Metrikler
Yayın
58
Açık Erişim
8
BM Sürdürülebilir Kalkınma Amaçları
Akademi Dışı Deneyim
1994 - 1996
1994 - 1996öğretmen
adana/yüreğir kiremithane end. mes.lis. ve tek lise , öğretmen
Makaleler
Tümü (54)
SCI-E, SSCI, AHCI (45)
SCI-E, SSCI, AHCI, ESCI (52)
ESCI (7)
Scopus (46)
TRDizin (18)
2022
20221. Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.
FUNCTIONAL & INTEGRATIVE GENOMICS
, cilt.22, sa.3, ss.291-315, 2022 (SCI-Expanded)
2021
20212. The cumulative effects of MEFV gene polymorphisms and mutations in patients with inflammatory bowel diseases
AĞIN M., BİŞGİN A., YILMAZ M., KONT ÖZHAN A., Mammadov F., TÜMGÖR G.
JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION
, cilt.71, sa.2, ss.479-483, 2021 (SCI-Expanded, Scopus)
2021
20213. Altered expression of apoptosis-related, circulating cell-free miRNAs in children with familial Mediterranean fever: a cross-sectional study
Karpuzoglu E. M., KIŞLA EKİNCİ R. M., Balci S., BİŞGİN A., YILMAZ M.
RHEUMATOLOGY INTERNATIONAL
, cilt.41, sa.1, ss.103-111, 2021 (SCI-Expanded, Scopus)
2021
20214. Twenty-Year Experience of a Single Referral Center on Pediatric Familial Mediterranean Fever What Has Changed Over the Last Decade?
KIŞLA EKİNCİ R. M., Balci S., Dogruel D., ALTINTAŞ D. U., YILMAZ M.
JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
, cilt.27, sa.1, ss.18-24, 2021 (SCI-Expanded, Scopus)
2020
20205. Clinical manifestations and outcomes of 420 children with Henoch Schonlein Purpura from a single referral center from Turkey: A three-year experience
KIŞLA EKİNCİ R. M., Balci S., MELEK E., KARABAY BAYAZIT A., DOĞRUEL D., ALTINTAŞ D. U., et al.
MODERN RHEUMATOLOGY
, cilt.30, sa.6, ss.1039-1046, 2020 (SCI-Expanded)
2020
20206. Retrospective Analysis of the Factors Affecting Growth Parameters in Turkish Children With Systemic Lupus Erythematosus
Balci S., KIŞLA EKİNCİ R. M., MELEK E., KARABAY BAYAZIT A., Dogruel D., ALTINTAŞ D. U., et al.
ARCHIVES OF RHEUMATOLOGY
, cilt.35, sa.3, ss.357-365, 2020 (SCI-Expanded, Scopus, TRDizin)
2020
20207. Growth Parameters of Turkish Children With an Autoinflammatory Disease Before and After Canakinumab Treatment
Balci S., KIŞLA EKİNCİ R. M., Dogruel D., ALTINTAŞ D. U., YILMAZ M.
INDIAN PEDIATRICS
, cilt.57, sa.7, ss.637-640, 2020 (SCI-Expanded, Scopus)
2020
20208. Pre-Pulseless Takayasu Arteritis in a Child Represented With Prolonged Fever of Unknown Origin and Successful Management With Concomitant Mycophenolate Mofetil and Infliximab
KIŞLA EKİNCİ R. M., Balci S., Piskin F. C., Varan C., ALINÇ ERDEM S., YILMAZ M.
ARCHIVES OF RHEUMATOLOGY
, cilt.35, sa.2, ss.278-282, 2020 (SCI-Expanded, Scopus, TRDizin)
2020
20209. Unicentric Castleman Disease Mimicking an Autoinflammatory Disorder: A Diagnostic Challenge in a Pediatric Patient With Recurrent Fever
KIŞLA EKİNCİ R. M., Balci S., ERGİN M., KÜPELİ S., BAYRAM İ., YILMAZ M., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.42, sa.3, ss.204-207, 2020 (SCI-Expanded, Scopus)
2020
202010. Phenotypic variability in two patients with tumor necrosis factor receptor associated periodic fever syndrome emphasizes a rare manifestation: Immunoglobulin A nephropathy
Balci S., KIŞLA EKİNCİ R. M., MELEK E., ATMIŞ B., BİŞGİN A., YILMAZ M.
