Neuronal intranuclear inclusion disease and juvenile parkinsonism

Movement Disorders

Volumn 15, Issue 5, 2000, Pages 990-995

  Garraux, Gaetan ^a,c   Salmon, Eric ^a   Peigneux, Philippe ^a   Kreisler, Alexandre ^b   Degueldre, Christian ^a   Lemaire, Christian ^a   Destée, Alain ^b   Franck, Georges ^a  

^a UNIVERSITY OF LIÈGE   (Belgium)

^b LILLE UNIVERSITY HOSPITAL   (France)

^c UNIVERSITY OF LIÈGE   (Belgium)

Author keywords

Intranuclear inclusion; Juvenile; Levodopa; Parkinsonism

Indexed keywords

CARBIDOPA PLUS LEVODOPA; UBIQUITIN;

ADOLESCENT; ADULT; ARTICLE; ASPIRATION PNEUMONIA; AUTOPSY; CARDIOPULMONARY INSUFFICIENCY; CASE REPORT; CELL LOSS; CELL NUCLEUS INCLUSION BODY; CLINICAL EXAMINATION; CLINICAL FEATURE; DEGENERATIVE DISEASE; DIFFERENTIAL DIAGNOSIS; DISEASE SEVERITY; DRUG WITHDRAWAL; DYSKINESIA; FAMILY HISTORY; FRONTAL CORTEX; HISTOPATHOLOGY; HUMAN; JUVENILE; LOCUS CERULEUS; MALE; MOTOR DYSFUNCTION; NERVE CELL; NEURONAL INTRANUCLEAR INCLUSION DISEASE; NEUROPATHOLOGY; ONSET AGE; PARKINSONISM; PRIORITY JOURNAL; SUBSTANTIA NIGRA;

ADOLESCENT; BRAIN; CASE REPORT; DIAGNOSIS, DIFFERENTIAL; FATAL OUTCOME; HUMAN; IMMUNOHISTOCHEMISTRY; INCLUSION BODIES; MALE; NEURODEGENERATIVE DISEASES; PARKINSONIAN DISORDERS; UBIQUITINS; VIDEOTAPE RECORDING;

EID: 0033809402     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8257(200009)15:5<990::AID-MDS1035>3.0.CO;2-I     Document Type: Article

References (39)

1. Young onset Parkinson's disease
2. A comparison of clinical and pathological features of young and old-onset Parkinson's disease
3. Early onset parkinsonism and parkin gene mutations
4. Widespread intranuclear neuronal corpuscles (Marinesco bodies) associated with a familial spinal degeneration with cranial and peripheral nerve involvement
5. An unusual degenerative disorder of neurons with a novel intranuclear inclusion (neuronal intranuclear hyaline inclusion disease): A clinicopathological study of a case
6. Neuronal intranuclear hyaline inclusion disease: Report of a case and review of the literature
7. Neuronal intranuclear inclusion disease in a child: Diagnosis by rectal biopsy
8. Neuronal intranuclear hyaline inclusion disease in a nine year old
9. Virus-like filaments in juvenile parkinsonism
10. Brain neurotransmitter abnormalities in neuronal intranuclear inclusion body disorder
11. Neuronal intranuclear hyaline inclusion disease associated with premature coronary atherosclerosis
12. Juvenile parkinsonism caused by chronic meningoencephalitis: A clinicopathological study
13. Progressive atrophy of the globus pallidus
14. Pallido-pyramidal disease
15. Contribution clinique et anatomique a l'etude de la paralysie agitante juvenile primitive
16. Familial paralysis agitans juvenilis. A clinical, anatomical and genetic study
17. Familial juvenile parkinsonism: Clinical and pathologic study in a family
18. Early-onset parkinsonism with diurnal fluctuation-clinical and pathological studies
19. Familial juvenile parkinsonism
20. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
21. Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q
22. Juvenile parkinsonism-some clinical, pharmacological, and neuropathological aspects
23. Doparesponsive dystonia with depigmentation of the substantia nigra and formation of Lewy bodies
24. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease
25. One autopsy case presenting a variety of neurological disorders such as oculogyric crises and kinesia paradoxale in conjunction with numerous neuronal intranuclear eosinophilic inclusions
26. Polyglutamine-containing aggregates in neuronal intranuclear inclusion disease
27. Late-onset neuronal intranuclear hyaline inclusion disease: A case report
28. Pupillary and electroretinographic abnormalities in a family with neuronal intranuclear hyaline inclusion disease
29. L-Dopa-induced peak-dose dyskinesias in patients with Parkinson's disease: A clinical pharmacological approach
30. Neuronal intranuclear inclusion disease in identical twins
31. Neuronal intranuclear hyaline inclusion disease presenting as Friedreich's ataxia
32. Familial neuronal intranuclear inclusion disease with ubiquitin positive inclusions
33. A familial neuronal disease presenting as intestinal pseudoobstruction
34. Intranuclear inclusion neuronal disease: Study of three members of a family
35. Familial visceral neuropathy with neuronal intranuclear inclusions: Diagnosis by rectal biopsy
36. Infantile multiple system atrophy with cytoplasmic and intranuclear glioneuronal inclusions
37. Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?
38. Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion disease
39. Ubiquitin carboxyl-terminal hydrolase (PGP 9.5) is selectively present in ubiquitinated inclusion bodies characteristic of human neurodegenerative diseases