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Lista de obras de Rabia Miray Kisla Ekinci

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

scientific article published on 14 September 2019

Canakinumab in Children with Familial Mediterranean Fever: A Single-Center, Retrospective Analysis

scientific article published on 01 October 2019

Clinical manifestations and outcomes of 420 children with Henoch Schönlein Purpura from a single referral center from Turkey: A three-year experience

artículo científico publicado en 2019

Decreased serum vitamin B12 and vitamin D levels affect sleep quality in children with familial Mediterranean fever.

artículo científico publicado en 2017

Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey

artículo científico publicado en 2020

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

scientific article published on 25 April 2019

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

scientific article published on 13 October 2020

Frequency of functional gastrointestinal disorders in children with familial Mediterranean fever

scientific article published on 31 January 2019

Hyperimmunoglobulinemia D syndrome with recurrent perianal abscess successfully treated with canakinumab

artículo científico publicado en 2019

Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in Gene: Experience from Southern Turkey

article

Is Henoch-Schönlein purpura a susceptibility factor for functional gastrointestinal disorders in children?

artículo científico publicado en 2018

MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience

artículo científico publicado en 2018

Phenotypic variability in two patients with tumor necrosis factor receptor associated periodic fever syndrome emphasizes a rare manifestation: Immunoglobulin A nephropathy

artículo científico publicado en 2019

Pre-Pulseless Takayasu Arteritis in a Child Represented With Prolonged Fever of Unknown Origin and Successful Management With Concomitant Mycophenolate Mofetil and Infliximab

artículo científico publicado en 2019

Recurrent Henoch Schönlein purpura without renal involvement successfully treated with methotrexate

artículo científico publicado en 2018

Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?

artículo científico publicado en 2020

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

scientific article published on 30 October 2017

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