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

Year Number of Results
2004 1
2006 1
2008 2
2009 3
2010 2
2011 3
2012 1
2013 7
2014 4
2015 15
2016 9
2017 6
2018 7
2019 6
2020 5
2021 12
2022 11
2023 8
2024 2

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93 results

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Page 1
Central Precocious Puberty in Italian Boys: Data From a Large Nationwide Cohort.
Cassio A, Marescotti G, Aversa T, Salerno M, Tornese G, Stancampiano M, Tuli G, Faienza MF, Cavarzere P, Fava D, Parpagnoli M, Bruzzi P, Ibba A, Calcaterra V, Mameli C, Grandone A, Cherubini V, Assirelli V, Franchina F, Capalbo D, Mase RD, Tamaro G, Cavasin J, Munarin J, Russo G, Wasniewska M; Physiopathology of Growth Processes and Puberty Study Group of the Italian Society for Pediatric Endocrinology and Diabetology. Cassio A, et al. Among authors: grandone a. J Clin Endocrinol Metab. 2024 Feb 3:dgae035. doi: 10.1210/clinem/dgae035. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38308814
XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH).
Seefried L, Alzahrani A, Arango Sancho P, Bacchetta J, Crowley R, Emma F, Gibbins J, Grandone A, Javaid MK, Mindler G, Raimann A, Rothenbuhler A, Tucker I, Zeitlin L, Linglart A. Seefried L, et al. Among authors: grandone a. Orphanet J Rare Dis. 2023 Oct 27;18(Suppl 2):333. doi: 10.1186/s13023-023-02883-3. Orphanet J Rare Dis. 2023. PMID: 37885021 Free PMC article. No abstract available.
DICER1 Syndrome: A Multicenter Surgical Experience and Systematic Review.
Spinelli C, Ghionzoli M, Sahli LI, Guglielmo C, Frascella S, Romano S, Ferrari C, Gennari F, Conzo G, Morganti R, De Napoli L, Quaglietta L, De Martino L, Picariello S, Grandone A, Luongo C, Gambale A, Patrizio A, Fallahi P, Antonelli A, Ferrari SM. Spinelli C, et al. Among authors: grandone a. Cancers (Basel). 2023 Jul 19;15(14):3681. doi: 10.3390/cancers15143681. Cancers (Basel). 2023. PMID: 37509342 Free PMC article.
De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling.
Morleo M, Venditti R, Theodorou E, Briere LC, Rosello M, Tirozzi A, Tammaro R, Al-Badri N, High FA, Shi J; Undiagnosed Diseases Network; Telethon Undiagnosed Diseases Program; Putti E, Ferrante L, Cetrangolo V, Torella A, Walker MA, Tenconi R, Iascone M, Mei D, Guerrini R, van der Smagt J, Kroes HY, van Gassen KLI, Bilal M, Umair M, Pingault V, Attie-Bitach T, Amiel J, Ejaz R, Rodan L, Zollino M, Agrawal PB, Del Bene F, Nigro V, Sweetser DA, Franco B. Morleo M, et al. Am J Hum Genet. 2023 Aug 3;110(8):1377-1393. doi: 10.1016/j.ajhg.2023.06.012. Epub 2023 Jul 13. Am J Hum Genet. 2023. PMID: 37451268 Free PMC article.
Editorial: Genetic, epigenetic and molecular landscaping of puberty.
Howard SR, Fanis P, Nicolaides NC, Grandone A. Howard SR, et al. Among authors: grandone a. Front Endocrinol (Lausanne). 2023 Mar 16;14:1178888. doi: 10.3389/fendo.2023.1178888. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37008930 Free PMC article. No abstract available.
Patients with DeSanto-Shinawi syndrome: Further extension of phenotype from Italy.
Pasquali D, Torella A, Grandone A, Luongo C, Morleo M, Peduto C, di Fraia R, Selvaggio LD, Allosso F, Accardo G, Zanobio MT, Maitz S, Mariani M, Selicorni A, Banfi S, Nigro V; TUDP Study Group. Pasquali D, et al. Among authors: grandone a. Am J Med Genet A. 2023 Mar;191(3):823-830. doi: 10.1002/ajmg.a.63061. Epub 2022 Nov 24. Am J Med Genet A. 2023. PMID: 36420948
93 results