Ramsay Hunt Paralysis Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
A recurrent mutation in PARK2 is associated with familial lung cancer.
|
25640678 |
2015 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
Methylmercury can induce Parkinson's-like neurotoxicity similar to 1-methyl-4- phenylpyridinium: a genomic and proteomic analysis on MN9D dopaminergic neuron cells.
|
26558463 |
2015 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Therapeutic
|
disease |
CTD_human |
A recurrent mutation in PARK2 is associated with familial lung cancer.
|
25640678 |
2015 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Methylmercury can induce Parkinson's-like neurotoxicity similar to 1-methyl-4- phenylpyridinium: a genomic and proteomic analysis on MN9D dopaminergic neuron cells.
|
26558463 |
2015 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
Low doses of paraquat and polyphenols prolong life span and locomotor activity in knock-down parkin Drosophila melanogaster exposed to oxidative stress stimuli: implication in autosomal recessive juvenile parkinsonism.
|
23046578 |
2013 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Low doses of paraquat and polyphenols prolong life span and locomotor activity in knock-down parkin Drosophila melanogaster exposed to oxidative stress stimuli: implication in autosomal recessive juvenile parkinsonism.
|
23046578 |
2013 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin protects against neurotoxicity in the 6-hydroxydopamine rat model for Parkinson's disease.
|
16914382 |
2006 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin protects against neurotoxicity in the 6-hydroxydopamine rat model for Parkinson's disease.
|
16914382 |
2006 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin disease: a phenotypic study of a large case series.
|
12764051 |
2003 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin disease: a phenotypic study of a large case series.
|
12764051 |
2003 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.
|
11254447 |
2001 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.
|
11254447 |
2001 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Therapeutic
|
disease |
CTD_human |
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
|
10894217 |
2000 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
|
10894217 |
2000 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Biomarker
|
disease |
CTD_human |
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
|
10072423 |
1999 |
Ramsay Hunt Paralysis Syndrome
|
0.300 |
Therapeutic
|
disease |
CTD_human |
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
|
10072423 |
1999 |