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Fügen Ersoy

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Tuba Turul-Ozgür; Gülten Türkkani-Asal; Ilhan Tezcan; Mustafa Yavuz Köker; Ayse Metin; Leman Yel; Fügen Ersoy; Ozden Sanal
Clinical features of chronic granulomatous disease: a series of 26 patients from a single center.
Mustafa Yavuz Köker; Ozden Sanal; Martin de Boer; Ilhan Tezcan; Ayse Metin; Fügen Ersoy; Dirk Roos
Mutations of chronic granulomatous disease in Turkish families.
Tuba Turul Ozgur; Gulten Turkkan Asal; Aytemiz Gurgey; Ilhan Tezcan; Fügen Ersoy; Ozden Sanal
Acquired factor VIII deficiency associated with a novel primary immunodeficiency suggestive of autosomal recessive hyper IgE syndrome.

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All Publications

2010: Tuba Turul-Ozgür; Gülten Türkkani-Asal; Ilhan Tezcan; Mustafa Yavuz Köker; Ayse Metin; Leman Yel; Fügen Ersoy; Ozden Sanal
Clinical features of chronic granulomatous disease: a series of 26 patients from a single center.
The Turkish journal of pediatrics 2010;52(6):576-81.
2007: Mustafa Yavuz Köker; Ozden Sanal; Martin de Boer; Ilhan Tezcan; Ayse Metin; Fügen Ersoy; Dirk Roos
Mutations of chronic granulomatous disease in Turkish families.
European journal of clinical investigation 2007;37(7):589-95.
2007: Tuba Turul Ozgur; Gulten Turkkan Asal; Aytemiz Gurgey; Ilhan Tezcan; Fügen Ersoy; Ozden Sanal
Acquired factor VIII deficiency associated with a novel primary immunodeficiency suggestive of autosomal recessive hyper IgE syndrome.
Journal of pediatric hematology/oncology 2007;29(5):327-9.
2007: Ozden Sanal; Gulten Turkkani; Fatma Gumruk; Leman Yel; Gulten Secmeer; Ilhan Tezcan; Ates Kara; Fügen Ersoy
A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis.
The Pediatric infectious disease journal 2007;26(4):366-8.
2006: Lütfiye Mesci; Hilal Ozdag; Tuba Turul; Fügen Ersoy; Ilhan Tezcan; Ozden Sanal
A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase.
The Turkish journal of pediatrics 2006;48(4):362-4.
2006: Mustafa Yavuz Köker; Ozden Sanal; Martin de Boer; Ilhan Tezcan; Ayse Metin; C Tan; Fügen Ersoy; Dirk Roos
Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one family.
European journal of clinical investigation 2006;36(4):257-64.
2006: Ozden Sanal; Tuba Turul; Tjitske de Boer; Esther van de Vosse; Işik Yalcin; Ilhan Tezcan; Cağman Sun; Leyla Memis; Tom H M Ottenhoff; Fügen Ersoy
Presentation of interleukin-12/-23 receptor beta1 deficiency with various clinical symptoms of Salmonella infections.
Journal of clinical immunology 2006;26(1):1-6.
2005: Benan Bayrakci; Fügen Ersoy; Ozden Sanal; Sebnem Kiliç; Ayse Metin; Ilhan Tezcan
The efficacy of immunoglobulin replacement therapy in the long-term follow-up of the B-cell deficiencies (XLA, HIM, CVID).
The Turkish journal of pediatrics 2005;47(3):239-46.
2005: Sevgi Yetgin; Idil Yenicesu; Fügen Ersoy
The effects of megadose methylprednisolone therapy on the immune system in childhood immune thrombocytopenia.
Pediatric hematology and oncology 2005;22(5):401-7.
2005: Ilhan Tezcan; Fügen Ersoy; Ozden Sanal; Tuba Turul; Duygu Uckan; Sevim Balci; Gonul Hicsonmez; Marguerite Prieur; S Caillat-Zucmann; Francois Le Deist; Geneviève de Saint Basile
Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment.
The Journal of pediatrics 2005;146(1):137-40.
2004: Ozden Sanal; Filiz Ozbaş-Gerçeker; Leman Yel; Fügen Ersoy; Ilhan Tezcan; A Izzet Berkel; Ayse Metin; Richard A Gatti
Defective anti-polysaccharide antibody response in patients with ataxia-telangiectasia.
The Turkish journal of pediatrics 2004;46(3):208-13.
2004: Yasemin Aksoy; Ozden Sanal; Ayse Metin; Ilhan Tezcan; Fügen Ersoy; Hamdi Oğüş; Nazmi Ozer
Antioxidant enzymes in red blood cells and lymphocytes of ataxia-telangiectasia patients.
The Turkish journal of pediatrics 2004;46(3):204-7.
2004: Ali Varan; Münevver Büyükpamukçu; Fügen Ersoy; Ozden Sanal; Canan Akyüz; Tezer Kutluk; Bilgehan Yalçin
Malignant solid tumors associated with congenital immunodeficiency disorders.