EUROPEAN JOURNAL OF MEDICAL GENETICS
, cilt.63, sa.4, 2020 (SCI-Expanded, Scopus)
2020
202011. Baricitinib experience on STING-associated vasculopathy with onset in infancy: A representative case from Turkey
Balci S., KIŞLA EKİNCİ R. M., de Jesus A. A., Goldbach-Mansky R., YILMAZ M.
CLINICAL IMMUNOLOGY
, cilt.212, ss.113-116, 2020 (SCI-Expanded)
2020
202012. Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey
KIŞLA EKİNCİ R. M., Balci S., Hershfield M., BİŞGİN A., DOĞRUEL D., ALTINTAŞ D. U., et al.
RHEUMATOLOGY
, cilt.59, sa.1, ss.254-256, 2020 (SCI-Expanded, Scopus)
2019
201913. Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency
Kiykim A., Öğülür İ., Dursun E., Charbonnier L. M., Nain E., Çekiç Ş., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE
, cilt.7, ss.2790-2815, 2019 (SCI-Expanded)
2019
201914. Canakinumab in Children with Familial Mediterranean Fever: A Single-Center, Retrospective Analysis
KIŞLA EKİNCİ R. M., Balci S., DOĞRUEL D., ALTINTAŞ D. U., YILMAZ M.
PEDIATRIC DRUGS
, cilt.21, sa.5, ss.389-395, 2019 (SCI-Expanded, Scopus)
2019
201915. Disease Severity and Genotype Affect Physical Growth in Children With Familial Mediterranean Fever
KIŞLA EKİNCİ R. M., Balci S., Akay E., DOĞRUEL D., ALTINTAŞ D. U., YILMAZ M.
ARCHIVES OF RHEUMATOLOGY
, cilt.34, sa.3, ss.288-293, 2019 (SCI-Expanded, Scopus, TRDizin)
2019
201916. Etanercept for the Treatment of Chronic Arthritis Related to Chronic Granulomatous Disease: A Case
Balci S., KIŞLA EKİNCİ R. M., SERBES M., DOĞRUEL D., ALTINTAŞ D. U., YILMAZ M.
PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY
, cilt.32, sa.3, ss.131-134, 2019 (SCI-Expanded, Scopus)
2019
201917. Hyperimmunoglobulinemia D syndrome with recurrent perianal abscess successfully treated with canakinumab
KIŞLA EKİNCİ R. M., Balci S., BİŞGİN A., TÜMGÖR G., DOĞRUEL D., YILMAZ M.
SCOTTISH MEDICAL JOURNAL
, cilt.64, sa.3, ss.103-107, 2019 (SCI-Expanded, Scopus)
2019
201918. Unusual and early onset IPEX syndrome: a case report
DOĞRUEL D., GÜRBÜZ F., TURAN İ., ALTINTAŞ D. U., YILMAZ M., YÜKSEL B.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.4, ss.580-584, 2019 (SCI-Expanded, Scopus, TRDizin)
2019
201919. Two years of newborn screening for cystic fibrosis in Turkey: Cukurova experience
Sasihuseyinoglu A. S., ALTINTAŞ D. U., BİŞGİN A., DOĞRUEL D., YILMAZ M., SERBES M.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.4, ss.505-512, 2019 (SCI-Expanded)
2019
201920. Recurrent Henoch Schonlein purpura without renal involvement successfully treated with methotrexate
KIŞLA EKİNCİ R. M., Balci S., SERBES M., Aycin G. D., DOĞRUEL D., ALTINTAŞ D. U., et al.
SCOTTISH MEDICAL JOURNAL
, cilt.64, sa.2, ss.74-77, 2019 (SCI-Expanded, Scopus)
2019
201921. Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent
ATMIŞ B., KIŞLA EKİNCİ R. M., MELEK E., BİŞGİN A., YILMAZ M., Anarat A., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.3, ss.444-448, 2019 (SCI-Expanded, Scopus, TRDizin)
2019
201922. Autoimmune Manifestations in Heterozygote Type I Complement 2 Deficiency: A Child Eventually Diagnosed With Systemic Lupus Erythematosus
KIŞLA EKİNCİ R. M., Balci S., BİŞGİN A., ATMIŞ B., DOĞRUEL D., YILMAZ M.
ARCHIVES OF RHEUMATOLOGY
, cilt.34, sa.1, ss.96-99, 2019 (SCI-Expanded, Scopus, TRDizin)
2019
201923. Evaluation of high resolution computed tomography findings of cystic fibrosis
Sasihuseyinoglu A. S., ALTINTAŞ D. U., SOYUPAK S., DOĞRUEL D., YILMAZ M., SERBES M., et al.
