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Wilson s disease
LE WE PMID CA
Wilson s disease1832Wilson Erkrankung

Adenine phosphoribosyl transferase

Atox1

ATP7A

ATP7B

Bedlington terrier

Copper

Ctr1

Cystinosis

Cystinuria

Drug repositioning

Fahr s disease

Fanconi s syndrome

Fructose intolerance

Huntington s disease

LEC rat

Lesch Nyhan syndrome

Liver (MRT)

Menkes s disease

Mitochondria (Mitochondriopathy)

Nephrolithiasis

Oxalosis

Phosphoribosylpyrophosphate synthetase

Triethylenetetramine ttCuChelator

Tyrosinemia

Wilson s disease

Xanthine

1970  
1
Hepatolenticular degeneration (Wilson's disease): observations in 7 cases and review of the literature.
[5415807] South Med J 63(1): 82-9 (1970)
1996  
2
Treatment of Wilson's disease: the historical background.
[8759497] QJM 89(7): 553-5 (1996)
1998  
3
Neuropsychiatric correlates and treatment of lenticulostriatal diseases: a review of the literature and overview of research opportunities in Huntington's, Wilson's, and Fahr's diseases. A report of the ANPA Committee on Research. American Neuropsychiatric Association.
[9706533] J Neuropsychiatry Clin Neurosci 10(3): 249-66 (1998)
1998  
4
Wilson disease and canine copper toxicosis.
[9587157] Am J Clin Nutr 67(5 Suppl): 1087S-1090S (1998)
1998  
5
Physiologic function of the Wilson disease gene product, ATP7B.
[9587140] Am J Clin Nutr 67(5 Suppl): 982S-987S (1998)
1996  
6
Wilson disease and idiopathic copper toxicosis.
[8615372] Am J Clin Nutr 63(5): 842S-5S (1996)
2007  
7
Wilson disease: not just a copper disorder. Analysis of a Wilson disease model demonstrates the link between copper and lipid metabolism.
[18000558] Mol Biosyst 3(12): 816-24 (2007)
2004  
8
Review article: diagnosis and current therapy of Wilson's disease.
[14723607] Aliment Pharmacol Ther 19(2): 157-65 (2004)
2009  
9
Systematic review: clinical efficacy of chelator agents and zinc in the initial treatment of Wilson disease.
[19210288] Aliment Pharmacol Ther 29(9): 947-58 (2009)
2000  
10
2001  
11
Copper control as an antiangiogenic anticancer therapy: lessons from treating Wilson's disease.
[11444102] Exp Biol Med (Maywood) 226(7): 665-73 (2001)
2003  
12
2000  
13
Recognition, diagnosis, and management of Wilson's disease.
[10632959] Proc Soc Exp Biol Med 223(1): 39-46 (2000)
2001  
14
Pharmacology of tetrandrine and its therapeutic use in digestive diseases.
[11819843] World J Gastroenterol 7(5): 627-9 (2001)
2008  
15
Diagnosis and treatment of Wilson disease: an update.
[18506894] Hepatology 47(6): 2089-111 (2008)
2003  
16
A practice guideline on Wilson disease.
[12774027] Hepatology 37(6): 1475-92 (2003)
2008  
17
2009  
18
Wilson's disease: a case report and a historical review.
[19623464] Arq Neuropsiquiatr 67(2B): 539-43 (2009)
2010  
19
Nephrolithiasis related to inborn metabolic diseases.
[19156444] Pediatr Nephrol 25(3): 415-24 (2010)
2007  
20
Introducing single-nucleotide polymorphism markers in the diagnosis of Wilson disease.
[17711999] Clin Chem 53(9): 1568-9 (2007)
2010  
21
Wilson disease and its current problems.
[20453398] Intern Med 49(9): 807-8 (2010)
2002  
22
Molecular mechanism of copper transport in Wilson disease.
[12426114] Environ Health Perspect 110 Suppl 5(-): 695-8 (2002)
2003  
23
Genetic defects in copper metabolism.
[12730458] J Nutr 133(5 Suppl 1): 1527S-31S (2003)
2010  
24
Clinical application of liver MR imaging in Wilson's disease.
[21076593] Korean J Radiol 11(6): 665-72 (2010)
2007  
25
Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.
[17717039] J Med Genet 44(11): 673-88 (2007)
2010  
26
Triethylenetetramine pharmacology and its clinical applications.
[20660601] Mol Cancer Ther 9(9): 2458-67 (2010)
PMC   
27
Wilson's disease: changes in methionine metabolism and inflammation affect global DNA methylation in early liver disease.
[22945834] Hepatology 57(2):555-65 (2013)
PMC   
28
Role of p38 Mapk in development of acute hepatic injury in Long-Evans Cinnamon (LEC) rats, an animal model of human Wilson's disease.
[23877843] J Vet Med Sci 75(12):1551-6 (2013)
PMC   
29
Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B.
[24706876] Proc Natl Acad Sci U S A 111(14):E1364-73 (2014)

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