Found: 5
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Phenotypic heterogeneity in patients with the same IL12RB1 mutation: screening of 3 families with patients with BCG infection.
- Published in:
- Turkish Journal of Immunology, 2016, v. 4, p. 20
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- Publication type:
- Article
Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss.
- Published in:
- Turkish Journal of Pediatrics, 2018, v. 60, n. 3, p. 270, doi. 10.24953/turkjped.2018.03.006
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- Publication type:
- Article
Defective pneumococcal antibody response in patients with recurrent respiratory tract infections.
- Published in:
- Turkish Journal of Pediatrics, 2017, v. 59, n. 5, p. 555, doi. 10.24953/turkjped.2017.05.008
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- Publication type:
- Article
Clinical and genetic features of IL12Rβ1 deficiency: Single center experience of 18 patients.
- Published in:
- Turkish Journal of Pediatrics, 2016, v. 58, n. 4, p. 356, doi. 10.24953/turkjped.2016.04.002
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- Publication type:
- Article
Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS.
- Published in:
- Turkish Journal of Pediatrics, 2015, v. 57, n. 2, p. 141
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- Article