KOREAN JOURNAL OF INTERNAL MEDICINE
, cilt.34, sa.2, ss.335-343, 2019 (SCI-Expanded, Scopus)
2019
201924. Clinical findings and genetic analysis of the patients with IL-12R beta 1 deficiency from southeast Turkey
DOĞRUEL D., ÖZGÜR GÜNDEŞLİOĞLU Ö., YILMAZ M., Alabaz D., ALTINTAŞ D. U., KOCABAŞ E.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.2, ss.174-179, 2019 (SCI-Expanded, Scopus, TRDizin)
2019
201925. Is Henoch-Schonlein purpura a susceptibility factor for functional gastrointestinal disorders in children?
KIŞLA EKİNCİ R. M., Balci S., Mart O. O., TÜMGÖR G., Yavuz S., Celik H., et al.
RHEUMATOLOGY INTERNATIONAL
, cilt.39, sa.2, ss.317-322, 2019 (SCI-Expanded)
2019
201926. Dendritic cell activation is blunted in patients with coronary artery disease and diabetes mellitus
Yetkin G. I., YÜCEL A. A., TEKİN İ. Ö., YILMAZ M., Atalay H., Yetkin E.
JOURNAL OF DIABETES AND ITS COMPLICATIONS
, cilt.33, sa.2, ss.134-139, 2019 (SCI-Expanded)
2019
201927. Does selective IgA deficiency have a good prognostic role on juvenile dermatomyositis? a case report
Balci S., KIŞLA EKİNCİ R. M., DOĞRUEL D., SERBES M., ALTINTAŞ D. U., YILMAZ M.
CUKUROVA MEDICAL JOURNAL
, cilt.44, sa.4, ss.1511-1514, 2019 (ESCI, TRDizin)
2018
201828. Term ve geç preterm bebeklerde kordon klempleme zamanının lenfosit alt grupları üzerine etkisi
BAHAR N., SATAR M., YILMAZ M., BÜYÜKKURT S., OZLU F., YAPICIOĞLU YILDIZDAŞ H., et al.
TURK PEDIATRI ARSIVI , cilt.53, sa.4, ss.214-221, 2018 (Scopus, TRDizin)
2018
201829. Renal Amyloidosis in Deficiency of Adenosine Deaminase 2: Successful Experience With Canakinumab
Kışla Ekinci R. M., Balci S., Bişgin A., Hershfield M., Atmış B., Doğruel D., et al.
PEDIATRICS
, cilt.142, sa.5, 2018 (SCI-Expanded, Scopus)
2018
201830. Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor beta 1 and biotinidase deficiencies
DOĞRUEL D., BULUT F. D., YILMAZ M., Onenli-Mungan N., ALTINTAŞ D. U.
TURKISH JOURNAL OF PEDIATRICS
, cilt.60, sa.5, ss.584-587, 2018 (SCI-Expanded)
2018
201831. Squamous Cell Carcinoma With Hyper-IgE Syndrome: A Case Report
Sasihuseyinoglu A. S., YILMAZ M., ALTINTAŞ D. U., DOĞRUEL D., SERBES M., Uguz A. H., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.40, sa.6, 2018 (SCI-Expanded)
2018
201832. A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome
BULUT F. D., KOR D., Yilmaz B. S., YILMAZ M., ALTINTAŞ D. U., Ceylaner S., et al.
JOURNAL OF PEDIATRIC RESEARCH
, cilt.5, sa.1, ss.54-56, 2018 (ESCI)
2018
201833. Ataxia-Telangiectasia Clinical and Laboratory Features: Single Center Results
Sasihuseyinoglu A. S., YILMAZ M., BİŞGİN A., DOĞRUEL D., ALTINTAŞ D. U., Duyuler G., et al.
PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY
, cilt.31, sa.1, ss.9-14, 2018 (SCI-Expanded, Scopus)
2018
201834. Juvenile mixed connective tissue disease: case series
KIŞLA EKİNCİ R. M., Balci S., Altintas D. U., YILMAZ M.
CUKUROVA MEDICAL JOURNAL
, cilt.43, sa.1, ss.235-240, 2018 (ESCI, TRDizin)
2018
201835. Effects of physical exercise on clinical and functional parameters in children with asthma
DOĞRUEL D., ALTINTAŞ D. U., YILMAZ M.
