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49 results for Karaca,+Neslihan+Edeer

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Successful management of colchicine resistant familial Mediterranean fever patients with a standardized canakinumab treatment protocol: a case series and literature review
Author / Creator:Eren Akarcan, Sanem ; Dogantan, Seyda ; Edeer Karaca, Neslihan ; Aksu, Guzide ; Kutukculer, Necil
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Rheumatology international, 2020-01, Vol.40 (1), p.161-168
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An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission
Author / Creator:Aytac, Gulcin ; Guven, Burcu ; Aydin, Ilyas ; Topyildiz, Ezgi ; Aykut, Ayca ; Durmaz, Asude ; Edeer Karaca, Neslihan ; Aksu, Guzide ; Kutukculer, Necil
Publisher:New York: Hindawi
Journal title:Case reports in immunology, 2023-04, Vol.2023, p.1-6
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22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management
Author / Creator:Ozen, Selime ; Akcal, Omer ; Taskirdi, Ilke ; Haci, Idil Akay ; Karaca, Neslihan Edeer ; Gulez, Nesrin ; Aksu, Guzide ; Genel, Ferah ; Kutukculer, Necil
Publisher:Singapore: Codon Publications
Journal title:Allergologia et immunopathologia, 2021-01, Vol.49 (1), p.95-100
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The Quality of Life and Mental Health in Children with Primary Immunodeficiency
Author / Creator:Ocakoglu, Binay Kayan ; Karaca, Neslihan Edeer ; Aksu, Guzide ; Erermis, Serpil
Publisher:Galenos Yayinevi Tic. Ltd
Journal title:The journal of pediatric research, 2019-03, Vol.6 (1), p.1-6
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Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy
Author / Creator:Aksu, Guzide ; Migaud, Melanie ; Karaca, Neslihan ; Moriya, Kunihiko ; Akarcan, Sanem ; Puel, Anne ; Kutukculer, Necil ; Casanova, Jean-Laurent
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case reports in immunology, 2019, Vol.2019 (2019), p.1-6
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Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies
Author / Creator:Casanova, Jean-Laurent ; Kutukculer, Necil ; Puel, Anne ; Evin Gurkan, Ferda ; Migaud, Melanie ; Aksu, Guzide ; Isik, Esra ; Karaca, Neslihan ; Ulusoy, Ezgi ; Akarcan, Sanem ; Azarsız, Elif
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case reports in immunology, 2017-01, Vol.2017 (2017), p.1-6
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Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?
Author / Creator:Memmedova, Lale ; Azarsiz, Elif ; Edeer Karaca, Neslihan ; Aksu, Guzide ; Kutukculer, Necil
Publisher:Italy: MDPI AG
Journal title:Pediatric reports, 2013-09, Vol.5 (3), p.e14-e14
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Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections
Author / Creator:Taskin, Raziye Burcu ; Topyıldız, Ezgi ; Edeer Karaca, Neslihan ; Aksu, Guzide ; Yılmaz Karapınar, Deniz ; Kutukculer, Necil
Publisher:Basel, Switzerland
Journal title:International archives of allergy and immunology, 2024-04, Vol.185 (4), p.392-401
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Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference
Author / Creator:Kutukculer, Necil ; Topyildiz, Ezgi ; Berdeli, Afig ; Guven Bilgin, Burcu ; Aykut, Ayca ; Durmaz, Asude ; Cogulu, Ozgur ; Aksu, Guzide ; Edeer Karaca, Neslihan
Publisher:England: John Wiley & Sons, Inc
Journal title:Clinical case reports, 2021-04, Vol.9 (4), p.2023-2031
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Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants
Author / Creator:Kütükçüler, Necil ; Bölük, Ezgi ; Tökmeci, Nazan ; Neslihan Edeer Karaca ; Azarsız, Elif ; Aksu, Güzide ; Aykut, Ayça
Publisher:Istanbul: Aves Yayincilik Ltd. STI
Journal title:Turkish archives of pediatrics, 2020-09, Vol.55 (3), p.320
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Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients
Author / Creator:Senol, Handan Duman ; Barlik, Meral ; Topyildiz, Ezgi ; Gulen, Figen ; Aksu, Guzide ; Kutukculer, Necil ; Demir, Esen ; Karaca, Neslihan Edeer
Publisher:Galenos Yayinevi Tic. Ltd
Journal title:The journal of pediatric research, 2024-06, Vol.11 (2), p.110-117
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A Novel BLNK Gene Mutation in a Four-Year-Old Child Who Presented with Late Onset of Severe Infections and High IgM Levels and Diagnosed and Followed as X-Linked Agammaglobulinemia for Two Years
Author / Creator:Topyildiz, Ezgi ; Edeer Karaca, Neslihan ; Aygun, Ayse ; Aykut, Ayca ; Durmaz, Asude ; Aksu, Guzide ; Kutukculer, Necil
Publisher:New York: Hindawi
Journal title:Case reports in immunology, 2022-06, Vol.2022, p.1-6
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Frequency of Mycobacterium bovis and mycobacteria in primary immunodeficiencies
Author / Creator:Ulusoy, Ezgi ; Karaca, Neslihan Edeer ; Aksu, Güzide ; Çavuşoğlu, Cengiz ; Kütükçüler, Necil
Publisher:Turkey: Turkish Pediatrics Association
Journal title:Turk Pediatri Arsivi, 2017-09, Vol.52 (3), p.138-144
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Consanguinity Rate and Delay in Diagnosis in Turkish Patients with Combined Immunodeficiencies: a Single-Center Study
Author / Creator:Azarsiz, Elif ; Gulez, Nesrin ; Edeer Karaca, Neslihan ; Aksu, Guzide ; Kutukculer, Necil
