Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Frederick Wooten"'
Autor:
John C. Morgan, Lillian J. Currie, Madaline B. Harrison, James P. Bennett, Joel M. Trugman, G. Frederick Wooten
Publikováno v:
Parkinson's Disease, Vol 2014 (2014)
Parkinson’s disease (PD) is associated with increased mortality despite many advances in treatment. Following the introduction of levodopa in the late 1960’s, many studies reported improved or normalized mortality rates in PD. Despite the remarka
Externí odkaz:
https://doaj.org/article/9d74ca4ba55c49dc85998908a9c3f64b
Autor:
Matthew J. Barrett, Antonia Pusso, Christopher L. Groth, Scott A. Sperling, W. Jeffrey Elias, G. Frederick Wooten, Diane S. Huss
Publikováno v:
The Journal of Neuropsychiatry and Clinical Neurosciences. 30:160-163
Psychosis is common in Parkinson's disease (PD), especially in advanced disease, and can lead to a number of psychotic symptoms, including delusions. One uncommon delusion is Capgras syndrome (CS). The authors report on three PD patients with a histo
Autor:
Nicholas E. F. Hać, Matthew J. Barrett, Madaline B. Harrison, Guofen Yan, G. Frederick Wooten
Publikováno v:
Movement Disorders. 30:733-735
Background The aim of this study was to determine whether age of onset of Parkinson disease (PD) is associated with differences in PD risk and PD age of onset in parents and siblings. Methods Clinical and detailed family history data were available f
Autor:
Charles K Jessup, Madaline B. Harrison, Wery P. M. van den Wildenberg, Daniel O. Claassen, Scott A. Wylie, K. Richard Ridderinkhof, G. Frederick Wooten
Publikováno v:
Behavioral Neuroscience, 125(4), 492-500. American Psychological Association
Risk-taking behavior is characterized by pursuit of reward in spite of potential negative consequences. Dopamine neurotransmission along the mesocorticolimbic pathway is a potential modulator of risk behavior. In patients with Parkinson's disease (PD
Autor:
John G. Nutt, G. Frederick Wooten
Publikováno v:
New England Journal of Medicine. 353:1021-1027
A 62-year-old man presents with an intermittent tremor in his left hand and some vague discomfort in the left arm. Physical examination shows a minimal rest tremor in the left hand that disappears with use of the limb, mild rigidity at the left wrist
Publikováno v:
The Journal of Neuropsychiatry and Clinical Neurosciences. 28:e31-e32
Autor:
Madaline B. Harrison, Lillian J. Currie, G. Frederick Wooten, John C. Morgan, Joel M. Trugman, James P. Bennett
Publikováno v:
Parkinson's Disease
Parkinson's Disease, Vol 2014 (2014)
Parkinson's Disease, Vol 2014 (2014)
Parkinson’s disease (PD) is associated with increased mortality despite many advances in treatment. Following the introduction of levodopa in the late 1960’s, many studies reported improved or normalized mortality rates in PD. Despite the remarka
Publikováno v:
Annals of Neurology. 50:537-540
Sex-linked male deafness and dystonia (Mohr-Tranebjaerg syndrome) arises from mutation of the deafness/dystonia peptide (DDP) gene. We describe a novel guanine deletion at nucleotide 108 of the DDP gene in a family with Mohr-Tranebjaerg syndrome, whi
Autor:
G. Frederick Wooten, John H. Dougherty, Janice K. Parks, James P. Bennett, Russell H. Swerdlow, W. Scott Bridges, David S. Cassarino, Lillian J. Currie, W. Davis Parker, Patricia A. Trimmer, John N. Davis
Publikováno v:
Annals of Neurology. 44:873-881
Recent data suggesting complex I dysfunction in Parkinson's disease (PD) arises from mitochondrial DNA (mtDNA) mutation does not conclusively answer whether the responsible genetic lesion is inherited (primary) or somatic (secondary). To address this
Autor:
David M. Sletten, Wolfgang Singer, Brad A. Racette, Matthew B. Stern, Jayawant N. Mandrekar, C.M. Tanner, Frederick Wooten, Phillip A. Low, S.G. Reich, Thomas C. Chelimsky, Sid Gilman, Peter Novak, Joseph Jankovic, C.W. Shults, Paola Sandroni, Frederick J. Marshall
Publikováno v:
Autonomic Neuroscience. 192:126-127
Background: Multiple system atrophy (MSA) is a fatal and poorly understood rare neurodegenerative disorder. Here we describe the baseline characteristics of patients with MSA enrolled in a prospective multicenter natural history study of the NIH-spon