-
1دورية أكاديمية
المؤلفون: Karaca, N., Azarsiz, E., Karaca, E., Aksu, G., Genel, F., Gulez, N., Ozen, S.
مصطلحات موضوعية: consanguinity, BCG vaccine, IL12Rβ1 deficiency, mendelian susceptibility to mycobacterial disease, primary immunodeficiency, antibiotic agent, gamma interferon receptor, gamma interferon receptor 1, I kappa B kinase gamma, interleukin 12 receptor beta1, protein gamma interferon receptor 2, recombinant gamma interferon, STAT1 protein, tuberculostatic agent, unclassified drug, Article, cellular parameters, child, clinical article, clinical feature, early diagnosis, family history, female, follow up, gene mutation, genetic analysis, human, immune deficiency, infant, infection sensitivity
العلاقة: Asian Pacific Journal of Allergy and Immunology; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11454/93140Test; https://doi.org/10.12932/ap-271219-0726Test; 41; 372; 378
-
2دورية أكاديمية
المؤلفون: Brogan, Paul A., Arch, B., Hickey, H., Anton, J., Iglesias, E., Baildam, E, Mahmood, K., Cleary, G., Moraitis, E., Papadopoulou, C., Beresford, M.W., Riley, P., Demir, S., Ozen, S., Culeddu, Giovanna, Hughes, Dyfrig, Dolezalova, P., Hampson, L., Whitehead, J., Jayne, D., Ruperto, N., Tudor-Smith, Catrin, Eleftheriou, D.
المصدر: Brogan , P A , Arch , B , Hickey , H , Anton , J , Iglesias , E , Baildam , E , Mahmood , K , Cleary , G , Moraitis , E , Papadopoulou , C , Beresford , M W , Riley , P , Demir , S , Ozen , S , Culeddu , G , Hughes , D , Dolezalova , P , Hampson , L , Whitehead , J , Jayne , D , Ruperto , N , Tudor-Smith , C & Eleftheriou , D 2021 , ' Mycophenolate Mofetil Versus ....
مصطلحات موضوعية: Polyarteritis nodosa, Child, Randomised control trial, Bayesian, Mycophenolate mofetil, Cyclophosphamide
وصف الملف: application/pdf
العلاقة: https://research.bangor.ac.uk/portal/en/researchoutputs/mycophenolate-mofetil-versus-cyclophosphamide-for-remission-induction-in-childhood-polyarteritis-nodosa-an-openlabel-randomized-bayesian-noninferiority-trialTest(60e76fc8-2665-47d9-afd1-efa4a8a37ecb).html
الإتاحة: https://doi.org/10.1002/art.41730Test
https://research.bangor.ac.uk/portal/en/researchoutputs/mycophenolate-mofetil-versus-cyclophosphamide-for-remission-induction-in-childhood-polyarteritis-nodosa-an-openlabel-randomized-bayesian-noninferiority-trialTest(60e76fc8-2665-47d9-afd1-efa4a8a37ecb).html
https://research.bangor.ac.uk/ws/files/37124365/2021_MYPAN_trial.pdfTest -
3دورية أكاديمية
المؤلفون: Brogan, PA, Arch, B, Hickey, H, Anton, J, Iglesias, E, Baildam, E, Mahmood, K, Cleary, G, Moraitis, E, Papadopoulou, C, Beresford, MW, Riley, P, Demir, S, Ozen, S, Culeddu, G, Hughes, DA, Dolezalova, P, Hampson, LV, Whitehead, J, Jayne, D, Ruperto, N, Tudur-Smith, C, Eleftheriou, D
المصدر: Arthritis & Rheumatology , 73 (9) pp. 1673-1682. (2021)
مصطلحات موضوعية: Bayesian, Child, Cyclophosphamide, Mycophenolate mofetil, Polyarteritis nodosa, Randomised controlled trial
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/10125340/9/Brogan_Arthritis%20%20%20Rheumatology%20-%202021%20-%20Brogan%20-%20Mycophenolate%20Mofetil%20Versus%20Cyclophosphamide%20for%20Remission%20Induction%20in.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10125340Test/
-
4دورية أكاديمية
المؤلفون: Evin, F., Goksen, D., Isik, E., Ozen, S., Atik, T., Ozkinay, F., Akcan, N.
