-
1
-
-
84963072124
-
Progressive lenticular degeneration: A familial nervous disease associated with cirrhosis of the liver
-
Wilson SAK. Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver. Brain 1912;34:295-509.
-
(1912)
Brain
, vol.34
, pp. 295-509
-
-
Wilson, S.A.K.1
-
3
-
-
0002201227
-
A genetical analysis of thiny families with Wilson's disease (hepatolenticular degeneration)
-
Bearn AG. A genetical analysis of thiny families with Wilson's disease (hepatolenticular degeneration). Ann Hum Genet 1960;24:33-43.
-
(1960)
Ann Hum Genet
, vol.24
, pp. 33-43
-
-
Bearn, A.G.1
-
4
-
-
0001435653
-
The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration
-
Cumings JN. The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration. Brain 1948;71:410-5.
-
(1948)
Brain
, vol.71
, pp. 410-415
-
-
Cumings, J.N.1
-
6
-
-
78651036626
-
The effect of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease)
-
Denny-Brown D, Porter H. The effect of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease). N Engl J Med 1951;245:917-25.
-
(1951)
N Engl J Med
, vol.245
, pp. 917-925
-
-
Denny-Brown, D.1
Porter, H.2
-
7
-
-
0000852301
-
Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease)
-
Scheinberg IH, Gitlin D. Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease). Science 1952;116: 484-5.
-
(1952)
Science
, vol.116
, pp. 484-485
-
-
Scheinberg, I.H.1
Gitlin, D.2
-
8
-
-
0021083002
-
Evidence for linkage between the loci for transferrin and ceruloplasmin in man
-
Weitkamp LR. Evidence for linkage between the loci for transferrin and ceruloplasmin in man. Ann Hum Genet 1983;47:293-7.
-
(1983)
Ann Hum Genet
, vol.47
, pp. 293-297
-
-
Weitkamp, L.R.1
-
9
-
-
0342372868
-
Assignment of the gene for Wilson's disease to chromosome 13: Linkage to the esterase D locus
-
Frydman M, Bonne-Tamir B, Farrer LA, et al. Assignment of the gene for Wilson's disease to chromosome 13: linkage to the esterase D locus. Proc Natl Acad Sci U S A 1985;82:1819-21.
-
(1985)
Proc Natl Acad Sci U S A
, vol.82
, pp. 1819-1821
-
-
Frydman, M.1
Bonne-Tamir, B.2
Farrer, L.A.3
-
10
-
-
77049283245
-
Penicillamine. A new oral therapy for Wilson's disease
-
Walshe JM. Penicillamine. A new oral therapy for Wilson's disease. Am J Med 1956;21:487-95.
-
(1956)
Am J Med
, vol.21
, pp. 487-495
-
-
Walshe, J.M.1
-
11
-
-
0014415177
-
Prevention of Wilson's disease in asymptomatic patients
-
Sternlieb I, Scheinberg IH. Prevention of Wilson's disease in asymptomatic patients. N Engl J Med 1968;278:352-9.
-
(1968)
N Engl J Med
, vol.278
, pp. 352-359
-
-
Sternlieb, I.1
Scheinberg, I.H.2
-
12
-
-
0023262532
-
The use of trientine in preventing the effects of interrupting penicillamine therapy in Wilson's disease
-
Scheinberg IH, Jaffe ME, Sternlieb I. The use of trientine in preventing the effects of interrupting penicillamine therapy in Wilson's disease. N Engl J Med 1987;317:209-13.
-
(1987)
N Engl J Med
, vol.317
, pp. 209-213
-
-
Scheinberg, I.H.1
Jaffe, M.E.2
Sternlieb, I.3
-
13
-
-
0027364961
-
The Wilson disease gene is a copper-transporting ATPase with homology to the Menkes disease gene
-
Tanzi RE, Petrukhin I, Chernov JL, et al. The Wilson disease gene is a copper-transporting ATPase with homology to the Menkes disease gene. Nature Genet 1993;5:344-50.
-
(1993)
Nature Genet
, vol.5
, pp. 344-350
-
-
Tanzi, R.E.1
Petrukhin, I.2
Chernov, J.L.3
-
14
-
-
0027427695
-
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
-
Petrukhin K, Fischer SG, Pirastu M, et al. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene. Nature Genet 1993;5:338-43.
-
(1993)
Nature Genet
, vol.5
, pp. 338-343
-
-
Petrukhin, K.1
Fischer, S.G.2
Pirastu, M.3
-
15
-
-
0027452091
-
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
-
Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nature Genet 1993;5:327-37.
-
(1993)
Nature Genet
, vol.5
, pp. 327-337
-
-
Bull, P.C.1
Thomas, G.R.2
Rommens, J.M.3
Forbes, J.R.4
Cox, D.W.5
-
16
-
-
0027507834
-
Polymorphic microsatellites and Wilson disease (WD)
-
Stewart EA, White A, Tomfohrde J, et al. Polymorphic microsatellites and Wilson disease (WD). Am J Hum Genet 1993;53:864-73.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 864-873
-
-
Stewart, E.A.1
White, A.2
Tomfohrde, J.3
-
18
-
-
0018888158
-
Copper and the liver
-
Sternlieb I. Copper and the liver. Gastroenterology 1980;78:1615-28.
