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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2004 1
2005 2
2006 2
2007 4
2008 3
2009 3
2010 2
2011 4
2012 5
2013 8
2014 4
2015 1
2016 3
2017 5
2018 5
2019 6
2020 6
2024 0

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56 results

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Page 1
Screening for celiac disease among children with overweight and obesity: toward exploring celiac iceberg.
Calcaterra V, Regalbuto C, Manuelli M, Klersy C, Pelizzo G, Albertini R, Vinci F, Larizza D, Leonard MM, Cena H. Calcaterra V, et al. Among authors: larizza d. J Pediatr Endocrinol Metab. 2020 Jul 13:/j/jpem.ahead-of-print/jpem-2020-0076/jpem-2020-0076.xml. doi: 10.1515/jpem-2020-0076. Online ahead of print. J Pediatr Endocrinol Metab. 2020. PMID: 32653877 Free article. Review.
New understandings of the genetic basis of isolated idiopathic central hypogonadism.
Bonomi M, Libri DV, Guizzardi F, Guarducci E, Maiolo E, Pignatti E, Asci R, Persani L; Idiopathic Central Hypogonadism Study Group of the Italian Societies of Endocrinology and Pediatric Endocrinology and Diabetes. Bonomi M, et al. Asian J Androl. 2012 Jan;14(1):49-56. doi: 10.1038/aja.2011.68. Epub 2011 Dec 5. Asian J Androl. 2012. PMID: 22138902 Free PMC article. Review.
A frequent oligogenic involvement in congenital hypothyroidism.
de Filippis T, Gelmini G, Paraboschi E, Vigone MC, Di Frenna M, Marelli F, Bonomi M, Cassio A, Larizza D, Moro M, Radetti G, Salerno M, Ardissino D, Weber G, Gentilini D, Guizzardi F, Duga S, Persani L. de Filippis T, et al. Among authors: larizza d. Hum Mol Genet. 2017 Jul 1;26(13):2507-2514. doi: 10.1093/hmg/ddx145. Hum Mol Genet. 2017. PMID: 28444304 Free article.
Small supernumerary marker chromosomes: A legacy of trisomy rescue?
Kurtas NE, Xumerle L, Leonardelli L, Delledonne M, Brusco A, Chrzanowska K, Schinzel A, Larizza D, Guerneri S, Natacci F, Bonaglia MC, Reho P, Manolakos E, Mattina T, Soli F, Provenzano A, Al-Rikabi AH, Errichiello E, Nazaryan-Petersen L, Giglio S, Tommerup N, Liehr T, Zuffardi O. Kurtas NE, et al. Among authors: larizza d. Hum Mutat. 2019 Feb;40(2):193-200. doi: 10.1002/humu.23683. Epub 2018 Nov 22. Hum Mutat. 2019. PMID: 30412329 Free article.
New case of 4H syndrome and a review of the literature.
Orcesi S, Tonduti D, Uggetti C, Larizza D, Fazzi E, Balottin U. Orcesi S, et al. Among authors: larizza d. Pediatr Neurol. 2010 May;42(5):359-64. doi: 10.1016/j.pediatrneurol.2010.01.015. Pediatr Neurol. 2010. PMID: 20399393 Review.
GCK-MODY and obesity: symptom overlap makes diagnosis difficult.
Calcaterra V, Regalbuto C, Delle Cave F, Larizza D, Iafusco D. Calcaterra V, et al. Among authors: larizza d. Acta Diabetol. 2020 May;57(5):627-629. doi: 10.1007/s00592-019-01473-9. Epub 2020 Jan 21. Acta Diabetol. 2020. PMID: 31965321 No abstract available.
Diet and Lifestyle Role in Homocysteine Metabolism in Turner Syndrome.
Calcaterra V, Larizza D, De Giuseppe R, De Liso F, Klersy C, Albertini R, Pozzebon I, Princis MP, Montalbano C, Madè A, Cena H. Calcaterra V, et al. Among authors: larizza d. Med Princ Pract. 2019;28(1):48-55. doi: 10.1159/000494138. Epub 2018 Oct 2. Med Princ Pract. 2019. PMID: 30278440 Free PMC article.
Smoke exposure and cardio-metabolic profile in youth with type 1 diabetes.
Calcaterra V, Winickoff JP, Klersy C, Schiano LM, Bazzano R, Montalbano C, Musella V, Regalbuto C, Larizza D, Cena H. Calcaterra V, et al. Among authors: larizza d. Diabetol Metab Syndr. 2018 Jul 6;10:53. doi: 10.1186/s13098-018-0355-0. eCollection 2018. Diabetol Metab Syndr. 2018. PMID: 29989097 Free PMC article.
Gender Differences at the Onset of Autoimmune Thyroid Diseases in Children and Adolescents.
Calcaterra V, Nappi RE, Regalbuto C, De Silvestri A, Incardona A, Amariti R, Bassanese F, Clemente AM, Vinci F, Albertini R, Larizza D. Calcaterra V, et al. Among authors: larizza d. Front Endocrinol (Lausanne). 2020 Apr 17;11:229. doi: 10.3389/fendo.2020.00229. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32362875 Free PMC article.
56 results