Therapeutic interventions for disease progression in Huntington's disease

scientific article

Therapeutic interventions for disease progression in Huntington's disease is …
instance of (P31):
meta-analysisQ815382
scholarly articleQ13442814

External links are
P356DOI10.1002/14651858.CD006455.PUB2
P3181OpenCitations bibliographic resource ID1484966
P932PMC publication ID7390161
P698PubMed publication ID19588392

P50authorCristina SampaioQ28359585
Tiago MestreQ28359619
Miguel M. CoelhoQ55232782
Joaquim FerreiraQ55232786
P2093author name stringMário Rosa
P2860cites workA novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.Q27860836
Assessing the quality of reports of randomized clinical trials: is blinding necessary?Q27860973
Trinucleotide repeat length and progression of illness in Huntington's diseaseQ33596210
Effect of fetal neural transplants in patients with Huntington's disease 6 years after surgery: a long-term follow-up studyQ33994217
Huntington's disease: present treatments and future therapeutic modalitiesQ34312421
Detection of Huntington's disease decades before diagnosis: the Predict-HD studyQ36941187
Influence of lamotrigine on progression of early Huntington disease: a randomized clinical trialQ39118783
Neuroprotective gene therapy for Huntington's disease, using polymer-encapsulated cells engineered to secrete human ciliary neurotrophic factor: results of a phase I study.Q40462605
A controlled trial of idebenone in Huntington's diseaseQ40929165
A controlled clinical trial of baclofen as protective therapy in early Huntington's diseaseQ41265980
MRI and neuropsychological improvement in Huntington disease following ethyl-EPA treatmentQ43940983
Minocycline for Huntington's disease: an open label studyQ44357409
Creatine therapy for Huntington's disease: clinical and MRS findings in a 1-year pilot study.Q44504149
Creatine supplementation in Huntington's disease: a placebo-controlled pilot trialQ44616594
The N-methyl-D-aspartate antagonist memantine retards progression of Huntington's disease.Q45049292
Neuroprotection in Huntington's disease: a 2-year study on minocyclineQ45108539
Creatine supplementation lowers brain glutamate levels in Huntington's diseaseQ45239341
George Huntington and hereditary choreaQ45288544
Trial of d-alpha-tocopherol in Huntington's diseaseQ45291405
Assessment of coenzyme Q10 tolerability in Huntington's diseaseQ45292398
High-dose creatine therapy for Huntington disease: a 2-year clinical and MRS study.Q45296832
Riluzole therapy in Huntington's disease (HD).Q45297539
Ethyl-EPA in Huntington disease: a double-blind, randomized, placebo-controlled trialQ45297817
CYTE-I-HD: phase I dose finding and tolerability study of cysteamine (Cystagon) in Huntington's diseaseQ45298950
Safety and tolerability assessment of intrastriatal neural allografts in five patients with Huntington's diseaseQ45299926
Porcine xenografts in Parkinson's disease and Huntington's disease patients: preliminary resultsQ45300364
Motor and cognitive improvements in patients with Huntington's disease after neural transplantationQ45301920
A randomized, placebo-controlled trial of coenzyme Q10 and remacemide in Huntington's diseaseQ45303631
Bilateral human fetal striatal transplantation in Huntington's disease.Q45305502
Riluzole in Huntington's disease: a 3-year, randomized controlled studyQ45305925
Unified Huntington's disease rating scale: Reliability and consistencyQ57422462
Vitamin E in treatment of Huntington's choreaQ66839991
P921main subjectHuntington's diseaseQ190564
P577publication date2009-07-08
P13046publication type of scholarly workreview articleQ7318358
P1433published inCochrane Database of Systematic ReviewsQ15750361
P1476titleTherapeutic interventions for disease progression in Huntington's disease

Reverse relations

cites work (P2860)
Q27335053A new drug design targeting the adenosinergic system for Huntington's disease
Q22305812Advances in the Pharmacological Management of Huntingtonʼs Disease
Q57178432Advances in the discovery of genetic risk factors for complex forms of neurodegenerative disorders: contemporary approaches, success, challenges and prospects
Q52311573Agreement between clinician-rated versus patient-reported outcomes in Huntington disease
Q35106341Automated structural imaging analysis detects premanifest Huntington's disease neurodegeneration within 1 year
Q37627670Cellular and molecular pathways triggering neurodegeneration in the spinocerebellar ataxias
Q54917713Chronic Caffeine Treatment Protects Against α-Synucleinopathy by Reestablishing Autophagy Activity in the Mouse Striatum.
Q36773397Cognitive Impairment in Huntington Disease: Diagnosis and Treatment
Q38332316Diagnosis and treatment of chorea syndromes
Q37386063Early Detection of Huntington Disease
Q37034726Huntington's Disease: The Most Curable Incurable Brain Disorder?
Q35140660Mitochondrial Medicine and the Neurodegenerative Mitochondriopathies
Q27004209Modeling Huntington's disease with induced pluripotent stem cells
Q38163877Neuroprotective effects of psychotropic drugs in Huntington's disease
Q55020670Population-specific genetic modification of Huntington's disease in Venezuela.
Q52685691Pridopidine: Overview of Pharmacology and Rationale for its Use in Huntington's Disease
Q42143817Recent advances in the management of choreas
Q30475466Sex-dependent changes in social behaviors in motor pre-symptomatic R6/1 mice
Q92583579Survival, Mortality, Causes and Places of Death in a European Huntington's Disease Prospective Cohort
Q37682680Targeting glial cells to elucidate the pathogenesis of Huntington's disease.
Q35597607The Current Status of Neural Grafting in the Treatment of Huntington's Disease. A Review
Q26764930The P42 peptide and Peptide-based therapies for Huntington's disease
Q22306292The importance of integrating basic and clinical research toward the development of new therapies for Huntington disease
Q45304275Therapies targeting DNA and RNA in Huntington's disease
Q38006434Therapy in Huntington’s Disease: Where Are We?

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