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Allergologia Et Immunopathologia
|
May 11, 2023
CD4+CD25+CD127<sup>lo</sup>FOXP3+ cell in food allergy: Does it predict anaphylaxis?
Semiha Bahceci Erdem, Ferah Genel, Hikmet Tekin Nacaroglu, et al.
Pediatric Allergy, Immunology, and Pulmonology
|
June 17, 2026
Clinical, Immunological Findings, and Outcomes of Children with Ataxia-Telangiectasia: A Single Center Experience
Serenay Cetinoglu, Selime Ozen, Idil Akay Haci, et al.
Scandinavian Journal of Immunology
|
December 4, 2018
Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages
Necil Kutukculer, Ayca Aykut, Neslihan E Karaca, et al.
Central-European Journal of Immunology
|
September 19, 2019
Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report
Yöntem Yaman, Sultan Aydin Köker, Fahri Yüce Ayhan, et al.
Allergologia Et Immunopathologia
|
February 2, 2021
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management
Selime Ozen, Omer Akcal, Ilke Taskirdi, et al.
Clinical and Experimental Medicine
|
May 22, 2009
Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID
Neslihan Edeer Karaca, Guzide Aksu, Ferah Genel, et al.
Tuberkuloz Ve Toraks
|
June 17, 2017
Tuberculosis masked by immunodeficiency: a review of two cases diagnosed with chronic granulomatous disease
Hikmet Tekin Nacaroğlu, Semiha Bahçeci Erdem, Nesrin Gülez, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 7, 2019
Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13
Melis Demir Köse, Mehtap Kagnici, Taha Reşit Özdemir, et al.
Jornal De Pediatria
|
August 25, 2016
Parameters indicative of persistence of valvular pathology at initial diagnosis in acute rheumatic carditis: the role of albumin and CD19 expression
Taliha Oner, Rahmi Ozdemir, Dildar Bahar Genc, et al.
Scandinavian Journal of Immunology
|
March 18, 2022
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants
Ayca Aykut, Asude Durmaz, Neslihan Karaca, et al.
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Search research articles
Search
Showing results (31-40 of 74) with videos related to
Sort By:
Page
of 8
Allergologia Et Immunopathologia
|
May 11, 2023
CD4+CD25+CD127<sup>lo</sup>FOXP3+ cell in food allergy: Does it predict anaphylaxis?
Semiha Bahceci Erdem, Ferah Genel, Hikmet Tekin Nacaroglu, et al.
Pediatric Allergy, Immunology, and Pulmonology
|
June 17, 2026
Clinical, Immunological Findings, and Outcomes of Children with Ataxia-Telangiectasia: A Single Center Experience
Serenay Cetinoglu, Selime Ozen, Idil Akay Haci, et al.
Scandinavian Journal of Immunology
|
December 4, 2018
Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages
Necil Kutukculer, Ayca Aykut, Neslihan E Karaca, et al.
Central-European Journal of Immunology
|
September 19, 2019
Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report
Yöntem Yaman, Sultan Aydin Köker, Fahri Yüce Ayhan, et al.
Allergologia Et Immunopathologia
|
February 2, 2021
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management
Selime Ozen, Omer Akcal, Ilke Taskirdi, et al.
Clinical and Experimental Medicine
|
May 22, 2009
Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID
Neslihan Edeer Karaca, Guzide Aksu, Ferah Genel, et al.
Tuberkuloz Ve Toraks
|
June 17, 2017
Tuberculosis masked by immunodeficiency: a review of two cases diagnosed with chronic granulomatous disease
Hikmet Tekin Nacaroğlu, Semiha Bahçeci Erdem, Nesrin Gülez, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 7, 2019
Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13
Melis Demir Köse, Mehtap Kagnici, Taha Reşit Özdemir, et al.
Jornal De Pediatria
|
August 25, 2016
Parameters indicative of persistence of valvular pathology at initial diagnosis in acute rheumatic carditis: the role of albumin and CD19 expression
Taliha Oner, Rahmi Ozdemir, Dildar Bahar Genc, et al.
Scandinavian Journal of Immunology
|
March 18, 2022
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants
Ayca Aykut, Asude Durmaz, Neslihan Karaca, et al.
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of 8