Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Phaedon G. Kaklamanis"'
Publikováno v:
Acta Medica Iranica, Vol 55, Iss 8 (2017)
Behçet’s disease is a chronic, recurrent, inflammatory disorder characterized by orogenital ulcers and skin lesions; serious manifestations also include ocular, large vessel, gastrointestinal and neurological involvement. Genetic and unknown envir
Externí odkaz:
https://doaj.org/article/5913fdbe59244b408af3c4523acd8d47
Autor:
M A Kanakis, G. Vaiopoulos, Aristeidis G. Vaiopoulos, Phaedon G. Kaklamanis, Michael Samarkos, Christos C. Zouboulis, Violetta Kapsimali
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADV. 33(2)
BACKGROUND/OBJECTIVES Musculoskeletal manifestations are frequent in Adamantiades-Behcet's disease (ABD) but only represent non-specific clinical findings. They have not been included in the two commonly used sets of classification criteria. The occu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e98d0c7c0163843c7a1cf5c66907e0c
https://pubmed.ncbi.nlm.nih.gov/30394611
https://pubmed.ncbi.nlm.nih.gov/30394611
Autor:
Phaedon G. Kaklamanis, Kyriaki Katsouri, Meletios A. Kanakis, George Vaiopoulos, Aristeides G. Vaiopoulos, Stavroula Kyriazi
Publikováno v:
Case Reports in Medicine
Case Reports in Medicine, Vol 2015 (2015)
Case Reports in Medicine, Vol 2015 (2015)
Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disease, which affects a wide variety of organs including the spleen. Splenic involvement in SLE includes conditions such as splenomegaly, hyposplenism, infarction, and spontaneous rupt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f677a379f1421820c9aa6d675a29326a
https://doi.org/10.1155/2015/414102
https://doi.org/10.1155/2015/414102
Autor:
F. Ramos, Ahmadreza Jamshidi, Carlo Salvarani, Khalifa E. Sharquie, M. Bastos, J. E. Crook, A. V. Elonakov, J. Graña Gil, C. Resende, I. Ben Ghorbel, Ali Akbar Haghdoost, Michael Schirmer, M. Sliti-Khanfir, Samir H. Assaad-Khalil, J. A. Correia, Athanassios Kyrgidis, Nicolò Pipitone, R. M. Hayani, Bahar Sadeghi-Abdollahi, Kenneth T. Calamia, E. Ben-Chetrit, Z. S. Alekberova, N. Ziaei, Ashok Kumar, M. V. De Queiroz, Zilong Zhang, K. Elmuntaser, Hormoz Shams, Wafa Madanat, L. Carvalho, Y. Dong, WenChieh Chen, Phaedon G. Kaklamanis, Ayşe Boyvat, Habib Houman, J. Vaz Patto, Abdolhadi Nadji, C. Vasconcelos, Joana Vedes, Shigeaki Ohno, F. Paixão-Duarte, Christos C. Zouboulis, M. Akhlagi, Kenichi Namba, M. J. Serra, T. Tribolet De Abreu, J. Crespo, E. Arromdee, Cheyda Chams-Davatchi, C. M. Rosa, Y. K. Cheng, T. Tzellos, M. Baltaci, Bertrand Wechsler, A. Altenburg, Farhad Shahram, A. A. Ali, A. Al-Dalaan, I. Olivieri, Fereydoun Davatchi, Carlos Tadeu dos Santos Dias, A. R. Isayeva, S. Benamour
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 28:338-347
Objective Behcet's disease (BD) is a chronic, relapsing, inflammatory vascular disease with no pathognomonic test. Low sensitivity of the currently applied International Study Group (ISG) clinical diagnostic criteria led to their reassessment. Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d6ef7ce594547ddb1e368df05e37484
https://doi.org/10.1111/jdv.12107
https://doi.org/10.1111/jdv.12107
Autor:
Petros P. Sfikakis, Kalliopi Fragiadaki, Evi Delicha, Phaedon G. Kaklamanis, Stylianos Masselos, Nikos N. Markomichelakis
Publikováno v:
Rheumatology. 50:593-597
To compare a single infusion of the anti-TNF antibody infliximab vs CSs for acute panuveitis attacks in Behçet's disease (BD).A prospective, observational study of patients with panuveitis, who received either an infliximab infusion (5 mg/kg, 19 eye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2394b0b53d42b74b2052273f34957487