-
(1980)
Gastroenterology
, vol.78
, pp. 1615-1628
-
-
Sternlieb, I.1
-
19
-
-
0018375555
-
The role of radiocopper in the diagnosis of Wilson's disease
-
Sternlieb I, Scheinberg IH. The role of radiocopper in the diagnosis of Wilson's disease. Gastroenterology 1979;77:138-42.
-
(1979)
Gastroenterology
, vol.77
, pp. 138-142
-
-
Sternlieb, I.1
Scheinberg, I.H.2
-
21
-
-
0015633326
-
Wilson's disease or chronic copper poisoning?
-
Walker-Smith JA, Bloomfield J. Wilson's disease or chronic copper poisoning? Arch Dis Child 1973;48:476-9.
-
(1973)
Arch Dis Child
, vol.48
, pp. 476-479
-
-
Walker-Smith, J.A.1
Bloomfield, J.2
-
22
-
-
0023262597
-
Fatal copper storage disease of the liver in a German infant resembling Indian childhood cirrhosis
-
Müller-Hocker J, Weiss M, Meyer U, et al. Fatal copper storage disease of the liver in a German infant resembling Indian childhood cirrhosis. Virchow Arch A Pathol Anat Histopathol 1987;411:379-85.
-
(1987)
Virchow Arch A Pathol Anat Histopathol
, vol.411
, pp. 379-385
-
-
Müller-Hocker, J.1
Weiss, M.2
Meyer, U.3
-
24
-
-
0023841577
-
Copper storage disease of the liver and chronic dietary intoxication in two further German infants mimicking Indian childhood cirrhosis
-
Müller-Höcker J, Meyer U, Wiebecke B, et al. Copper storage disease of the liver and chronic dietary intoxication in two further German infants mimicking Indian childhood cirrhosis. Pathol Res Pract 1988; 183:39-45.
-
(1988)
Pathol Res Pract
, vol.183
, pp. 39-45
-
-
Müller-Höcker, J.1
Meyer, U.2
Wiebecke, B.3
-
26
-
-
0028215447
-
Indian childhood cirrhosis-like liver disease in an Arab child. A brief report
-
Aljajeh IA, Mughal S, Al-Tahou B, Ajrawi T, Ismail EA, Nayak NC. Indian childhood cirrhosis-like liver disease in an Arab child. A brief report. Virchow Arch 1994;424:225-7.
-
(1994)
Virchow Arch
, vol.424
, pp. 225-227
-
-
Aljajeh, I.A.1
Mughal, S.2
Al-Tahou, B.3
Ajrawi, T.4
Ismail, E.A.5
Nayak, N.C.6
-
28
-
-
2942697281
-
High water copper content associated with Indian childhood cirrhosis in European children
-
abstr
-
Gormally SM, Baker A, Portmann B, Mowat A, Drumm B. High water copper content associated with Indian childhood cirrhosis in European children. Gastroenterology 1994;106:A900(abstr).
-
(1994)
Gastroenterology
, vol.106
-
-
Gormally, S.M.1
Baker, A.2
Portmann, B.3
Mowat, A.4
Drumm, B.5
-
29
-
-
0019985357
-
Hepatic copper overload and features of Indian childhood cirrhosis in an American sibship
-
Lefkowitch JH, Honig CL, King ME, Hagstrom JWC. Hepatic copper overload and features of Indian childhood cirrhosis in an American sibship. N Engl J Med 1982;307:271-7.
-
(1982)
N Engl J Med
, vol.307
, pp. 271-277
-
-
Lefkowitch, J.H.1
Honig, C.L.2
King, M.E.3
Hagstrom, J.W.C.4
-
30
-
-
0026575948
-
Indian childhood cirrhosis in an American child
-
Adamson M, Reiner B, Olsen JL, et al. Indian childhood cirrhosis in an American child. Gastroenterology 1992;102:1771-7.
-
(1992)
Gastroenterology
, vol.102
, pp. 1771-1777
-
-
Adamson, M.1
Reiner, B.2
Olsen, J.L.3
-
31
-
-
15844384725
-
Indian childhood cirrhosis
-
Tanner S, ed. London: Churchill Livingstone
-
Tanner S. Indian childhood cirrhosis. In: Tanner S, ed. Paediatric hepatology. London: Churchill Livingstone 1989:214-7.
-
(1989)
Paediatric Hepatology
, pp. 214-217
-
-
Tanner, S.1
-
32
-
-
0018785658
-
Cytoplasmic copper and its toxic effects: Studies in Indian childhood cirrhosis
-
Popper H, Goldfischer S, Sternlieb I, Nayak NC, Madhavan TV. Cytoplasmic copper and its toxic effects: studies in Indian childhood cirrhosis. Lancet 1979;1:1205-8.
-
(1979)
Lancet
, vol.1
, pp. 1205-1208
-
-
Popper, H.1
Goldfischer, S.2
Sternlieb, I.3
Nayak, N.C.4
Madhavan, T.V.5
-
33
-
-
0028122983
-
Is non-Indian childhood cirrhosis caused by excess dietary copper?
-
Scheinberg IH, Sternlieb I Is non-Indian childhood cirrhosis caused by excess dietary copper? Lancet 1994;344 1002-4.
-
(1994)
Lancet
, vol.344
, pp. 1002-1004
-
-
Scheinberg, I.H.1
Sternlieb, I.2
|