يعرض 1 - 10 نتائج من 54 نتيجة بحث عن '"García Serrano JL"', وقت الاستعلام: 1.00s تنقيح النتائج
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
    دورية أكاديمية
  6. 6

    المساهمون: [Cénti,MC, Márquez,A, Martín,J] Instituto de Parasitología y Biomedicina López-Neyra, IPBLN, CSIC, Granada, Spain. [Cordero-Coma,M] Ophthalmology Department, Hospital de León, León, Spain. [Gorroño-Echebarría, MB] Ophthalmology Department, Hospital Universitario Principe de Asturias, Alcalá de Henares, Spain. [Fonollosa,A, Martínez-Berriotxoa,A] Internal Medicine Department, Hospital de Cruces, Bilbao, Spain. [Adán,A, Molins,B] Ophthalmology Department, Hospital Clinic, Barcelona, Spain. [DÍaz Valle,D] Ophthalmology Department, Hospital Clínico San Carlos, Madrid, Spain. [Pato,E] Rheumatology Department, Hospital Clínico San Carlos, Madrid, Spain. [Blanco,R] Rheumatology Department, Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain. [Cañal,J] Ophthalmology Department, Hospital Marqués de Valdecilla, Santander, Spain. [Díaz-Llopis,M] Ophthalmology Department, Hospital Universitario La Fe, Valencia, Spain. [García Serrano,JL] Ophthalmology Department, Hospital Clínico San Cecilio, Granada, Spain. [Ramón de, E] Internal Medicine Department, Hospital Carlos Haya, Málaga, Spain. [Río del,MJ] Ophthalmology Department, Hospital Carlos Haya, Málaga, Spain. [Martín-Villa,JM] Immunology Department, Facultad de Medicina, Universidad Complutense de Madrid, Spain. [Ortego-Centeno,N] Internal Medicine Department, Hospital Clínico San Cecilio, Granada, Spain.

    المصدر: Digital.CSIC. Repositorio Institucional del CSIC
    instname
    PLoS ONE
    PLoS ONE, Vol 8, Iss 11, p e72892 (2013)

    مصطلحات موضوعية: Phenomena and Processes::Immune System Phenomena::Immunity::Autoimmunity [Medical Subject Headings], Male, Polimorfismo de nucleótido simple, Polimorfismo genético, Autoimmunity, Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings], medicine.disease_cause, Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Gene Frequency, Genotype, STAT4, Multidisciplinary, Receptores de interleucina, Middle Aged, STAT4 Transcription Factor, Phenotype, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Membrane Proteins::Receptors, Cell Surface::Receptors, Immunologic::Receptors, Cytokine::Receptors, Interleukin [Medical Subject Headings], Medicine, Female, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Alelos, Uveitis, Research Article, Adult, musculoskeletal diseases, Science, Check Tags::Male [Medical Subject Headings], Autoinmunidad, Biology, Polymorphism, Single Nucleotide, Factores de transcripción, IL23R protein, human, Named Groups::Persons::Age Groups::Adult [Medical Subject Headings], medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, Allele, Allele frequency, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Alleles, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], Polymorphism, Genetic, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intracellular Signaling Peptides and Proteins::Adaptor Proteins, Signal Transducing::STAT Transcription Factors [Medical Subject Headings], Receptors, Interleukin, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], medicine.disease, Uveítis, Check Tags::Female [Medical Subject Headings], Immunology, Genotipo, Diseases::Eye Diseases::Uveal Diseases::Uveitis [Medical Subject Headings]

