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期刊名:Pediatric nephrology

缩写:PEDIATR NEPHROL

ISSN:0931-041X

e-ISSN:1432-198X

IF/分区:2.6/Q1

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共收录本刊相关文章索引6087
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Nergis Akay,Bagdagul Aksu,Zeynep Yuruk Yildirim et al. Nergis Akay et al.
Background: Chronic kidney disease (CKD) in children is associated with substantial morbidity and risk of progression to kidney failure in some cases. Identifying clinical predictors of kidney function decline is essentia...
Derya Cevizli,Emre Leventoğlu,Özlem Gül Kırkaş et al. Derya Cevizli et al.
Hemolytic uremic syndrome (HUS) in infancy may be difficult to classify because infection-associated HUS and genetic thrombotic microangiopathies (TMAs) can present with similar findings. We report a 7-month-old boy admitted with pneumonia,...
Moran Plonsky Toder,Shirley Pollack,Rami Tibi et al. Moran Plonsky Toder et al.
Background: Temporary discontinuation of mycophenolate mofetil (MMF) is frequently required in pediatric kidney transplant recipients, most often in response to viral complications. However, data regarding the long-term s...
María Herrero-Goñi,Mireia Aguirre Meñica,Alejandro Zarauza Santoveña et al. María Herrero-Goñi et al.
Background: The shortage of pediatric kidney donors has increased interest in donation after circulatory death (DCD) as an alternative for transplantation. ...
Eduardo Gutiérrez,Ángel M Sevillano,Fernando Caravaca-Fontán et al. Eduardo Gutiérrez et al.
Hematuria has traditionally been considered a benign sign of glomerular injury, as reported in autosomal dominant type IV collagen-related nephropathy. However, growing clinical and experimental evidence suggests that it may be an active dr...
Agnieszka Prytuła,Lars Pape,Zainab Arslan et al. Agnieszka Prytuła et al.
Children after kidney transplantation (KTx) are prone to mineral and bone disease (MBD) including growth restriction, bone pain, skeletal deformities, fractures, and vascular calcifications. We present a position paper on the diagnosis and ...
Stephan Przygodda,Laura Celine Brieger,Alina Verena Bohlen et al. Stephan Przygodda et al.
Background: X-linked hypophosphatemia (XLH) is the most common form of inherited rickets, resulting in short stature despite treatment with oral phosphate and active vitamin D. Detailed data of anthropometric parameters a...
Daniel Heydari,Sheldon Langlois,Mahboobeh Norouzi et al. Daniel Heydari et al.
Background: Discovery of autoantibodies in steroid-sensitive nephrotic syndrome (SSNS) has transformed our understanding of SSNS as an immune-mediated disease; however, mechanisms underlying autoantibody production are un...