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Parvovirus B19 infection in a hypogammaglobulinemic infant with neurologic disorders and anemia: successful immunoglobulin therapy.
Nigro G, D'Eufemia P, Zerbini M, Krzysztofiak A, Finocchiaro R, Giardini O. Nigro G, et al. Among authors: finocchiaro r. Pediatr Infect Dis J. 1994 Nov;13(11):1019-21. Pediatr Infect Dis J. 1994. PMID: 7845728 No abstract available.
High levels of serum prostaglandin E2 in children with osteogenesis imperfecta are reduced by neridronate treatment.
D'Eufemia P, Finocchiaro R, Celli M, Zambrano A, Tetti M, Villani C, Persiani P, Mari E, Zicari A. D'Eufemia P, et al. Among authors: finocchiaro r. Pediatr Res. 2008 Feb;63(2):203-6. doi: 10.1203/PDR.0b013e31815efd63. Pediatr Res. 2008. PMID: 18091347
Neutrophil glutamine deficiency in relation to genotype in children with cystic fibrosis.
D'Eufemia P, Finocchiaro R, Celli M, Tote J, Ferrucci V, Zambrano A, Troiani P, Quattrucci S. D'Eufemia P, et al. Among authors: finocchiaro r. Pediatr Res. 2006 Jan;59(1):13-6. doi: 10.1203/01.pdr.0000191139.17987.5a. Epub 2005 Dec 2. Pediatr Res. 2006. PMID: 16327011
Serum brain-type creatine kinase increases in children with osteogenesis imperfecta during neridronate treatment.
D'Eufemia P, Finocchiaro R, Villani C, Zambrano A, Lodato V, Palombaro M, Properzi E, Celli M. D'Eufemia P, et al. Among authors: finocchiaro r. Pediatr Res. 2014 May;75(5):626-30. doi: 10.1038/pr.2014.20. Epub 2014 Feb 11. Pediatr Res. 2014. PMID: 24518563
Low-dosage immunoglobulins for an infant with hypogammaglobulinemia, maple syrup urine disease, and parvovirus B19-associated aplastic crisis.
D'Eufemia P, Nigro G, Celli M, Finocchiaro R, Iannetti P, Giardini O. D'Eufemia P, et al. Among authors: finocchiaro r. J Pediatr Hematol Oncol. 2000 Sep-Oct;22(5):485-7. doi: 10.1097/00043426-200009000-00026. J Pediatr Hematol Oncol. 2000. PMID: 11037872 No abstract available.
Autoimmune thyroiditis in a case of tyrosinaemia type III.
D'Eufemia P, Giardini O, Cantani A, Martino F, Finocchiaro R. D'Eufemia P, et al. Among authors: finocchiaro r. J Inherit Metab Dis. 1992;15(6):861-2. doi: 10.1007/BF01800222. J Inherit Metab Dis. 1992. PMID: 1293381 No abstract available.
Immunological abnormalities in a patient with tyrosinaemia type III.
D'Eufemia PD, Finocchiaro R, Celli M, Viozzi L, Giardini O. D'Eufemia PD, et al. Among authors: finocchiaro r. J Inherit Metab Dis. 1995;18(3):355-6. doi: 10.1007/BF00710429. J Inherit Metab Dis. 1995. PMID: 7474904 No abstract available.
Abnormal intestinal permeability in children with autism.
D'Eufemia P, Celli M, Finocchiaro R, Pacifico L, Viozzi L, Zaccagnini M, Cardi E, Giardini O. D'Eufemia P, et al. Among authors: finocchiaro r. Acta Paediatr. 1996 Sep;85(9):1076-9. doi: 10.1111/j.1651-2227.1996.tb14220.x. Acta Paediatr. 1996. PMID: 8888921
Vitamin D deficiency rickets in five "at-risk" children.
D'Eufemia P, Parisi P, Celli M, Finocchiaro R, Roggini M, Raccio I, Zambrano A, Villa MP. D'Eufemia P, et al. Among authors: finocchiaro r. Pediatr Int. 2012 Feb;54(1):152-5. doi: 10.1111/j.1442-200X.2011.03408.x. Pediatr Int. 2012. PMID: 22335329 No abstract available.
Reduction of plasma taurine level in children affected by osteogenesis imperfecta during bisphosphonate therapy.
D'Eufemia P, Finocchiaro R, Zambrano A, Tetti M, Ferrucci V, Celli M. D'Eufemia P, et al. Among authors: finocchiaro r. Biomed Pharmacother. 2007 May;61(4):235-40. doi: 10.1016/j.biopha.2006.11.005. Epub 2006 Dec 29. Biomed Pharmacother. 2007. PMID: 17275249
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