Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation

ERMAN B., Bal S. K., Aydoğmuş Ç., Ersoy G. Z., Boztug K.
Journal of Clinical Immunology , cilt.44, sa.3, 2024 (SCI-Expanded) identifier identifier

Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre.

Karaatmaca B., Cagdas D. N., Esenboga S., Erman B., Tan C., Ozgur T. T., et al.
Clinical and experimental immunology , cilt.215, sa.2, ss.160-176, 2024 (SCI-Expanded) identifier identifier

A Novel Homozygous Germline Mutation in Transferrin Receptor 1 (TfR1) Leads to Combined Immunodeficiency and Provides New Insights into Iron-Immunity Axis

Aba Ü., MASLAK İ. C., İpşir C., Pehlivan D., Warnock N. I., Tumes D. J., et al.
Journal of Clinical Immunology , cilt.44, sa.2, 2024 (SCI-Expanded) identifier identifier

Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients.

Yakici N., Kreins A. Y., Catak M. C., Babayeva R., Erman B., Kenney H., et al.
Clinical immunology (Orlando, Fla.) , cilt.255, ss.109757, 2023 (SCI-Expanded) identifier identifier

COVID-19 Induced Hemophagocytic Lymphohistiocytosis in a Patient with Novel Homozygous UNC13D Gene Variant.

Tekeli S., Erman B., Kurucu B., Tanir G., Aytekin C.
Klinische Padiatrie , cilt.235, sa.4, ss.258-260, 2023 (SCI-Expanded) identifier identifier

Experimental Investigation of Microfluidic Device for Platelet Activation.

Demir N. Y., Bozyel I., Erman B., Gokcen D., Duman M.
IEEE transactions on bio-medical engineering , cilt.70, sa.3, ss.954-961, 2023 (SCI-Expanded) identifier identifier identifier

Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.

Lévy R., Gothe F., Momenilandi M., Magg T., Materna M., Peters P., et al.
The Journal of experimental medicine , cilt.220, sa.2, 2023 (SCI-Expanded) Creative Commons License identifier identifier identifier

Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency.

Sefer A. P., Abolhassani H., Ober F., Kayaoglu B., Bilgic Eltan S., Kara A., et al.
Journal of clinical immunology , cilt.42, ss.634-652, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

A novel frameshift mutation in Malt1 gene resulted in defective TCR signaling and impaired immune response to fungal ligands

KAYAOĞLU B., Yilmaz N., Baydemir I., Aydin Y., Yilmaz A. P., ERMAN B., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.329, 2021 (SCI-Expanded) identifier

Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency.

Ghosh S., Köstel B., Edwards E., Pillay B., Jimenez-Heredia R., Rao G., et al.
Blood , cilt.136, ss.2638-2655, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

Invasive Saprochaete capitata Infection in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature

Erman B., Firtina S., Aksoy B. A., Aydogdu S., Genc G. E., Dogan O., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.40, sa.3, ss.466-474, 2020 (SCI-Expanded) identifier identifier identifier

Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency

Erman B., Firtina S., Fisgin T., Bozkurt C., Cipe F. E.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.40, sa.3, ss.539-542, 2020 (SCI-Expanded) identifier identifier identifier

Genetic Screening of the Patients with Primary Immunodeficiency by Whole-Exome Sequencing

Erman B., Cipe F.
PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY , cilt.33, sa.1, ss.19-24, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

IgE and IgG4 binding to lentil epitopes in children with red and green lentil allergy

Sackesen C., Erman B., Gimenez G., Grishina G., Yilmaz O., Yavuz S., et al.
PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.31, sa.2, ss.158-166, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Two siblings with PRKDC defect who presented with cutaneous granulomas and review of the literature

Esenboga S., AKAL C., Karaatmaca B., Erman B., Dogan S., ORHAN D., et al.
CLINICAL IMMUNOLOGY , cilt.197, ss.1-5, 2018 (SCI-Expanded) identifier identifier identifier

