المؤلفون: Haralambous, E., Weiss, H. A., Radalowicz, A., Hibberd, M. L., Booy, R., Levin, M.

المصدر: Epidemiology and Infection, 2003 Jun 01. 130(3), 413-418.

URL الوصول: https://www.jstor.org/stable/3865458

المؤلفون: Callaghan, M J, Rockett, K, Banner, C, Haralambous, E, Betts, H, Faust, S, Maiden, M C J, Kroll, J S, Levin, M, Kwiatkowski, D P, Pollard, A J

المصدر: Genes & Immunity ; volume 9, issue 1, page 30-37 ; ISSN 1466-4879 1476-5470

الاتاحة: http://dx.doi.org/10.1038/sj.gene.6364442
https://www.nature.com/articles/6364442.pdf
https://www.nature.com/articles/6364442

المؤلفون: Cremers, F. P M, Kimberling, W. J, Kulm, M., de Brouwer, A. P, van Wijk, E., te Brinke, H., Cremers, C. W R J, Hoefsloot, L. H, Banfi, S., Simonelli, F., Fleischhauer, J. C, Berger, W., Kelley, P. M, Haralambous, E., Bitner-Glindzicz, M., Webster, A. R, Saihan, Z., De Baere, E., Leroy, B. P, Silvestri, G., McKay, G. J, Koenekoop, R. K, Millan, J. M, Rosenberg, T., Joensuu, T., Sankila, E.-M., Weil, D., Weston, M. D, Wissinger, B., Kremer, H.

المصدر: Journal of Medical Genetics ; volume 44, issue 2, page 153-160 ; ISSN 1468-6244

الاتاحة: http://dx.doi.org/10.1136/jmg.2006.044784
https://syndication.highwire.org/content/doi/10.1136/jmg.2006.044784

المؤلفون: Valavanidis, A., Haralambous, E.

المصدر: Redox Report ; volume 6, issue 3, page 161-171 ; ISSN 1351-0002 1743-2928

الاتاحة: http://dx.doi.org/10.1179/135100001101536274
http://www.tandfonline.com/doi/pdf/10.1179/135100001101536274

المؤلفون: Haralambous, E, Dolly, S, Hibberd, M, Litt, D, Udalova, I, O'dwyer, C, Langford, P, Simon Kroll, J, Levin, M

Relation: https://ora.ox.ac.uk/objects/uuid:1eabca63-6d9e-427e-bd45-f7e1b3aa9992; https://doi.org/10.1080/00365540600643203

الاتاحة: https://doi.org/10.1080/00365540600643203
https://ora.ox.ac.uk/objects/uuid:1eabca63-6d9e-427e-bd45-f7e1b3aa9992

المؤلفون: Renner, P., Roger, T., Bochud, P.Y., Sprong, T., Sweep, C.G.J., Bochud, M., Faust, S.N., Haralambous, E., Betts, H., Chanson, A.L., Reymond, M.K., Mermel, E., Erard, V., Deuren, M. van, Read, R.C., Levin, M., Calandra, T

المصدر: The Faseb Journal, 26, 2, pp. 907-16

مصطلحات موضوعية: IGMD 6: Hormonal regulation ONCOL 5: Aetiology, screening and detection, N4i 1: Pathogenesis and modulation of inflammation

Relation: http://hdl.handle.net/2066/110607; https://doi.org/10.1096/fj.11-195065

الاتاحة: http://hdl.handle.net/2066/110607
https://doi.org/10.1096/fj.11-195065

المؤلفون: Emonts, Marieke, Vermont, CE, Houwing-Duistermaat, JJ, Haralambous, E, Gaast-de Jongh, CE, Hazelzet, Jan, Faust, SN, Betts, H, Hermans, PWM, Levin, M, Groot, Ronald

المصدر: Emonts , M , Vermont , CE , Houwing-Duistermaat , JJ , Haralambous , E , Gaast-de Jongh , CE , Hazelzet , J , Faust , SN , Betts , H , Hermans , PWM , Levin , M & Groot , R 2010 , ' Polymorphisms in PARP, IL1B, IL4, C1INH, DEFB1 and DEFA4 in meningococcal disease in three populations ' , Shock , vol. 34 , no. 1 , pp. 17-22 . https://doi.org/10.1097/SHK.0b013e3181ce2c7d

مصطلحات موضوعية: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMM045408A, name=EMC MM-04-54-08-A, /dk/atira/pure/keywords/researchprograms/AFL001000/EMCOR025406, name=EMC OR-02-54-06

Relation: https://pure.eur.nl/en/publications/12ef6dcc-f7ae-4087-9202-9e27c249cd94

