Issue 12/2007
Content (24 Articles)
Molecular mechanism of edema formation in nephrotic syndrome: therapeutic implications
Alain Doucet, Guillaume Favre, Georges Deschênes
Chronic kidney disease in children: the global perspective
Bradley A. Warady, Vimal Chadha
Teaching molecular genetics: chapter 4—positional cloning of genetic disorders
Aldamaria Puliti, Gianluca Caridi, Roberto Ravazzolo, Gian Marco Ghiggeri
NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome
Afig Berdeli, Sevgi Mir, Onder Yavascan, Erkin Serdaroglu, Mustafa Bak, Nejat Aksu, Ayse Oner, Ali Anarat, Osman Donmez, Nurhan Yildiz, Lale Sever, Yilmaz Tabel, Ruhan Dusunsel, Ferah Sonmez, Nilgun Cakar
Reduced albumin levels and utilization of arteriovenous access in pediatric patients with systemic lupus erythematosus (SLE)
Sangeeta D. Sule, Jeffrey J. Fadrowski, Barbara A. Fivush, Gregory Gorman, Susan L. Furth
Identification of a urinary proteomic signature for lupus nephritis in children
Michiko Suzuki, Gary F. Ross, Kristina Wiers, Shannen Nelson, Michael Bennett, Murray H. Passo, Prasad Devarajan, Hermine I. Brunner
Treatment with mycophenolate mofetil and prednisolone for steroid-dependent nephrotic syndrome
Kamran Afzal, Arvind Bagga, Shina Menon, Pankaj Hari, Stanley C. Jordan
Serum levels of galactose-deficient IgA in children with IgA nephropathy and Henoch-Schönlein purpura
Keith K. Lau, Robert J. Wyatt, Zina Moldoveanu, Milan Tomana, Bruce A. Julian, Ronald J. Hogg, Jeannette Y. Lee, Wen-Qiang Huang, Jiri Mestecky, Jan Novak
Efficacy of urine screening at school: experience in Shanghai, China
Yi-Hui Zhai, Hong Xu, Guang-Hua Zhu, Min-Jiang Wei, Bing-Chun Hua, Qian Shen, Jia Rao, Jie Ge
Antenatal and postnatal risk factors for neonatal hypertension and infant follow-up
Wael A. Seliem, Michael C. Falk, Bruce Shadbolt, Alison L. Kent
NGAL is an early predictive biomarker of contrast-induced nephropathy in children
Russel Hirsch, Catherine Dent, Holly Pfriem, Janene Allen, Robert H. Beekman III, Qing Ma, Sudha Dastrala, Michael Bennett, Mark Mitsnefes, Prasad Devarajan
Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder
Ajay P. Sharma, Cheryl R. Greenberg, Asuri N. Prasad, Chitra Prasad
Hemodialysis in children weighing less than 15 kg: a single-center experience
Yael Kovalski, Roxana Cleper, Irit Krause, Miriam Davidovits
Correlation between finger-prick and venous ciclosporin levels: association with gingival overgrowth and hypertrichosis
Nicholas J. A. Webb, Malcolm G. Coulthard, Richard S. Trompeter, Margaret M. Fitzpatrick, Suzanne Stephens, Jan Dudley, Heather Maxwell, Simon Waller, Graham C. Smith, Alan R. Watson, David A. Hughes, Brian G. Keevil, Janice S. Ellis
Cystic renal dysplasia as a leading sign of inherited metabolic disease
Felix Distelmaier, Markus Vogel, Ute Spiekerkötter, Klaus Gempel, Dirk Klee, Stefan Braunstein, Heinz-Peter Groneck, Ertan Mayatepek, Udo Wendel, Bernd Schwahn
Thrombotic microangiopathy as a complication in a patient with focal segmental glomerulosclerosis
Kerstin Benz, Kerstin Amann, Katalin Dittrich, Jörg Dötsch
Perinatal asphyxia may present with features of neonatal atypical hemolytic uremic syndrome
Valérie Biran, Sébastien Fau, Taleb Jamal, Frédérique Veinberg, Sylvain Renolleau, Francis Gold, Albert Bensman, Tim Ulinski
WT1 mutation and podocyte molecular expression in a Chinese Frasier syndrome patient
Jianguo Li, Dan Zhao, Jie Ding, Huijie Xiao, Na Guan, Qingfeng Fan, Hongwen Zhang
Splenic peliosis in the course of IgA nephropathy
Vesna Stojanović, Igor Mitić, Radoica Jokić, Nada Vučković, Aleksandra Doronjski, Gordana Vijatov, Biljana Milošević, Milesa Djapić
Rabson-Mendenhall syndrome: medullary sponge kidney, a new component
Andrew M. Harris, Bryan Hall, Vesna M. Kriss, John L. Fowlkes, Stefan G. Kiessling