CUKUROVA MEDICAL JOURNAL
, cilt.43, sa.2, ss.457-462, 2018 (ESCI, TRDizin)
2018
201836. T helper, cytotoxic T, and natural killer T cell profiles and their association with clinical prognosis in children with sickle cell anemia
ATMIŞ B., KILINÇ Y., YILMAZ M., Atmis A., Karagun B. S., ŞAŞMAZ H. İ.
CUKUROVA MEDICAL JOURNAL
, cilt.43, sa.4, ss.1002-1007, 2018 (ESCI, TRDizin)
2017
201737. Hematopoietic stem cell transplantation from unrelated donors in children with DOCK8 deficiency
Uygun D. F. K., Uygun V., REİSLİ İ., KELEŞ S., Ozen A., YILMAZ M., et al.
PEDIATRIC TRANSPLANTATION
, cilt.21, sa.7, 2017 (SCI-Expanded, Scopus)
2017
201738. Distribution of Allergen Sensitization in Childhood with the Skin Test
Sasihuseyinoglu A. S., Kont Ozhan A., SERBES M., Duyuler G. A., BINGOL G., YILMAZ M., et al.
ASIM ALLERJI IMMUNOLOJI
, cilt.15, sa.1, ss.43-48, 2017 (ESCI, TRDizin)
2017
201739. Yenidoğan döneminde sağlık bakımı ile ilişkili enfeksiyon geçirmiş ve geniş spektrumlu antibiyotik kullanmış olmanın erken çocukluk döneminde gözlenen astma, allerjik rinit ve atopik dermatit üzerine etkisi
YAPICIOĞLU YILDIZDAŞ H., ÖZCAN A., YILMAZ M., SERTDEMİR Y.
CUKUROVA MEDICAL JOURNAL , cilt.42, sa.1, ss.132-139, 2017 (TRDizin)
2017
201740. Effect of healthcare associated infections and broad spectrum antibiotic use in newborn period on development of asthma, allergic rhinitis and atopic dermatitis in early childhood
YILDIZDAS H. Y., OEZCAN A., Sertdemir Y., Yilmaz M.
CUKUROVA MEDICAL JOURNAL
, cilt.42, sa.1, ss.132-139, 2017 (ESCI, TRDizin)
2015
201541. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
Engelhardt K. R., Gertz M. E., Keles S., Schaeffer A. A., Sigmund E. C., Glocker C., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
, cilt.136, sa.2, ss.402-412, 2015 (SCI-Expanded, Scopus)
2014
201442. Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion
YILMAZ M., Cagdas D., Grandin V., ALTINTAŞ D. U., Tezcan I., de Saint Basile G., et al.
PEDIATRIC ALLERGY AND IMMUNOLOGY
, cilt.25, sa.8, ss.817-819, 2014 (SCI-Expanded, Scopus)
2014
201443. A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc
Cagdas D., YILMAZ M., KANDEMİR N., Tezcan I., Etzioni A., Sanal O.
JOURNAL OF CLINICAL IMMUNOLOGY
, cilt.34, sa.8, ss.1009-1014, 2014 (SCI-Expanded, Scopus)
2014
201444. AUTOIMMUNE HEPATITIS AND SCLERODERMA IN A PATIENT WITH X-LINKED AGAMMAGLOBULINAEMIA
YILMAZ M., BİNGÖL KARAKOÇ G., ALTINTAŞ D. U., Kotil A.
JOURNAL OF CLINICAL IMMUNOLOGY
, cilt.34, sa.6, ss.723, 2014 (SCI-Expanded, Scopus)
2014
201445. EFFECTS OF ANTIDOTAL THERAPY ON TESTIS TISSUE IN ORGANOPHOSPHATE POISONING
GUMUSAY U., SEBE A., SATAR D. A., AY M. O., Yilmaz M., METE U. Ö.
ACTA MEDICA MEDITERRANEA
, cilt.30, sa.2, ss.435-439, 2014 (SCI-Expanded, Scopus)
2014
201446. Correlation between nasal eosinophils and nasal airflows in children with asthma and/or rhinitis monosensitised to house dust mites
Yukselen A., Kendirli S. G., YILMAZ M., ALTINTAŞ D. U., BİNGÖL KARAKOÇ G.