Role of natural killer cells in lung cancer

Aktas O. N., Ozturk A. B., Erman B., Erus S., Tanju S., Dilege S.
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY , cilt.144, sa.6, ss.997-1003, 2018 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin Lymphoma

Gokturk B., Casanova J. L., Picard C., Ayvaz C. D., ERMAN B., Tezcan I., et al.
JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY , cilt.28, sa.4, ss.271-273, 2018 (SCI-Expanded) Creative Commons License identifier identifier

Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD

Esenboga S., EMİRALİOĞLU N., Cagdas D. N., Erman B., De Boer M., OĞUZ B., et al.
Journal of Clinical Immunology , cilt.37, sa.3, ss.269-272, 2017 (SCI-Expanded) identifier identifier identifier

Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing

ERMAN B., Bilic I., Hirschmugl T., Salzer E., Boztug H., Sanal O., et al.
SCANDINAVIAN JOURNAL OF IMMUNOLOGY , cilt.85, sa.3, ss.227-234, 2017 (SCI-Expanded) identifier identifier identifier

Defective pneumococcal antibody response in patients with recurrent respiratory tract infections.

Erman B., Demirtaş D., Bildik H., Çağdaş-Ayvaz D. N., Sanal Ö., Tezcan İ.
The Turkish journal of pediatrics , cilt.59, sa.5, ss.555-560, 2017 (SCI-Expanded) Creative Commons License identifier identifier identifier

Course of IL-2-inducible T-cell kinase deficiency in a family: lymphomatoid granulomatosis, lymphoma and allogeneic bone marrow transplantation in one sibling; and death in the other

ÇAĞDAŞ AYVAZ D. N., ERMAN B., Hanoglu D., Tavil B., KUŞKONMAZ B. B., AYDIN G. B., et al.
BONE MARROW TRANSPLANTATION , cilt.52, sa.1, ss.126-129, 2017 (SCI-Expanded) identifier identifier identifier

Statins and IL-1 beta, IL-10, and MPO Levels in Gingival Crevicular Fluid: Preliminary Results

ARI V. C., İLARSLAN Y. D., Erman B., Sarkarati B., TEZCAN I., KARABULUT E., et al.
INFLAMMATION , cilt.39, sa.4, ss.1547-1557, 2016 (SCI-Expanded) identifier identifier identifier

Successful outcome with second hematopoietic stem cell transplantation in a patient with IL-10R deficiency

KUŞKONMAZ B. B., Ayvaz D. N., Aydemir Y., Erman B., Tavil B., ÖZEN H., et al.
BONE MARROW TRANSPLANTATION , cilt.51, sa.4, ss.615-616, 2016 (SCI-Expanded) Creative Commons License identifier identifier identifier

STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation

HALACLI S. O., AYVAZ D. N., Sun-Tan C., Erman B., Uz E., YILMAZ D. Y., et al.
CLINICAL IMMUNOLOGY , cilt.161, sa.2, ss.316-323, 2015 (SCI-Expanded) identifier identifier identifier

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R.

Erman B., Bilic I., Hirschmugl T., Salzer E., ÇAĞDAŞ AYVAZ D. N., Esenboga S., et al.
Haematologica , cilt.100, sa.6, 2015 (SCI-Expanded) identifier identifier identifier

Necessity of Keratinized Tissues for Dental Implants: A Clinical, Immunological, and Radiographic Study

Askin S. B., Berker E., Akincibay H., UYSAL S., Erman B., Tezcan I., et al.
CLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH , cilt.17, sa.1, ss.1-12, 2015 (SCI-Expanded) identifier identifier identifier

C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma

TOPALOĞLU R., TASKIRAN E. Z., TAN Ç., Erman B., ÖZALTIN F., SANAL O.
CLINICAL RHEUMATOLOGY , cilt.31, sa.7, ss.1123-1126, 2012 (SCI-Expanded) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

Investigation of causative genetic defects in patients with primary immunodeficiency by next generation sequencing

