TY  - JOUR
AU  - López-Mejías, Raquel
AU  - Genre, Fernanda
AU  - Remuzgo-Martínez, Sara
AU  - Sevilla Pérez, Belén
AU  - Castañeda, Santos
AU  - Llorca, Javier
AU  - Ortego-Centeno, Norberto
AU  - Ubilla, Begoña
AU  - Mijares, Verónica
AU  - Pina, Trinitario
AU  - Calvo-Río, Vanesa
AU  - Palmou, Natalia
AU  - Miranda-Filloy, José A
AU  - Navas Parejo, Antonio
AU  - Argila, Diego
AU  - Sánchez-Pérez, Javier
AU  - Rubio, Esteban
AU  - León Luque, Manuel
AU  - Blanco-Madrigal, Juan María
AU  - Galíndez-Aguirregoikoa, Eva
AU  - Ocejo-Vinyals, J Gonzalo
AU  - Martín, Javier
AU  - Blanco, Ricardo
AU  - González-Gay, Miguel A
PY  - 2015
DO  - 10.1186/s13075-015-0796-x
SN  - 1478-6354
UR  - http://hdl.handle.net/10668/2556
T2  - Arthritis research & therapy
AB  - INTRODUCTIONTo determine whether the PTPN22 (protein tyrosine phosphatase nonreceptor 22)/CSK (c-src tyrosine kinase) pathway is implicated in the susceptibility and clinical heterogeneity of Henoch-Schönlein purpura (HSP) in the largest series of...
LA  - en
PB  - BioMed Central
KW  - Niño
KW  - Femenino
KW  - Frecuencia de los genes
KW  - Adulto
KW  - Predisposición genética a la enfermedad
KW  - Genotipo
KW  - Humanos
KW  - Masculino
KW  - Polimorfismo de nucleótido simple
KW  - Proteína tirosina fosfatasa no receptora tipo 22
KW  - Púrpura de Schoenlein-Henoch
KW  - Reacción en cadena en tiempo real de la polimerasa
KW  - España
KW  - Medical Subject Headings::Named Groups::Persons::Age Groups::Child
KW  - Medical Subject Headings::Check Tags::Female
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Gene Frequency
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype
KW  - Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans
KW  - Medical Subject Headings::Check Tags::Male
KW  - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide
KW  - Medical Subject Headings::Diseases::Hemic and Lymphatic Diseases::Hematologic Diseases::Blood Coagulation Disorders::Purpura::Purpura, Schoenlein-Henoch
KW  - Medical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Nucleic Acid Amplification Techniques::Polymerase Chain Reaction::Real-Time Polymerase Chain Reaction
KW  - Medical Subject Headings::Geographicals::Geographic Locations::Europe::Spain
KW  - Medical Subject Headings::Named Groups::Persons::Age Groups::Adult
TI  - Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis).
TY  - research article
ER  -