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Makale detayı · 2017 · article

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

YÖKSİS OpenAlex Açık erişim · gold
Yıl2017
Atıf10OpenAlex
Yüzdelik%52,4
FWCI0,31,00 = dünya ortalaması
Scopus (SJR)Q3
WoS (JCR)Q2

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıInternational Journal of Immunopathology and Pharmacology
  • Katalog eşleşmesi (ISSN)International Journal of Immunopathology and Pharmacology
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

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 different primary immunodeficiency diseases. The objective of this study was to establish national reference values for B-lymphocyte co-receptors and some surface markers, CD20, CD22, CD27, as well as classic lymphocyte subsets in the peripheral blood of healthy children. A total of 90 healthy children were included in this study. Complete blood counts were performed and cells with CD3, CD4, CD8, CD19, CD16/56, CD20, CD21, CD22, CD27, and CD81 surface markers were simultaneously detected by flow cytometry. The children were evaluated in three age subgroups, 0-1, 1-6, and >6 years, and minimum, maximum, mean, mean minus standard deviation, and 2.5-97.5 percentile values were all determined. By establishing reliable reference ranges for these surface markers, we hoped to help identifying and classifying some primary immunodeficiency patients, especially those defined as unclassified hypogammaglobulinemia and those without definite diagnosis.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

10atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 16 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2017 Gain-of-Function Mutations inSTAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined ImmunodeficienciesAtıf 39 · OpenAlex
  2. 2017 Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined ImmunodeficienciesAtıf 39 · OpenAlex
  3. 2017 Gain-of-Function Mutations in STAT1: A RecentlyDefined Cause for Chronic Mucocutaneous CandidiasisDisease Mimicking Combined ImmunodeficienciesAtıf 39 · OpenAlex
  4. 2017 title Gain-of-Function Mutations in iSTAT1/i : A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies/titleAtıf 39 · OpenAlex
  5. 2017 Gain-of-Function Mutations inSTAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined ImmunodeficienciesAtıf 39 · OpenAlex
  6. 2017 Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined ImmunodeficienciesAtıf 39 · OpenAlex
  7. 2018 Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndromeAtıf 19 · OpenAlex
  8. 2018 Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndromeAtıf 19 · OpenAlex
  9. 2018 Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndromeAtıf 19 · OpenAlex
  10. 2018 Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndromeAtıf 19 · OpenAlex

Yazarlar

4
  1. Elif Azarsiz 1
  2. NESLİHAN KARACA EGE ÜNİVERSİTESİ 2
  3. Guzide Aksu 3
  4. Necil Kutukculer 4