Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
2002 3
2003 5
2004 1
2005 2
2006 3
2007 2
2008 1
2009 4
2010 2
2011 1
2012 3
2013 1
2014 2
2015 6
2016 2
2017 3
2018 4
2019 2
2020 3
Text availability
Article attribute
Article type
Publication date

Search Results

47 results
Results by year
Filters applied: . Clear all
Page 1
Clinical features and outcome of 6 new patients carrying de novo KCNB1 gene mutations.
Marini C, Romoli M, Parrini E, Costa C, Mei D, Mari F, Parmeggiani L, Procopio E, Metitieri T, Cellini E, Virdò S, De Vita D, Gentile M, Prontera P, Calabresi P, Guerrini R. Marini C, et al. Among authors: gentile m. Neurol Genet. 2017 Dec 11;3(6):e206. doi: 10.1212/NXG.0000000000000206. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264397 Free PMC article.
Risk of Fetal Loss in Pregnancies Undergoing Midtrimester Amniocentesis after Inconclusive Chorionic Villus Sampling.
Salsi G, Grati FR, Bellussi F, Pompilii E, Maggi F, Simoni G, D'Ambrosi F, Orsi M, Gentile M, Rembouskos G, Zuliani G, Volpe P, Pilu G. Salsi G, et al. Among authors: gentile m. Fetal Diagn Ther. 2019;46(3):149-152. doi: 10.1159/000493206. Epub 2018 Oct 23. Fetal Diagn Ther. 2019. PMID: 30352439
Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant.
Borghesi A, Mencarelli MA, Memo L, Ferrero GB, Bartuli A, Genuardi M, Stronati M, Villani A, Renieri A, Corsello G; their respective Scientific Societies. Borghesi A, et al. Ital J Pediatr. 2017 Nov 3;43(1):100. doi: 10.1186/s13052-017-0418-0. Ital J Pediatr. 2017. PMID: 29100554 Free PMC article. Review.
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients.
Zollino M, Marangi G, Ponzi E, Orteschi D, Ricciardi S, Lattante S, Murdolo M, Battaglia D, Contaldo I, Mercuri E, Stefanini MC, Caumes R, Edery P, Rossi M, Piccione M, Corsello G, Della Monica M, Scarano F, Priolo M, Gentile M, Zampino G, Vijzelaar R, Abdulrahman O, Rauch A, Oneda B, Deardorff MA, Saitta SC, Falk MJ, Dubbs H, Zackai E. Zollino M, et al. Among authors: gentile m. J Med Genet. 2015 Dec;52(12):804-14. doi: 10.1136/jmedgenet-2015-103184. Epub 2015 Sep 30. J Med Genet. 2015. PMID: 26424144
Clinical biomarkers for cancer recognition and prevention: A novel approach with optical measurements.
Latini G, De Felice C, Barducci A, Dipaola L, Gentile M, Andreassi MG, Correale M, Bianciardi G. Latini G, et al. Among authors: gentile m. Cancer Biomark. 2018;22(2):179-198. doi: 10.3233/CBM-170050. Cancer Biomark. 2018. PMID: 29689703 Review.
Pulmonary alveolar microlithiasis: review of the 1022 cases reported worldwide.
Castellana G, Castellana G, Gentile M, Castellana R, Resta O. Castellana G, et al. Among authors: gentile m. Eur Respir Rev. 2015 Dec;24(138):607-20. doi: 10.1183/16000617.0036-2015. Eur Respir Rev. 2015. PMID: 26621975 Free article. Review.
Genomic changes of chromosomes 8p23.1 and 1q21: Novel mutations in malignant mesothelioma.
Serio G, Vimercati L, Pennella A, Gentile M, Cavone D, Buonadonna AL, Scattone A, Fortarezza F, De Palma A, Marzullo A. Serio G, et al. Among authors: gentile m. Lung Cancer. 2018 Dec;126:106-111. doi: 10.1016/j.lungcan.2018.10.012. Epub 2018 Oct 27. Lung Cancer. 2018. PMID: 30527173
Age and sex prevalence estimate of Joubert syndrome in Italy.
Nuovo S, Bacigalupo I, Ginevrino M, Battini R, Bertini E, Borgatti R, Casella A, Micalizzi A, Nardella M, Romaniello R, Serpieri V, Zanni G, Valente EM, Vanacore N; JS Italian Study Group. Nuovo S, et al. Neurology. 2020 Feb 25;94(8):e797-e801. doi: 10.1212/WNL.0000000000008996. Epub 2020 Jan 22. Neurology. 2020. PMID: 31969461 Free PMC article. Clinical Trial.
Novel exostosin-2 missense variants in a family with autosomal recessive exostosin-2-related syndrome: further evidences on the phenotype.
Gentile M, Agolini E, Cocciadiferro D, Ficarella R, Ponzi E, Bellacchio E, Antonucci MF, Novelli A. Gentile M, et al. Clin Genet. 2019 Jan;95(1):165-171. doi: 10.1111/cge.13458. Epub 2018 Oct 24. Clin Genet. 2019. PMID: 30288735
Autism spectrum disorders in XYY syndrome: two new cases and systematic review of the literature.
Margari L, Lamanna AL, Craig F, Simone M, Gentile M. Margari L, et al. Among authors: gentile m. Eur J Pediatr. 2014 Mar;173(3):277-83. doi: 10.1007/s00431-014-2267-9. Epub 2014 Jan 25. Eur J Pediatr. 2014. PMID: 24464091 Review.
47 results
Jump to page
Feedback