Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1) von Ménasché, Gaël, Ho, Chen Hsuan, Sanal, Ozden, Feldmann, Jérôme, Tezcan, Ilhan, Ersoy, Fügen, Houdusse, Anne, Fischer, Alain, Basile, Geneviève de Saint

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Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome von Certain, Stéphanie, Le Deist, Françoise, Feldmann, Jérôme, Fischer, Alain, de Saint Basile, Geneviève, Ménasché, Gaël, Pastural, Elodie, Wulffraat, Nico, Dupuis, Sophie, Ersoy, Fügen, Bianchi, Diana

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Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2) von Revy, Patrick, Muto, Taro, Levy, Yves, Geissmann, Frédéric, Plebani, Alessandro, Sanal, Ozden, Catalan, Nadia, Forveille, Monique, Dufourcq-Lagelouse, Rémi, Gennery, Andrew, Tezcan, Ilhan, Ersoy, Fugen, Kayserili, Hulya, Ugazio, Alberto G, Brousse, Nicole, Muramatsu, Masamichi, Notarangelo, Luigi D, Kinoshita, Kazuo, Honjo, Tasuku, Fischer, Alain, Durandy, Anne

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Transient hypogammaglobulinemia of infancy: Clinical and immunologic features of 40 new cases von Kiliç, S Şebnem, Tezcan, İlhan, Sanal, Özden, Metin, Ayşe, Ersoy, Fügen

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Mutations in Igα (CD79a) result in a complete block in B-cell development von Minegishi, Yoshiyuki, Coustan-Smith, Elaine, Rapalus, Lisa, Ersoy, Fügen, Campana, Dario, Conley, Mary Ellen

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Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1) von Ménasché, Gaël, Ho, Chen Hsuan, Sanal, Ozden, Feldmann, Jérôme, Tezcan, Ilhan, Ersoy, Fügen, Houdusse, Anne, Fischer, Alain, de Saint Basile, Geneviève

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Clinical features of chronic granulomatous disease: a series of 26 patients from a single center von Turul-Ozgür, Tuba, Türkkani-Asal, Gülten, Tezcan, Ilhan, Köker, M Yavuz, Metin, Ayşe, Yel, Leman, Ersoy, Fügen, Sanal, Ozden

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A family with hyperimmunoglobulin M syndrome and systemic amyloidosis von Öner, Ayşe, Demircin, Gülay, Erdoğan, Özlem, Bülbül, Mehmet, Memiş, Leyla, Arda, Nilüfer, Ersoy, Fügen

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Griscelli disease: Genotype-phenotype correlation in an array of clinical heterogeneity von SANAL, Ozden, ERSOY, Fugen, TEZCAN, Ilhan, METIN, Ayse, YEL, Leman, MENASCHE, Gaël, GÜRGEY, Aytemiz, BERKEL, Izzet, DE SAINT BASILE, Geneviève

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The efficacy of immunoglobulin replacement therapy in the long-term follow-up of the B-cell deficiencies (XLA, HIM, CVID) von Bayrakci, Benan, Ersoy, Fügen, Sanal, Ozden, Kiliç, Sebnem, Metin, Ayşe, Tezcan, Ilhan

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Polymorphism of the Fourth Component of Complement in Turks von METIN, AYŞE, SANAL, ÖZDEN, ERSOY, FÜGEN, TEZCAN, İLHAN, BERKEL, A. İZZET, IRKEÇ, CEYLA

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Localization of an ataxia-telangiectasia gene to chromosome 11q22-23 von Gatti, Richard A, Berkel, Izzet, Boder, Elena, Braedt, Gary, Charmley, Patrick, Concannon, Patrick, Ersoy, Fugen, Foroud, Tatiana, Jaspers, Nicholas G. J, Lange, Kenneth, Lathrop, G. Mark, Leppert, Mark, Nakamura, Yusuke, O'Connell, Peter, Paterson, Malcolm, Salser, Winston, Sanal, Ozden, Silver, Jack, Sparkes, Robert S, Susi, Ellen, Weeks, Daniel E, Wei, Shan, White, Ray, Yoder, Freda

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The European Society for Immunodeficiencies (ESID) registry 2014 von Grimbacher, B.

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Lack of association between TLR4 polymorphism and severe gram-negative bacterial infection in neonates von ÖZGÜR, Tuba TURUL

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Association of tumour necrosis factor-alpha -308 G/A polymorphism with primary open-angle glaucoma von Bozkurt, Banu, Mesci, Lutfiye, Irkec, Murat, Ozdag, Burcin B, Sanal, Ozden, Arslan, Umut, Ersoy, Fugen, Tezcan, Ilhan

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Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1) von Ménasché, Gaël, Hsuan Ho, Chen, Sanal, Ozden, Feldmann, Jérôme, Tezcan, Ilhan, Ersoy, Fügen, Houdusse, Anne, Fischer, Alain, de Saint Basile, Geneviève

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Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1) von Menasche, G.

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A CASE OF INTERLEUKIN-12 RECEPTOR β-1 DEFICIENCY WITH RECURRENT LEISHMANIASIS von Sanal, Ozden, Turkkani, Gulten, Gumruk, Fatma, Yel, Leman, Secmeer, Gulten, Tezcan, Ilhan, Kara, Ates, Ersoy, Fugen

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Common variable immunodeficiency in a patient with neurofibromatosis von Kiliç, Şebnem, Tezcan, Ilhan, Sanal, Özden, Ersoy, Fügen

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Altered apoptotic profiles in irradiated patients with increased toxicity von Crompton, Nigel E.A, Miralbell, Raymond, Rutz, Hans-Peter, Ersoy, Fügen, Sanal, Özden, Wellmann, Danielle, Bieri, Sabine, Coucke, Philippe A, Emery, Gillian C, Shi, Yu-Quan, Blattmann, Hans, Ozsahin, Mahmut

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