Epidemiologic study of hepatolenticular degeneration (Wilson's disease) in Sardinia (1902–1983)

Acta Neurologica Scandinavica

Volumn 72, Issue 1, 1985, Pages 43-55

  Giagheddu, A ^a,b   Demelia, L ^a,b   Puggioni, G ^a,b   Nurchi, A M ^a,b   Contu, L ^a,b   Pirari, G ^a,b   Deplano, A ^a,b   Rachele, M G ^a,b  

^a UNIVERSITY OF CAGLIARI   (Italy)

^b UNIVERSITY OF SASSARI   (Italy)

Author keywords

Cupric metabolism; extrapyramidal diseases; hepatoneurologic diseases; hereditary dismetabolic diseases; Wilson's disease

Indexed keywords

CENTRAL NERVOUS SYSTEM; CLINICAL ARTICLE; DIAGNOSIS; EPIDEMIOLOGY; GEOGRAPHIC DISTRIBUTION; HUMAN; PRIORITY JOURNAL; WILSON DISEASE;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CROSS-SECTIONAL STUDIES; FEMALE; HEPATOLENTICULAR DEGENERATION; HUMANS; ITALY; MALE; PEDIGREE; SEX FACTORS;

EID: 0022392888     PISSN: 00016314     EISSN: 16000404     Source Type: Journal    
DOI: 10.1111/j.1600-0404.1985.tb01546.x     Document Type: Article

References (38)

1. Zur Ätiologie und Nosologie der Pseudosclerose Westphal‐Wilson
2. Genetic and biochemical aspects of Wilson's disease
3. Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease)
4. Studies on copper metabolism in demye‐linating diseases of the central nervous system
5. The copper and iron content of brain and liver in the normal and in hepatolenticular degeneration
6. Studies on copper metabolism. XIII. Hepatolenticular degeneration
7. A clinical and biochemical study of hepatolenticular degeneration
8. Tissue copper levels in Chinese patients with Wilson's disease
9. Hepatolenticular degeneration. Clinical and biochemical study of three cases
10. Wilson's disease: new oral therapy
11. Prevention of Wilson's disease in asymptomatic patients
12. Wilson's disease. Report of ten cases
13. A genetic, biochemical and clinical study of Wilson's disease among Chinese in Taiwan
14. A genetic aspect of Wilson's disease in Japan
15. Genetic studies of Wilson's disease in Japan
16. Wilson's disease in India. I. Geographic, genetic and clinical aspects in 16 families
17. A genetic study of Wilson's disease: evidence for heterogeneity
18. Die Wilsonsche Krankheit in der Schweiz. Klinische, genetische und bio‐chemische Untersuchungen
19. Wilson's disease in Turkey, a review of 49 cases in 39 families
20. Heterogeneity of Wilson's disease in Israel
21. Untersuchungen zur Wilsonschen Erkrankung in der DDR
22. An assessment of efficiency in potential screening for Wilson's disease
23. Epidemiologic study of amyotrophic lateral sclerosis in Sardinia, Italy
24. Sulla degenerazione lenticolare progressiva (malattia di Wilson)
25. Uber die hepatolentikuläre Degeneration (Wilson‐Westphal‐Strömpell)
26. The pathogenesis and evolution of Wilson's disease
27. Clinical spectrum of Wilson's disease (hepatolenticuiar degeneration)
28. A genetical analysis of thirty families with Wilson's disease (hepatolenticular degeneration)
29. The dual role of the liver in Wilson's disease
30. Wilson's disease. The presenting symptoms
31. Genetic considerations in Wilson's disease
32. La consanguineità umana nell'isola di Sardegna dal secolo XVIII al secolo XX
33. Genetical studies of Wilson's disease. 2. Mode of inheritance and gene frequency in Japan
34. Prevention of Wilson's disease in asymptomatic patients