Publisher:Boston: Springer US
Journal title:Journal of clinical immunology, 2011-02, Vol.31 (1), p.106-111
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A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature
Author / Creator:Darcan, Şükran ; Kütükçüler, Necil ; Aksu, Güzide ; Edeer Karaca, Neslihan ; Gökşen, Damla ; Özen, Samim ; Ata, Aysun ; Onay, Hüseyin
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case reports in immunology, 2020-09, Vol.2020 (2020), p.1-5
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An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation
Author / Creator:Pariltay, Erhan ; Aykut, Ayca ; Aksu, Guzide ; Karaca, Neslihan ; Kutukculer, Necil ; Cogulu, Ozgur
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case reports in immunology, 2018-01, Vol.2018 (2018), p.1-4
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Granulomatous Skin Lesions, Severe Scrotal and Lower Limb Edema Due to Mycobacterial Infections in a Child with Complete IFN-γ Receptor-1 Deficiency
Author / Creator:Edeer Karaca, Neslihan ; Boisson-Dupuis, Stephanie ; Aksu, Güzide ; Bustamante, Jacinta ; Kandiloglu, Gulsen ; Ozsan, Nazan ; Hekimgil, Mine ; Casanova, Jean-Laurent ; Kutukculer, Necil
Publisher:Future Medicine Ltd
Journal title:Immunotherapy, 2012-11, Vol.4 (11), p.1121-1127
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Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases
Author / Creator:Kansoy, Savas ; Boztug, Kaan ; Kutukculer, Necil ; Gulez, Nesrin ; Akarcan, Sanem ; Genel, Ferah ; Gozmen, Salih ; Aksoylar, Serap ; Ulusoy, Ezgi ; Aksu, Guzide ; Karaca, Neslihan ; Hirschmugl, Tatjana
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case reports in immunology, 2016-01, Vol.2016 (2016), p.1-5
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An unusual manifestation: Papillary thyroid carcinoma in a patient with ataxia-telengiectasia
Author / Creator:Ulusoy, Ezgi ; Edeer-Karaca, Neslihan ; Özen, Samim ; Ertan, Yeşim ; Gökşen, Damla ; Aksu, Güzide ; Darcan, Şükran ; Kütükçüler, Necil
Publisher:Turkey: Hacettepe University Faculty of Medicine
Journal title:Turkish journal of pediatrics, 2016, Vol.58 (4), p.442-445
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Clinical, Laboratory and Molecular Approach to Ten Children with Congenital Neutropenia
Author / Creator:Edeer Karaca, Neslihan ; Aksu, Güzide ; Gülez, Nesrin ; Azarsız, Elif ; Kavaklı, Kaan ; Klein, Christoph ; Kütükçüler, Necil
Journal title:The journal of pediatric research, 2016-04, Vol.3 (1), p.7-12
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Showing 1 to 20 of 49 results

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Successful management of colchicine resistant familial Mediterranean fever patients with a standardized canakinumab treatment protocol: a case series and literature review

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An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission

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22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management

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The Quality of Life and Mental Health in Children with Primary Immunodeficiency

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Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy

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Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies

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Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?

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Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections

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Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference

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Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants

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Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients

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A Novel BLNK Gene Mutation in a Four-Year-Old Child Who Presented with Late Onset of Severe Infections and High IgM Levels and Diagnosed and Followed as X-Linked Agammaglobulinemia for Two Years

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Frequency of Mycobacterium bovis and mycobacteria in primary immunodeficiencies

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Consanguinity Rate and Delay in Diagnosis in Turkish Patients with Combined Immunodeficiencies: a Single-Center Study

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A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature

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An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation

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Granulomatous Skin Lesions, Severe Scrotal and Lower Limb Edema Due to Mycobacterial Infections in a Child with Complete IFN-γ Receptor-1 Deficiency

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Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases

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An unusual manifestation: Papillary thyroid carcinoma in a patient with ataxia-telengiectasia

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Clinical, Laboratory and Molecular Approach to Ten Children with Congenital Neutropenia

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