Erman B., Arıkoğlu T., Kont Özhan A., Demirhan A., Tökmeci N., Aydoğmuş Ç., et al.
Annals of Medical Research , cilt.28, sa.5, ss.1038-1043, 2021 (Hakemli Dergi) Creative Commons License

Immune Reconstitution in the Patients with Talasemia Major after Hematopoietic Stem Cell Transplantation

Erman B., Adakli Aksoy B.
TURKISH JOURNAL OF IMMUNOLOGY , cilt.8, sa.3, ss.113-119, 2020 (ESCI) identifier identifier

Apoptosis in Autoimmune Lymphoproliferative Syndrome Suspected Patients with Clinical and Laboratory Findings

ERMAN B., ÇAĞDAŞ AYVAZ D. N., Metin A., Tezcan I., Sanal O.
TURKISH JOURNAL OF IMMUNOLOGY , cilt.1, sa.1, ss.5-12, 2013 (ESCI) identifier identifier

Klinik ve Laboratuvar Özellikleri ile Otoimmün Lenfoproliferatif Sendrom Düşünülen Hastalarda Apoptoz

ERMAN B., ÇAĞDAŞ AYVAZ D. N., Metin A., TEZCAN F. İ., SANAL Ş. Ö.
TURKISH JOURNAL OF IMMUNOLOGY , cilt.1, sa.1, ss.5-12, 2013 (Scopus)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Investigation of heat and matrix effect on milk proteins' allergenicity and the development of hypoallergenic food products

Suer H., Yazici D., ERMAN B., Sackesen C.
Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Munich, Almanya, 26 - 30 Mayıs 2018, cilt.73, ss.428-429 identifier

Çok nadir iki sendromun birlikteliği: Noonan syndrome like with loose anagen hair ile ICF2 sendromu

AKGÜN DOĞAN Ö., ŞİMŞEK KİPER P. Ö., Lissewski C., Erman B., ÇAĞDAŞ AYVAZ D. N., Boztuğ K., et al.
3.Ulusal Çocuk Genetik Sempozyumu, Antalya, Türkiye, 11 - 13 Ekim 2017

Activated PI3KCD Syndrome Same Dominant Activating Mutation in Four Patients From 3 Families from Turkey

ÇAĞDAŞ AYVAZ D. N., Erman B., Karaatmaca B., ESENBOĞA S., YILDIRAN A., ARIKOĞLU T., et al.
ESID 2016, 21 - 24 Eylül 2016

Succesful Hematopoietic stem cell Transplantation in children with IL 2 inducible T cell kinase ITK deficiency

KUŞKONMAZ B. B., ÇAĞDAŞ AYVAZ D. N., erman B., Hanoğlu D., TAVİL E. B., AYDIN G. B., et al.
EBMT 2016, 3 - 06 Nisan 2016

Diskoid lupus tanısı ile izlenen erişkin bir hastada, kronik granulomatöz hastalık: İmmünoloji konsültasyonunun önemi

ESENBOĞA S., ERMAN B., TAN Ç., Çelik Başaran N., DOĞAN GÜNAYDIN S., ÇAĞDAŞ AYVAZ D. N., et al.
2. Klinik İmmünoloji Kongresi, Antalya, Türkiye, 31 Mart - 03 Nisan 2016

Ciltte granüloma oluşumu ile başvuran ve DNA-PKcs defekti saptanan kombine immün yetmezlikli iki kardeş

aker c., ESENBOĞA S., ERMAN B., karaatmaca b., ÇAĞDAŞ AYVAZ D. N., Boztug K., et al.
2. Klinik İmmünoloji Kongresi, Antalya, Türkiye, 31 Mart - 03 Nisan 2016

Primer immün yetmezlikli hastalarda hastalığa neden olan genetik defektlerin yeni nesil dizileme yöntemiyle araştırılması

ERMAN B., Bilic I., Hirschmugl T., ÇAĞDAŞ AYVAZ D. N., SANAL Ş. Ö., TEZCAN F. İ., et al.
2. Klinik İmmünoloji Kongresi, Antalya, Türkiye, 31 Mart 2016

