Výsledky vyhledávání - "I.H Scheinberg"

Is non-Indian childhood cirrhosis caused by excess dietary copper?

Autor: I.H Scheinberg, I Sternlieb

Publikováno v: Lancet (London, England). 344(8928)

Indian childhood cirrhosis is generally believed to be caused by toxic excesses of hepatic copper derived from milk boiled in copper vessels. Sporadic cases of a disorder indistinguishable from Indian childhood cirrhosis have appeared in other countr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9591aa007089a1bae42cbf1ba87dc9c5
https://pubmed.ncbi.nlm.nih.gov/7968155

Zobrazit plný text záznamu

Plný text ve formátu HTML

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Publikováno v: Nature Genetics
Nature Genetics, Nature Publishing Group, 1993, 5 (4), pp.344-350. ⟨10.1038/ng1293-344⟩
Nature genetics
5 (1993): 344–350. doi:10.1038/ng1293-344
info:cnr-pdr/source/autori:Tanzi R.E.; Petrukhin K.; Chernov I.; Pellequer J.L.; Wasco W.; Ross B.; Romano D.M.; Parano E.; Pavone L.; Brzustowicz L.M.; Devoto M.; Peppercorn J.; Bush A.I.; Sternlieb I.; Pirastu M.; Gusella J.F.; Evgrafov O.; Penchaszadeh G.K.; Gilliam T.C./titolo:The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene/doi:10.1038%2Fng1293-344/rivista:Nature genetics (Print)/anno:1993/pagina_da:344/pagina_a:350/intervallo_pagine:344–350/volume:5

Wilson disease (WD) is an autosomal recessive disorder characterized by the toxic accumulation of copper in a number of organs, particularly the liver and brain. As shown in the accompanying paper, linkage disequilibrium and haplotype analysis confir

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::403bdaac8bcabdd4c3c152ef6c89b86d
http://hdl.handle.net/11573/497083

Zobrazit plný text záznamu

Physical and Chemical Studies on Ceruloplasmin

Autor: I Sternlieb, Gilbert Ashwell, R A Irvine, I.H. Scheinberg, A G Morell

Publikováno v: Journal of Biological Chemistry. 243:155-159

Injection into rabbits of radioactive ceruloplasmin from which sialic acid had been removed enzymatically resulted in a rapid disappearance of the asialoceruloplasmin from the serum and its appearance in parenchymal cells, but not in Kupffer cells, o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2cd601dc33723da4eb77b2afc3ca3041
https://doi.org/10.1016/s0021-9258(18)99337-3

Zobrazit plný text záznamu

THE INCORPORATION OF COPPER INTO CERULOPLASMIN IN VIVO: STUDIES WITH COPPER64 AND COPPER67*

Autor: W.D. Tucker, M.W. Greene, Anatol G. Morell, I.H. Scheinberg, Irmin Sternlieb

Publikováno v: Journal of Clinical Investigation. 40:1834-1840

The hypothesis that ceruloplasmin exchanges its copper for ionic copper in vivo was tested, by means of ceruloplasmin labeled with copper-64 and copper- 67, in two patients with Wilson's disease and in two control subjects. No indication of exchange

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a83dcb0c8ac06b1ef3245b3011f99812
https://doi.org/10.1172/jci104407

Zobrazit plný text záznamu

ORTHOTOPIC LIVER TRANSPLANTATION FOR WILSON'S DISEASE

Autor: R.S. Dubois, Irmin Sternlieb, C.G. Halgrimson, J. Lilly, G. Martineau, G. Shroter, Thomas E. Starzl, I.H. Scheinberg, D.O. Rodgerson, G. Giles

Publikováno v: The Lancet. 297:505-508

An 11-year-old boy with terminal hepatic failure due to Wilson's disease was treated 18 months ago with orthotopic liver transplantation. Postoperatively, there has been evidence of clearance of body copper stores but without accumulation of copper i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1028a26432188522760c3843c11ee22b
https://doi.org/10.1016/s0140-6736(71)91121-4

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání