Results 231 to 240 of about 4,891,805 (263)
Correction: F2,6BP restores mitochondrial genome integrity in Huntington's disease. [PDF]
J Biol ChemChakraborty A +13 more
europepmc +1 more source
Huntington's Disease-Like 2 in a European Caucasian Patient. [PDF]
Mov Disord Clin PractRodrigues CC +5 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
BMJ, 2010
#### Summary points Huntington’s disease is a devastating inherited neurodegenerative disease characterised by progressive motor, cognitive, and psychiatric symptoms. Patients may present with any of these symptoms, and familiarity with the phenotype is therefore important.
Marianne J U, Novak, Sarah J, Tabrizi
+9 more sources
#### Summary points Huntington’s disease is a devastating inherited neurodegenerative disease characterised by progressive motor, cognitive, and psychiatric symptoms. Patients may present with any of these symptoms, and familiarity with the phenotype is therefore important.
Marianne J U, Novak, Sarah J, Tabrizi
+9 more sources
Seminars in Cell Biology, 1995
Early in 1993, an unstable, expanded trinucleotide repeat in a novel gene of unknown function was identified on HD chromosomes. This discovery unleased a flurry of experimentation that has established the expanded CAG repeat the almost universal cause of the characteristic neurologic symptoms and pathology of this neurodegenerative disorder of midlife ...
J F, Gusella, M E, MacDonald
openaire +2 more sources
Early in 1993, an unstable, expanded trinucleotide repeat in a novel gene of unknown function was identified on HD chromosomes. This discovery unleased a flurry of experimentation that has established the expanded CAG repeat the almost universal cause of the characteristic neurologic symptoms and pathology of this neurodegenerative disorder of midlife ...
J F, Gusella, M E, MacDonald
openaire +2 more sources
Science of Aging Knowledge Environment, 2003
In this case study, we describe the symptoms, neurological exam, neuropsychological test results, and brain pathology of a man who died with Huntington's disease (HD). HD is a rare neurodegenerative disease. Like other movement disorders involving the basal ganglia, HD affects motor, cognitive, and psychiatric functioning.
Mark, Grove +3 more
openaire +4 more sources
In this case study, we describe the symptoms, neurological exam, neuropsychological test results, and brain pathology of a man who died with Huntington's disease (HD). HD is a rare neurodegenerative disease. Like other movement disorders involving the basal ganglia, HD affects motor, cognitive, and psychiatric functioning.
Mark, Grove +3 more
openaire +4 more sources
Annual Review of Medicine, 1975
Huntington'S disease (HD) is an autosomal dominant disorder associated with neuronal degeneration especially involving the basal ganglia and cerebral cortex. The cardinal signs of dementia and involuntary movements usually appear in middle life. Although the pathogenesis of this disease remains unknown, its course progres sive, and the efficacy of ...
I, Shoulson, T N, Chase
openaire +2 more sources
Huntington'S disease (HD) is an autosomal dominant disorder associated with neuronal degeneration especially involving the basal ganglia and cerebral cortex. The cardinal signs of dementia and involuntary movements usually appear in middle life. Although the pathogenesis of this disease remains unknown, its course progres sive, and the efficacy of ...
I, Shoulson, T N, Chase
openaire +2 more sources