    وصف الملف: application/pdf

  7. 7

    المساهمون: [Márquez,A, Cénit,MC, Martín,J] Instituto de Parasitología y Biomedicina López-Neyra, IPBLN, CSIC, Granada, Spain. [Cordero-Coma,M] Ophthalmology Department, Hospital de León, Spain. [Ortego-Centeno,N] Internal Medicine Department, Hospital Clínico San Cecilio, Granada, Spain. [Adán,A, Llorenç,V] Ophthalmology Department, Hospital Clínic, Barcelona, Spain. [Fonollosa,A, Artaraz,J] Ophthalmology Department, Hospital de Cruces, Bilbao, Spain. [Díaz Valle,D] Ophthalmology Department, Hospital Clínico San Carlos, Madrid, Spain. [Pato,E] Rheumatology Department, Hospital Clínico San Carlos, Madrid, Spain. [Blanco,R] Rheumatology Department, Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain. [Cañal,J] Ophthalmology Department, Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain. [Díaz-Llopis,M] Ophthalmology Department, Hospital La Fe, Valencia, Spain.[Ramón,E de] Internal Medicine Department, Hospital Carlos Haya, Málaga, Spain. [Rio,MJ del] Ophthalmology Department, Hospital Carlos Haya, Málaga, Spain. [García Serrano,JL] Ophthalmology Department, Hospital Clínico San Cecilio, Granada, Spain. [Martín-Villa,JM] Immunology Department, Facultad de Medicina, Universidad Complutense de Madrid, Spain. [Gorroño-Echebarría,MB] Ophthalmology Department, Hospital Principe de Asturias, Alcalá de Henares, Spain., Universitat de Barcelona

    المصدر: PLoS ONE
    Dipòsit Digital de la UB
    Universidad de Barcelona
    PLoS ONE, Vol 8, Iss 10, p e76777 (2013)
    Digital.CSIC. Repositorio Institucional del CSIC
    instname
    Recercat. Dipósit de la Recerca de Catalunya

    مصطلحات موضوعية: Male, Phenomena and Processes::Genetic Phenomena::Phenotype [Medical Subject Headings], Polimorfismo de nucleótido simple, lcsh:Medicine, Interferó, Autoimmunity, Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings], medicine.disease_cause, Linkage Disequilibrium, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Gene Frequency, Interferon, Diseases::Eye Diseases::Uveal Diseases::Uveitis::Panuveitis::Uveitis, Anterior [Medical Subject Headings], lcsh:Science, Multidisciplinary, Autoimmunitat, Middle Aged, Phenomena and Processes::Genetic Phenomena::Genetic Linkage::Linkage Disequilibrium [Medical Subject Headings], Uveitis, Anterior, Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease [Medical Subject Headings], Modelos logísticos, Phenotype, Diseases::Eye Diseases::Retinal Diseases::Retinal Degeneration::Macular Degeneration::Macular Edema [Medical Subject Headings], Oftalmologia, Interferon Regulatory Factors, Female, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Fenotipo, Uveitis, Research Article, medicine.drug, Adult, Genotype, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intracellular Signaling Peptides and Proteins::Adaptor Proteins, Signal Transducing::Interferon Regulatory Factors [Medical Subject Headings], Check Tags::Male [Medical Subject Headings], Biology, Polymorphism, Single Nucleotide, Macular Edema, Genetic variation, Edema macular, medicine, Named Groups::Persons::Age Groups::Adult [Medical Subject Headings], Humans, Genetic Predisposition to Disease, Macular edema, Health Care::Health Care Quality, Access, and Evaluation::Quality of Health Care::Health Care Evaluation Mechanisms::Statistics as Topic::Models, Statistical::Logistic Models [Medical Subject Headings], Alleles, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], lcsh:R, medicine.disease, Uveítis anterior, Ophthalmology, Logistic Models, Factores reguladores del interferón, Haplotypes, Desequilibrio de ligamiento, Check Tags::Female [Medical Subject Headings], Genetic marker, Immunology, lcsh:Q, Phenomena and Processes::Genetic Phenomena::Gene Frequency [Medical Subject Headings], IRF5, Interferon regulatory factors