مصطلحات موضوعية: Monogenic diabetes, IFIH1, Targeted next generation sequencing analysis (NGS), Whole exome sequencing (WES), ABCC8 gene, adolescent, adult, Article, BLK gene, child, clinical feature, controlled study, CTRC gene, diabetes mellitus, family history, female, GCK gene, gene, gene identification, genetic variability, heterozygosity, high throughput sequencing, HNF1A gene, human, hyperglycemia, IFIH1 gene, incidental finding, infant, INSR gene, IRS1 gene
العلاقة: Diabetes Research and Clinical Practice; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11454/92747Test; https://doi.org/10.1016/j.diabres.2023.110953Test; 205
-
5دورية أكاديمية
المؤلفون: Jelusic M., Sestan M., Cimaz R., Ozen S.
المساهمون: M. Jelusic, M. Sestan, R. Cimaz, S. Ozen
مصطلحات موضوعية: Biopsy, Children, Glomerulonephriti, Henoch-Schönlein purpura, Histology, IgA Vasculiti, Child, Preschool, Human, Kidney, Nephriti, Purpura, Schoenlein-Henoch, Settore MED/16 - Reumatologia, Settore MED/38 - Pediatria Generale e Specialistica
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30819179; info:eu-repo/semantics/altIdentifier/wos/WOS:000460081400001; volume:17; issue:1; firstpage:1; lastpage:7; numberofpages:7; journal:PEDIATRIC RHEUMATOLOGY ONLINE JOURNAL; http://hdl.handle.net/2434/666687Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85062345597
-
6دورية أكاديمية
المؤلفون: De Benedetti, F., Gattorno, M., Anton, J., Ben-Chetrit, E., Frenkel, J., Hoffman, H.M., Koné-Paut, I., Lachmann, H.J., Ozen, S., Simon, A., Zeft, A., Calvo Penades, I., Moutschen, M., Quartier, P., Kasapcopur, O., Shcherbina, A., Hofer, M., Hashkes, P.J., Van der Hilst, J., Hara, R., Bujan-Rivas, S., Constantin, T., Gul, A., Livneh, A., Brogan, P., Cattalini, M., Obici, L., Lheritier, K., Speziale, A., Junge, G.
المصدر: The New England journal of medicine, vol. 378, no. 20, pp. 1908-1919
مصطلحات موضوعية: Adolescent, Adult, Antibodies, Monoclonal/administration & dosage, Monoclonal/adverse effects, Monoclonal/therapeutic use, Child, Preschool, Dose-Response Relationship, Drug, Double-Blind Method, Familial Mediterranean Fever/drug therapy, Female, Fever/drug therapy, Hereditary Autoinflammatory Diseases/drug therapy, Humans, Injections, Subcutaneous, Interleukin-1beta/antagonists & inhibitors, Male, Mevalonate Kinase Deficiency/drug therapy, Young Adult
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29768139; info:eu-repo/semantics/altIdentifier/eissn/1533-4406; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_0FBB82A8DEDF0; https://serval.unil.ch/notice/serval:BIB_0FBB82A8DEDFTest; urn:issn:0028-4793; https://serval.unil.ch/resource/serval:BIB_0FBB82A8DEDF.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_0FBB82A8DEDF0Test
الإتاحة: https://doi.org/10.1056/NEJMoa1706314Test
https://serval.unil.ch/notice/serval:BIB_0FBB82A8DEDFTest
https://serval.unil.ch/resource/serval:BIB_0FBB82A8DEDF.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_0FBB82A8DEDF0Test -
7دورية أكاديمية
المؤلفون: Groot, N, de Graeff, N, Avcin, T, Bader-Meunier, B, Dolezalova, P, Feldman, B, Kenet, G, Koné-Paut, I, Lahdenne, P, Marks, SD, McCann, L, Pilkington, CA, Ravelli, A, van Royen-Kerkhof, A, Uziel, Y, Vastert, SJ, Wulffraat, NM, Ozen, S, Brogan, P, Kamphuis, S, Beresford, MW
المصدر: Annals of the Rheumatic Diseases , 76 (10) pp. 1637-1641. (2017)
مصطلحات موضوعية: Antiphospholipid Antibodies, Antiphospholipid Syndrome, Autoantibodies, Systemic Lupus Erythematosus, Treatment, Adolescent, Child, Preschool, Evidence-Based Medicine, Humans, Infant, Newborn
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/10049138/1/Groot_European_evidence-based_recommendations_paediatric_antiphospholipid.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10049138Test/
-
8دورية أكاديمية