https://doi.org/10.1093/rheumatology/keq366
https://doi.org/10.1093/rheumatology/keq366
Autor:
Marwen Ghabra, Farida Fortune, Neslihan Abaci, Phaedon G. Kaklamanis, Oznur Aglar, Oliver J. Brand, John M O'Shea, Ahmet Gül, Benjamin D. Korman, Miles Stanford, Hulya Azakli, Colleen Satorius, Dongsik Bang, Young-Hun Cho, Ilknur Tugal-Tutkun, Elaine F. Remmers, Virginia G. Kaklamani, Gulsen Akman-Demir, Michael B. Dizon, Afet Akdag Kose, Burak Erer, Graham R. Wallace, Daniel L. Kastner, Duran Ustek, Massimo Gadina, Wei-Wei Chen, William E R Ollier, Christopher I. Amos, Aris Cakiris, Julie M. Le, Eldad Ben-Chetrit, Fulya Cosan, Michael J. Ombrello, Yohei Kirino, Zeliha Emrence, Gülsevim Azizlerli, Barbara Yang
Publikováno v:
Nature genetics
Behçet's disease is a genetically complex disease of unknown etiology characterized by recurrent inflammatory attacks affecting the orogenital mucosa, eyes and skin. We performed a genome-wide association study with 311,459 SNPs in 1,215 individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5be1fd6ac9b45f9ffccab1cd283931b1
https://doi.org/10.1038/ng.625
https://doi.org/10.1038/ng.625
Publikováno v:
Current Rheumatology Reports. 10:349-355
Behçet's disease (BD) is a chronic, multisystem, inflammatory disorder that is classified among the systemic vasculitidies. Its cause has yet to be determined, but genetic and environmental factors and immune dysregulation are thought to play a role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a2a51fcbb88301392b16dd8864e18c0
https://doi.org/10.1007/s11926-008-0057-y
https://doi.org/10.1007/s11926-008-0057-y
Autor:
H. Yazici, Petros P. Sfikakis, Erkan Alpsoy, Christos C. Zouboulis, Ahmet Gül, N. Pipitone, B. Wechsler, Phaedon G. Kaklamanis, Shigeaki Ohno, Michael Schirmer, Nikos N. Markomichelakis, Miles Stanford, Bahram Bodaghi, Samir H. Assaad-Khalil
Publikováno v:
Rheumatology. 46:736-741
Summary and conclusions The published evidence on the use of anti-TNF agents in BDconsists mainly of reports of the open use of infliximab,principally evaluated as an add-on therapy. The majority ofpatients suffered from relapsing, posterior segment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0aa80f149a028f8fb186275297ebe15f
https://doi.org/10.1093/rheumatology/kem034
https://doi.org/10.1093/rheumatology/kem034
Autor:
Aristeidis G, Vaiopoulos, Petros P, Sfikakis, Meletios A, Kanakis, George, Vaiopoulos, Phaedon G, Kaklamanis
Publikováno v:
Clinical and experimental rheumatology. 32(4 Suppl 84)
Behçet's disease is a chronic, recurrent, inflammatory disorder characterized by orogenital ulcers and skin lesions; serious manifestations also include ocular, large vessel, gastrointestinal and neurological involvement. Genetic and unknown environ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a5595299178ebc51787ee4facb5b9c17
https://pubmed.ncbi.nlm.nih.gov/25268668
https://pubmed.ncbi.nlm.nih.gov/25268668
Autor:
E Kaklamani, C. Caroline Blackwell, Phaedon G. Kaklamanis, Y Koumandaki, Klea Katsouyanni, L Sparos, D Karalis, D Trichopoulos, Donald M. Weir
Publikováno v:
FEMS Microbiology Letters. 76:151-158
The phagocytic activity of mononuclear phagocytes of A/J mice and Wistar rats was estimated by the carbon clearance test following injection of Mycoplasma arthritidis. In mice, the overall phagocytic activity was significantly increased at the end of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c549a23030fcd5573a93c3753b8f728d
https://doi.org/10.1111/j.1574-6968.1991.tb04208.x
https://doi.org/10.1111/j.1574-6968.1991.tb04208.x