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kw.\*:("Wilson disease")

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Genetic defects in copper metabolismSHIM, Hoon; HARRIS, Z. Leah.The Journal of nutrition. 2003, Vol 133, Num 5, pp 1527S-1531S, issn 0022-3166, SUP1Conference Paper

Unithiol in Wilson's diseaseWALSHE, J. M.British medical journal (1857). 1985, Vol 290, Num 6469, pp 673-674, issn 0007-1447Article

Wilson's disease: evoked potentials and computed tomographyROACH, E. S; FORD, C. S; SPUDIS, E. V et al.Journal of neurology. 1985, Vol 232, Num 1, pp 20-23, issn 0340-5354Article

Genomic studies of gene expression: regulation of the Wilson disease geneBOCHUKOVA, Elena G; JEFFERSON, Andrew; FRANCIS, Michael J et al.Genomics (San Diego, Calif.). 2003, Vol 81, Num 6, pp 531-542, issn 0888-7543, 12 p.Article

Proteomic analysis of sera of asymptomatic, early-stage patients with Wilson's diseasePARK, Jung-Young; JOO HEE MUN; BEOM HEE LEE et al.Proteomics. Clinical applications (Print). 2009, Vol 3, Num 10, pp 1185-1190, issn 1862-8346, 6 p.Article

LA MALADIE DE WILSON. HISTOIRE D'UN CAS.FINDLAY D.1976; REV. ASS. PSYCHIATRES CANADA; CANADA; DA. 1976; VOL. 21; NO 2; PP. 117-121; ABS. ANGL.; BIBL. 9 REF.Article

PHYSOSTIGMINE IN WILSON DISEASE.TARSY D; MAHONEY JF; CUMMINGS JL et al.1978; ANN. NEUROL.; U.S.A.; DA. 1978; VOL. 3; NO 4; PP. 372-373; BIBL. 2 REF.Article

LES 13 DESSERTS DE NOEL. REVELATION INATTENDUE D'UNE MALADIE DE WILSONBETEND B; CHATELAIN P; PINARD et al.1983; ARCHIVES FRANCAISES DE PEDIATRIE; ISSN 0003-9764; FRA; DA. 1983; VOL. 40; NO 2; PP. 101-102; ABS. ENG; BIBL. 18 REF.Article

BESTIMMUNG VON KUPFER IN LEBERPUNKTATEN ZUR DIAGNOSE DES MORBUS WILSON = DOSAGE DU CUIVRE DANS LE PRODUIT DE JONCTIONS DU FOIE EN VUE DU DIAGNOSTIC DE LA MALADIE DE WILSONWAWSCHINEK O; BEYER W.1982; JOURNAL OF CLINICAL CHEMISTRY AND CLINICAL BIOCHEMISTRY; ISSN 0340-076X; DEU; DA. 1982; VOL. 20; NO 12; PP. 929-930; ABS. ENG; BIBL. 11 REF.Article

Determination of triethylenetetramine dihydrochloride in aqueous solution by reversed-phase ion-pairing high performance liquid chromatography and conductivity detectionHANSEN, E. B. JR; RUSHING, L. G; THOMPSON, H. C. JR et al.Journal of analytical toxicology. 1985, Vol 9, Num 4, pp 167-171, issn 0146-4760Article

Oral zinc therapy for Wilson's diseaseBREWER, G. J; HILL, G. M; PRASAD, A. S et al.Annals of internal medicine. 1983, Vol 99, Num 3, pp 314-320, issn 0003-4819Article

Critical roles for the COOH terminus of the Cu-ATPase ATP7B in protein stability, trans-Golgi network retention, copper sensing, and retrograde traffickingBRAITERMAN, L; NYASAE, L; LEVES, F et al.American journal of physiology. Gastrointestinal and liver physiology. 2011, Vol 64, Num 1, issn 0193-1857, G69-G81Article

Withdrawal of penicillamine from zinc sulphate-penicillamine maintenance therapy in Wilson's disease : Promising, safe and cheapSINHA, S; TALY, A. B.Journal of the neurological sciences. 2008, Vol 264, Num 1-2, pp 129-132, issn 0022-510X, 4 p.Article

New novel mutation of the ATP7B gene in a family with Wilson diseaseLEE, Jun-Young; KIM, Young-Hyun; KIM, Tae-Woo et al.Journal of the neurological sciences. 2012, Vol 313, Num 1-2, pp 129-131, issn 0022-510X, 3 p.Article

The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysisSTAPELBROEK, Janneke M; BOLLEN, Casper W; PLOOS VAN AMSTEL, Johannes K et al.Journal of hepatology. 2004, Vol 41, Num 5, pp 758-763, issn 0168-8278, 6 p.Article

Quality of Life in Patients with Treated and Clinically Stable Wilson's DiseaseSVETEL, Marina; PEKMEZOVIC, Tatjana; TOMIC, Aleksandra et al.Movement disorders. 2011, Vol 26, Num 8, pp 1503-1508, issn 0885-3185, 6 p.Article

Wilson diseaseKITZBERGER, Reinhard; MADL, Christian; FERENCI, Peter et al.Metabolic brain disease. 2005, Vol 20, Num 4, pp 295-302, issn 0885-7490, 8 p.Conference Paper

D-Penicillamin-induzierter IgA-Mangel bei der Therapie der Wilsonschen ErkrankungIBEL, H; FEIST, D; ENDRES, W et al.Klinische Pädiatrie. 1990, Vol 202, Num 6, pp 427-429, issn 0300-8630Article

Aspects psychiatriques de la maladie de Wilson = Psychiatric aspects of Wilson diseaseCROCQ, M. A; FURTOS, J.Actualités psychiatriques. 1985, Vol 15, Num 5, pp 89-93, issn 0300-8274Article

Hudson memorial lecture: Wilson's disease: genetics and biochemistry ― their relevance to therapyWALSHE, J. M.Journal of inherited metabolic disease. 1983, Vol 6, pp 51-58, issn 0141-8955, suppl. 1Article

Pathological case of the monthBARNESS, L; GILBERT-BARNESS, E.American journal of diseases of children (1960). 1992, Vol 146, Num 1, pp 111-112, issn 0002-922XArticle

Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's diseaseFARRER, L. A; BONNE-TAMIR, B; FRYDMAN, M et al.Human genetics. 1988, Vol 79, Num 2, pp 109-117, issn 0340-6717Article

Hepatic copper and metallothionein distribution in Wilson's disease (hepatolenticular degeneration)NARTEY, N. O; FREI, J. V; CHERIAN, M. G et al.Laboratory investigation. 1987, Vol 57, Num 4, pp 397-401, issn 0023-6837Article

Sensory evoked potentials in Wilson's diseaseNAI-SHIN CHU.Brain. 1986, Vol 109, Num 3, pp 491-507, issn 0006-8950Article

A genetic study of Wilson's disease in the United KingdomCOFFEY, Alison J; DURKIE, Miranda; MIELI-VERGANI, Giorgina et al.Brain. 2013, Vol 136, pp 1476-1487, issn 0006-8950, 12 p., 5Article

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