Pediatric hematology and oncology 2004;21(5):441-51.
2004: Ozden Sanal; Fügen Ersoy; Ilhan Tezcan; Ayse Metin; Tuba Turul; Semra Gariboglu; Leman Yel
Antibody response to a seven-valent pneumococcal conjugated vaccine in patients with ataxia-telangiectasia.
Journal of clinical immunology 2004;24(4):411-7.
2004: Pierre Quartier; Jacinta Bustamante; Ozden Sanal; Alessandro Plebani; Marianne Debré; Anne Deville; Jiri Litzman; Jacov Levy; Jean-Paul Fermand; Peter Lane; Gerd Horneff; Guzide Aksu; Isik Yalçin; Graham Davies; Ilhan Tezcan; Fügen Ersoy; Nadia Catalan; Kohsuhe Imai; Alain Fischer; Anne Durandy
Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency.
Clinical immunology (Orlando, Fla.) 2004;110(1):22-9.
2003: E Nazli Gonc; Tuba Turul; Nursen Yordam; Fügen Ersoy
Trimethoprim-sulfamethoxazole induced prolonged hypoglycemia in an infant with MHC class II deficiency: diazoxide as a treatment option.
Journal of pediatric endocrinology & metabolism : JPEM 2003;16(9):1307-9.
2003: Tevfik Karagoz; Turgay Coskun; Imran Ozalp; Ethem Ozkaya; Fügen Ersoy
Immune function in children with classical phenylketonuria and tetrahydrobiopterin deficiencies.
Indian pediatrics 2003;40(9):822-33.
2003: Gaël Ménasché; Chen Hsuan Ho; Ozden Sanal; Jérôme Feldmann; Ilhan Tezcan; Fügen Ersoy; Anne Houdusse; Alain Fischer; Geneviève de Saint Basile
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).
The Journal of clinical investigation 2003;112(3):450-6.
2003: Filiz Ozbaş-Gerçeker; Ilhan Tezcan; A Izzet Berkel; Seref Ozkara; Ayşenaz Ozcan; Fügen Ersoy; Ozden Sanal; Meral Ozgüç
The effect of mannose-binding protein gene polymorphisms in recurrent respiratory system infections in children and lung tuberculosis.
The Turkish journal of pediatrics 2003;45(2):95-8.
2003: Tolga F Tözüm; Ezel Berker; Fügen Ersoy; Ilhan Tezcan; Ozden Sanal
The relationship between periodontal status and peripheral levels of neutrophils in two consanguineous siblings with severe congenital neutropenia: case reports.
Quintessence international (Berlin, Germany : 1985) 2003;34(3):221-6.
2003: Elgin G R Lichtenauer-Kaligis; Tjitske de Boer; Frank A W Verreck; Sjaak van Voorden; Marieke A Hoeve; Esther van de Vosse; Fügen Ersoy; Ilhan Tezcan; Jaap T van Dissel; Ozden Sanal; Tom H M Ottenhoff
Severe Mycobacterium bovis BCG infections in a large series of novel IL-12 receptor beta1 deficient patients and evidence for the existence of partial IL-12 receptor beta1 deficiency.
European journal of immunology 2003;33(1):59-69.
2002: S Sebnem Kiliç; Ozden Sanal; Ilhan Tezcan; Fügen Ersoy
Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome.
The Turkish journal of pediatrics 2002;44(4):357-9.
2002: Ozden Sanal; Fügen Ersoy; Ilhan Tezcan; Ayse Metin; Leman Yel; Gaël Ménasché; Aytemiz Gürgey; Izzet Berkel; Geneviève de Saint Basile
Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.
Journal of clinical immunology 2002;22(4):237-43.
2001: Sebnem Kiliç; Ilhan Tezcan; Ozden Sanal; Fügen Ersoy
Common variable immunodeficiency in a patient with neurofibromatosis.
Pediatrics international : official journal of the Japan Pediatric Society 2001;43(6):691-3.
2000: Sebnem Kiliç; Ilhan Tezcan; Ozden Sanal; Ayse Metin; Fügen Ersoy
Transient hypogammaglobulinemia of infancy: clinical and immunologic features of 40 new cases.
Pediatrics international : official journal of the Japan Pediatric Society 2000;42(6):647-50.
2000: Patrick Revy; T Muto; Y Levy; Frederic Geissmann; Alessandro Plebani; Ozden Sanal; Nadia Catalan; Monique Forveille; R Dufourcq-Labelouse; A Gennery; Ilhan Tezcan; Fügen Ersoy; H Kayserili; Alberto G Ugazio; Nicole Brousse; Masamichi Muramatsu; Luigi D Notarangelo; Kazuo Kinoshita; Tasuku Honjo; Alain Fischer; Anne Durandy
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2).
Cell 2000;102(5):565-75.
2000: Ozden Sanal; Leman Yel; T Kucukali; E Gilbert-Barnes; M Tardieu; I Texcan; Fügen Ersoy; Ayse Metin; Geneviève de Saint Basile
An allelic variant of Griscelli disease: presentation with severe hypotonia, mental-motor retardation, and hypopigmentation consistent with Elejalde syndrome (neuroectodermal melanolysosomal disorder).
