Neutropenia in congenital nephrotic syndrome of the Finnish type: role of urinary ceruloplasmin loss.
Ulinski, Tim; Aoun, Bilal; Toubiana, Julie; Vitkevic, Renata; Bensman, Albert; Donadieu, Jean.
; 113(19): 4820-1, 2009 May 07.
Artigo em Inglês | MEDLINE | ID: mdl-19423745
Anemia in congenital nephrotic syndrome: role of urinary copper and ceruloplasmin loss.
Differentially expressed urinary biomarkers in children with idiopathic nephrotic syndrome.
Renal biopsy criterion in idiopathic nephrotic syndrome with microscopic hematuria at onset.
Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children.
[Nutritional management of kidney diseases in children].
Stezenie lamininy i fibronektyny w moczu dzieci z zespolem nerczycowym.
The role of bioelectrical impedance analysis, NT-ProBNP and inferior vena cava sonography in the assessment of body fluid volume in children with nephrotic syndrome
Elevated Urinary Levels of 8-Hydroxy-2'-deoxyguanosine in a Japanese Child of Xeroderma Pigmentosum/Cockayne Syndrome Complex with Infantile Onset of Nephrotic Syndrome.
Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis.
Therapy-resistant anaemia in congenital nephrotic syndrome of the Finnish type--implication of EPO, transferrin and transcobalamin losses.