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WDWestern Digital
WDWidth
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WDWalt Disney
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WDWorking Draft
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WDWestern Economic Diversification Canada (Canada)
WDWeb Design
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WDWhite Dwarf
WDWithdrawn
WDWatford (UK postal Code)
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WDWithout Doubt
WDWound Debridement
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WDWilson Disease
WDWorking Dog
WDWatership Down (novel)
WDWebster's Dictionary
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WDWater Deficit (agriculture)
WDWoody Debris
WDWhirling Disease (Rainbow Trout disease)
WDWide Differential (SCSI)
WDWeibull Distribution
WDWhen Discovered (Nalcomis)
WDWeapons Director
WDWeapon Data
WDWet Dock (DD3)
WDWrist-Disarticulation (amputation)
WDWireless Directive (US DoD)
WDWestminster Dragoons (UK Territorial Army)
WDWafer Defect(s)
WDWord Displacement
WDWeak Dipole
WDWorld Devastator (Star Wars)
WDWarm Dielectric (high temperature superconducting cables)
WDWestern Economic Development Canada
WDWet/Dry Index
WDWDS Processing (Tartar Module)
WDWord Disparity
WDWorld Domination Recordings (Capitol Records)
WDWeekend Dykes
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References in periodicals archive ?
As seen in the current case, low alkaline phosphatase activity is also seen in fulminant hepatitis due to Wilson disease. Because none of the other causes of low alkaline phosphatase activity would be associated with jaundice or hemolytic anemia, the combination of these findings should lead the astute laboratorian to contact the clinicians to make sure that they consider Wilson disease as a diagnostic possibility.
High prevalence of the very rare Wilson disease gene mutation Leu708Pro in the Island of Gran Canaria (Canary Islands, Spain): a genetic and clinical study.
Wilson disease in Septuagenarian siblings: raising the bar of diagnosis.
Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus.
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations, and genotype-phenotype correlation in Indian patients.
Biopharmaceutical company Wilson Therapeutics AB (STO:WTX) announced on Monday the successful conclusion of its discussions with the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) regarding the study protocol for the single pivotal Phase 3 FOCuS trial for WTX101 in Wilson Disease.
No patient was subsequently diagnosed by the requesting clinicians as having Wilson disease; accordingly, we were unable to calculate indices of diagnostic accuracy (with confidence intervals) such as sensitivity/ specificity, likelihood ratios, and areas under ROC curves (9).
Molecular characterization of Wilson disease in the Sardinian population-evidence of a founder effect.
This chapter also introduces the major genetic disorders of copper metabolism: Menkes and Wilson diseases and aceruloplasminemia.
M2 EQUITYBITES-December 15, 2017-Wilson Therapeutics' WTX101 granted Fast Track designation by the US FDA for Wilson Disease treatment
The company's lead product, WTX101, is in development as a novel treatment for Wilson Disease. A Phase 2 clinical study has been successfully completed and preparations for a pivotal Phase 3 study are ongoing.