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

Year Number of Results
1975 2
1977 2
1978 1
1979 1
1981 3
1982 2
1983 3
1984 1
1985 2
1986 7
1987 1
1988 1
1989 6
1990 5
1991 3
1992 2
1993 5
1994 5
1996 4
1997 3
1998 3
1999 1
2000 2
2001 5
2002 3
2003 1
2004 1
2005 4
2006 3
2007 6
2008 5
2009 8
2010 4
2011 9
2012 7
2013 12
2014 5
2015 1
2016 3
2017 5
2018 5
2019 7
2020 7
2024 0

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152 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.
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.
Pheochromocytoma and diabetes mellitus.
Lorini R, Larizza D, Cammareri V, Severi F. Lorini R, et al. Among authors: larizza d. Clin Endocrinol (Oxf). 1983 Aug;19(2):275-6. doi: 10.1111/j.1365-2265.1983.tb02990.x. Clin Endocrinol (Oxf). 1983. PMID: 6883740 No abstract available.
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.
Thrombophilic screening in Turner syndrome.
Calcaterra V, Gamba G, Montani N, de Silvestri A, Terulla V, Lanati G, Larizza D. Calcaterra V, et al. Among authors: larizza d. J Endocrinol Invest. 2011 Oct;34(9):676-9. doi: 10.3275/7724. Epub 2011 May 17. J Endocrinol Invest. 2011. PMID: 21586893
An analysis of Xq deletions.
Maraschio P, Tupler R, Barbierato L, Dainotti E, Larizza D, Bernardi F, Hoeller H, Garau A, Tiepolo L. Maraschio P, et al. Among authors: larizza d. Hum Genet. 1996 Mar;97(3):375-81. doi: 10.1007/BF02185777. Hum Genet. 1996. PMID: 8786087
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.
152 results