Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degeneration

Archives of Neurology

Volumn 59, Issue 8, 2002, Pages 1319-1326

  Zannolli, Raffaella ^a   Gilman, Sid ^c   Rossi, Simone ^a   Volpi, Nila ^b   Bernini, Andrea ^a   Galluzzi, Paolo ^a   Galimberti, Daniela ^a   Pucci, Lucia ^a   D'Ambrosio, Alfonso ^a   Morgese, Guido ^a   Giannini, Fabio ^a  

^a UNIVERSITY HOSPITAL OF SIENA   (Italy)

^b UNIVERSITY OF SIENA   (Italy)

^c UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTONOMIC NERVOUS SYSTEM FUNCTION; BRAIN ELECTROPHYSIOLOGY; CASE REPORT; CENTRAL NERVOUS SYSTEM DISEASE; CEREBELLUM ATROPHY; CEREBELLUM DEGENERATION; CLINICAL EXAMINATION; DEGENERATIVE DISEASE; DYSMETRIA; ELECTROMYOGRAPHY; ERECTILE DYSFUNCTION; EVOKED BRAIN STEM RESPONSE; EVOKED MUSCLE RESPONSE; EVOKED SOMATOSENSORY RESPONSE; EVOKED VISUAL RESPONSE; FAMILIAL DISEASE; FECES INCONTINENCE; FEMALE; HEARING TEST; HEREDITARY NEURONAL INTRANUCLEAR INCLUSION DISEASE; HUMAN; IMMUNOHISTOCHEMISTRY; INCIDENCE; MALE; MOLECULAR GENETICS; MONOZYGOTIC TWINS; NERVE CONDUCTION; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; ORTHOSTATIC HYPOTENSION; PATHOLOGICAL ANATOMY; PATHOPHYSIOLOGY; PERIPHERAL NERVOUS SYSTEM; PRIORITY JOURNAL; RECURRENT DISEASE; SKELETAL MUSCLE; SPHINCTER; URINE INCONTINENCE; VESTIBULAR TEST;

ADULT; AUTONOMIC NERVOUS SYSTEM DISEASES; BIOPSY; CELL NUCLEUS; CEREBELLAR DISEASES; CEREBELLUM; ELECTROENCEPHALOGRAPHY; FAMILY HEALTH; FEMALE; HUMANS; INCLUSION BODIES; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; NERVE DEGENERATION; NEURONS;

EID: 0036340640     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.59.8.1319     Document Type: Article

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