Marco Zaffanello
Department of Life and Reproduction Sciences
Section of Pediatrics
University of Verona
Verona
Italy
Name/email consistency: high
- Genetic susceptibility to renal scar formation after urinary tract infection: a systematic review and meta-analysis of candidate gene polymorphisms. Zaffanello, M., Tardivo, S., Cataldi, L., Fanos, V., Biban, P., Malerba, G. Pediatr. Nephrol. (2011)
- Long-term effects of neonatal drugs on the kidney. Zaffanello, M., Bassareo, P.P., Cataldi, L., Antonucci, R., Biban, P., Fanos, V. J. Matern. Fetal. Neonatal. Med. (2010)
- Evidence-based treatment limitations prevent any therapeutic recommendation for acute poststreptococcal glomerulonephritis in children. Zaffanello, M., Cataldi, L., Franchini, M., Fanos, V. Med. Sci. Monit. (2010)
- Genetic risk for recurrent urinary tract infections in humans: a systematic review. Zaffanello, M., Malerba, G., Cataldi, L., Antoniazzi, F., Franchini, M., Monti, E., Fanos, V. J. Biomed. Biotechnol. (2010)
- Acute non-oliguric kidney failure and cholestatic hepatitis induced by ibuprofen and acetaminophen: a case report. Zaffanello, M., Brugnara, M., Angeli, S., Cuzzolin, L. Acta Paediatr. (2009)
- Evaluating kidney damage from vesico-ureteral reflux in children. Zaffanello, M., Franchini, M., Brugnara, M., Fanos, V. Saudi. J. Kidney. Dis. Transpl (2009)
- Prophylaxis with AT III for thromboembolism in nephrotic syndrome: why should it be done? Zaffanello, M., Brugnara, M., Fanos, V., Franchini, M. Int. Urol. Nephrol (2009)
- Hidden high-grade vesicoureteral reflux is the main risk factor for chronic renal damage in children under the age of two years with first urinary tract infection. Zaffanello, M., Cataldi, L., Brugnara, M., Franchini, M., Bruno, C., Fanos, V. Scand. J. Urol. Nephrol. (2009)
- Are children with congenital solitary kidney at risk for lifelong complications? A lack of prediction demands caution. Zaffanello, M., Brugnara, M., Zuffante, M., Franchini, M., Fanos, V. Int. Urol. Nephrol (2009)
- Treatment-based literature of Henoch-Schönlein purpura nephritis in childhood. Zaffanello, M., Fanos, V. Pediatr. Nephrol. (2009)
- Early diagnosis of Acute Kidney Injury with urinary biomarkers in the newborn. Zaffanello, M., Antonucci, R., Cuzzolin, L., Cataldi, L., Fanos, V. J. Matern. Fetal. Neonatal. Med. (2009)
- Renal involvement in children with vesicoureteral reflux: are prenatal detection and surgical approaches preventive? Zaffanello, M., Brugnara, M., Cecchetto, M., Fedrizzi, M., Fanos, V. Scand. J. Urol. Nephrol. (2008)
- TCF2 gene mutation leads to nephro-urological defects of unequal severity: an open question. Zaffanello, M., Brugnara, M., Franchini, M., Fanos, V. Med. Sci. Monit. (2008)
- Pelvi-ureteric junction obstruction and renal function after pyeloplasty: a retrospective study in 29 children. Zaffanello, M., Cecchetto, M., Brugnara, M., Martone, E., Zuffante, M., Fedrizzi, M., Fanos, V. Minerva. Urol. Nefrol (2008)
- New therapeutic strategies with combined renin-angiotensin system inhibitors for pediatric nephropathy. Zaffanello, M., Franchini, M., Fanos, V. Pharmacotherapy (2008)
- Is serum procalcitonin able to predict long-term kidney morbidity from urinary tract infections in children?. Zaffanello, M., Brugnara, M., Franchini, M., Fanos, V. Clin. Chem. Lab. Med. (2008)
- Is serum Cystatin-C a suitable marker of renal function in children? Zaffanello, M., Franchini, M., Fanos, V. Ann. Clin. Lab. Sci. (2007)
- Therapeutic options in childhood nocturnal enuresis. Zaffanello, M., Giacomello, L., Brugnara, M., Fanos, V. Minerva. Urol. Nefrol (2007)
- Therapy for children with henoch-schonlein purpura nephritis: a systematic review. Zaffanello, M., Brugnara, M., Franchini, M. ScientificWorldJournal (2007)
- Thromboembolism in childhood nephrotic syndrome: a rare but serious complication. Zaffanello, M., Franchini, M. Hematology (2007)
- Urological complications and copper replacement therapy in childhood Menkes syndrome. Zaffanello, M., Maffeis, C., Fanos, V., Franchini, M., Zamboni, G. Acta Paediatr. (2006)
- Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern Italian neonatal screening. Zaffanello, M., Zamboni, G., Maselli, M., Gandini, A., Camilot, M., Maffeis, C., Burlina, A.B., Tatò, L. Genet. Test. (2005)
- Therapeutic approach in a case of Pearson's syndrome. Zaffanello, M., Zamboni, G. Minerva Pediatr. (2005)
- Complex glycerol kinase deficiency leads to psychomotor and body-growth failure. Zaffanello, M., Zamboni, G., Tonin, P., Solero, G.P., Tatò, L. J. Paediatr. Child. Health (2004)
- Neonatal screening for glucose-6-phosphate dehydrogenase deficiency fails to detect heterozygote females. Zaffanello, M., Rugolotto, S., Zamboni, G., Gaudino, R., Tatò, L. Eur. J. Epidemiol. (2004)
- A case of partial biotinidase deficiency associated with autism. Zaffanello, M., Zamboni, G., Fontana, E., Zoccante, L., Tatò, L. Child. Neuropsychol (2003)
- Neonatal birth parameters of positive newborns at PKU screening as predictors of false-positive and positive results at recall-testing. Zaffanello, M., Zamboni, G., Maffeis, C., Tatò, L. J. Med. Screen (2003)
- Growth parameters in newborns with hyperphenylalaninaemia. Zaffanello, M., Zamboni, G., Tatò, L. Paediatr. Perinat. Epidemiol (2002)