الاتاحة: https://pure.eur.nl/en/publications/12ef6dcc-f7ae-4087-9202-9e27c249cd94
https://doi.org/10.1097/SHK.0b013e3181ce2c7d
http://hdl.handle.net/1765/64528

المؤلفون: Emonts, M., Vermont, C.L., Houwing-Duistermaat, J.J., Haralambous, E., Gaast-de Jongh, C.E., Hazelzet, J.A., Faust, S.N., Betts, H., Hermans, P.W.M., Levin, M., Groot, R. de, St Mary's Imperial Coll Grp, Erasmus MC-Sophia Children's Hosp

المصدر: Shock. Injury,Inflammation and Sepsis

مصطلحات موضوعية: Meningococcal infection immune response genetic variation pediatric infectious disease transmission disequilibrium test prognostic score serine-protease septic shock c1 inhibitor children sepsis gene association susceptibility interleukin-4

Relation: lumc-id: 5001954; https://hdl.handle.net/1887/110326

الاتاحة: https://hdl.handle.net/1887/110326

المؤلفون: Callaghan, M.J., Rockett, K., Banner, C., Haralambous, E., Betts, H., Faust, S., Maiden, M.C.J., Kroll, J. S., Levin, M., Kwiatkowski, D.P., Pollard, A.J.

Relation: Callaghan, M.J., Rockett, K., Banner, C., Haralambous, E., Betts, H., Faust, S., Maiden, M.C.J., Kroll, J. S., Levin, M., Kwiatkowski, D.P. and Pollard, A.J. (2008) Haplotypic diversity in human CEACAM genes: effects on susceptibility to meningococcal disease. Genes and Immunity, 9 (1), 30-37. (doi:10.1038/sj.gene.6364442 ). (PMID:17960155 )

الاتاحة: https://eprints.soton.ac.uk/70815/

المؤلفون: Haralambous, E, Hibberd, ML, Hermans, PWM, Ninis, N, Nadel, S, Levin, M

المصدر: Haralambous , E , Hibberd , ML , Hermans , PWM , Ninis , N , Nadel , S & Levin , M 2003 , ' Role of functional plasminogen-activator-inhibitor-1 4G/5G promoter polymorphism in susceptibility, severity, and outcome of meningococcal disease in Caucasian children ' , Critical Care Medicine , vol. 31 , no. 12 , pp. 2788-2793 . https://doi.org/10.1097/01.CCM.0000100122.57249.5D

مصطلحات موضوعية: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMM045408A, name=EMC MM-04-54-08-A

الاتاحة: https://pure.eur.nl/en/publications/11bd0a7e-8256-4eaa-bc98-0b97193e87d6
https://doi.org/10.1097/01.CCM.0000100122.57249.5D
http://hdl.handle.net/1765/61569

المؤلفون: Haralambous, E, Weiss, HA, Radalowicz, A, Hibberd, ML, Booy, R, Levin, M

وصف الملف: text

Relation: https://researchonline.lshtm.ac.uk/id/eprint/16124/1/EI9.pdf; Haralambous, E; Weiss, HA ; Radalowicz, A; Hibberd, ML ; Booy, R; Levin, M; (2003) Sibling familial risk ratio of meningococcal disease in UK Caucasians. Epidemiology and infection, 130 (3). pp. 413-418. ISSN 0950-2688 DOI: https://doi.org/10.1017/s0950268803008513

الاتاحة: https://researchonline.lshtm.ac.uk/id/eprint/16124/
https://researchonline.lshtm.ac.uk/id/eprint/16124/1/EI9.pdf

المؤلفون: Hosangady, A., Haralambous, E., Levin, M., Hibberd, M.

المصدر: Journal of Infection ; volume 44, issue 2, page 127 ; ISSN 0163-4453

الاتاحة: http://dx.doi.org/10.1016/s0163-4453(02)90360-9
https://api.elsevier.com/content/article/PII:S0163445302903609?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0163445302903609?httpAccept=text/plain

المؤلفون: Dolly, S., Haralambous, E., Levin, M., Hibberd, M.

المصدر: Journal of Infection ; volume 44, issue 2, page 107 ; ISSN 0163-4453

الاتاحة: http://dx.doi.org/10.1016/s0163-4453(02)90280-x
https://api.elsevier.com/content/article/PII:S016344530290280X?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S016344530290280X?httpAccept=text/plain

المؤلفون: Valavanidis, A Haralambous, E

مصطلحات موضوعية: complex mixtures

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2127::d79ab786a732dffc66328332b99d0101
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3054583

المؤلفون: Cremers, F.P.M., Kimberling, W.J., Kulm, M., Brouwer, A.P.M. de, Wijk, E. van, Brinke, H. te, Cremers, C.W.R.J., Hoefsloot, L.H., Banfi, S., Simonelli, F., Fleischhauer, J.C., Berger, W., Kelley, P.M., Haralambous, E., Bitner-Glindzicz, M., Webster, A.R., Saihan, Z., Baere, E. de, Leroy, B.P., Silvestri, G., McKay, G.J., Koenekoop, R.K., Millan, J.M., Rosenberg, T., Joensuu, T., Sankila, E.M., Weil, D., Weston, M.D., Wissinger, B., Kremer, H.

