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Results by year

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

Year Number of Results
1948 3
1950 6
1951 3
1952 5
1953 4
1954 5
1955 10
1956 3
1957 7
1959 2
1960 4
1961 1
1962 1
1963 1
1964 1
1965 1
1968 3
1969 2
1971 1
1972 4
1973 1
1974 4
1975 6
1976 3
1977 7
1978 6
1979 8
1980 10
1981 7
1982 4
1983 2
1984 1
1985 5
1986 4
1987 4
1988 13
1989 6
1990 7
1991 9
1992 7
1993 8
1994 10
1995 7
1996 3
1997 10
1998 10
1999 15
2000 5
2001 2
2002 7
2003 7
2004 9
2005 10
2006 3
2007 12
2008 14
2009 10
2010 8
2011 11
2012 11
2013 10
2014 15
2015 18
2016 14
2017 10
2018 4
2019 12
2020 7
2021 5
2022 6
2023 2

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424 results

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Page 1
Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndrome.
Motta M, Solman M, Bonnard AA, Kuechler A, Pantaleoni F, Priolo M, Chandramouli B, Coppola S, Pizzi S, Zara E, Ferilli M, Kayserili H, Onesimo R, Leoni C, Brinkmann J, Vial Y, Kamphausen SB, Thomas-Teinturier C, Guimier A, Cordeddu V, Mazzanti L, Zampino G, Chillemi G, Zenker M, Cavé H, den Hertog J, Tartaglia M. Motta M, et al. Among authors: mazzanti l. Hum Mol Genet. 2022 Aug 23;31(16):2766-2778. doi: 10.1093/hmg/ddac071. Hum Mol Genet. 2022. PMID: 35348676 Free PMC article.
Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum.
Motta M, Pannone L, Pantaleoni F, Bocchinfuso G, Radio FC, Cecchetti S, Ciolfi A, Di Rocco M, Elting MW, Brilstra EH, Boni S, Mazzanti L, Tamburrino F, Walsh L, Payne K, Fernández-Jaén A, Ganapathi M, Chung WK, Grange DK, Dave-Wala A, Reshmi SC, Bartholomew DW, Mouhlas D, Carpentieri G, Bruselles A, Pizzi S, Bellacchio E, Piceci-Sparascio F, Lißewski C, Brinkmann J, Waclaw RR, Waisfisz Q, van Gassen K, Wentzensen IM, Morrow MM, Álvarez S, Martínez-García M, De Luca A, Memo L, Zampino G, Rossi C, Seri M, Gelb BD, Zenker M, Dallapiccola B, Stella L, Prada CE, Martinelli S, Flex E, Tartaglia M. Motta M, et al. Among authors: mazzanti l. Am J Hum Genet. 2020 Sep 3;107(3):499-513. doi: 10.1016/j.ajhg.2020.06.018. Epub 2020 Jul 27. Am J Hum Genet. 2020. PMID: 32721402 Free PMC article.
Endocrinological manifestations in RASopathies.
Tamburrino F, Scarano E, Schiavariello C, Perri A, Pession A, Mazzanti L. Tamburrino F, et al. Among authors: mazzanti l. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):471-477. doi: 10.1002/ajmg.c.32013. Epub 2022 Nov 19. Am J Med Genet C Semin Med Genet. 2022. PMID: 36401574 Review.
Editorial: Endocrine aspects of Noonan syndrome and related syndromes.
Radetti G, Edouard T, Mazzanti L, Tartaglia M, Zenker M. Radetti G, et al. Among authors: mazzanti l. Front Endocrinol (Lausanne). 2023 Jan 5;13:1127686. doi: 10.3389/fendo.2022.1127686. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36686494 Free PMC article. No abstract available.
Developmental syndromes: growth hormone deficiency and treatment.
Mazzanti L, Tamburrino F, Bergamaschi R, Scarano E, Montanari F, Torella M, Ballarini E, Cicognani A. Mazzanti L, et al. Endocr Dev. 2009;14:114-34. doi: 10.1159/000207481. Epub 2009 Feb 27. Endocr Dev. 2009. PMID: 19293579 Review.
Alzheimer's disease and diabetes: new insights and unifying therapies.
Vignini A, Giulietti A, Nanetti L, Raffaelli F, Giusti L, Mazzanti L, Provinciali L. Vignini A, et al. Among authors: mazzanti l. Curr Diabetes Rev. 2013 May;9(3):218-27. doi: 10.2174/1573399811309030003. Curr Diabetes Rev. 2013. PMID: 23363296 Review.
Neuropsychiatric phenotype in a child with pseudohypoparathyroidism.
Visconti P, Posar A, Scaduto MC, Russo A, Tamburrino F, Mazzanti L. Visconti P, et al. Among authors: mazzanti l. J Pediatr Neurosci. 2016 Jul-Sep;11(3):267-270. doi: 10.4103/1817-1745.193373. J Pediatr Neurosci. 2016. PMID: 27857805 Free PMC article.
424 results