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

Year Number of Results
2006 1
2007 1
2008 1
2009 1
2010 1
2011 3
2012 1
2013 1
2014 2
2015 2
2016 2
2019 3
2020 3
2021 6
2022 4
2023 4
2024 0

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29 results

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Page 1
Genes and Microbiota Interaction in Monogenic Autoimmune Disorders.
Costa F, Beltrami E, Mellone S, Sacchetti S, Boggio E, Gigliotti CL, Stoppa I, Dianzani U, Rolla R, Giordano M. Costa F, et al. Among authors: mellone s. Biomedicines. 2023 Apr 8;11(4):1127. doi: 10.3390/biomedicines11041127. Biomedicines. 2023. PMID: 37189745 Free PMC article. Review.
A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature.
Mancioppi V, Daffara T, Romanisio M, Ceccarini G, Pelosini C, Santini F, Bellone S, Mellone S, Baricich A, Rabbone I, Aimaretti G, Akinci B, Giordano M, Prodam F. Mancioppi V, et al. Among authors: mellone s. Front Endocrinol (Lausanne). 2023 Jul 12;14:1212729. doi: 10.3389/fendo.2023.1212729. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37501786 Free PMC article. Review.
Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort.
De Rienzo F, Mellone S, Bellone S, Babu D, Fusco I, Prodam F, Petri A, Muniswamy R, De Luca F, Salerno M, Momigliano-Richardi P, Bona G, Giordano M; Italian Study Group on Genetics of CPHD. De Rienzo F, et al. Among authors: mellone s. Clin Endocrinol (Oxf). 2015 Dec;83(6):849-60. doi: 10.1111/cen.12849. Epub 2015 Aug 6. Clin Endocrinol (Oxf). 2015. PMID: 26147833 Review.
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: mellone s. 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.
Temporal correlation between the first melanoma and the first noncutaneous tumor in CKDN2A genotyped patients.
Gironi LC, Esposto E, Zottarelli F, Giorgione R, Farinelli P, Zavattaro E, Cammarata E, Di Cristo N, Ogliara P, Camillo L, Giordano M, Mellone S, Pasini B, Ambrosi A, Savoia P. Gironi LC, et al. Among authors: mellone s. Melanoma Res. 2023 Oct 1;33(5):425-430. doi: 10.1097/CMR.0000000000000906. Epub 2023 Jun 21. Melanoma Res. 2023. PMID: 37352544
The Usefulness of a Targeted Next Generation Sequencing Gene Panel in Providing Molecular Diagnosis to Patients With a Broad Spectrum of Neurodevelopmental Disorders.
Mellone S, Puricelli C, Vurchio D, Ronzani S, Favini S, Maruzzi A, Peruzzi C, Papa A, Spano A, Sirchia F, Mandrile G, Pelle A, Rasmini P, Vercellino F, Zonta A, Rabbone I, Dianzani U, Viri M, Giordano M. Mellone S, et al. Front Genet. 2022 Aug 11;13:875182. doi: 10.3389/fgene.2022.875182. eCollection 2022. Front Genet. 2022. PMID: 36035117 Free PMC article.
COVID-19 first lockdown and outpatient hospital setting: a single center, real life study focusing on pattern changes in patients' ethnicities and treated dermatoses.
Gironi LC, Esposto E, Giorgione R, Zavattaro E, Farinelli P, Giordano M, Mellone S, Buja A, Pigatto PD, Damiani G, Savoia P. Gironi LC, et al. Among authors: mellone s. Ital J Dermatol Venerol. 2022 Oct;157(5):414-418. doi: 10.23736/S2784-8671.22.07357-1. Epub 2022 Jun 6. Ital J Dermatol Venerol. 2022. PMID: 35666665 Free article.
29 results