Lipopolisakkarit e duyarlı beige benzeri Protein LRBA Defekti Bulunan Hastaların Klinik ve Laboratuvar Bulgularının Değerlendirilmesi Hacettepe Serisi

ÇAĞDAŞ AYVAZ D. N., KARAATMACA B., ESENBOĞA S., YILMAZ T., ERMAN B., TAN Ç., et al.
2. Klinik İmmünoloji Kongresi, Türkiye, 31 Mart - 03 Nisan 2016

Successful hematopoietic stem cell trasnplantation in children with IL-2-inducible T-cell Kinase (ITK) deficiency

KUŞKONMAZ B. B., ÇAĞDAŞ AYVAZ D. N., ERMAN B., Hanoglu D., Tavil B., AYDIN G. B., et al.
42nd Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation, Valencia, İspanya, 3 - 06 Nisan 2016, cilt.51 identifier

STK4 (MST1) deficiency in three families with the clinical and immunologic features of AR-HIES

ÇAĞDAŞ AYVAZ D. N., Halacli S. O., TAN Ç., ERMAN B., UZ YILDIRIM E., Yilmaz D. Y., et al.
4th International Forum on Immunology Research, 08 Ekim 2015

STK 4 MST1 Deficiency in Three Families with the Clinical and Immunological Features of AR HIES

ÇAĞDAŞ AYVAZ D. N., oskay S., TAN Ç., Erman B., UZ E., ÖZGÜL R. K., et al.
International Forum on Immunology Research, 8 - 10 Ekim 2015

Kütanöz Granümların Eşlik Ettiği Primer İmmün Yetmezlik Olgu Örnekleri

ESENBOĞA S., ÇAĞDAŞ AYVAZ D. N., ERMAN B., TAN Ç., ERSOY EVANS S., TEZCAN F. İ.
1. Klinik İmmünoloji Kongresi, Türkiye, 9 - 12 Nisan 2015

IL-10 RECEPTOR DEFECT IN A PATIENT WHO PRESENTED WITH EARLY-ONSET INFANTILE INFLAMATORY BOWEL DISEASE

Ayvaz D. N., ERMAN B., TAN Ç., KUŞKONMAZ B. B., Hizal G., Berberoglu B., et al.
15th Biennial Meeting European-Society-for-Immunodeficiency (ESID), Florence, İtalya, 3 - 06 Ekim 2012, cilt.32, ss.69 identifier

İnflamatuvar barsak hastalığı ile prezente olan bir olguda interlökin-10 reseptör defekti

ÇAĞDAŞ AYVAZ D. N., ERMAN B., TAN Ç., KUŞKONMAZ B. B., HIZAL G., Berberoğlu B., et al.
Allerjik Hastalıklar ve Klinik İmmünolojide Tedavi, Antalya, Türkiye, 01 Kasım 2011

Chronic granulomatous disease CGD subgroup analysis of patients by FACScan with specific anti human NADPH oxidase components antibodies

KÖKER M. Y., ÖZDEN S., TEZCAN F. İ., ERSOY F., METIN A., TAN Ç., et al.
1st Joint Meeting of European National Societies of Immunology -16th European Congress of Immunology, (EFİS), 6 - 09 Eylül 2006 Sürdürülebilir Kalkınma

Kitap & Kitap Bölümleri

Kısım 11: İmmünolojik Hastalıklar, Bölüm 10: Primer İmmün Yetmezliklerin Tanısında Kullanılan İlk Basamak Laboratuvar Testleri

Demirtaş D., Tan Ç., Erman B., Tezcan F. İ.
Yurdakök Pediatri, Murat Yurdakök, Editör, Güneş Tıp Kitabevleri, Ankara, ss.2185-2188, 2017

Metrikler

Yayın

47

Atıf (WoS)

316

H-İndeks (WoS)

10

Atıf (Scopus)

443

H-İndeks (Scopus)

11

Proje

13

Açık Erişim

7
BM Sürdürülebilir Kalkınma Amaçları