Wilsonova bolezen (Slovenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Wilsonova bolezen" in Slovenian language version.

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2oxfordjournals.org

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1cobiss.net

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archive.org

Walshe, J.M. (1996). »Treatment of Wilson's disease: the historical background«. QJM. 89 (7): 553–5. PMID 8759497.

bmj.com

gut.bmj.com

Merle U.; Schaefer M.; Ferenci P.; Stremmel W. (2007). »Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study«. Gut. 56 (1): 115–20. doi:10.1136/gut.2005.087262. PMID 16709660.

jmg.bmj.com

de Bie P.; Muller P.; Wijmenga C.; Klomp L.W. (2007). »Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes«. J. Med. Genet. 44 (11): 673–88. doi:10.1136/jmg.2007.052746. PMID 17717039.

cobiss.net

plus.cobiss.net

Gelehrter, T.D.; Collins, F.S. (1990). Principles of Medical Genetics. Baltimore, Hong Kong, London, Sydney: Williams & Wilkins. str. 284–5. COBISS 852756. ISBN 0-683-03447-2.

doi.org

Kinnier Wilson, S.A. (1912). »Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver« (PDF). Brain. 34 (1): 295–507. doi:10.1093/brain/34.4.295.
Cumings, J.N. (1948). »The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration« (PDF). Brain. 71 (Dec): 410–5. doi:10.1093/brain/71.4.410. PMID 18124738.
Cumings, J.N. (1951). »The effects of B.A.L. in hepatolenticular degeneration«. Brain. 74 (1): 10–22. doi:10.1093/brain/74.1.10. PMID 14830662.
Walshe, J.M. (1956). »Wilson's disease; new oral therapy«. Lancet. 267 (6906): 25–6. doi:10.1016/S0140-6736(56)91859-1. PMID 13279157.
Bull, Peter C.; Thomas, Gordon R.; Rommens, Johanna M.; Forbes, John R.; Cox, Diane Wilson (1. december 1993). »The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene«. Nature Genetics. 5 (4): 327–337. doi:10.1038/ng1293-327.
Tanzi, R.E.; Petrukhin, K.; Chernov, I.; Pellequer, J.L.; Wasco, W.; in sod. (1993). »The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene«. Nature Genetics. 5 (4): 344–350. doi:10.1038/ng1293-344.
Merle U.; Schaefer M.; Ferenci P.; Stremmel W. (2007). »Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study«. Gut. 56 (1): 115–20. doi:10.1136/gut.2005.087262. PMID 16709660.
Grubenbecher S.; Stüve O.; Hefter H.; Korth C. (2006). »Prion protein gene codon 129 modulates clinical course of neurological Wilson disease«. Neuroreport. 17 (5): 549–52. doi:10.1097/01.wnr.0000209006.48105.90. PMID 16543824.
de Bie P.; Muller P.; Wijmenga C.; Klomp L.W. (2007). »Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes«. J. Med. Genet. 44 (11): 673–88. doi:10.1136/jmg.2007.052746. PMID 17717039.
Roberts EA; Schilsky ML (2003). »A practice guideline on Wilson disease« (PDF). Hepatology. 37 (6): 1475–92. doi:10.1053/jhep.2003.50252. PMID 12774027.^{[mrtva povezava]}
Shaver WA; Bhatt H; Combes B (1986). »Low serum alkaline phosphatase activity in Wilson's disease«. Hepatology. 6 (5): 859–63. doi:10.1002/hep.1840060509. PMID 3758940.
van de Sluis, B. (1. januar 2002). »Identification of a new copper metabolism gene by positional cloning in a purebred dog population«. Human Molecular Genetics. 11 (2): 165–173. doi:10.1093/hmg/11.2.165.
Müller, Thomas; van de Sluis, Bart; Zhernakova, Alexandra; van Binsbergen, Ellen; Janecke, Andreas R.; in sod. (2003). »The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis«. Journal of Hepatology. 38 (2): 164–168. doi:10.1016/s0168-8278(02)00356-2.

nih.gov

pubmed.ncbi.nlm.nih.gov

Cumings, J.N. (1948). »The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration« (PDF). Brain. 71 (Dec): 410–5. doi:10.1093/brain/71.4.410. PMID 18124738.
Cumings, J.N. (1951). »The effects of B.A.L. in hepatolenticular degeneration«. Brain. 74 (1): 10–22. doi:10.1093/brain/74.1.10. PMID 14830662.
Denny-Brown, D.; Porter, H. (1951). »The effect of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease)«. N. Engl. J. Med. 245 (24): 917–25. PMID 14882450.
Walshe, J.M. (1956). »Wilson's disease; new oral therapy«. Lancet. 267 (6906): 25–6. doi:10.1016/S0140-6736(56)91859-1. PMID 13279157.
Merle U.; Schaefer M.; Ferenci P.; Stremmel W. (2007). »Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study«. Gut. 56 (1): 115–20. doi:10.1136/gut.2005.087262. PMID 16709660.
Grubenbecher S.; Stüve O.; Hefter H.; Korth C. (2006). »Prion protein gene codon 129 modulates clinical course of neurological Wilson disease«. Neuroreport. 17 (5): 549–52. doi:10.1097/01.wnr.0000209006.48105.90. PMID 16543824.
de Bie P.; Muller P.; Wijmenga C.; Klomp L.W. (2007). »Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes«. J. Med. Genet. 44 (11): 673–88. doi:10.1136/jmg.2007.052746. PMID 17717039.
Roberts EA; Schilsky ML (2003). »A practice guideline on Wilson disease« (PDF). Hepatology. 37 (6): 1475–92. doi:10.1053/jhep.2003.50252. PMID 12774027.^{[mrtva povezava]}
Shaver WA; Bhatt H; Combes B (1986). »Low serum alkaline phosphatase activity in Wilson's disease«. Hepatology. 6 (5): 859–63. doi:10.1002/hep.1840060509. PMID 3758940.
Walshe, J.M. (1996). »Treatment of Wilson's disease: the historical background«. QJM. 89 (7): 553–5. PMID 8759497.
Sternlieb, I.; Twedt, D.C.; Johnson, G.F.; Gilbertson, S.; Korotkin, E.; Quintana, N.; Scheinberg, I.H. (1977). »Inherited copper toxicity of the liver in Bedlington terriers«. Proc. R. Soc. Med. 70 (Suppl. 3): 8–9. PMC 1543595. PMID 122681.

ncbi.nlm.nih.gov

Sternlieb, I.; Twedt, D.C.; Johnson, G.F.; Gilbertson, S.; Korotkin, E.; Quintana, N.; Scheinberg, I.H. (1977). »Inherited copper toxicity of the liver in Bedlington terriers«. Proc. R. Soc. Med. 70 (Suppl. 3): 8–9. PMC 1543595. PMID 122681.

oxfordjournals.org

brain.oxfordjournals.org

Kinnier Wilson, S.A. (1912). »Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver« (PDF). Brain. 34 (1): 295–507. doi:10.1093/brain/34.4.295.
Cumings, J.N. (1948). »The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration« (PDF). Brain. 71 (Dec): 410–5. doi:10.1093/brain/71.4.410. PMID 18124738.

wiley.com

www3.interscience.wiley.com

Roberts EA; Schilsky ML (2003). »A practice guideline on Wilson disease« (PDF). Hepatology. 37 (6): 1475–92. doi:10.1053/jhep.2003.50252. PMID 12774027.^{[mrtva povezava]}