    وصف الملف: application/pdf

  8. 8

    المساهمون: [Cénit,MC, Márquez,A, Martín,J] Instituto de Parasitología y Biomedicina López-Neyra, IPBLN, CSIC, Armilla, Granada, Spain. [Cordero-Coma,M] Ophthalmology Department, Hospital de León, Spain. [Fonollosa,A, Martínez-Berriotxoa,A] Internal Medicine Department, Hospital de Cruces, Bilbao, Spain. [Adán,A, Llorenç,V] Ophthalmology Department, Hospital Clinic, Barcelona, Spain. [Díaz Valle,D] Ophthalmology Department, Hospital Clínico San Carlos, Madrid, Spain. [Blanco,R] Rheumatology Department, Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain. [Cañal,J] Ophthalmology Department, Hospital Marqués de Valdecilla, Santander, Spain. [Díaz-Llopis,M] Ophthalmology Department, Hospital Universitario La Fe, Valencia, Spain. [García Serrano,JL] Ophthalmology Department, Hospital Clínico San Cecilio, Granada, Spain. [Ramón,E de] Internal Medicine Department, Hospital Carlos Haya, Málaga, Spain. [Rio,MJ del] Ophthalmology Department, Hospital Carlos Haya, Málaga, Spain. [Gorroño- Echebarría,MB] Ophthalmology Department, Hospital Universitario Principe de Asturias, Alcalá de Henares, Spain. [Martín-Villa,JM] Immunology Department, Facultad de Medicina, Universidad Complutense de Madrid, Spain. [Ortego-Centeno,N] Internal Medicine Department, Hospital Clínico San Cecilio, Granada, Spain.

    المصدر: Digital.CSIC. Repositorio Institucional del CSIC
    instname
    BMC Medical Genetics

    مصطلحات موضوعية: Male, Polimorfismo de nucleótido simple, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intercellular Signaling Peptides and Proteins::Cytokines::Interleukins [Medical Subject Headings], Health Care::Health Care Quality, Access, and Evaluation::Quality of Health Care::Health Care Evaluation Mechanisms::Statistics as Topic::Models, Statistical [Medical Subject Headings], Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings], medicine.disease_cause, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Membrane Proteins::Receptors, Cell Surface::Receptors, Immunologic::Receptors, Cytokine::Receptors, Interleukin::Receptors, Interleukin-2::Interleukin-2 Receptor beta Subunit [Medical Subject Headings], Autoimmunity, Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], 0302 clinical medicine, Modelos estadísticos, Genotype, Genetics(clinical), Genetics (clinical), IL21, Genetics, 0303 health sciences, Predisposición genética a la enfermedad, Middle Aged, 3. Good health, Association study, Female, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation [Medical Subject Headings], Uveitis, Research Article, Adult, Interleucina-2, Check Tags::Male [Medical Subject Headings], Biology, Variación genética, Subunidad alfa del receptor de interleucina-2, Polymorphism, Single Nucleotide, Health Care::Health Care Quality, Access, and Evaluation::Quality of Health Care::Health Care Evaluation Mechanisms::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Case-Control Studies [Medical Subject Headings], 03 medical and health sciences, Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Susceptibility::Genetic Predisposition to Disease [Medical Subject Headings], Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intercellular Signaling Peptides and Proteins::Cytokines::Interleukins::Interleukin-2 [Medical Subject Headings], Genetic variation, Genetic predisposition, medicine, Genetic susceptibility, Named Groups::Persons::Age Groups::Adult [Medical Subject Headings], Humans, Genetic Predisposition to Disease, Allele, Named Groups::Persons::Age Groups::Adult::Aged [Medical Subject Headings], Alleles, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Aged, 030304 developmental biology, IL2RB, Models, Statistical, IL2, Polymorphism, Genetic, IL2RA, Interleukins, Interleukin-2 Receptor alpha Subunit, Genetic Variation, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], medicine.disease, Human genetics, Interleukin-2 Receptor beta Subunit, Uveítis, stomatognathic diseases, Check Tags::Female [Medical Subject Headings], Case-Control Studies, Immunology, 030221 ophthalmology & optometry, Interleukin-2, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Membrane Proteins::Receptors, Cell Surface::Receptors, Immunologic::Receptors, Cytokine::Receptors, Interleukin::Receptors, Interleukin-2::Interleukin-2 Receptor alpha Subunit [Medical Subject Headings], Polymorphisms, Genotipo, Diseases::Eye Diseases::Uveal Diseases::Uveitis [Medical Subject Headings]

