A controlled clinical trial of baclofen as protective therapy in early Huntington's disease

scientific article published on March 1989

A controlled clinical trial of baclofen as protective therapy in early Huntington's disease is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/ANA.410250308
P698PubMed publication ID2524992

P2093author name stringMiller C
Behr J
Goldblatt D
Kennedy J
Shoulson I
Rubin A
Bamford K
Caine E
Oakes D
Odoroff C
P2860cites workNon-cholinergic synaptic excitation in neostriatum: pharmacological evidence for mediation by a glutamate-like transmitterQ35887348
Two types of gamma-aminobutyric acid receptor on embryonic sensory neuronesQ39931499
Huntington's disease in Venezuela: neurologic features and functional declineQ45297315
Normal caudate glucose metabolism in persons at risk for Huntington's diseaseQ45298212
Huntington disease: functional capacities in patients treated with neuroleptic and antidepressant drugsQ45303724
Multiple sclerosis in Iceland: 1. Evidence of a postwar epidemicQ50590075
P433issue3
P921main subjectHuntington's diseaseQ190564
P304page(s)252-259
P577publication date1989-03-01
P1433published inAnnals of NeurologyQ564414
P1476titleA controlled clinical trial of baclofen as protective therapy in early Huntington's disease
P478volume25

Reverse relations

cites work (P2860)
Q35753388A review of the treatment options for Huntington's disease
Q38624994Advancing pharmacotherapy for treating Huntington's disease: a review of the existing literature
Q30660685An overview of psychiatric symptoms in Huntington's disease
Q38248687Animal models of Huntington's disease for translation to the clinic: best practices
Q45290173Antidopaminergic Medication is Associated with More Rapidly Progressive Huntington's Disease
Q45295617Differential responses of extracellular GABA to intrastriatal perfusions of 3-nitropropionic acid and quinolinic acid in the rat
Q38792714Discovery of Therapeutic Approaches for Polyglutamine Diseases: A Summary of Recent Efforts
Q37488273Emerging drug therapies in Huntington's disease
Q41628677Huntington Disease and the Related Disorder, Dentatorubral-Pallidoluysian Atrophy (DRPLA)
Q34247413Huntington's Disease: Advocacy Driving Science
Q33921449Huntington's disease: pathogenesis, diagnosis and treatment
Q40612866Huntington's disease: update and review of neuropsychiatric aspects
Q45305483Motor, cognitive, and functional declines contribute to a single progressive factor in early HD.
Q38163877Neuroprotective effects of psychotropic drugs in Huntington's disease
Q41258822Pharmacological options for the management of dyskinesias
Q45297193Prospectives for cell and gene therapy in Huntington's disease
Q45288751Psychopathological changes preceding motor symptoms in Huntington's disease: a report on four cases
Q45300446Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease
Q58574520Rating Scales and Performance-based Measures for Assessment of Functional Ability in Huntington's Disease: Critique and Recommendations
Q92978549Resting-state connectivity stratifies premanifest Huntington's disease by longitudinal cognitive decline rate
Q37131233Symptomatic treatment of Huntington disease
Q35597607The Current Status of Neural Grafting in the Treatment of Huntington's Disease. A Review
Q36684263The corticostriatal pathway in Huntington's disease
Q38202178The most appropriate primary outcomes to design clinical trials on Huntington's disease: meta-analyses of cohort studies and randomized placebo-controlled trials
Q33790829Therapeutic Strategies in Huntington's Disease
Q24239973Therapeutic interventions for disease progression in Huntington's disease
Q34205521Therapeutic opportunities in polyglutamine disease
Q36277195Therapeutics development for triplet repeat expansion diseases
Q53716390Therapy development in Huntington disease: From current strategies to emerging opportunities.
Q35479486Topography of cerebral atrophy in early Huntington's disease: a voxel based morphometric MRI study.
Q33596210Trinucleotide repeat length and progression of illness in Huntington's disease

Search more.