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array:23 [ "pii" => "S2173574310700101" "issn" => "21735743" "doi" => "10.1016/S2173-5743(10)70010-1" "estado" => "S300" "fechaPublicacion" => "2010-01-01" "aid" => "70010" "copyright" => "Sociedad Española de Reumatología and Colegio Mexicano de Reumatología" "copyrightAnyo" => "2010" "documento" => "simple-article" "crossmark" => 0 "subdocumento" => "cor" "cita" => "Reumatol Clin. 2010;6:53-5" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 2197 "formatos" => array:3 [ "EPUB" => 36 "HTML" => 1338 "PDF" => 823 ] ] "itemSiguiente" => array:18 [ "pii" => "S2173574310700113" "issn" => "21735743" "doi" => "10.1016/S2173-5743(10)70011-3" "estado" => "S300" "fechaPublicacion" => "2010-01-01" "aid" => "70011" "copyright" => "Sociedad Española de Reumatología and Colegio Mexicano de Reumatología" "documento" => "simple-article" "crossmark" => 0 "subdocumento" => "cor" "cita" => "Reumatol Clin. 2010;6:56-7" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 2083 "formatos" => array:3 [ "EPUB" => 48 "HTML" => 1355 "PDF" => 680 ] ] "en" => array:10 [ "idiomaDefecto" => true "titulo" => "Response to rituximab in a patient with Wegener's granulomatosis refractory to conventional therapies" "tienePdf" => "en" "tieneTextoCompleto" => 0 "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "56" "paginaFinal" => "57" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Respuesta a rituximab en un paciente con granulomatosis de Wegener refractaria a terapia convencional" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Inmaculada Macías Fernández" "autores" => array:1 [ 0 => array:2 [ "nombre" => "Inmaculada" "apellidos" => "Macías Fernández" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173574310700113?idApp=UINPBA00004M" "url" => "/21735743/0000000600000001/v1_201305061603/S2173574310700113/v1_201305061603/en/main.assets" ] "itemAnterior" => array:18 [ "pii" => "S2173574310700095" "issn" => "21735743" "doi" => "10.1016/S2173-5743(10)70009-5" "estado" => "S300" "fechaPublicacion" => "2010-01-01" "aid" => "70009" "copyright" => "Sociedad Española de Reumatología and Colegio Mexicano de Reumatología" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Reumatol Clin. 2010;6:49-52" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 1840 "formatos" => array:3 [ "EPUB" => 54 "HTML" => 1244 "PDF" => 542 ] ] "en" => array:10 [ "idiomaDefecto" => true "titulo" => "New advances on diagnostic imaging in spinal pathology" "tienePdf" => "en" "tieneTextoCompleto" => 0 "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "49" "paginaFinal" => "52" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Nuevos avances en el diagnóstico por imagen de la enfermedad del raquis" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Joan C. Vilanova" "autores" => array:1 [ 0 => array:2 [ "nombre" => "Joan C." "apellidos" => "Vilanova" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173574310700095?idApp=UINPBA00004M" "url" => "/21735743/0000000600000001/v1_201305061603/S2173574310700095/v1_201305061603/en/main.assets" ] "en" => array:14 [ "idiomaDefecto" => true "titulo" => "Septic arthritis in a case of hyper-IgE syndrome" "tieneTextoCompleto" => 0 "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "53" "paginaFinal" => "55" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "Inmaculada Macías Fernández" "autores" => array:1 [ 0 => array:3 [ "nombre" => "Inmaculada" "apellidos" => "Macías Fernández" "email" => array:1 [ 0 => "imaciasfdez@hotmail.com" ] ] ] "afiliaciones" => array:1 [ 0 => array:1 [ "entidad" => "Sección de Reumatología, Hospital Universitario Puerta del Mar, Cádiz, Spain" ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Artritis séptica en un caso de síndrome de hiperinmunoglobulinemia E" ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2008-12-08" "fechaAceptado" => "2009-01-27" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec112333" "palabras" => array:5 [ 0 => "Hiper-IgE syndrome" 1 => "Infections" 2 => "Diagnosis" 3 => "Septic artritis" 4 => "Cutaneous infections" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec112332" "palabras" => array:5 [ 0 => "Síndrome de hiperinmunoglobulinemia E" 1 => "Infecciones" 2 => "Diagnóstico" 3 => "Artritis séptica" 4 => "Infecciones cutáneas" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Hyper-IgE syndrome (HIES) is characterized by recurrent skin and pulmonary infections (mainly bacterial), eczematous dermatitis and elevated serum IgE levels. Associated abnormalities in some patients include coarse facial features, failure or delay of shedding of primary teeth, recurrent fractures, hyperextensible joints, and scoliosis. Laboratory abnormalities include elevated total serum IgE levels, typically ranging from 1,000 to greater than 50,000<span class="elsevierStyleHsp" style=""></span>IU/ml and variable eosynophilia. The diagnosis of HIES is based upon the presence of suggestive clinical and laboratory findings. A definitive laboratory test is not commercially available at present. Management of patients with HIES is focused on skin care, prevention of infection, prompt and complete treatment of infections that do develop, and control of pulmonary complications.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">El síndrome de hiperinmunoglobulinemia E (HIES) se caracteriza por infecciones recurrentes cutáneas y pulmonares (principalmente bacterianas), dermatitis eccematosa y elevados niveles séricos de IgE. Anomalías asociadas en algunos pacientes incluyen rasgos faciales toscos, fracaso o retraso de la caída de los dientes primarios, fracturas recurrentes, hiperlaxitud en las articulaciones y escoliosis. Anormalidades de laboratorio son niveles elevados de IgE total en suero, generalmente, de 1.000 a más de 50.000<span class="elsevierStyleHsp" style=""></span>U/ml y eosinofilia variable. El diagnóstico de HIES se basa en la presencia de característicos hallazgos clínicos y de laboratorio. Un test diagnóstico definitivo no existe en la actualidad. El manejo de los pacientes con HIES se centra en el cuidado de la piel, la prevención de la infección, el tratamiento precoz de las infecciones que se desarrollan y el control de las complicaciones pulmonares.</p>" ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:10 [ 0 => array:3 [ "identificador" => "bib1" "etiqueta" => "1." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Extreme hyperimmunoglobulinemia E and undue susceptibility to infection" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "R.H. Buckley" 1 => "B.B. Wray" 2 => "E.Z. 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