Zobrazeno 1 - 10
of 20
pro vyhledávání: '"M. Cem Mat"'
Publikováno v:
Behçet Syndrome ISBN: 9783030241308
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68179752ba5481dd36cd06b7e5c66029
https://doi.org/10.1007/978-3-030-24131-5_4
https://doi.org/10.1007/978-3-030-24131-5_4
Autor:
Elif, Dincses, Sinem Nihal, Esatoglu, Yesim, Ozguler, Ugur, Uygunoglu, Vedat, Hamuryudan, Emire, Seyahi, Melike, Melikoglu, Izzet, Fresko, Didar, Ucar, Yilmaz, Ozyazgan, Zekayi, Kutlubay, M Cem, Mat, Sebahattin, Yurdakul, Aksel, Siva, Gulen, Hatemi
Publikováno v:
Clinical and experimental rheumatology. 37(6)
The efficacy and safety of biosimilar infliximab (bio-IFX) was shown in randomised controlled trials and it was approved for all indications of the reference product in several countries. However, a previous case series of 3 patients with Behçet's s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac420c0b9669c75c74b013f3c9aae57a
https://pubmed.ncbi.nlm.nih.gov/31856937
https://pubmed.ncbi.nlm.nih.gov/31856937
Autor:
M. Cem Mat
Publikováno v:
Türkderm, Vol 43, Iss Suppl 2, Pp 92-97 (2009)
Behcet disease is a chronic disease of unknown etiology. It is a systemic vasculitis which can affect many systems and the disease course may be severe in young males. The main aim of treatment is to reduce inflammation and control symptoms of the di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::b718c2430bf226cfe1a9a426d0fa7d75
http://www.journalagent.com/z4/download_fulltext.asp?pdir=turkderm&plng=tur&un=TURKDERM-88700
http://www.journalagent.com/z4/download_fulltext.asp?pdir=turkderm&plng=tur&un=TURKDERM-88700
Publikováno v:
Clinics in dermatology. 32(3)
Behcet's disease usually begins with cutaneous manifestations, such as recurrent aphthous stomatitis, genital ulcers, erythema nodosum-like lesions, papulopustular findings, and pathergy phenomenon. Recurrent aphthous stomatitis is generally the firs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d08962b78cae6c94f162a98c5b56e994
https://pubmed.ncbi.nlm.nih.gov/24767193
https://pubmed.ncbi.nlm.nih.gov/24767193
Publikováno v:
International Journal of Dermatology. 45:554-556
Background Although genital ulceration with or without scar formation is an important manifestation of Behcet's syndrome, formal data on the rate of genital scarring are lacking. Objective To study prospectively the frequency of genital scar formatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb33cedb22c8723af890ba1071aa4088
https://doi.org/10.1111/j.1365-4632.2006.02859.x
https://doi.org/10.1111/j.1365-4632.2006.02859.x
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 9:161-165
Background Intraepidermal IgA pustulosis is a rare vesiculopustular condition characterized by intercellular IgA deposits, neutrophilic infiltration and mild acantholysis. This condition is usually reported in middle-aged or elderly people. We presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::417ff85c104abc9f5ec090125f85fc28
https://doi.org/10.1016/s0926-9959(97)00040-8
https://doi.org/10.1016/s0926-9959(97)00040-8
Publikováno v:
The American Journal of dermatopathology. 36(4)
Rosai-Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a benign proliferative disorder of histiocytes with an unknown etiology. It is a rare disease characterized by overproduction and accumulation of histiocytes wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3546d7538fe045cc6bbf71a184adc85
https://pubmed.ncbi.nlm.nih.gov/23863552
https://pubmed.ncbi.nlm.nih.gov/23863552
Publikováno v:
International Journal of Nanomedicine
M Sedef Erdal,1 Gül Özhan,2 M Cem Mat,3 Yıldız Özsoy,1 Sevgi Güngör1 1Department of Pharmaceutical Technology, 2Department of Pharmaceutical Toxicology, Faculty of Pharmacy, 3Department of Dermatology, Cerrahpasa Medical Faculty, Istanbul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65a5dcf2626ef18dcdfc4e85c17ae5cd
https://doi.org/10.2147/ijn.s96243
https://doi.org/10.2147/ijn.s96243
Autor:
Cuyan Demirkesen, M. Cem Mat, Mehmet Agirbasli, Zehra Aşiran Serdar, Mesut Eren, Douglas E. Vaughan, Dilek Seckin, Tuba Zara, Fatih Eren, Sheila B. Murphy
Publikováno v:
Journal of thrombosis and thrombolysis. 32(1)
Livedoid vasculopathy (LV) is a chronic, recurrent, painful cutaneous disease with distinctive clinical features and an uncertain etiology. The skin lesions are recognizable by focal purpura, depigmentation and shallow ulcers. Thrombophilic condition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c10d7bf74355ef9b469a57fca262206d
https://pubmed.ncbi.nlm.nih.gov/21311952
https://pubmed.ncbi.nlm.nih.gov/21311952
Publikováno v:
Behçet’s Syndrome ISBN: 9781441956408
The diagnosis of Behcet’s disease is based on clinical features. There is no specific diagnostic test. Skin-mucosa lesions like recurrent aphtous stomatitis, genital ulcers, and various cutaneous lesions are its foremost manifestations. The presenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88d38c8fa2d0c3d12ab901a6f75e786e
https://doi.org/10.1007/978-1-4419-5641-5_4
https://doi.org/10.1007/978-1-4419-5641-5_4