المؤلفون: Groot, N, de Graeff, N, Avcin, T, Bader-Meunier, B, Brogan, P, Dolezalova, P, Feldman, B, Kone-Paut, I, Lahdenne, P, Marks, SD, McCann, L, Ozen, S, Pilkington, C, Ravelli, A, Royen-Kerkhof, AV, Uziel, Y, Vastert, B, Wulffraat, N, Kamphuis, S, Beresford, MW
المصدر: Annals of the Rheumatic Diseases , 76 (11) pp. 1788-1796. (2017)
مصطلحات موضوعية: Autoantibodies, Corticosteroids, Disease Activity, Systemic Lupus Erythematosus, Treatment, Adolescent, Age of Onset, Child, Europe, Evidence-Based Medicine, Humans, International Cooperation, Lupus Erythematosus, Systemic, Practice Guidelines as Topic, Young Adult
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/10049136/1/Groot_European_evidence-based_recommendations_lupus_erythematosus.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10049136Test/
-
9دورية أكاديمية
المؤلفون: Ombrello M. J., Remmers E. F., Tachmazidou I., Grom A., Foell D., Haas J. -P., Martini A., Gattorno M., Ozen S., Prahalad S., Zeft A. S., Bohnsack J. F., Mellins E. D., Ilowite N. T., Russo R., Len C., Hilario M. O. E., Oliveira S., Yeung R. S. M., Rosenberg A., Wedderburn L. R., Anton J., Schwarza T., Hinksb A., Bilginer Y., Park J., Cobb J., Satorius C. L., Han B., Baskin E., Signa S., Duerr R. H., Achkar J. P., Kamboh M. I., Kaufman K. M., Kottyan L. C., Pinto D., Scherer S. W., Alarcon-Riquelme M. E., Docampo E., Estivill X., Gul A., De Bakker P. I. W., Raychaudhuri S., Langefeld C. D., Thompson S., Zeggini E., Thomson W., Kastner D. L., Woo P.
المساهمون: Ombrello, M. J., Remmers, E. F., Tachmazidou, I., Grom, A., Foell, D., Haas, J. -P., Martini, A., Gattorno, M., Ozen, S., Prahalad, S., Zeft, A. S., Bohnsack, J. F., Mellins, E. D., Ilowite, N. T., Russo, R., Len, C., Hilario, M. O. E., Oliveira, S., Yeung, R. S. M., Rosenberg, A., Wedderburn, L. R., Anton, J., Schwarza, T., Hinksb, A., Bilginer, Y., Park, J., Cobb, J., Satorius, C. L., Han, B., Baskin, E., Signa, S., Duerr, R. H., Achkar, J. P., Kamboh, M. I., Kaufman, K. M., Kottyan, L. C., Pinto, D., Scherer, S. W., Alarcon-Riquelme, M. E., Docampo, E., Estivill, X., Gul, A., De Bakker, P. I. W., Raychaudhuri, S., Langefeld, C. D., Thompson, S., Zeggini, E., Thomson, W., Kastner, D. L., Woo, P.
مصطلحات موضوعية: Autoinflammation, Human leukocyte antigen, Still's disease, Systemic juvenile idiopathic arthriti, Arthritis, Juvenile, Child, Gene Frequency, Genetic Predisposition to Disease, Genotype, HLA-DRB1 Chain, Haplotype, Histocompatibility Antigens Class II, Human, Linkage Disequilibrium, Meta-Analysis as Topic, Odds Ratio, Risk Factor, Polymorphism, Single Nucleotide
وصف الملف: STAMPA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26598658; info:eu-repo/semantics/altIdentifier/wos/WOS:000367234700064; volume:112; firstpage:15970; lastpage:15975; numberofpages:6; journal:PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA; http://hdl.handle.net/11567/964445Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84952685055
-
10دورية أكاديمية
المؤلفون: Guran, T, Buonocore, F, Saka, N, Ozbek, MN, Aycan, Z, Bereket, A, Bas, F, Darcan, S, Bideci, A, Guven, A, Demir, K, Akinci, A, Buyukinan, M, Aydin, BK, Turan, S, Agladioglu, SY, Atay, Z, Abali, ZY, Tarim, O, Catli, G, Yuksel, B, Akcay, T, Yildiz, M, Ozen, S, Doger, E, Demirbilek, H, Ucar, A, Isik, E, Ozhan, B, Bolu, S, Ozgen, IT, Suntharalingham, JP, Achermann, JC
المصدر: Journal of Clinical Endocrinology and Metabolism , 101 (1) pp. 284-292. (2016)
مصطلحات موضوعية: Adolescent, Adrenal Insufficiency, Age of Onset, Child, Preschool, Cohort Studies, DNA, Female, Gene Expression, Genetic Variation, Humans, Infant, Newborn, Male, Mutation, Turkey
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/1483638/1/jc%252E2015-3250.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1483638Test/