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S Lincoln

Showing results (31-40 of 60) with videos related to

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Neurology|September 15, 2005
LRRK2 mutations in Parkinson diseaseM Farrer, J Stone, I F Mata, et al.
American Journal of Clinical Oncology|February 1, 1997
A phase II trial of edatrexate in previously treated squamous cell cervical cancer: a Gynecologic Oncology Group studyE R Broun, K A Iseminger, P G Rose, et al.
Journal of Medical Genetics|February 27, 2004
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein functionP J Lockhart, S Lincoln, M Hulihan, et al.
Neuroreport|April 15, 1999
Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's diseaseS Lincoln, J Vaughan, N Wood, et al.
Neurology|September 18, 2007
alpha-Synuclein and Parkinson disease susceptibilityS Winkler, J Hagenah, S Lincoln, et al.
Journal of Rehabilitation and Assistive Technologies Engineering|June 13, 2019
Direct measurement of plantarflexion resistive moments and angular positions of an articulated ankle-foot orthosis while walking in individuals post stroke: A preliminary studyToshiki Kobayashi, Michael S Orendurff, Madeline L Singer, et al.
Gynecologic Oncology|September 1, 1990
Treatment of 29 patients with bulky squamous cell carcinoma of the cervix with simultaneous cisplatin, 5-fluorouracil, and split-course hyperfractionated radiation therapyD Heaton, E Yordan, S Reddy, et al.
American Journal of Medical Genetics|May 2, 1997
Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysisS Rajangam, R C Michaelis, G V Velagaleti, et al.
The Annals of Thoracic Surgery|September 1, 1984
Management of penetrating cardiac injuries: the role of emergency room thoracotomyS Tavares, J R Hankins, A L Moulton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Linkage exclusion in French families with probable Parkinson' s diseaseM Farrer, T Destée, E Becquet, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Neurology|September 15, 2005
LRRK2 mutations in Parkinson diseaseM Farrer, J Stone, I F Mata, et al.
American Journal of Clinical Oncology|February 1, 1997
A phase II trial of edatrexate in previously treated squamous cell cervical cancer: a Gynecologic Oncology Group studyE R Broun, K A Iseminger, P G Rose, et al.
Journal of Medical Genetics|February 27, 2004
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein functionP J Lockhart, S Lincoln, M Hulihan, et al.
Neuroreport|April 15, 1999
Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's diseaseS Lincoln, J Vaughan, N Wood, et al.
Neurology|September 18, 2007
alpha-Synuclein and Parkinson disease susceptibilityS Winkler, J Hagenah, S Lincoln, et al.
Journal of Rehabilitation and Assistive Technologies Engineering|June 13, 2019
Direct measurement of plantarflexion resistive moments and angular positions of an articulated ankle-foot orthosis while walking in individuals post stroke: A preliminary studyToshiki Kobayashi, Michael S Orendurff, Madeline L Singer, et al.
Gynecologic Oncology|September 1, 1990
Treatment of 29 patients with bulky squamous cell carcinoma of the cervix with simultaneous cisplatin, 5-fluorouracil, and split-course hyperfractionated radiation therapyD Heaton, E Yordan, S Reddy, et al.
American Journal of Medical Genetics|May 2, 1997
Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysisS Rajangam, R C Michaelis, G V Velagaleti, et al.
The Annals of Thoracic Surgery|September 1, 1984
Management of penetrating cardiac injuries: the role of emergency room thoracotomyS Tavares, J R Hankins, A L Moulton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Linkage exclusion in French families with probable Parkinson' s diseaseM Farrer, T Destée, E Becquet, et al.
Pageof 6