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Results: 1-15 |
Results: 15
CHARACTERIZATION OF CERULOPLASMIN IN WILSONS-DISEASE PATIENTS AND NEONATES
Authors: HELLEBY L VERNON GM DAS SR SCHEINBERG IH
Citation: L. Helleby et al., CHARACTERIZATION OF CERULOPLASMIN IN WILSONS-DISEASE PATIENTS AND NEONATES, The FASEB journal, 11(9), 1997, pp. 3265-3265
IDENTIFICATION AND ANALYSIS OF MUTATIONS IN THE WILSON-DISEASE GENE (ATP7B) - POPULATION FREQUENCIES, GENOTYPE-PHENOTYPE CORRELATION, AND FUNCTIONAL ANALYSES
Authors: SHAH AB CHERNOV I ZHANG HT ROSS BM DAS K LUTSENKO S PARANO E PAVONE L EVGRAFOV O IVANOVASMOLENSKAYA IA ANNEREN G WESTERMARK K URRUTIA FH PENCHASZADEH GK STERNLIEB I SCHEINBERG IH GILLIAM TC PETRUKHIN K
Citation: Ab. Shah et al., IDENTIFICATION AND ANALYSIS OF MUTATIONS IN THE WILSON-DISEASE GENE (ATP7B) - POPULATION FREQUENCIES, GENOTYPE-PHENOTYPE CORRELATION, AND FUNCTIONAL ANALYSES, American journal of human genetics, 61(2), 1997, pp. 317-328
EXCESS ZINC ASSOCIATED WITH CHOLESTASIS
Authors: SCHEINBERG IH STERNLIEB I
Citation: Ih. Scheinberg et I. Sternlieb, EXCESS ZINC ASSOCIATED WITH CHOLESTASIS, Lancet, 347(9011), 1996, pp. 1331-1331
WILSON DISEASE AND IDIOPATHIC COPPER TOXICOSIS
Authors: SCHEINBERG IH STERNLIEB I
Citation: Ih. Scheinberg et I. Sternlieb, WILSON DISEASE AND IDIOPATHIC COPPER TOXICOSIS, The American journal of clinical nutrition, 63(5), 1996, pp. 842-845
RATE OF INFORMATION-PROCESSING IN PATIENTS WITH WILSONS-DISEASE
Authors: LITTMAN E MEDALIA A SENIOR G SCHEINBERG IH
Citation: E. Littman et al., RATE OF INFORMATION-PROCESSING IN PATIENTS WITH WILSONS-DISEASE, The Journal of neuropsychiatry and clinical neurosciences, 7(1), 1995, pp. 68-71
TREATMENT OF THE NEUROLOGIC MANIFESTATIONS OF WILSONS-DISEASE
Authors: SCHEINBERG IH STERNLIEB L
Citation: Ih. Scheinberg et L. Sternlieb, TREATMENT OF THE NEUROLOGIC MANIFESTATIONS OF WILSONS-DISEASE, Archives of neurology, 52(4), 1995, pp. 339-340
MUTATION ANALYSIS OF THE WILSON DISEASE GENE IN VARIOUS ETHNIC POPULATIONS
Authors: SHAH AB PETRUKHIN K CHERNOV I ZHANG HT ROSS BM PARANO E PAVANO L EVGRAFOV O IVANOVASMOLENKAYA IA ANNEREN G WESTERMARK K PENCHASZADEH GK STERNLIEB I SCHEINBERG IH GILLIAM TC
Citation: Ab. Shah et al., MUTATION ANALYSIS OF THE WILSON DISEASE GENE IN VARIOUS ETHNIC POPULATIONS, American journal of human genetics, 57(4), 1995, pp. 982-982
LIVER-TRANSPLANTATION FOR WILSONS-DISEASE - INDICATIONS AND OUTCOME
Authors: SCHILSKY ML SCHEINBERG IH STERNLIEB I
Citation: Ml. Schilsky et al., LIVER-TRANSPLANTATION FOR WILSONS-DISEASE - INDICATIONS AND OUTCOME, Hepatology, 19(3), 1994, pp. 583-587
IS NON-INDIAN CHILDHOOD CIRRHOSIS CAUSED BY EXCESS DIETARY COPPER
Authors: SCHEINBERG IH STERNLIEB I
