Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Belgin Kesim"'
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Akademický článek
Outcomes of long term treatments of type I hereditary angioedema in a Turkish family
Autor: Gulsen Akoglu, Belgin Kesim, Gokhan Yildiz, Ahmet Metin
Publikováno v: Anais Brasileiros de Dermatologia, Vol 92, Iss 5, Pp 655-660 (2017)
Abstract: Background: Hereditary angioedema is a rare autosomal dominantly inherited immunodeficiency disorder characterized by potentially life-threatening angioedema attacks. Objective: We aimed to investigate the clinical and genetic features of a
Externí odkaz: https://doaj.org/article/f3a00b22c3414b6f9d1992d1dc0a8935
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2
Outcomes of long term treatments of type I hereditary angioedema in a Turkish family
Autor: Belgin Kesim, Gokhan Yildiz, Ahmet Metin, Gulsen Akoglu
Publikováno v: Anais Brasileiros de Dermatologia v.92 n.5 2017
Anais brasileiros de dermatologia
Sociedade Brasileira de Dermatologia (SBD)
instacron:SBD
Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Volume: 92, Issue: 5, Pages: 655-660, Published: OCT 2017
Anais Brasileiros de Dermatologia, Vol 92, Iss 5, Pp 655-660 (2017)
Background: Hereditary angioedema is a rare autosomal dominantly inherited immunodeficiency disorder characterized by potentially life-threatening angioedema attacks. Objective: We aimed to investigate the clinical and genetic features of a family wi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02ef4609e784937547d1e30f463238ac
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962017000500655
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3
Content Vol. 156, 2011
Autor: Jean-François Nicolas, Asghar Aghamohammadi, Zehra Oya Uyguner, Jan Walter Schroeder, P. Schöpf, G. Sahin, Tamara Vorobjova, Ferhan Özşeker, Mahroo Mirahmadian, M. Russello, Nima Rezaei, T. Herzinger, Gül Karakaya, Satz Mengensatzproduktion, M. Pagani, Shiro Amano, A. Antico, Sarah Abolmaali, Julia Rodriguez, Junichiro Morioka, Annice Heratizadeh, Sara Pasqualetti, Kaupo Teesalu, Franco Frati, Mikiro Mori, Carmen Burbano, Murat Dal, Kazumi Kodaira, Tomohiko Usui, Diana Mamerow, Joseph Haddad, Cristoforo Incorvaia, Hiromi Yano, Hironori Sagara, Karim Allaf, Philippe Moingeon, J. Mullol, Kenya Kohyama, Bahattin Çolakoğlu, Chi-Chih Huang, Takao Nagano, Shyuzo Abe, Bertrand Dubois, Nihal Mete Gökmen, Füsun Erdenen, Ambra Mascheri, Mohammad Biglari, Michele Nichelatti, E. Compalati, Chao-Chien Wu, Tsu-Nai Wang, Meng-Chih Lin, Marina Panarina, Okan Gülbahar, Dominique Kaiserlian, Motohiro Kurosawa, Tung-Heng Wang, Christophe Dercamp, Mercedes M. Pedrosa, Mamoru Tanaka, Hideharu Funatsu, Ming-Shyan Huang, Maryam Tabatabaeiyan, Hiroaki Inamura, Tsu-Yu Yuan, Laura Farioli, Thomas Werfel, Elide A. Pastorello, Alessandro Marocchi, Mercedes Muzquiz, Shao-Hua Lu, Laura Primavesi, Tatsuo Yukawa, Ying-Chin Ko, F. Ruëff, Valerio Pravettoni, Aytül Sin, Li-Ling Yang, Reem Kanjarawi, Chrysi Stafylaraki, Karine Adel-Patient, Soichiro Hozawa, Yasuko Kato, L.E. Walther, Hossein Asgarian-Omran, Imke Satzger, Kaire Heilman, O. Pfaar, Marina Mauro, Kasra Moazzami, Ömür Ardeniz, Ivi Ojakivi, Mayumi Ota, K. Hörmann, Ken Haruma, B. Przybilla, G. Passalacqua, Yen-Hsiung Liao, Jesus F. Crespo, L. Klimek, Claude André, Belgin Kesim, Nathalie Etchart, P.P. Vescovi, Tatsuya Mimura, Aslı Gelincik, Gianbattista Gazzola, Druck Reinhardt Druck Basel, Chin-Chou Wang, Oivi Uibo, Hidetaka Noma, Hassan Abolhassani, Linda Borgonovo, Raivo Uibo, Nima Parvaneh, Beatriz Cabanillas, Marta Piantanida, Margarete Niebuhr, Suna Büyüköztürk, Lawrence B. Schwartz, Joseph Scibilia, Carmen Cuadrado
Publikováno v: International Archives of Allergy and Immunology. 156:I-IV
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2db039bd29769d481fecdbe5e0f3e0b1
https://doi.org/10.1159/000331122