ALLERGOLOGIA ET IMMUNOPATHOLOGIA
, cilt.42, sa.1, ss.50-55, 2014 (SCI-Expanded)
2013
201347. Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
KÖKER M. Y., Camcioglu Y., van Leeuwen K., KILIÇ S. Ş., Barlan I., YILMAZ M., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
, cilt.132, sa.5, ss.1156-1168, 2013 (SCI-Expanded, Scopus)
2011
201148. Evaluation of efficacy of immunotherapy in children with asthma monosensitized to Alternaria
Kilic M., ALTINTAŞ D. U., YILMAZ M., BİNGÖL KARAKOÇ G., Burgut R., Guneser-Kendirli S.
TURKISH JOURNAL OF PEDIATRICS
, cilt.53, sa.3, ss.285-294, 2011 (SCI-Expanded, Scopus)
2010
201049. Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling
LI Y., LAUE K., TEMTAMY S., AGLAN M., KOTAN L. D., YIGIT G., et al.
AMERICAN JOURNAL OF HUMAN GENETICS
, cilt.87, sa.6, ss.757-767, 2010 (SCI-Expanded, Scopus)
2009
200950. Exhaled Breath Condensate MMP-9 Levels in Children With Bronchiectasis
BİNGÖL KARAKOÇ G., Inal A., YILMAZ M., ALTINTAŞ D. U., Kendirli S. G.
PEDIATRIC PULMONOLOGY
, cilt.44, sa.10, ss.1010-1016, 2009 (SCI-Expanded, Scopus)
2009
200951. The clinical and genetical features of 124 children with Familial Mediterranean fever: experience of a single tertiary center
Inal A., YILMAZ M., Kendirli S. G., ALTINTAŞ D. U., BİNGÖL KARAKOÇ G.
RHEUMATOLOGY INTERNATIONAL
, cilt.29, sa.11, ss.1279-1285, 2009 (SCI-Expanded, Scopus)
2009
200952. Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome
Al Khatib S., Keles S., Garcia-Lioret M., Koc-Aydiner E. K., Reisli I., ARTAÇ H., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
, cilt.124, sa.2, ss.342-348, 2009 (SCI-Expanded, Scopus)
2009
200953. Exposure to house dust endotoxin and allergic sensitization in allergic and nonallergic children living in Adana, Turkey
YILMAZ M., ALTINTAŞ D. U., BİNGÖL KARAKOÇ G., Inal A., Kilic M., Sutolukta Z., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.51, sa.3, ss.225-231, 2009 (SCI-Expanded)
2008
200854. Effect of outdoor fungus concentrations on symptom severity of children with asthma and/or rhinitis monosensitized to molds
Inal A., BİNGÖL KARAKOÇ G., ALTINTAŞ D. U., Pinar M., Ceter T., YILMAZ M., et al.
ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY
, cilt.26, sa.1, ss.11-17, 2008 (SCI-Expanded)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2021
20211. The evaluation of rare and low-frequency genetic variants in common variable immune deficiency (CVID) patients together with CV/RVCD (common variant/rare variant, common disease) hypothesis for final interpretation
BİŞGİN A., SÖNMEZLER Ö., BOGA İ., YILMAZ M.
6. Uluslararası Katılımlı Erciyes Tıp Tibbi Genetik Kongresi, Türkiye, 16 Eylül 2021, (Özet Bildiri)
2018
20182. geç preterm ve term bebeklerde kordon klempleme zamanının lenfosit alt gruplarına etkisi
Bahar N., Satar M., Yılmaz M., Büyükkurt S., Ozlu F., Yapıcıoğlu Yıldızdaş H.
UNEKO-26, İskele, Kıbrıs (Kktc), 14 - 18 Nisan 2018, (Tam Metin Bildiri)
2017
20173. Nöroihtiyotik Sendromlar: Bir Vaka Serisi
İNCECİK F., HERGÜNER M. Ö., GÜNGÖR S., YILMAZ M., BEŞEN Ş., GÜL MERT G.
19.Ulusal Çocuk Nörolojisi Kongresi, Türkiye, 19 - 23 Nisan 2017, (Özet Bildiri)
2014
20144. AUTOIMMUNE HEPATITIS AND SCLERODERMA IN A PATIENT WITH X-LINKED AGAMMAGLOBULINAEMIA
YILMAZ M., BİNGÖL KARAKOÇ G., ALTINTAŞ D. U., Kotil A.
100th J Project Meeting, Antalya, Türkiye, 12 - 14 Mart 2014, cilt.34, ss.723, (Özet Bildiri)