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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

Molecular and cellular aspects of Copper transport in developing mammalsMERCER, Julian F. B; LLANOS, Roxana M.The Journal of nutrition. 2003, Vol 133, Num 5, pp 1481S-1484S, 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

Do cytokines have any role in Wilson's disease?GOYAL, M. K; SINHA, S; PATIL, S. A et al.Clinical and experimental immunology (Print). 2008, Vol 154, Num 1, pp 74-79, issn 0009-9104, 6 p.Article

Diagnostic de la maladie de Wilson: quinze observations = Diagnosis of Wilson's diseaseMALLET, B; VESCO-GUILLAUME, O; GAMBINI, M et al.La Presse médicale (1983). 1984, Vol 13, Num 39, issn 0755-4982, 2389Article

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

Studies in pancreatic secretion. VIII: Pancreatic function in patients with Wilson's diseaseDREILING, D. A; GRATERON, H.The Mount Sinai journal of medicine. 1983, Vol 50, Num 4, pp 335-337, issn 0027-2507Article

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

Soy protein isolate enhances hepatic copper accumulation and cell damage in LEC ratsYONEZAWA, Kayo; NUNOMIYA, Sachiko; DAIGO, Mitsue et al.The Journal of nutrition. 2003, Vol 133, Num 5, pp 1250-1254, issn 0022-3166, 5 p.Article

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

Proteomic analysis of the hepatic tissue of Long―Evans Cinnamon (LEC) rats according to the natural course of Wilson diseaseLEE, Beom H; KIM, Jae-Min; HEO, Sun H et al.Proteomics (Weinheim. Print). 2011, Vol 11, Num 18, pp 3698-3705, issn 1615-9853, 8 p.Article

Diagnostic significance of reduced serum caeruloplasmin concentration in neurological diseaseWALSHE, John M.Movement disorders. 2005, Vol 20, Num 12, pp 1658-1661, issn 0885-3185, 4 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

PLASMA AMINE OXIDASES IN WILSON'S DISEASEBOMBARDIER G; BEVILACQUA E; CONTI LR et al.1981; LIFE SCI. (1973); ISSN 0024-3205; GBR; DA. 1981; VOL. 29; NO 2; PP. 117-120; BIBL. 15 REF.Article

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