Ausgabe 7/2017
Inhalt (26 Artikel)
C4d deposits in IgA nephropathy: where does complement activation come from?
Rosanna Coppo
Oral paricalcitol: expanding therapeutic options for pediatric chronic kidney disease patients
Michael Freundlich, Carolyn L. Abitbol
Genetic causes of hypomagnesemia, a clinical overview
Daan H. H. M Viering, Jeroen H. F. de Baaij, Stephen B. Walsh, Robert Kleta, Detlef Bockenhauer
Treatment of renal angiomyolipoma in tuberous sclerosis complex (TSC) patients
S. Brakemeier, F. Bachmann, K. Budde
Peritoneal dialysis for the management of pediatric patients with acute kidney injury
Anil Vasudevan, Kishore Phadke, Hui-Kim Yap
Congenital eyelid ptosis, decreased glomerular filtration, and orthostatic hypotension: Questions
Tessa Wassenberg, Michèl Willemsen, Henry Dijkman, Jaap Deinum, Leo Monnens
Congenital eyelid ptosis, decreased glomerular filtration, and orthostatic hypotension: Answers
Tessa Wassenberg, Michèl Willemsen, Henry Dijkman, Jaap Deinum, Leo Monnens
An atypical case of a 2-year-old boy with acute kidney injury: a race against time. Questions
Werner Keenswijk, Johan Vande Walle
An atypical case of a 2-year-old boy with acute kidney injury: a race against time. Answers
Werner Keenswijk, Johan Vande Walle
Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome
Fang Wang, Yanqin Zhang, Jianhua Mao, Zihua Yu, Zhuwen Yi, Li Yu, Jun Sun, Xiuxiu Wei, Fangrui Ding, Hongwen Zhang, Huijie Xiao, Yong Yao, Weizhen Tan, Svjetlana Lovric, Jie Ding, Friedhelm Hildebrandt
Clinical outcomes in children with Henoch–Schönlein purpura nephritis without crescents
Jean Daniel Delbet, Julien Hogan, Bilal Aoun, Iulia Stoica, Rémi Salomon, Stéphane Decramer, Isabelle Brocheriou, Georges Deschênes, Tim Ulinski
The ISKDC classification and a new semiquantitative classification for predicting outcomes of Henoch–Schönlein purpura nephritis
Mikael Koskela, Elisa Ylinen, Elli-Maija Ukonmaanaho, Helena Autio-Harmainen, Päivi Heikkilä, Jouko Lohi, Outi Jauhola, Jaana Ronkainen, Timo Jahnukainen, Matti Nuutinen
Mesangial C4d deposition may predict progression of kidney disease in pediatric patients with IgA nephropathy
Rafaela Cabral Gonçalves Fabiano, Stanley de Almeida Araújo, Eduardo Alves Bambirra, Eduardo Araújo Oliveira, Ana Cristina Simões e Silva, Sérgio Veloso Brant Pinheiro
Efficacy and safety of paricalcitol in children with stages 3 to 5 chronic kidney disease
Nicholas J. A. Webb, Gary Lerner, Bradley A. Warady, Katherine M. Dell, Larry A. Greenbaum, Gema Ariceta, Bernd Hoppe, Peter Linde, Ho-Jin Lee, Ann Eldred, Matthew B. Dufek
Dietary sources of energy and nutrient intake among children and adolescents with chronic kidney disease
Wen Chen, Kirstie Ducharme-Smith, Laura Davis, Wun Fung Hui, Bradley A. Warady, Susan L. Furth, Alison G. Abraham, Aisha Betoko
Association among prematurity (<30 weeks’ gestational age), blood pressure, urinary albumin, calcium, and phosphate in early childhood
Namrata Vashishta, Vidya Surapaneni, Sanjay Chawla, Gaurav Kapur, Girija Natarajan
Membrane pressures predict clotting of pediatric continuous renal replacement therapy circuits
Aadil Kakajiwala, Thomas Jemielita, John Z. Hughes, Kimberly Windt, Michelle Denburg, Stuart L. Goldstein, Benjamin Laskin
Unusual severe case of hemolytic uremic syndrome due to Shiga toxin 2d-producing E. coli O80:H2
Kioa L. Wijnsma, Anne M. Schijvens, John W. A. Rossen, A. M. D. (Mirjam) Kooistra-Smid, Michiel F. Schreuder, Nicole C. A. J. van de Kar
Challenges in establishing genotype–phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations
Kathrin Ebner, Claudia Dafinger, Nadina Ortiz-Bruechle, Friederike Koerber, Bernhard Schermer, Thomas Benzing, Jörg Dötsch, Klaus Zerres, Lutz Thorsten Weber, Bodo B. Beck, Max Christoph Liebau
Polycythemia, capillary rarefaction, and focal glomerulosclerosis in two adolescents born extremely low birth weight and premature
Nariaki Asada, Takanori Tsukahara, Megumi Furuhata, Daisuke Matsuoka, Shunsuke Noda, Kuniaki Naganuma, Akinori Hashiguchi, Midori Awazu
Children with Henoch–Schönlein purpura with low complement levels: follow-up for >6 years
Qiang Lin, Xiaozhong Li
Conversion from immediate- to extended-release cysteamine may decrease disease control and increase additional side effects
Sören Bäumner, Lutz T. Weber
Erratum to: mesangial C4d deposition may predict progression of kidney disease in pediatric patients with IgA nephropathy
Rafaela Cabral Gonçalves Fabiano, Stanley de Almeida Araújo, Eduardo Alves Bambirra, Eduardo Araújo Oliveira, Ana Cristina Simões e Silva, Sérgio Veloso Brant Pinheiro
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability
Brendan D. Crawford, Christopher E. Gillies, Catherine C. Robertson, Matthias Kretzler, Edgar A. Otto, Virginia Vega-Warner, Matthew G. Sampson