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Posts
- Category: Articles (continued)
- Parkinson's, Huntington's disease research makes advances with stem cells: Discoveries
- PBT2 recommended for orphan designation in Europe
- Penn Biologists Identify a Key Enzyme Involved in Protecting Nerves From Degeneration
- Phosphodiesterase inhibitors: new HD drugs entering trials soon
- Planning a ‘Dancing at the Vatican’ screening to celebrate the global Huntington’s disease community’s journey
- Possible role for Huntington’s gene discovered
- Postdoctoral Fellowship, Huntington's Disease
- Potential new treatments for depression uncovered by research into Huntington's
- Potential Therapeutic Target for Huntington’s Disease
- Potential Treatment for Huntington's Disease, Found Effective, Safe in Mice, Monkeys, Enters Clinical Testing
- Potential treatment for Huntington’s disease discovered by NUIG researchers
- Prana Alzheimer's disease data features at world leading conference
- Prana Announces Successful Phase 2 Results in Huntington Disease Trial
- Prana Biotechnology Investor Presentation and Audio Recording - Phase 2 HD trial
- Prana Completes Phase 2 Huntington Disease Trial with PBT2
- Prana Completes Recruitment in Huntington Trial
- Prana drug treatment PBT2 named one of TopNeuroscience Projects to Watch
- Prana Enrolls First Patient in the “Reach2HD” Phase II Huntington Disease Trial
- Prana presents new benchmark test to assess Huntington’s Disease patients in clinical trials
- Prana Provides Huntington Disease Trial Update
- Prana receives FDA Orphan Drug Designation for PBT2 for Huntington Disease
- Prana to present at New York Academy of Science Symposium on November 29 th
- Prana Updates Progress on PBT2 Trials in Alzheimer’s and Huntington’sDiseases
- Prana's PBT2 receives FDA Orphan Drug designation for treatment of Huntington diseaseread more
- Prana’s Huntington Disease trial analysis to feature at global movement disorder conference
- Prana’s PBT2 presented at the Huntington’s Disease Society of America National Convention
- Predict the onset and course of Huntington's disease
- Premio Nobel per la Fisiologia o Medicina 2012: un approfondimento
- Pride-HD Study Enrolling Patients Globally to Further Evaluate Pridopidine for the Symptomatic Treatment of Huntington’s Disease
- PRIME designation granted by European Medicines Agency for RG6042 for treatment of Huntington’s disease
- Production of toxic protein causes common neurodegenerative disorder
- Programme Leader: Professor Giovanna Mallucci MD PhD
- Proposed drug may reverse Huntington's disease symptoms
- Protein aggregates save cells during aging
- Proteomic analysis of wild-type and mutant huntingtin associated proteins in mouse brains identifies unique interactions and involvement in protein synthesis
- PTC Therapeutics and CHDI Foundation Announce a Collaboration on a Small-Molecule Therapeutic for Huntington's Disease
- QR Pharma Begins Collaboration on Posiphen and Huntington’s disease
- Quanterix to Host Webinar on Predicting the Progression of Neurodegeneration with a Blood Test
- Quantitative connection between polyglutamine aggregation kinetics and neurodegenerative process in patients with Huntington's disease
- R6/2 Huntington's Disease Mice Develop Early and Progressive Abnormal Brain Metabolism and Seizures
- Rallentare il processo di invecchiamento combatte Alzheimer, Parkinson e Huntington
- Range of brain diseases could be treated by single drug
- Raptor Announces Clinical Results With RP103 in Huntington's Disease Phase 2/3 Trial
- Raptor Pharmaceutical Completes Enrollment in Phase 2/3 Clinical Trial of RP103 for the Potential Treatment of Huntington's Disease
- Raptor Plans to Advance RP103 in a Registration Study in Huntington's Disease Based on Favorable Treatment Effects at 36 Months in CYST-HD Trial
- Raptor Receives Orphan Drug Designation for Cysteamine Bitartrate in Huntington's Disease From the European Commission
- Rare, Orphan And Neglected Neurodegenerative Diseases - New Research Announced
- Reach2HD, a Phase II study in Huntington's disease, launched
- Reaching out to the ‘HD family’ at the World Congress on Huntington’s Disease
- Reading University team working to beat Huntingdon's disease
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