    وصف الملف: application/pdf

  9. 9

    المساهمون: [Cénit,MC, Márquez,A, Martín,J] Instituto de Parasitología y Biomedicina López-Neyra, IPBLN, CSIC, Granada, Spain. [Cordero-Coma,M] Ophthalmology Department, Hospital de León, León, Spain. [Fonollosa,A, Artaraz,J] Ophthalmology Department, Hospital de Cruces, Bilbao, Spain. [Llorenç,V] Ophthalmology Department, Hospital Clínic, Barcelona, Spain. [Díaz Valle, D] Ophthalmology Department, Hospital Clínico San Carlos, Madrid, Spain. [Blanco,R] Rheumatology Department, Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain. [Cañal,J] Ophthalmology Department, Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain. [Salom,D] Ophthalmology Department, Hospital Universitario La Fe, Valencia, Spain. [García Serrano,JL] Ophthalmology Department, Hospital Clínico San Cecilio, Granada, Spain. [Ramon,E de] Internal Medicine Department, Hospital Carlos Haya, Málaga, Spain. [Rio,MJ del] Ophthalmology Department, Hospital Carlos Haya, Málaga, Spain. [Gorroño-Echebarría,MB] Ophthalmology Department, Hospital Universitario Principe de Asturias, Alcalá de Henares, Spain. [Martín-Villa,JM] Immunology Department, Facultad de Medicina, Universidad Complutense de Madrid, Spain. [Molins,B] Instituto de Investigaciones Biomédicas, IDIBAPS, Hospital Clinic, Barcelona, Spain. [Ortego-Centeno,N] Internal Medicine Department, Hospital Clínico San Cecilio, Granada, Spain.

    المصدر: Europe PubMed Central
    Scopus-Elsevier
    MOLECULAR VISION
    r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
    instname
    Molecular Vision
    ResearcherID

    مصطلحات موضوعية: Male, Proteína tirosina fosfatasa no receptora de tipo 22, España, Health Care::Population Characteristics::Demography [Medical Subject Headings], Check Tags::Male [Medical Subject Headings], Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings], Proteínas mutantes, Polymorphism, Single Nucleotide, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Genetic Association Studies [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Intracellular Signaling Peptides and Proteins::Protein Tyrosine Phosphatases, Non-Receptor::Protein Tyrosine Phosphatase, Non-Receptor Type 22 [Medical Subject Headings], Gene Frequency, Humans, Demografía, Genetic Predisposition to Disease, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Mutant Proteins [Medical Subject Headings], Diseases::Eye Diseases::Uveal Diseases::Uveitis::Panuveitis::Uveitis, Anterior [Medical Subject Headings], Alleles, Genetic Association Studies, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Demography, Geographicals::Geographic Locations::Europe::Spain [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Processes::Mutagenesis::Amino Acid Substitution [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], Estudios de casos y controles, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Case-Control Studies [Medical Subject Headings], Estudios de asociación genética, Predisposición genética a la enfermedad, Protein Tyrosine Phosphatase, Non-Receptor Type 22, Middle Aged, Uveitis, Anterior, Polimorfismo de nucleótido único, Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease [Medical Subject Headings], eye diseases, Frecuencia génica, Uveítis anterior, Amino Acid Substitution, Check Tags::Female [Medical Subject Headings], Spain, Case-Control Studies, Female, Mutant Proteins, Alelos, Phenomena and Processes::Genetic Phenomena::Gene Frequency [Medical Subject Headings], Research Article

    وصف الملف: application/pdf

  10. 10
    دورية أكاديمية

    المؤلفون: García-Serrano JL; Department of Surgery, University of Granada, Ophthalmology Service, San Cecilio Clinical Hospital, Granada, Spain., Fernández-Marín E; Neonatal Intensive Care Unit, Medicine Faculty, San Cecilio Clinical Hospital, Granada, Spain., Domech-Serrano T; Department of Surgery, University of Granada, Ophthalmology Service, San Cecilio Clinical Hospital, Granada, Spain., Stevens BR; University of Manchester, Manchester, UK., Uberos Fernández J; Neonatal Intensive Care Unit, Medicine Faculty, San Cecilio Clinical Hospital, Granada, Spain.

    المصدر: Acta ophthalmologica [Acta Ophthalmol] 2024 Jun; Vol. 102 (4), pp. e628-e634. Date of Electronic Publication: 2023 Dec 26.

    نوع المنشور: Journal Article; Comparative Study

    بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101468102 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1755-3768 (Electronic) Linking ISSN: 1755375X NLM ISO Abbreviation: Acta Ophthalmol Subsets: MEDLINE