Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

77 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Why do premature newborn infants display elevated blood adenosine levels?
Panfoli I, Cassanello M, Bruschettini M, Colella M, Cerone R, Ravera S, Calzia D, Candiano G, Ramenghi L. Panfoli I, et al. Among authors: cerone r. Med Hypotheses. 2016 May;90:53-6. doi: 10.1016/j.mehy.2016.03.007. Epub 2016 Mar 12. Med Hypotheses. 2016. PMID: 27063086
Effect of carnitine supplementation on lipid profile and anemia in children on chronic dialysis.
Verrina E, Caruso U, Calevo MG, Emma F, Sorino P, De Palo T, Lavoratti G, Turrini Dertenois L, Cassanello M, Cerone R, Perfumo F; Italian Registry of Pediatric Chronic Dialysis. Verrina E, et al. Among authors: cerone r. Pediatr Nephrol. 2007 May;22(5):727-33. doi: 10.1007/s00467-006-0408-8. Epub 2007 Feb 3. Pediatr Nephrol. 2007. PMID: 17277954 Clinical Trial.
Newborn screening for homocystinurias: Recent recommendations versus current practice.
Keller R, Chrastina P, Pavlíková M, Gouveia S, Ribes A, Kölker S, Blom HJ, Baumgartner MR, Bártl J, Dionisi-Vici C, Gleich F, Morris AA, Kožich V, Huemer M; individual contributors of the European Network and Registry for Homocystinurias and Methylation Defects (E-HOD); Barić I, Ben-Omran T, Blasco-Alonso J, Bueno Delgado MA, Carducci C, Cassanello M, Cerone R, Couce ML, Crushell E, Delgado Pecellin C, Dulin E, Espada M, Ferino G, Fingerhut R, Garcia Jimenez I, Gonzalez Gallego I, González-Irazabal Y, Gramer G, Juan Fita MJ, Karg E, Klein J, Konstantopoulou V, la Marca G, Leão Teles E, Leuzzi V, Lilliu F, Lopez RM, Lund AM, Mayne P, Meavilla S, Moat SJ, Okun JG, Pasquini E, Pedron-Giner CC, Racz GZ, Ruiz Gomez MA, Vilarinho L, Yahyaoui R, Zerjav Tansek M, Zetterström RH, Zeyda M. Keller R, et al. Among authors: cerone r. J Inherit Metab Dis. 2019 Jan;42(1):128-139. doi: 10.1002/jimd.12034. J Inherit Metab Dis. 2019. PMID: 30740731 Free article.
Phenylketonuria: diet for life or not?
Cerone R, Schiaffino MC, Di Stefano S, Veneselli E. Cerone R, et al. Acta Paediatr. 1999 Jun;88(6):664-6. doi: 10.1080/08035259950169350. Acta Paediatr. 1999. PMID: 10419254
Computed tomography in maple syrup urine disease.
Taccone A, Schiaffino MC, Cerone R, Fondelli MP, Romano C. Taccone A, et al. Among authors: cerone r. Eur J Radiol. 1992 May-Jun;14(3):207-12. doi: 10.1016/0720-048x(92)90089-r. Eur J Radiol. 1992. PMID: 1563430
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.
Cassio A, Corbetta C, Antonozzi I, Calaciura F, Caruso U, Cesaretti G, Gastaldi R, Medda E, Mosca F, Pasquini E, Salerno MC, Stoppioni V, Tonacchera M, Weber G, Olivieri A; Italian Society for Pediatric Endocrinology and Diabetology; Italian Society for the Study of Metabolic Diseases and Neonatal Screening; Italian National Institute of Health; Italian National Coordinating Group for Congenital Hypothyroidism; Italian Thyroid Association; Italian Society of Pediatrics; Italian Society of Neonatology; Italian Society of Endocrinology; Associazione Medici Endocrinologi. Cassio A, et al. J Endocrinol Invest. 2013 Mar;36(3):195-203. doi: 10.3275/8849. Epub 2013 Feb 12. J Endocrinol Invest. 2013. PMID: 23404215 Review.
77 results