Literals
- ou:categoriaPDI
- 00063-PROFESOR CONTRATADO DOCTOR
- aiiso:code
- 44654ba5f4dfc6efcc21b5766fa0212c
- ou:dedicacionPDI
- TIEMPO COMPLETO
- foaf:firstName
- PEDRO
- ou:indiceHscopus
- 18
- foaf:lastName
- AYUSO PAREJO
- foaf:name
- PEDRO AYUSO PAREJO
- vivo:scopusId
- 22733336400
Typed Literals
- ou:esDoctor
- True (xsd:boolean)
- ou:personalActual
- True (xsd:boolean)
Relations
- teach:teacherOf
- ou:tienePublicacion
- A Nonsynonymous FCER1B SNP is Associated with Risk of Developing Allergic Rhinitis and with IgE Levels
- A lower dose of efavirenz can be coadministered with rifampicin and isoniazid in tuberculosis patients
- A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease
- Advanced phenotyping in hypersensitivity drug reactions to NSAIDs
- An association study between heme oxygenase-1 genetic variants and Parkinson’s disease
- An update on the pharmacogenetic considerations when prescribing dopamine receptor agonists for Parkinson’s disease
- Analysis of the functional polymorphism in the cytochrome P450 CYP2C8 gene rs11572080 with regard to colorectal cancer risk
- Assessment of nonsteroidal anti-inflammatory drug-induced hepatotoxicity
- Association study of genetic variants in PLA2G4A, PLCG1, LAT, SYK, and TNFRS11A genes in NSAIDs-induced urticaria and/or angioedema patients
- Asthma and allergic rhinitis associate with the rs2229542 variant that induces a p.Lys90Glu mutation and compromises AKR1B1 protein levels
- Clinical pharmacogenomics in asthma therapy
- Copy number variation in ALOX5 and PTGER1 is associated with NSAIDs-induced urticaria and/or angioedema
- Delta-amino-levulinic acid dehydratase gene and essential tremor
- Diamine oxidase rs10156191 and rs2052129 variants are associated with the risk for migraine
- Editorial: Editor’s feature: negative findings in pharmacogenetics and pharmacogenomics
- Eicosanoid mediator profiles in different phenotypes of nonsteroidal anti-inflammatory drug-induced urticaria
- Genetic variability of histamine receptors in patients with Parkinson's disease
- Genetic variability of human diamine oxidase: Occurrence of three nonsynonymous polymorphisms and study of their effect on serum enzyme activity
- Genetic variants in arachidonic acid pathway genes associated with NSAID-exacerbated respiratory disease
- Genetic variants of alcohol metabolizing enzymes and alcohol-related liver cirrhosis risk
- Genetic variants of thymic stromal lymphopoietin in nonsteroidal anti-inflammatory drug-induced urticaria/ angioedema
- Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor
- Histamine pharmacogenomics
- Hypersensitivity reactions to nonsteroidal anti-inflammatory drugs: An update on pharmacogenetics studies
- Improved analytical sensitivity reveals the occurrence of gender-related variability in diamine oxidase enzyme activity in healthy individuals
- Lack of Association between Common LAG3/CD4 Variants and Risk of Migraine
- Mediator release after nasal aspirin provocation supports different phenotypes in subjects with hypersensitivity reactions to NSAIDs
- Meta-analysis of the effect of CYP2B6, CYP2A6, UGT2B7 and CAR polymorphisms on efavirenz plasma concentrations
- Modulation of GSTP1-1 oligomerization by electrophilic inflammatory mediators and reactive drugs.
- Molecular monitoring of patient response to painkiller drugs
- Polymorphisms in eicosanoid-related biosynthesis enzymes associated with acute urticaria/angioedema induced by nonsteroidal anti-inflammatory drug hypersensitivity
- Response to the Letter to the Editor regarding Improved analytical sensitivity reveals the occurrence of gender-related variability in diamine oxidase enzyme activity in healthy individuals
- Serum Trace Elements Concentrations in Patients with Restless Legs Syndrome
- The Diamine Oxidase Gene Is Associated with Hypersensitivity Response to Non-Steroidal Anti-Inflammatory Drugs
- The study of severe cutaneous drug hypersensitivity reactions from a systems biology perspective
- Variability in histamine receptor genes HRH1, HRH2 and HRH4 in patients with hypersensitivity to NSAIDs
- Variability of the L-Histidine decarboxylase gene in allergic rhinitis
- Variability of the genes involved in the cellular redox status and their implication in drug hypersensitivity reactions
- Variants of CEP68 gene are associated with acute urticaria/angioedema induced by multiple non-steroidal anti-inflammatory drugs
- Vitamin D receptor and binding protein genes variants in patients with migraine
- ou:perteneceAGrupoInvestigacion
- ou:imparteDocenciaEnArea
- ou:adscritoACentro
- ou:adscritoADepartamento