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Toplam kayıt 30, listelenen: 11-20
Surgical Management Of Renovascular Hypertension In Children And Young Adults: A 13-Year Experience
(2019)
OBJECTIVES: In this study, we aimed to evaluate the early and mid-term outcomes of surgery for renovascular hypertension (RVH) at our institution, within the last 13years. METHODS: We retrospectively reviewed 19 patients ...
Rituximab For Children With Difficult-To-Treat Nephrotic Syndrome: Its Effects On Disease Progression And Growth
(2019)
Background: Since the early 2000s rituximab (RTX) has been thought of as an alternative treatment for steroid-sensitive nephrotic syndrome (SSNS) and steroid-resistant nephrotic syndrome (SRNS)., Objective: This study aimed ...
Bk Virus Associated Nephropathy And Severe Pneumonia In A Kidney Transplanted Adolescent With Schimke Immune-Osseous-Dysplasia
(2019)
Patients with juvenile onset Schimke immune-osseous-dysplasia (SIOD) have less severe symptoms and can survive in the second and third decade of life. We present an 18 year-old adolescent with juvenile onset SIOD who was ...
Mutations In Emp2 Cause Childhood-Onset Nephrotic Syndrome
(Cell Press, 2014)
Nephrotic syndrome (NS) is a genetically heterogeneous group of diseases that are divided into steroid-sensitive NS (SSNS) and steroid-resistant NS (SRNS). SRNS inevitably leads to end-stage kidney disease, and no curative ...
The Bone and Mineral Disorder of Children Undergoing Chronic Peritoneal Dialysis
(Elsevier Science Inc, 2010)
The mineral and bone disorder of chronic kidney disease remains a challenging complication in pediatric end-stage renal disease. Here, we assessed symptoms, risk factors and management of this disorder in 890 children and ...
Turkish Pediatric Atypical Hemolytic Uremic Syndrome Registry: Initial Analysis Of 146 Patients
(2017)
Background Atypical hemolytic uremic syndrome (aHUS) is a devastating disease with significant morbidity and mortality. Its genetic heterogeneity impacts its clinical presentation, progress, and outcome, and there is no ...
ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS
(Amer Soc Nephrology, 2016)
Hereditary defects of coenzyme Q(10) biosynthesis cause steroid-resistant nephrotic syndrome (SRNS) as part of multiorgan involvement but may also contribute to isolated SRNS. Here, we report 26 patients from 12 families ...
Respiratory-Chain Deficiency Presenting As Diffuse Mesangial Sclerosis with Nphs3 Mutation
(Springer, 2011)
Renal manifestations of mitochondrial cytopathies have been described, but nephrotic syndrome with respiratory-chain disorders have been described extremely rarely. We report a 9-month-old boy with a mitochondrial cytopathy ...