Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Differentiating children with familial Mediterranean fever from other recurrent fever syndromes: The utility of new Eurofever/PRINTO classification criteria

KIŞLA EKİNCİ R. M., Balci S., Erol A. H., Karagoz D., ALTINTAŞ D. U., BİŞGİN A.
ARCHIVES OF RHEUMATOLOGY , cilt.36, sa.4, ss.493-498, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier

Clinical features of childhood uveitis at a tertiary referral center in Southern Turkey

Esen E., Sızmaz S., Balci S., Kışla Ekinci R. M., Demircan N.
INTERNATIONAL OPHTHALMOLOGY , cilt.41, sa.6, ss.2073-2081, 2021 (SCI-Expanded) identifier identifier identifier

Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey

KIŞLA EKİNCİ R. M., Balci S., Dogan H., Ceylaner S., Varan C., ALINÇ ERDEM S., et al.
MOLECULAR SYNDROMOLOGY , cilt.12, sa.2, ss.112-117, 2021 (SCI-Expanded) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

Evaluation of different classification criteria in children with Behcet disease: results from a single referral center

KIŞLA EKİNCİ R. M., ESEN E., Erol A. H., SIZMAZ S., Karagoz D., ALTINTAŞ D. U., et al.
EXPERT REVIEW OF CLINICAL IMMUNOLOGY , cilt.16, sa.11, ss.1093-1097, 2020 (SCI-Expanded) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

Different clinical manifestations of three prime repair exonuclease 1 mutation: A case series

İNCECİK F., Balci S., KIŞLA EKİNCİ R. M., Herguner O. M., BİŞGİN A., YILMAZ M.
ANNALS OF INDIAN ACADEMY OF NEUROLOGY , cilt.23, sa.5, ss.699-703, 2020 (SCI-Expanded) identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia

EKINCI R. M. K., Balci S., BİŞGİN A., ŞAŞMAZ I., LEBLEBİSATAN G., İNCECİK F., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.36, sa.6, ss.376-381, 2019 (SCI-Expanded) identifier identifier identifier

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) identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

Do practical laboratory indices predict the outcomes of children with Henoch-Schonlein purpura?

EKINCI R. M. K., Balci S., GOKAY S. S., YILMAZ H. L., DOĞRUEL D., ALTINTAŞ D. U., et al.
POSTGRADUATE MEDICINE , cilt.131, sa.4, ss.295-298, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Juvenile systemic lupus erythematosus: a single-center experience from southern Turkey

Balci S., Ekinci R., Bayazit A., Melek E., Dogruel D., Altintas D. U., et al.
CLINICAL RHEUMATOLOGY , cilt.38, sa.5, ss.1459-1468, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier

Frequency of functional gastrointestinal disorders in children with familial Mediterranean fever

Ekinci R. M., Balcı S., AKAY E., Tumgor G., DOGRUEL D., Altintas D. U., et al.
CLINICAL RHEUMATOLOGY , cilt.38, sa.3, ss.921-926, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in <i>GALNT3</i> Gene: Experience from Southern Turkey

Kışla E., Gürbüz F., BALCI S., Bişgin A., TAŞTAN M., Yüksel B., et al.
Journal of clinical research in pediatric endocrinology , cilt.11, ss.94-99, 2019 (SCI-Expanded) identifier identifier identifier

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) Sürdürülebilir Kalkınma identifier identifier identifier

MEW gene variants in children with Henoch-Schonlein purpura and association with clinical manifestations: a singie-center Mediterranean experience

Ekinci R. M., Balci S., Bisgin A., Atmis B., Dogruel D., Altintas D. U., et al.
POSTGRADUATE MEDICINE , cilt.131, sa.1, ss.68-72, 2019 (SCI-Expanded) identifier identifier identifier

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) Creative Commons License identifier identifier identifier

Decreased serum vitamin B-12 and vitamin D levels affect sleep quality in children with familial Mediterranean fever

Ekinci R., Balci S., Serbes M., Dogruel D., Altintas D. U., Yilmaz M.
RHEUMATOLOGY INTERNATIONAL , cilt.38, sa.1, ss.83-87, 2018 (SCI-Expanded) identifier identifier identifier

A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.

Kisla E., Balci S., Bisgin A., Altintas D. U., Yilmaz M.
European journal of medical genetics , cilt.60, ss.690-694, 2017 (SCI-Expanded) identifier identifier identifier

The Influence of Concomitant Disorders on Disease Severity of Familial Mediterranean Fever in Children.

