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

Year Number of Results
2004 2
2006 1
2008 5
2009 6
2010 3
2011 3
2012 3
2013 8
2014 4
2015 18
2016 12
2017 6
2018 8
2019 7
2020 5
2021 12
2022 13
2023 4
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105 results
Results by year
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Page 1
New treatment modalities for obesity.
Grandone A, Di Sessa A, Umano GR, Toraldo R, Miraglia Del Giudice E. Grandone A, et al. Best Pract Res Clin Endocrinol Metab. 2018 Aug;32(4):535-549. doi: 10.1016/j.beem.2018.06.007. Epub 2018 Jun 25. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30086873 Review.
Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height.
Libraro A, D'Ascanio V, Cappa M, Chiarito M, Digilio MC, Einaudi S, Grandone A, Maghnie M, Mazzanti L, Mussa A, Patti G, Scarano E, Spinuzza A, Vannelli S, Wasniewska MG, Ferrero GB, Faienza MF. Libraro A, et al. Among authors: grandone a. Front Endocrinol (Lausanne). 2021 Dec 22;12:761171. doi: 10.3389/fendo.2021.761171. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 35002956 Free PMC article.
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders.
Giugliano T, Santoro C, Torella A, Del Vecchio Blanco F, Grandone A, Onore ME, Melone MAB, Straccia G, Melis D, Piccolo V, Limongelli G, Buono S, Perrotta S, Nigro V, Piluso G. Giugliano T, et al. Among authors: grandone a. Genes (Basel). 2019 Jul 31;10(8):580. doi: 10.3390/genes10080580. Genes (Basel). 2019. PMID: 31370276 Free PMC article.
MKRN3 role in regulating pubertal onset: the state of art of functional studies.
Palumbo S, Cirillo G, Aiello F, Papparella A, Miraglia Del Giudice E, Grandone A. Palumbo S, et al. Among authors: grandone a. Front Endocrinol (Lausanne). 2022 Sep 16;13:991322. doi: 10.3389/fendo.2022.991322. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36187104 Free PMC article. Review.
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype.
Palumbo S, Cirillo G, Sanchez G, Aiello F, Fachin A, Baldo F, Pellegrin MC, Cassio A, Salerno M, Maghnie M, Faienza MF, Wasniewska M, Fintini D, Giacomozzi C, Ciccone S, Miraglia Del Giudice E, Tornese G, Grandone A. Palumbo S, et al. Among authors: grandone a. J Endocrinol Invest. 2022 Dec 28. doi: 10.1007/s40618-022-01997-y. Online ahead of print. J Endocrinol Invest. 2022. PMID: 36577869
Variants in the 5'UTR reduce SHOX expression and contribute to SHOX haploinsufficiency.
Babu D, Vannelli S, Fanelli A, Mellone S, Baffico AM, Corrado L, Essa WA, Grandone A, Bellone S, Monzani A, Vinci G, De Sanctis L, Stuppia L, Prodam F, Giordano M. Babu D, et al. Among authors: grandone a. Eur J Hum Genet. 2021 Jan;29(1):110-121. doi: 10.1038/s41431-020-0676-y. Epub 2020 Jul 9. Eur J Hum Genet. 2021. PMID: 32647378 Free PMC article.
MKRN3 circulating levels in Prader-Willi syndrome: a pilot study.
Mariani M, Fintini D, Cirillo G, Palumbo S, Del Giudice EM, Bocchini S, Manco M, Cappa M, Grandone A. Mariani M, et al. Among authors: grandone a. J Endocrinol Invest. 2022 Nov;45(11):2165-2170. doi: 10.1007/s40618-022-01860-0. Epub 2022 Jul 19. J Endocrinol Invest. 2022. PMID: 35854182
105 results