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British Journal of Clinical Pharmacology|October 24, 2002
Entacapone improves the availability of L-dopa in plasma by decreasing its peripheral metabolism independent of L-dopa/carbidopa doseHelena Heikkinen, Anu Varhe, Tarmo Laine, et al.
Neuroreport|April 2, 2002
Memory-based comparison process not attenuated by haloperidol: a combined MEG and EEG studyEero Pekkone, Jyrki Hirvonen, Jyrki Ahveninen, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 5, 2002
Dopamine modulates involuntary attention shifting and reorienting: an electromagnetic studySeppo Kähkönen, Jyrki Ahveninen, Eero Pekkonen, et al.
Neurobiology of Aging|April 22, 2014
Novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathologyPetra Pasanen, Liisa Myllykangas, Maija Siitonen, et al.
European Journal of Clinical Pharmacology|February 21, 2009
Comparison of pharmacokinetic profile of levodopa throughout the day between levodopa/carbidopa/entacapone and levodopa/carbidopa when administered four or five times dailyMikko Kuoppamäki, Kirsi Korpela, Reijo Marttila, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 6, 2014
Gut microbiota are related to Parkinson's disease and clinical phenotypeFilip Scheperjans, Velma Aho, Pedro A B Pereira, et al.
Human Molecular Genetics|February 4, 2017
ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegiaHelen M Cooper, Yang Yang, Emil Ylikallio, et al.
American Journal of Human Genetics|August 5, 2005
Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European originAnna H Hakonen, Silja Heiskanen, Vesa Juvonen, et al.
Neurobiology of Aging|November 14, 2016
SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish populationPetra Pasanen, Eino Palin, Risto Pohjolan-Pirhonen, et al.
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