Citation: Ih. Scheinberg et I. Sternlieb, IS NON-INDIAN CHILDHOOD CIRRHOSIS CAUSED BY EXCESS DIETARY COPPER, Lancet, 344(8928), 1994, pp. 1002-1004
MAPPING, CLONING AND GENETIC-CHARACTERIZATION OF THE REGION CONTAINING THE WILSON DISEASE GENE
Authors: PETRUKHIN K FISCHER SG PIRASTU M TANZI RE CHERNOV I DEVOTO M BRZUSTOWICZ LM CAYANIS E VITALE E RUSSO JJ MATSEOANE D BOUKHGALTER B WASCO W FIGUS AL LOUDIANOS J CAO A STERNLIEB I EVGRAFOV O PARANO E PAVONE L WARBURTON D OTT J PENCHASZADEH GK SCHEINBERG IH GILLIAM TC
Citation: K. Petrukhin et al., MAPPING, CLONING AND GENETIC-CHARACTERIZATION OF THE REGION CONTAINING THE WILSON DISEASE GENE, Nature genetics, 5(4), 1993, pp. 338-343
THE WILSON DISEASE GENE IS A COPPER TRANSPORTING ATPASE WITH HOMOLOGYTO THE MENKES DISEASE GENE
Authors: TANZI RE PETRUKHIN K CHERNOV I PELLEQUER JL WASCO W ROSS B ROMANO DM PARANO E PAVONE L BRZUSTOWICZ LM DEVOTO M PEPPERCORN J BUSH AI STERNLIEB I PIRASTU M GUSELLA JF EVGRAFOV O PENCHASZADEH GK HONIG B EDELMAN IS SOARES MB SCHEINBERG IH GILLIAM TC
Citation: Re. Tanzi et al., THE WILSON DISEASE GENE IS A COPPER TRANSPORTING ATPASE WITH HOMOLOGYTO THE MENKES DISEASE GENE, Nature genetics, 5(4), 1993, pp. 344-350
PENICILLAMINE (PCA) PROPHYLAXIS FOR ASYMPTOMATIC CHILDREN WITH WILSONS-DISEASE (WD)
Authors: COLLINS JC SCHEINBERG IH STERNLIEB I
Citation: Jc. Collins et al., PENICILLAMINE (PCA) PROPHYLAXIS FOR ASYMPTOMATIC CHILDREN WITH WILSONS-DISEASE (WD), Hepatology, 18(4), 1993, pp. 10000128-10000128
POLYMORPHIC MICROSATELLITES AND WILSON DISEASE (WD)
Authors: STEWART EA WHITE A TOMFOHRDE J OSBORNELAWRENCE S PRESTRIDGE L BONNETAMIR B SCHEINBERG IH STGEORGEHYSLOP P GIAGHEDDU M KIM JW SEO JK LO WHY IVANOVASMOLENSKAYA IA LIMBORSKA SA CAVALLISFORZA LL FARRER LA BOWCOCK AM
Citation: Ea. Stewart et al., POLYMORPHIC MICROSATELLITES AND WILSON DISEASE (WD), American journal of human genetics, 53(4), 1993, pp. 864-873
MAPPING THE WILSONS-DISEASE GENE
Authors: PETRUHKIN K TANZI RE FISCHER S PIRASTU M CHERNOV I BOUKHGALTER B CYANIS E WASCO W BRZUSTOWICZ LM MATSEOANE D DEVOTO M FIGLIS AL LOLIDIHNOS J CAO A CHUMAKOV I EVGRAFOV G STERNLIEB I WARBURTON D PENCHASZADEH G SCHEINBERG IH GILLIAM TC
Citation: K. Petruhkin et al., MAPPING THE WILSONS-DISEASE GENE, American journal of human genetics, 53(3), 1993, pp. 55-55
ISOLATION AND CHARACTERIZATION OF A CANDIDATE GENE FOR WILSONS-DISEASE
Authors: TANZI RE PETRUHKIN K SOARES B WASCO W ROMANO D ROSS B CHERNOV I PIRASTU M HYSLOP PG GUSELLA JF SCHEINBERG IH GILLIAM TC
Citation: Re. Tanzi et al., ISOLATION AND CHARACTERIZATION OF A CANDIDATE GENE FOR WILSONS-DISEASE, American journal of human genetics, 53(3), 1993, pp. 228-228
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