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

Year Number of Results
1982 1
1984 1
1988 1
1989 3
1990 2
1994 3
1998 1
2001 4
2003 2
2005 5
2006 1
2007 4
2008 4
2009 4
2010 3
2011 1
2013 2
2014 1
2015 1
2016 2
2017 2
2019 2
2020 1
2021 3
2022 1
2023 3
2024 3

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56 results

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Page 1
GNB1-Related Rod-Cone Dystrophy: A Case Report.
Conti GM, Cancellieri F, Quinodoz M, Kaminska K, Vaclavik V, Rivolta C, Tran HV. Conti GM, et al. Among authors: cancellieri f. Case Rep Ophthalmol. 2024 Mar 18;15(1):230-237. doi: 10.1159/000537997. eCollection 2024 Jan-Dec. Case Rep Ophthalmol. 2024. PMID: 38500542 Free PMC article.
Recommendations on menopausal hormone replacement therapy.
Cagnacci A, Gambacciani M, Gallo M, Lello S; Executive Committee of the Italian Society of Menopause (SIM) and of the Italian Society of Gynecology of the Third Age (SIGiTE). Cagnacci A, et al. Minerva Ginecol. 2019 Dec;71(6):395-403. doi: 10.23736/S0026-4784.19.04500-3. Minerva Ginecol. 2019. PMID: 32064823 No abstract available.
Endothelial damage in septic shock patients as evidenced by circulating syndecan-1, sphingosine-1-phosphate and soluble VE-cadherin: a substudy of ALBIOS.
Piotti A, Novelli D, Meessen JMTA, Ferlicca D, Coppolecchia S, Marino A, Salati G, Savioli M, Grasselli G, Bellani G, Pesenti A, Masson S, Caironi P, Gattinoni L, Gobbi M, Fracasso C, Latini R; ALBIOS Investigators. Piotti A, et al. Crit Care. 2021 Mar 19;25(1):113. doi: 10.1186/s13054-021-03545-1. Crit Care. 2021. PMID: 33741039 Free PMC article. Clinical Trial.
Cardiovascular effects of raloxifene hydrochloride.
Saitta A, Morabito N, Frisina N, Cucinotte D, Corrado F, D'Anna R, Altavilla D, Squadrito G, Minutoli L, Arcoraci V, Cancellieri F, Squadrito F. Saitta A, et al. Among authors: cancellieri f. Cardiovasc Drug Rev. 2001 Spring;19(1):57-74. doi: 10.1111/j.1527-3466.2001.tb00183.x. Cardiovasc Drug Rev. 2001. PMID: 11314601 Review.
Anesthesia mumps after thyroidectomy.
Cozzaglio L, Pizzocaro A, Cancellieri F. Cozzaglio L, et al. Among authors: cancellieri f. J Endocrinol Invest. 2017 Mar;40(3):335-336. doi: 10.1007/s40618-016-0598-2. Epub 2016 Dec 20. J Endocrinol Invest. 2017. PMID: 28000179 No abstract available.
Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype.
Jurkute N, Cancellieri F, Pohl L, Li CHZ, Heaton RA, Reurink J, Bellingham J, Quinodoz M, Yioti G, Stefaniotou M, Weener M, Zuleger T, Haack TB, Stingl K; Genomics England Research Consortium; Hoyng CB, Mahroo OA, Hargreaves I, Raymond FL, Michaelides M, Rivolta C, Kohl S, Roosing S, Webster AR, Arno G. Jurkute N, et al. Among authors: cancellieri f. NPJ Genom Med. 2022 Oct 20;7(1):60. doi: 10.1038/s41525-022-00330-z. NPJ Genom Med. 2022. PMID: 36266294 Free PMC article.
Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies.
Daich Varela M, Bellingham J, Motta F, Jurkute N, Ellingford JM, Quinodoz M, Oprych K, Niblock M, Janeschitz-Kriegl L, Kaminska K, Cancellieri F, Scholl HPN, Lenassi E, Schiff E, Knight H, Black G, Rivolta C, Cheetham ME, Michaelides M, Mahroo OA, Moore AT, Webster AR, Arno G. Daich Varela M, et al. Among authors: cancellieri f. Hum Mol Genet. 2023 Jan 27;32(4):595-607. doi: 10.1093/hmg/ddac227. Hum Mol Genet. 2023. PMID: 36084042 Free PMC article.
Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies.
Rehman AU, Sepahi N, Bedoni N, Ravesh Z, Salmaninejad A, Cancellieri F, Peter VG, Quinodoz M, Mojarrad M, Pasdar A, Asad AG, Ghalamkari S, Piran M, Piran M, Superti-Furga A, Rivolta C. Rehman AU, et al. Among authors: cancellieri f. Sci Rep. 2021 Sep 29;11(1):19332. doi: 10.1038/s41598-021-98677-3. Sci Rep. 2021. PMID: 34588515 Free PMC article.
PCSK9 is associated with mortality in patients with septic shock: data from the ALBIOS study.
Vecchié A, Bonaventura A, Meessen J, Novelli D, Minetti S, Elia E, Ferrara D, Ansaldo AM, Scaravilli V, Villa S, Ferla L, Caironi P, Latini R, Carbone F, Montecucco F; ALBIOS Biomarkers Study Investigators. Vecchié A, et al. J Intern Med. 2021 Feb;289(2):179-192. doi: 10.1111/joim.13150. Epub 2020 Jul 30. J Intern Med. 2021. PMID: 32686253 Free article. Clinical Trial.
The first genetic landscape of inherited retinal dystrophies in Portuguese patients identifies recurrent homozygous mutations as a frequent cause of pathogenesis.
Peter VG, Kaminska K, Santos C, Quinodoz M, Cancellieri F, Cisarova K, Pescini Gobert R, Rodrigues R, Custódio S, Paris LP, Sousa AB, Coutinho Santos L, Rivolta C. Peter VG, et al. Among authors: cancellieri f. PNAS Nexus. 2023 Feb 13;2(3):pgad043. doi: 10.1093/pnasnexus/pgad043. eCollection 2023 Mar. PNAS Nexus. 2023. PMID: 36909829 Free PMC article.
56 results