of ApuliaCeleste Sassi, Rosa Capozzo, Monia Hammer, et al.
Annals of Neurology|July 29, 2008
Neurofibrillary tau pathology modulated by genetic variation of alpha-synucleinTerhi Peuralinna, Minna Oinas, Tuomo Polvikoski, et al.
The Journal of Trauma and Acute Care Surgery|November 6, 2019
Ultrasonographic inferior vena cava diameter response to trauma resuscitation after 1 hour predicts 24-hour fluid requirementJay Joseph Doucet, Paula Ferrada, Sarah Murthi, et al.
Pageof 29

Showing results (91-100 of 286) with videos related to

Sort By:
Pageof 29
Movement Disorders : Official Journal of the Movement Disorder Society|February 24, 2004
Exercise-induced dystonia as a preceding symptom of familial Parkinson's diseaseMichiko K Bruno, Bernard Ravina, Gaetan Garraux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 9, 2008
Novel progranulin mutation: screening for PGRN mutations in a Portuguese series of FTD/CBS casesRita Joao Guerreiro, Isabel Santana, Jose Miguel Bras, et al.
BMC Neurology|July 11, 2006
Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohortRita J Guerreiro, Jose M Bras, Isabel Santana, et al.
Human Molecular Genetics|September 13, 2015
A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's diseaseCelia Kun-Rodrigues, Christos Ganos, Rita Guerreiro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 3, 2002
Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and CaucasiansS H Subramony, Dena Hernandez, Amanda Adam, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2005
Taiwanese cases of SCA2 are derived from a single founderParastoo Momeni, Chin-Song Lu, Yah-Huei Wu Chou, et al.
Annals of Medicine|April 3, 2008
Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy studyMaarit Tanskanen, Terhi Peuralinna, Tuomo Polvikoski, et al.
Scientific Reports|March 19, 2021
Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of ApuliaCeleste Sassi, Rosa Capozzo, Monia Hammer, et al.
Annals of Neurology|July 29, 2008
Neurofibrillary tau pathology modulated by genetic variation of alpha-synucleinTerhi Peuralinna, Minna Oinas, Tuomo Polvikoski, et al.
The Journal of Trauma and Acute Care Surgery|November 6, 2019
Ultrasonographic inferior vena cava diameter response to trauma resuscitation after 1 hour predicts 24-hour fluid requirementJay Joseph Doucet, Paula Ferrada, Sarah Murthi, et al.
Pageof 29