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The Turkish Hereditary Angioedema Pilot Study (TURHAPS): The First Turkish Series of Hereditary Angioedema
Autor: Füsun Erdenen, Aytül Sin, Ferhan Özşeker, Belgin Kesim, Suna Büyüköztürk, Ömür Ardeniz, Aslı Gelincik, Zehra Oya Uyguner, Nihal Mete Gökmen, Okan Gülbahar, Gül Karakaya, Murat Dal, Bahattin Çolakoğlu
Publikováno v: International Archives of Allergy and Immunology. 156:443-450
Background: No published data presently exist concerning hereditary angioedema (HAE) in Turkey. The aim of the study was to initiate a preliminary multicentric evaluation about HAE and to determine the genetic properties of Turkish patients. Methods:
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f426f8033951c3c8b463b5ff1112e6a6
https://doi.org/10.1159/000323915
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5
Novel ubiquitin protein ligase E3 component N-Recognin 1 gene mutation in johanson–blizzard syndrome: Development of hypothyroidism during infancy
Autor: Ali Bulbul, Belgin Kesim, Maja Sukalo, Özgür Kirbiyik, Martin Zenker, Muhittin Çelik, Sinan Uslu
Publikováno v: Journal of Clinical Neonatology. 6:179
Johanson–Blizzard syndrome (JBS) is a rare autosomal recessive disorder, characterized by exocrine pancreatic deficiency and a wide range of other abnormalities. Here, we present an infant with failure to thrive, exocrine pancreatic deficiency, dev
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bd7b4a53bbeb958f4af4aeb0c030598d
https://doi.org/10.4103/jcn.jcn_204_15
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7
Subject Index Vol. 156, 2011
Autor: Chrysi Stafylaraki, K. Hörmann, Thomas Werfel, Sarah Abolmaali, Meng-Chih Lin, Kaupo Teesalu, Tamara Vorobjova, Maryam Tabatabaeiyan, Tatsuo Yukawa, Kazumi Kodaira, Nima Rezaei, Reem Kanjarawi, Jesus F. Crespo, Shao-Hua Lu, Nihal Mete Gökmen, Takao Nagano, Cristoforo Incorvaia, Füsun Erdenen, Hironori Sagara, Chi-Chih Huang, Bahattin Çolakoğlu, Laura Farioli, Nathalie Etchart, Imke Satzger, Elide A. Pastorello, Zehra Oya Uyguner, Tsu-Nai Wang, Mercedes Muzquiz, Alessandro Marocchi, Druck Reinhardt Druck Basel, Oivi Uibo, P.P. Vescovi, Valerio Pravettoni, Mercedes M. Pedrosa, Li-Ling Yang, G. Passalacqua, Laura Primavesi, Mamoru Tanaka, L.E. Walther, Linda Borgonovo, O. Pfaar, Tatsuya Mimura, Mayumi Ota, Aslı Gelincik, Claude André, Belgin Kesim, Raivo Uibo, P. Schöpf, Nima Parvaneh, Beatriz Cabanillas, Gianbattista Gazzola, Ferhan Özşeker, Yen-Hsiung Liao, Mahroo Mirahmadian, M. Russello, Annice Heratizadeh, T. Herzinger, Chin-Chou Wang, Hidetaka Noma, Ming-Shyan Huang, Kasra Moazzami, Ömür Ardeniz, Tomohiko Usui, Ivi Ojakivi, Junichiro Morioka, Karine Adel-Patient, Franco Frati, Ken Haruma, B. Przybilla, Hossein Asgarian-Omran, Marina Mauro, Michele Nichelatti, Hassan Abolhassani, Karim Allaf, Asghar Aghamohammadi, Jean-François Nicolas, Jan Walter Schroeder, Shiro Amano, A. Antico, Ambra Mascheri, Mohammad Biglari, Mikiro Mori, J. Mullol, Okan Gülbahar, Hideharu Funatsu, Ying-Chin Ko, F. Ruëff, Soichiro Hozawa, Yasuko Kato, Kaire Heilman, Joseph Haddad, Philippe Moingeon, Shyuzo Abe, Bertrand Dubois, Chao-Chien Wu, Aytül Sin, Dominique Kaiserlian, Sara Pasqualetti, Motohiro Kurosawa, Gül Karakaya, Satz Mengensatzproduktion, Murat Dal, Diana Mamerow, Hiromi Yano, Tung-Heng Wang, Christophe Dercamp, Marta Piantanida, Margarete Niebuhr, G. Sahin, Julia Rodriguez, Marina Panarina, Tsu-Yu Yuan, Lawrence B. Schwartz, Joseph Scibilia, Carmen Burbano, Carmen Cuadrado, Suna Büyüköztürk, Hiroaki Inamura, L. Klimek, Kenya Kohyama, E. Compalati, M. Pagani
Publikováno v: International Archives of Allergy and Immunology. 156:471-472
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::93bb2929f2dab9fdcecec47d580fd2df
https://doi.org/10.1159/000331121
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