المصدر: Journal of Medical Genetics; 153; 160; 0022-2593; 2; 44; ~Journal of Medical Genetics~153~160~~~0022-2593~2~44~~

URL: http://hdl.handle.net/2066/52397

المؤلفون: Haralambous, E., Hibberd, M.L., Hermans, P.W.M., Ninis, N., Nadel, S., Levin, M.

المصدر: Critical Care Medicine; 2788; 93; 0090-3493; 31; ~Critical Care Medicine~2788~93~~~0090-3493~~31~~

URL: http://hdl.handle.net/2066/185167
https://doi.org/10.1097/01.CCM.0000100122.57249.5D

المؤلفون: Callaghan, M. J., Rockett, K., Banner, C., Haralambous, E., Betts, H., Faust, S., Maiden, M. C. J., Kroll, J. S., Levin, M., Kwiatkowski, D. P., Pollard, A. J.

المصدر: Genes & Immunity; Jan2008, Vol. 9 Issue 1, p30-37, 8p, 2 Diagrams

مصطلحات موضوعية: DISEASE susceptibility, GENETIC polymorphisms, DISEASES, GENETICS education, CARCINOEMBRYONIC antigen, NEISSERIA meningitidis, BACTERIAL diseases, PLEOMORPHIC fungi, IMMUNITY, EDUCATION

المؤلفون: Andrew R. Webster, Robert K. Koenekoop, Zubin Saihan, P.M. Kelley, Elfride De Baere, Arjan P.M. de Brouwer, Maigi Külm, Elene Haralambous, Eeva-Marja Sankila, Erwin van Wijk, Johannes Fleischhauer, Sandro Banfi, Michael D. Weston, William J. Kimberling, Dominique Weil, Gareth J. McKay, Bart P. Leroy, José M. Millán, Lies H. Hoefsloot, Francesca Simonelli, Cor W. R. J. Cremers, Tarja Joensuu, Thomas Rosenberg, Giuliana Silvestri, Heleen te Brinke, Bernd Wissinger, Maria Bitner-Glindzicz, Hannie Kremer, Wolfgang Berger, Frans P.M. Cremers

المساهمون: Cremers, Fp, Kimberling, Wj, Kulm, M, DE BROUWER, A, VAN WIJK, E, TE BRINKE, H, Cremers, Cw, Hoefsloot, Lh, Banfi, Sandro, Simonelli, Francesca, Fleischhauer, Jc, Berger, W, Kelley, Pm, Haralambous, E, BITNER GLINDZICZ, M, Webster, Ar, Saihan, Z, DE BAERE, E, Leroy, Bp, Silvestri, G, Mckay, G, Koenekoop, Rk, Millan, Jm, Rosenberg, T, Joensuu, T, Sankila, Em, Weil, D, Weston, Md, Wissinger, B, Kremer, H.

المصدر: JOURNAL OF MEDICAL GENETICS
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Journal of Medical Genetics, 44, 153-60
Journal of Medical Genetics, 44, 2, pp. 153-60

مصطلحات موضوعية: RECESSIVE RETINITIS-PIGMENTOSA, Microarray, Genetics and epigenetic pathways of disease [NCMLS 6], Genotype, Hearing loss, Usher syndrome, LEBER CONGENITAL AMAUROSIS, Biology, USH2A GENE, EAR SENSORY CELLS, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, SYNDROME TYPE 1F, MUTATION DETECTION, SYNDROME-TYPE-II, Retinitis pigmentosa, Genetics, medicine, Medicine and Health Sciences, Perception and Action [DCN 1], otorhinolaryngologic diseases, Neurosensory disorders [UMCN 3.3], Humans, Genotyping, Genetics (clinical), 030304 developmental biology, DNA Primers, Oligonucleotide Array Sequence Analysis, 0303 health sciences, Genetic heterogeneity, HEARING-LOSS, 030305 genetics & heredity, Genetic Variation, DNA, medicine.disease, ARRAYED PRIMER EXTENSION, eye diseases, 3. Good health, MYOSIN VIIA GENE, Europe, Genetic defects of metabolism [UMCN 5.1], sense organs, medicine.symptom, Functional Neurogenomics [DCN 2], Usher Syndromes, PCDH15, Letter to JMG

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1907102e04096faab331e49feaf22c1
https://hdl.handle.net/2066/52397