ExLibris header image
SFX Logo
Title: A prospective study of transmission by transfusion of HTLV-I and risk factors associated with seroconversion
Source:

International Journal of Cancer [0020-7136] Manns, Angela yr:1992


Collapse list of basic services Basic
Full text
Full text available via Wiley Online Library All Journals
GO
Full text available via Wiley Online Library STM 2011
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Waters, G A A. "HTLV type I/II in British Columbia Amerindians: a seroprevalence study and sequence characterization of an HTLV type IIa isolate." AIDS research and human retroviruses 16.9 (2000): 883-92. Link to SFX for this item
2. Lai, H. "Demyelination and ethnicity: experience at the University of British Columbia Multiple Sclerosis Clinic with special reference to HTLV-I-associated myelopathy in British Columbian natives." Annals of neurology 36 (1994): 22-4. Link to Full Text for this item Link to SFX for this item
3. Macmillan, C. "Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect." American journal of human genetics 66.1 (2000): 332-335. Link to Full Text for this item Link to SFX for this item
4. Petrou, R H H. "Long-term effect of prospective detection of high genetic risk on couples' reproductive life: Data for thalassaemia." Prenatal diagnosis 20.6 (2000): 469-474. Link to Full Text for this item Link to SFX for this item
5. Dupuy, F. "Anti-HIV antibodies and other serological and immunological parameters among normal Haitians in Montreal." Journal of acquired immune deficiency syndromes 3.2 (1990): 166-172. Link to SFX for this item
6. Watanabe T, T. "Current status of HTLV-1 infection." International journal of hematology 94.5 (2011): 430-434. Link to SFX for this item
7. Weiss, K M M. "James V. Neel, M.D., Ph.D. (March 22, 1915-January 31, 2000): founder effect." American journal of human genetics 66.3 (2000): 755-60. Link to Full Text for this item Link to SFX for this item
8. Kirkham, T. "Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy." Neurology 50.2 (1998): 417-422. Link to SFX for this item
9. Chagnon, P. "Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French-Canadian founder population." American journal of medical genetics 85.1 (1999): 20-30. Link to Full Text for this item Link to SFX for this item
10. Kountouras J, J. "Helicobacter pylori may hold a variable role in multiple sclerosis based on ethnicity." Medical Hypotheses 71.4: 614-5. Link to SFX for this item
11. Steele. "Effect of sibship position on reproductive behaviour of couples after the birth of a genetically handicapped child." Clinical genetics 30.4 (1986): 328-334. Link to SFX for this item
12. Smith, R J J. "Survey of attitudes of pregnant women towards Down syndrome screening." Prenatal diagnosis 20.1 (1999): 23-9. Link to Full Text for this item Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced