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Year Number of Results
2005 1
2006 3
2007 2
2008 1
2009 2
2010 4
2011 3
2012 2
2013 4
2014 3
2015 4
2016 4
2017 3
2018 5
2019 2
2020 1
2021 3
2022 1
2023 2
2024 0

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39 results

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Page 1
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence).
Baldelli I, Baccarani A, Barone C, Bedeschi F, Bianca S, Calabrese O, Castori M, Catena N, Corain M, Costanzo S, Barbato GP, De Stefano S, Divizia MT, Feletti F, Formica M, Lando M, Lerone M, Lorenzetti F, Martinoli C, Mellini L, Nava MB, Porcellini G, Puliti A, Romanini MV, Rondoni F, Santi P, Sartini S, Senes F, Spada L, Tarani L, Valle M, Venturino C, Zaottini F, Torre M, Crimi M. Baldelli I, et al. Among authors: puliti a. Orphanet J Rare Dis. 2020 Aug 5;15(1):201. doi: 10.1186/s13023-020-01481-x. Orphanet J Rare Dis. 2020. PMID: 32758259 Free PMC article. Review.
Genetic Downregulation of the Metabotropic Glutamate Receptor Type 5 Dampens the Reactive and Neurotoxic Phenotype of Adult ALS Astrocytes.
Torazza C, Provenzano F, Gallia E, Cerminara M, Balbi M, Bonifacino T, Tessitore S, Ravera S, Usai C, Musante I, Puliti A, Van Den Bosch L, Jafar-Nejad P, Rigo F, Milanese M, Bonanno G. Torazza C, et al. Among authors: puliti a. Cells. 2023 Jul 27;12(15):1952. doi: 10.3390/cells12151952. Cells. 2023. PMID: 37566031 Free PMC article.
FGF23 and Fetuin-A Interaction in the Liver and in the Circulation.
Mattinzoli D, Ikehata M, Tsugawa K, Alfieri CM, Dongiovanni P, Trombetta E, Valenti L, Puliti A, Lazzari L, Messa P. Mattinzoli D, et al. Among authors: puliti a. Int J Biol Sci. 2018 Apr 25;14(6):586-598. doi: 10.7150/ijbs.23256. eCollection 2018. Int J Biol Sci. 2018. PMID: 29904273 Free PMC article.
Purkinje neuron Ca2+ influx reduction rescues ataxia in SCA28 model.
Maltecca F, Baseggio E, Consolato F, Mazza D, Podini P, Young SM Jr, Drago I, Bahr BA, Puliti A, Codazzi F, Quattrini A, Casari G. Maltecca F, et al. Among authors: puliti a. J Clin Invest. 2015 Jan;125(1):263-74. doi: 10.1172/JCI74770. Epub 2014 Dec 8. J Clin Invest. 2015. PMID: 25485680 Free PMC article.
Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing.
Rosti G, Boeri S, Divizia MT, Pisciotta L, Mancardi MM, Lerone M, Cerminara M, Servetti M, Spirito G, Vozzi D, Fontana M, Gustincich S, Nobili L, Zara F, Puliti A. Rosti G, et al. Among authors: puliti a. Mol Syndromol. 2023 Oct;14(5):433-438. doi: 10.1159/000529408. Epub 2023 May 9. Mol Syndromol. 2023. PMID: 37915395 Free PMC article.
Assessment of copy number variations in 120 patients with Poland syndrome.
Vaccari CM, Tassano E, Torre M, Gimelli S, Divizia MT, Romanini MV, Bossi S, Musante I, Valle M, Senes F, Catena N, Bedeschi MF, Baban A, Calevo MG, Acquaviva M, Lerone M, Ravazzolo R, Puliti A. Vaccari CM, et al. Among authors: puliti a. BMC Med Genet. 2016 Nov 25;17(1):89. doi: 10.1186/s12881-016-0351-x. BMC Med Genet. 2016. PMID: 27884122 Free PMC article.
39 results