Cargando…

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

In order to evaluate B-lymphocyte subsets of patients with primary immunodeficiencies, the normal values for national healthy children have to be used as a reference. Recently, B-cell co-receptor markers (CD19, CD21, and CD81) and CD20, CD22, and CD27 deficiencies have been reported in relation with...

Descripción completa

Detalles Bibliográficos
Autores principales:	Azarsiz, Elif, Karaca, Neslihan Edeer, Aksu, Guzide, Kutukculer, Necil
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2017
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806800/ https://www.ncbi.nlm.nih.gov/pubmed/28449602 http://dx.doi.org/10.1177/0394632017707609

Ejemplares similares

TNFRSF13B/TACI Alterations in Turkish Patients with Common Variable Immunodeficiency and IgA Deficiency
por: Karaca, Neslihan Edeer, et al.
Publicado: (2018)

Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis
por: Ulusoy, Ezgi, et al.
Publicado: (2016)

Does Intravenous Immunoglobulin Therapy Prolong Immunodeficiency in Transient Hypogammaglobulinemia of Infancy?
por: Memmedova, Lale, et al.
Publicado: (2013)

Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants
por: Kütükçüler, Necil, et al.
Publicado: (2020)

A Clinical and Laboratory Approach to the Evaluation of Innate Immunity in Pediatric CVID Patients
por: Kutukculer, Necil, et al.
Publicado: (2015)

Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients
por: Karaca, Neslihan Edeer, et al.
Publicado: (2018)

Novel mutatıons and diverse clinical phenotypes in recombınase-activating gene 1 deficiency
por: Kutukculer, Necil, et al.
Publicado: (2012)

X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis
por: Gulez, Nesrin, et al.
Publicado: (2011)

Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report
por: Ulusoy, Ezgi, et al.
Publicado: (2015)

An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation
por: Kutukculer, Necil, et al.
Publicado: (2018)

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
por: Topyildiz, Ezgi, et al.
Publicado: (2022)

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, et al.
Publicado: (2019)

Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies
por: Eren Akarcan, Sanem, et al.
Publicado: (2017)

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, et al.
Publicado: (2020)

Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report
por: Karaca, Neslihan, et al.
Publicado: (2010)

Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndrome
por: Eren Akarcan, Sanem, et al.
Publicado: (2018)

An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission
por: Aytac, Gulcin, et al.
Publicado: (2023)

Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference
por: Kutukculer, Necil, et al.
Publicado: (2021)

Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant
por: Kutukculer, Necil, et al.
Publicado: (2021)

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, et al.
Publicado: (2016)

Are Proteinase 3 and Cathepsin C Enzymes Related to Pathogenesis of Periodontitis?
por: Türkoğlu, Oya, et al.
Publicado: (2014)

Necrotizing Liver Granuloma/Abscess and Constrictive Aspergillosis Pericarditis with Central Nervous System Involvement: Different Remarkable Phenotypes in Different Chronic Granulomatous Disease Genotypes
por: Eren Akarcan, Sanem, et al.
Publicado: (2017)

Early Immunomodulatory Effects of Different Natural Surfactant Preparations in Preterms With Respiratory Distress
por: Yalaz, Mehmet, et al.
Publicado: (2022)

D-bifunctional Protein Deficiency: A Case Report of a Turkish Child
por: Incecik, Faruk, et al.
Publicado: (2019)

Reference values for T and B lymphocyte subpopulations in Turkish children and adults
por: BESCİ, Özge, et al.
Publicado: (2021)

Determination of reference values for tricuspid annular plane systolic excursion in healthy Turkish children
por: Uysal, Fahrettin, et al.
Publicado: (2016)

Birth Weight Reference Percentiles by Gestational Age for Turkish Twin Neonates
por: Al-Mendalawi, Mahmood D.
Publicado: (2021)

β-Thalassemia Mutation At Codon 37 (Tgg>>Tga) Detected In A Turkish Family
por: Güleç, Derya, et al.
Publicado: (2013)

Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family
por: Hançer, Veysel Sabri, et al.
Publicado: (2018)

Levels of ll-37 antimicrobial peptide in the gingival crevicular fluid of young and middle-aged subjects with or without gingivitis
por: Turkoglu, Oya, et al.
Publicado: (2017)

Z-Score Reference Values for Height in Turkish Children Aged 6 to 18 Years
por: Günöz, Hülya, et al.
Publicado: (2014)

Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children
por: Neyzi, Olcay, et al.
Publicado: (2015)

Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child
por: Ozcanyuz, Duygu G., et al.
Publicado: (2020)

Awareness About Dental Amalgam Among Turkish Dentists and Patients: A Questionnaire and Search Engine Based Cross-Sectional Study
por: Erçin, Özlem, et al.
Publicado: (2021)

Clause Chaining and Discourse Continuity in Turkish Children's Narratives
por: Ögel-Balaban, Hale, et al.
Publicado: (2020)

Craspedostaurosnazmii sp. nov., a new diatom species (Bacillariophyta) from the Turkish Coast of the Black Sea
por: Yılmaz, Elif, et al.
Publicado: (2023)

Anogenital Distance in Turkish Newborns
por: Oğuz Kutlu, Alev
Publicado: (2012)

Evaluation of the relation between the pulp stones and direct restorations using cone beam computed tomography in a Turkish subpopulation
por: Sezgin, Güzide Pelin, et al.
Publicado: (2021)

Novel Mutation p.Asp374Val of SERPINC1 in a Turkish Family with Inherited Antithrombin Deficiency
por: Aslan, Deniz
Publicado: (2021)

Spinocerebellar Ataxia-21 in a Turkish Child
por: Incecik, Faruk, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_t8npptn9qf2ib0sinbv5g7q2a3