Reference values for B-cell surface markers and co-receptors associated with primary immune deficiencies in healthy Turkish children

por Azarsiz, Elif, Karaca, Neslihan Edeer, Aksu, Guzide, Kutukculer, Necil
Publicado 2017

Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report

por Karaca, Neslihan, Aksu, Guzide, Ozturk, Can, Gulez, Nesrin, Kutukculer, Necil
Publicado 2010

Novel mutatıons and diverse clinical phenotypes in recombınase-activating gene 1 deficiency

por Kutukculer, Necil, Gulez, Nesrin, Karaca, Neslihan Edeer, Aksu, Guzide, Berdeli, Afig
Publicado 2012

Does Intravenous Immunoglobulin Therapy Prolong Immunodeficiency in Transient Hypogammaglobulinemia of Infancy?

por Memmedova, Lale, Azarsiz, Elif, Edeer Karaca, Neslihan, Aksu, Guzide, Kutukculer, Necil
Publicado 2013

A Clinical and Laboratory Approach to the Evaluation of Innate Immunity in Pediatric CVID Patients

por Kutukculer, Necil, Azarsiz, Elif, Karaca, Neslihan Edeer, Ulusoy, Ezgi, Koturoglu, Guldane, Aksu, Guzide
Publicado 2015

Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis

por Ulusoy, Ezgi, Karaca, Neslihan Edeer, Azarsiz, Elif, Berdeli, Afig, Aksu, Guzide, Kutukculer, Necil
Publicado 2016

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

por Kutukculer, Necil, Karaca, Neslihan Edeer, Aksu, Guzide, Aykut, Ayca, Pariltay, Erhan, Cogulu, Ozgur
Publicado 2018

X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis

por Gulez, Nesrin, Aksu, Guzide, Berdeli, Afig, Karaca, Neslihan, Tanrıverdi, Sema, Kutukculer, Necil, Azarsiz, Elif
Publicado 2011

Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report

por Ulusoy, Ezgi, Karaca, Neslihan Edeer, El-Shanti, Hatem, Kilicoglu, Erhan, Aksu, Guzide, Kutukculer, Necil
Publicado 2015

TNFRSF13B/TACI Alterations in Turkish Patients with Common Variable Immunodeficiency and IgA Deficiency

por Karaca, Neslihan Edeer, Severcan, Ezgi Ulusoy, Guven, Burcu, Azarsiz, Elif, Aksu, Guzide, Kutukculer, Necil
Publicado 2018

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

por Kütükçüler, Necil, Bölük, Ezgi, Tökmeci, Nazan, Karaca, Neslihan Edeer, Azarsız, Elif, Aksu, Güzide, Aykut, Ayça
Publicado 2020

Early Immunomodulatory Effects of Different Natural Surfactant Preparations in Preterms With Respiratory Distress

por Yalaz, Mehmet, Tanriverdi, Sema, Uygur, Özgün, Altun Köroğlu, Özge, Azarsiz, Elif, Aksu, Guzide, Kültürsay, Nilgün
Publicado 2022

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...

por Topyildiz, Ezgi, Edeer Karaca, Neslihan, Aygun, Ayse, Aykut, Ayca, Durmaz, Asude, Aksu, Guzide, Kutukculer, Necil
Publicado 2022

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

por Ata, Aysun, Özen, Samim, Gökşen, Damla, Edeer Karaca, Neslihan, Aksu, Güzide, Kütükçüler, Necil, Onay, Hüseyin, Darcan, Şükran
Publicado 2020

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

por Aytac, Gulcin, Guven, Burcu, Aydin, Ilyas, Topyildiz, Ezgi, Aykut, Ayca, Durmaz, Asude, Edeer Karaca, Neslihan, Aksu, Guzide, Kutukculer, Necil
Publicado 2023

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

por Kutukculer, Necil, Puel, Anne, Eren Akarcan, Sanem, Moriya, Kunihiko, Edeer Karaca, Neslihan, Migaud, Melanie, Casanova, Jean-Laurent, Aksu, Guzide
Publicado 2019

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

por Kutukculer, Necil, Topyildiz, Ezgi, Berdeli, Afig, Guven Bilgin, Burcu, Aykut, Ayca, Durmaz, Asude, Cogulu, Ozgur, Aksu, Guzide, Edeer Karaca, Neslihan
Publicado 2021

Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients

por Karaca, Neslihan Edeer, Severcan, Ezgi Ulusoy, Bilgin, Burcu Guven, Azarsiz, Elif, Akarcan, Sanem, Gunaydın, Nursen Cigerci, Gulez, Nesrin, Genel, Ferah, Aksu, Guzide, Kutukculer, Necil
Publicado 2018

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

por Karaca, Neslihan Edeer, Aksu, Guzide, Ulusoy, Ezgi, Aksoylar, Serap, Gozmen, Salih, Genel, Ferah, Akarcan, Sanem, Gulez, Nesrin, Hirschmugl, Tatjana, Kansoy, Savas, Boztug, Kaan, Kutukculer, Necil
Publicado 2016

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

por Eren Akarcan, Sanem, Ulusoy Severcan, Ezgi, Edeer Karaca, Neslihan, Isik, Esra, Aksu, Guzide, Migaud, Mélanie, Evin Gurkan, Ferda, Azarsiz, Elif, Puel, Anne, Casanova, Jean-Laurent, Kutukculer, Necil
Publicado 2017