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

Year Number of Results
1972 3
1973 2
1974 3
1987 1
1988 2
1998 1
2004 2
2005 1
2007 1
2008 6
2009 3
2010 5
2014 1
2015 4
2016 7
2017 3
2019 4
2020 8
2021 8
2022 3
2023 7
2024 8

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73 results

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Page 1
Assessing the landscape of STXBP1-related disorders in 534 individuals.
Xian J, Parthasarathy S, Ruggiero SM, Balagura G, Fitch E, Helbig K, Gan J, Ganesan S, Kaufman MC, Ellis CA, Lewis-Smith D, Galer P, Cunningham K, O'Brien M, Cosico M, Baker K, Darling A, Veiga de Goes F, El Achkar CM, Doering JH, Furia F, García-Cazorla Á, Gardella E, Geertjens L, Klein C, Kolesnik-Taylor A, Lammertse H, Lee J, Mackie A, Misra-Isrie M, Olson H, Sexton E, Sheidley B, Smith L, Sotero L, Stamberger H, Syrbe S, Thalwitzer KM, van Berkel A, van Haelst M, Yuskaitis C, Weckhuysen S, Prosser B, Son Rigby C, Demarest S, Pierce S, Zhang Y, Møller RS, Bruining H, Poduri A, Zara F, Verhage M, Striano P, Helbig I. Xian J, et al. Among authors: furia f. Brain. 2022 Jun 3;145(5):1668-1683. doi: 10.1093/brain/awab327. Brain. 2022. PMID: 35190816 Free PMC article.
Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood.
Stamberger H, Crosiers D, Balagura G, Bonardi CM, Basu A, Cantalupo G, Chiesa V, Christensen J, Dalla Bernardina B, Ellis CA, Furia F, Gardiner F, Giron C, Guerrini R, Klein KM, Korff C, Krijtova H, Leffler M, Lerche H, Lesca G, Lewis-Smith D, Marini C, Marjanovic D, Mazzola L, McKeown Ruggiero S, Mochel F, Ramond F, Reif PS, Richard-Mornas A, Rosenow F, Schropp C, Thomas RH, Vignoli A, Weber Y, Palmer E, Helbig I, Scheffer IE, Striano P, Møller RS, Gardella E, Weckhuysen S. Stamberger H, et al. Among authors: furia f. Neurology. 2022 Jul 19;99(3):e221-e233. doi: 10.1212/WNL.0000000000200715. Epub 2022 Jun 3. Neurology. 2022. PMID: 35851549 Free PMC article.
IRF2BPL as a novel causative gene for progressive myoclonus epilepsy.
Gardella E, Michelucci R, Christensen HM, Fenger CD, Reale C, Riguzzi P, Pasini E, Albini-Riccioli L, Papa V, Foschini MP, Cenacchi G, Furia F, Marjanovic D, Hammer TB, Møller RS, Rubboli G. Gardella E, et al. Among authors: furia f. Epilepsia. 2023 Aug;64(8):e170-e176. doi: 10.1111/epi.17634. Epub 2023 Jun 8. Epilepsia. 2023. PMID: 37114479
Trends in the epidemiology of childhood nephrotic syndrome in Africa: A systematic review.
Wine R, Vasilevska-Ristovska J, Banh T, Knott J, Noone D, Gbadegesin R, Ilori TO, Okafor HU, Furia F, Ulasi I, Solarin AU, Esezobor C, Batte A, Raji Y, Olanrewaju TO, Muoneke U, Adetunji AE, Boima V, Amira O, Osafo C, Guemkam G, Ajayi S, Makusidi MA, Anigilaje EA, Ruggajo P, Asinobi AO, Ademola AD, Parekh RS; H3 Africa Kidney Disease Research Network. Wine R, et al. Among authors: furia f. Glob Epidemiol. 2021 Aug 25;3:100061. doi: 10.1016/j.gloepi.2021.100061. eCollection 2021 Nov. Glob Epidemiol. 2021. PMID: 37635724 Free PMC article. Review.
Sleep and sleep disorders during pregnancy and postpartum: The Life-ON study.
Manconi M, van der Gaag LC, Mangili F, Garbazza C, Riccardi S, Cajochen C, Mondini S, Furia F, Zambrelli E, Baiardi S, Giordano A, Rizzo N, Fonti C, Viora E, D'Agostino A, Cicolin A, Cirignotta F; Life-ON Study Group; Group of Milan (Italy); Aquilino D, Barassi A, Del Giudice R, Fior G, Gambini O, Giordano B, Martini A, Serrati C, Stefanelli R, Scarone S, Canevini M, Fanti V, Stein HC, Marconi AM; Group of Turin (Italy); Raimondo E, Viglietta E; Group of Bologna (Italy); Santoro R, Simonazzi G, Bianconcini A; Group of Lugano (Switzerland); Meani F, Piazza N, Filippakos F, Gyr T. Manconi M, et al. Among authors: furia f. Sleep Med. 2024 Jan;113:41-48. doi: 10.1016/j.sleep.2023.10.021. Epub 2023 Nov 11. Sleep Med. 2024. PMID: 37984016
Multiomic analysis of HER2-enriched and AR-positive breast carcinoma with apocrine differentiation and an oligometastatic course: a case report.
Poggiali B, Ponzetti A, Malerba M, Landuzzi F, Furia F, Charrance D, Trova S, Perseghin V, Falcone PA, Alliod V, Malossi A, Carassai P, Familiari U, Vecchi M, Gustincich S, Schena M, Cavalli A, Coppe A. Poggiali B, et al. Among authors: furia f. Front Oncol. 2023 Jul 31;13:1240865. doi: 10.3389/fonc.2023.1240865. eCollection 2023. Front Oncol. 2023. PMID: 37583932 Free PMC article.
Management of idiopathic childhood nephrotic syndrome in sub-Saharan Africa: Ibadan consensus statement.
Esezobor C, Ademola AD, Adetunji AE, Anigilaje EA, Batte A, Jiya-Bello FN, Furia FF, Muoneke U, McCulloch M, Nourse P, Obiagwu P, Odetunde O, Okyere P, Solarin A, Tannor EK, Noone D, Gbadegesin R, Parekh RS; Human Hereditary and Health in Africa Kidney Disease Research Network. Esezobor C, et al. Among authors: furia ff. Kidney Int. 2021 Jan;99(1):59-67. doi: 10.1016/j.kint.2020.07.045. Epub 2020 Aug 29. Kidney Int. 2021. PMID: 32866504 Free PMC article. No abstract available.
73 results