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

Year Number of Results
1974 1
1978 1
1981 1
1985 1
1986 1
1988 1
1990 1
1991 3
1993 1
1994 1
1995 1
1997 3
1998 2
1999 2
2000 4
2001 1
2003 1
2004 1
2005 1
2008 1
2010 5
2011 4
2012 3
2013 6
2014 5
2015 7
2016 3
2017 3
2018 2
2019 2
2020 2
2021 2
2022 4
2023 7
2024 1

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74 results

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Page 1
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease.
Calì E, Lin SJ, Rocca C, Sahin Y, Al Shamsi A, El Chehadeh S, Chaabouni M, Mankad K, Galanaki E, Efthymiou S, Sudhakar S, Athanasiou-Fragkouli A, Çelik T, Narlı N, Bianca S, Murphy D, De Carvalho Moreira FM; SYNaPS Study Group; Andrea Accogli, Petree C, Huang K, Monastiri K, Edizadeh M, Nardello R, Ognibene M, De Marco P, Ruggieri M, Zara F, Striano P, Şahin Y, Al-Gazali L, Abi Warde MT, Gerard B, Zifarelli G, Beetz C, Fortuna S, Soler M, Valente EM, Varshney G, Maroofian R, Salpietro V, Houlden H. Calì E, et al. Genet Med. 2022 Oct;24(10):2194-2203. doi: 10.1016/j.gim.2022.07.013. Epub 2022 Aug 24. Genet Med. 2022. PMID: 36001086 Free PMC article.
Fortification of maternal milk for preterm infants.
Di Natale C, Coclite E, Di Ventura L, Di Fabio S. Di Natale C, et al. Among authors: di fabio s. J Matern Fetal Neonatal Med. 2011 Oct;24 Suppl 1:41-3. doi: 10.3109/14767058.2011.607569. Epub 2011 Sep 2. J Matern Fetal Neonatal Med. 2011. PMID: 21883045 Review.
Revised recommendations concerning palivizumab prophylaxis for respiratory syncytial virus (RSV).
Bollani L, Baraldi E, Chirico G, Dotta A, Lanari M, Del Vecchio A, Manzoni P, Boldrini A, Paolillo P, Di Fabio S, Orfeo L, Stronati M, Romagnoli C; Italian Society of Neonatology. Bollani L, et al. Among authors: di fabio s. Ital J Pediatr. 2015 Dec 15;41:97. doi: 10.1186/s13052-015-0203-x. Ital J Pediatr. 2015. PMID: 26670908 Free PMC article. Review.
Vaccines against HIV.
Verani P, Titti F, Corrias F, Belli R, Di Fabio S, Geraci A, Konga-Mogtomo M, Maggiorella MT, Sernicola L. Verani P, et al. Among authors: di fabio s. J Biol Regul Homeost Agents. 1997 Jan-Jun;11(1-2):82-7. J Biol Regul Homeost Agents. 1997. PMID: 9418170 Review. No abstract available.
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.
Salpietro V, Maroofian R, Zaki MS, Wangen J, Ciolfi A, Barresi S, Efthymiou S, Lamaze A, Aughey GN, Al Mutairi F, Rad A, Rocca C, Calì E, Accogli A, Zara F, Striano P, Mojarrad M, Tariq H, Giacopuzzi E, Taylor JC, Oprea G, Skrahina V, Rehman KU, Abd Elmaksoud M, Bassiony M, El Said HG, Abdel-Hamid MS, Al Shalan M, Seo G, Kim S, Lee H, Khang R, Issa MY, Elbendary HM, Rafat K, Marinakis NM, Traeger-Synodinos J, Ververi A, Sourmpi M, Eslahi A, Khadivi Zand F, Beiraghi Toosi M, Babaei M, Jackson A; SYNAPS Study Group; Bertoli-Avella A, Pagnamenta AT, Niceta M, Battini R, Corsello A, Leoni C, Chiarelli F, Dallapiccola B, Faqeih EA, Tallur KK, Alfadhel M, Alobeid E, Maddirevula S, Mankad K, Banka S, Ghayoor-Karimiani E, Tartaglia M, Chung WK, Green R, Alkuraya FS, Jepson JEC, Houlden H. Salpietro V, et al. Am J Hum Genet. 2024 Jan 4;111(1):200-210. doi: 10.1016/j.ajhg.2023.11.012. Epub 2023 Dec 20. Am J Hum Genet. 2024. PMID: 38118446 Free PMC article.
Increase of Parkin and ATG5 plasmatic levels following perinatal hypoxic-ischemic encephalopathy.
Tarocco A, Morciano G, Perrone M, Cafolla C, Ferrè C, Vacca T, Pistocchi G, Meneghin F, Cocchi I, Lista G, Cetin I, Greco P, Garani G, Stella M, Natile M, Ancora G, Savarese I, Campi F, Bersani I, Dotta A, Tiberi E, Vento G, Chiodin E, Staffler A, Maranella E, Di Fabio S, Wieckowski MR, Giorgi C, Pinton P. Tarocco A, et al. Among authors: di fabio s. Sci Rep. 2022 May 12;12(1):7795. doi: 10.1038/s41598-022-11870-w. Sci Rep. 2022. PMID: 35551488 Free PMC article.
74 results