Kişla E., Balci S., Ufuk A., Yilmaz M.
Archives of rheumatology , cilt.33, ss.282-287, 2017 (SCI-Expanded) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

The adherence of parents regarding epinephrine auto-injector use in anaphylaxis management: a real-life study

Serbes M., Sasihuseyinoglu A. S., ÖZCAN D., Kisla Ekinci R. M., BALCI S., Altintas D. U.
Cukurova Medical Journal , cilt.48, sa.1, ss.234-242, 2023 (ESCI) Creative Commons License identifier

Retrospective analyzes of adverse events during biologic agents in children with juvenile idiopathic arthritis from a single center in Turkey

BALCI ÇETİNKAYA S., DEMİR İ., SERBES M., ÖZCAN D., ALTINTAŞ D. U., KIŞLA EKİNCİ R. M.
RHEUMATOLOGIA , cilt.58, sa.6, ss.367-374, 2020 (Scopus) identifier

Frequency of functional gastrointestinal disorders in children with juvenile idiopathic arthritis

BALCI ÇETİNKAYA S., KIŞLA EKİNCİ R. M., DEMİR İ., SERBES M., ÖZCAN D., ALTINTAŞ D. U., et al.
CUKUROVA MEDICAL JOURNAL , cilt.45, sa.4, ss.1768-1774, 2020 (ESCI) identifier

The frequency of avascular necrosis in juvenile systemic lupus erythematosus

Balci S., Kışla Ekinci R. M., Piskin F. C., Melek E., Atmış B., Doğruel D., et al.
CUKUROVA MEDICAL JOURNAL , cilt.45, ss.200-207, 2020 (ESCI) Creative Commons License identifier

Growth parameters of Turkish children with juvenile idiopathic arthritis

Balci S., Calkan M., Dilek S. O., Dogruel D., Altintas D. U., KIŞLA EKİNCİ R. M.
CUKUROVA MEDICAL JOURNAL , cilt.45, sa.2, ss.495-501, 2020 (ESCI) identifier

Complement C2 polymorphisms in children with Henoch Schonlein Purpura

KIŞLA EKİNCİ R. M., Balci S., ATMIŞ B., KARABAY BAYAZIT A., DOĞRUEL D., ALTINTAŞ D. U., et al.
CUKUROVA MEDICAL JOURNAL , cilt.45, sa.1, ss.89-95, 2020 (ESCI) identifier

Symptomatic multifocal avascular necrosis in an adolescent with neuropsychiatric systemic lupus erythematosus

Ekinci R. M., Balcı S., ÇELİK G., DOĞRUEL D., ALTINTAŞ D. U., YILMAZ M.
Reumatologia , cilt.57, sa.3, ss.182-187, 2019 (Scopus) identifier identifier

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) identifier

Çocukluk çağı Miks Konnektif Doku Hastalığı: tek merkez deneyimi

KIŞLA EKİNCİ R. M., BALCI S., ALTINTAŞ D. U., YILMAZ M.
CUKUROVA MEDICAL JOURNAL , cilt.43, sa.2, ss.1, 2018 (Hakemli Dergi)

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) identifier

Juvenile idiopathic inflammatory myopathy: single center data

Balci S., Ekinci R. M. K., ALTINTAŞ D. U., YILMAZ M.
CUKUROVA MEDICAL JOURNAL , cilt.43, sa.3, ss.685-691, 2018 (ESCI) identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Genotype-phenotype correlation of patients with familial mediterranean fever in childhood: Experience of a single center

DOĞRUEL D., KIŞLA EKİNCİ R. M., BALCI S., YILMAZ M., ALTINTAŞ D. U.
9. International Congress of Familial Mediterranean Fever and Systemic Auto Inflammatory Diseases, Kıbrıs (Kktc), 4 - 07 Mayıs 2017

Kitap & Kitap Bölümleri

Juvenil Dermatomiyozit

KIŞLA EKİNCİ R. M., BALCI ÇETİNKAYA S.
Klinik Romatoloji, Kısacık Bünyamin, Bes Cemal, Koca Süleyman Serdar, Kasapçopur Özgür, Editör, EMA TIP KİTABEVİ, ss.768-777, 2023

Metrikler

Yayın

45

Atıf (WoS)

112

H-İndeks (WoS)

6

Atıf (Scopus)

148

H-İndeks (Scopus)

7

Proje

3

Açık Erişim

5
BM Sürdürülebilir Kalkınma Amaçları