Fullerton / Neuroreport / Cleveland / Bethesda / Honolulu / Santa Cruz / Yi Yang / Coralville / Valencia / La Jolla / Atlanta / Cologne / /
Company
GraphPad Software Inc / Qiagen / Neurology Research Group / David C. Asselin MD Memorial Fund / Marian Falk Medical Research Trust / Beckman Coulter / IDT / Case / /
Country
Germany / /
Currency
ANG / / /
Facility
Northwestern University / Institute of Human Genetics / /
IndustryTerm
crucial phosphorylation site / Internet server / web-based tool / autophagy machinery / blood using standard protocols / http /
MedicalCondition
Motor Neuron Diseases / dementia / neurological disorders / Dysfunction / ALS / amyotrophic lateral sclerosis / very specific disease / memory loss / Paget disease / Pick disease / Patients With Amyotrophic Lateral Sclerosis / parkinsonism / Parkinson disease / human tauopathies / inclusion body myopathy / Paget’s disease / diseases / Valosin-containing protein disease / Optic Atrophy / sporadic and familial amyotrophic lateral sclerosis / Patients With Sporadic Amyotrophic Lateral Sclerosis / Neuromuscular Diseases / fatal paralytic disorder / sporadic and non-SOD1 familial amyotrophic lateral sclerosis / MS / common diseases / motor neuron disease / neurodegenerative disorders / frontotemporal lobar degeneration / sporadic disease / ALS/dementia / spinal muscular atrophy / disease / apparently sporadic disease / Lateral Sclerosis / tumor necrosis / protein aggregation diseases / allelic disorders / familial amyotrophic lateral sclerosis / neurological diseases / Alzheimer disease / fronto-temporal dementia / Patients With Familial Amyotrophic Lateral Sclerosis / familial and sporadic amyotrophic lateral sclerosis / syndrome / /
MedicalTreatment
AID / /
OperatingSystem
XP / Microsoft Windows / /
Organization
American Academy of Neurology / Genome-wide association / World Federation of Neurology Research Group / Center for Biomolecular Science & Engineering / Florence C. Wenske Foundation / Feinberg School of Medicine / FALS SALS / Institute of Human Genetics / Vena E. Schaff ALS Research Fund / Ralph / Les Turner ALS Foundation / Division of Neuromuscular Medicine / Department of Cell and Molecular Biology / Northwestern University / Chicago / Centers for Disease Control and Prevention / revised El Escorial World Federation / National Center for Biotechnology Information / Feinberg School of Medicine / and Interdepartmental Neuroscience Program / American Medical Association / El Escorial World Federation of Neurology / Ruth Davee Department of Neurology and Clinical Neurological Sciences / /
Person
Senda Ajroud-Driss / Ann Neurol / Robert L. Sufit / Jian Guo Zheng / Sandra Donkervoort / Erdong Liu / Arch Neurol / EADPRLI EADPRLI EADPRLI EADPRLI EADPRLI / Han-Xiang Deng / Wenjie Chen / Ruth Davee / Yong Shi / Hasan Arrat / Arch Ital Biol / Shin J. Molecular / Ken Davee / T. Siddique / Sclerosis Faisal Fecto / Lamar Seibenhener / Messrs Vemula / Teepu Siddique / Drs Fecto / Scott L. Heller / Jianhua Yan / / /
Position
Bone Miner / Author / Singer / Fisher / /
ProvinceOrState
Ohio / Hawaii / Mississippi / California / Georgia / Maryland / Illinois / Iowa / /
ORIGINAL CONTRIBUTION SQSTM1 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis Faisal Fecto, MD; Jianhua Yan, MD, PhD; S. Pavan Vemula; Erdong Liu, MD; Yi Yang, MS; Wenjie Chen, MD; Jian Guo Zheng, MD; Yo