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Volumn 34, Issue 3, 2014, Pages 309-313
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Definite familial multiple system atrophy with unknown genetics
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Author keywords
COQ2; Glial cytoplasmic inclusion; Multiple system atrophy (MSA); SNCA; synuclein
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Indexed keywords
ALPHA SYNUCLEIN;
ADULT;
ANHIDROSIS;
ARTICLE;
ASPIRATION PNEUMONIA;
ATAXIA;
AUTOPSY;
BLADDER CATHETERIZATION;
BRADYKINESIA;
BRAIN ATROPHY;
BRAIN SPONGIOSIS;
BRAIN VENTRICLE DILATATION;
BURNING SENSATION;
CASE REPORT;
CAUDATE NUCLEUS;
CEREBELLUM ATROPHY;
COMPUTER ASSISTED TOMOGRAPHY;
CONSANGUINITY;
CONSTIPATION;
DEPIGMENTATION;
DYSARTHRIA;
ENTERIC FEEDING;
FAMILIAL DISEASE;
FEMALE;
GENE MUTATION;
GENETIC SCREENING;
GENETICS;
GLIOSIS;
HUMAN;
HUMAN TISSUE;
IMMOBILITY;
IMMUNOREACTIVITY;
LOCUS CERULEUS;
MALE;
MIDDLE AGED;
NERVE CELL;
NEUROPATHOLOGY;
NUCLEAR MAGNETIC RESONANCE IMAGING;
ORTHOSTATIC HYPOTENSION;
PARKINSONISM;
PERCUTANEOUS ENDOSCOPIC GASTROSTOMY;
PONS;
PRIORITY JOURNAL;
PROSTATE HYPERTROPHY;
PUTAMEN;
SHY DRAGER SYNDROME;
SUBSTANTIA NIGRA;
TRANSURETHRAL RESECTION;
URINE INCONTINENCE;
URINE RETENTION;
AGED;
FATALITY;
MULTIPLE SYSTEM ATROPHY;
PEDIGREE;
AGED;
FATAL OUTCOME;
HUMANS;
MALE;
MULTIPLE SYSTEM ATROPHY;
PEDIGREE;
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EID: 84901689513
PISSN: 09196544
EISSN: 14401789
Source Type: Journal
DOI: 10.1111/neup.12092 Document Type: Article |
Times cited : (27)
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References (12)
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