Journal of neurology 2000;247(7):570-2.
2000: Ayse Metin; Ozden Sanal; Fügen Ersoy; Ilhan Tezcan; A Izzet Berkel; C Irkeç
Polymorphism of the fourth component of complement in Turks.
Human biology 2000;72(3):527-33.
2000: Gaël Ménasché; E Pastural; Jérôme Feldmann; Stéphanie Certain; Fügen Ersoy; Stéphanie Dupuis; Nico M Wulffraat; D Bianchi; Alain Fischer; Françoise Le Deist; Geneviève de Saint Basile
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.
Nature genetics 2000;25(2):173-6.
2000: Ozden Sanal; G Morgan; Ayhan Göçmen; V Novelli; N Klein; Ilhan Tezcan; Fügen Ersoy; A Izzet Berkel; Leman Yel
Isolated cutaneous response to granulocyte-monocyte colony stimulating factor in fatal idiopathic disseminated Bacillus-Calmette-Guerin infection.
European journal of pediatrics 2000;159(3):149-52.
2000: E Pastural; Fügen Ersoy; Nevin Yalman; Nico M Wulffraat; E Grillo; F Ozkinay; Ilhan Tezcan; G Gediköglu; N Philippe; Alain Fischer; Geneviève de Saint Basile
Two genes are responsible for Griscelli syndrome at the same 15q21 locus.
Genomics 2000;63(3):299-306.
2000: Ayse Metin; Fügen Ersoy; Keriman Tinaztepe; N Beşbaş; Ilhan Tezcan; Ozden Sanal
Cyclic neutropenia complicated by renal AA amyloidosis.
The Turkish journal of pediatrics 2000;42(1):61-4.
1999: Ilhan Tezcan; Ozden Sanal; Fügen Ersoy; Duygu Uckan; Sebnem Kiliç; Ayse Metin; Mualla Cetin; Ridvan Akin; Cihan Oner; Ayfer Tuncer
Successful bone marrow transplantation in a case of Griscelli disease which presented in accelerated phase with neurological involvement.
Bone marrow transplantation 1999;24(8):931-3.
1999: Ozden Sanal; Fügen Ersoy; Leman Yel; Ilhan Tezcan; Ayse Metin; Hamit Ozyürek; Semra Gariboglu; S Fikrig; A Izzet Berkel; Ger T Rijkers; BJ Zegers
Impaired IgG antibody production to pneumococcal polysaccharides in patients with ataxia-telangiectasia.
Journal of clinical immunology 1999;19(5):326-34.
1999: Ayse Metin; Ozden Sanal; Ilhan Tezcan; Fügen Ersoy; A Izzet Berkel
Gastric antral stricture in a patient with chronic granulomatous disease.
The Turkish journal of pediatrics 1999;41(3):369-73.
1999: Sebnem Kiliç; Fügen Ersoy; Ozden Sanal; D Türkbay; Ilhan Tezcan
Alopecia universalis in a patient with common variable immunodeficiency.
Pediatric dermatology 1999;16(4):305-7.
1998: Ilhan Tezcan; W Xu; Aytemiz Gurgey; M Tuncer; Mualla Cetin; Cihan Oner; Sevgi Yetgin; Fügen Ersoy; GI Aizencang; Kenneth H Astrin; Robert J Desnick
Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation.
Blood 1998;92(11):4053-8.
1998: Ilhan Tezcan; A Izzet Berkel; Fügen Ersoy; Ozden Sanal; Güler Kanra
Fc gamma receptor allotypes in children with bacterial meningitis. A preliminary study.
The Turkish journal of pediatrics 1998;40(4):533-8.
1998: Ilhan Tezcan; Fügen Ersoy; Ozden Sanal; E N Gönc; Mustafa ARICI; I Berkel
A case of X linked agammaglobulinaemia complicated with systemic amyloidosis.
Archives of disease in childhood 1998;79(1):94.
1998: H Hastürk; Ilhan Tezcan; Leman Yel; Fügen Ersoy; Ozden Sanal; Nermin Yamalik; Ezel Berker
A case of chronic severe neutropenia: oral findings and consequences of short-term granulocyte colony-stimulating factor treatment.
Australian dental journal 1998;43(1):9-13.
1997: Ilhan Tezcan; Y Yilmaz; Filiz Oner; Leman Yel; Ozden Sanal; Fügen Ersoy; Metin Onerci; A Izzet Berkel
Defective serum opsonization activity in children aged 6-48 months having acute purulent otitis media.
The Turkish journal of pediatrics 1997;39(4):453-7.
1997: A Izzet Berkel; Franz Petry; Ozden Sanal; Keriman Tinaztepe; Fügen Ersoy; Aysin Bakkaloglu; Michael Loos
Development of systemic lupus erythematosus in a patient with selective complete C1q deficiency.
European journal of pediatrics 1997;156(2):113-5.