Diagnostic criteria for Parkinson disease

DJ Gelb, E Oliver, S Gilman - Archives of neurology, 1999 - jamanetwork.com
The clinical diagnosis of Parkinson disease (PD) is based on the identification of some
combination of the cardinal motor signs of bradykinesia, rigidity, tremor, and postural instability, …

Second consensus statement on the diagnosis of multiple system atrophy

S Gilman, GK Wenning, PA Low, DJ Brooks… - Neurology, 2008 - AAN Enterprises
Background: A consensus conference on multiple system atrophy (MSA) in 1998 established
criteria for diagnosis that have been accepted widely. Since then, clinical, laboratory, …

Consensus statement on the diagnosis of multiple system atrophy

S Gilman, P Low, N Quinn, A Albanese… - Clinical autonomic …, 1998 - Springer
We report the results of a consensus conference on the diagnosis of multiple system
atrophy (MSA). We describe the clinical features of the disease, which include four domains: …

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

…, DH Geschwind, B Ghetti, JR Gilbert, S Gilman… - Nature …, 2011 - nature.com
The Alzheimer Disease Genetics Consortium (ADGC) performed a genome-wide association
study of late-onset Alzheimer disease using a three-stage design consisting of a discovery …

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference

…, MZ Jones, CJ D'Amato, S Gilman… - Annals of …, 1997 - Wiley Online Library
We held an international consensus conference on frontotemporal dementia, behavioral
disturbances, and parkinsonism linked to chromosome 17 to determine whether these are …

Development and validation of the unified multiple system atrophy rating scale (UMSARS)

…, T Scaravilli, M Bozi, C Colosimo, S Gilman… - Movement …, 2004 - Wiley Online Library
We aimed to develop and validate a novel rating scale for multiple system atrophy (Unified
Multiple System Atrophy Rating Scale ‐ UMSARS). The scale comprises the following …

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

…, J Grafman, J Hodges, MG Spillantini, S Gilman… - Nature …, 2010 - nature.com
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile
dementia. The predominant neuropathology is FTLD with TAR DNA-binding protein (TDP-43) …

Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes

…, DH Geschwind, B Ghetti, S Gilman… - Archives of …, 2010 - jamanetwork.com
Objectives: To determine whether genotypes at CLU, PICALM, and CR1 confer risk for
Alzheimer disease (AD) and whether risk for AD associated with these genes is influenced by …

Presynaptic monoaminergic vesicles in Parkinson's disease and normal aging

…, TM Vander Borght, RL Albin, S Gilman… - Annals of Neurology …, 1996 - Wiley Online Library
We present development and human application of a method for determining the regional
cerebral density of the type 2 vesicular monoamine transporter (VMAT2) using positron …

Natural history of multiple system atrophy in the USA: a prospective cohort study

…, MB Stern, P Novak, CM Tanner, S Gilman… - The Lancet …, 2015 - thelancet.com
Background Multiple system atrophy is a rare, fatal neurodegenerative disorder with symptoms
of autonomic failure plus parkinsonism, cerebellar ataxia, or both. We report results of the …