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Year Number of Results
2002 1
2008 1
2010 3
2011 1
2012 2
2013 6
2014 8
2015 7
2016 6
2017 13
2018 4
2019 4
2020 13
2021 5
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Showing results for andrea bartuli
Search for Andreja Bartulić instead (1 results)
Evolocumab in Pediatric Heterozygous Familial Hypercholesterolemia.
Santos RD, Ruzza A, Hovingh GK, Wiegman A, Mach F, Kurtz CE, Hamer A, Bridges I, Bartuli A, Bergeron J, Szamosi T, Santra S, Stefanutti C, Descamps OS, Greber-Platzer S, Luirink I, Kastelein JJP, Gaudet D; HAUSER-RCT Investigators. Santos RD, et al. Among authors: bartuli a. N Engl J Med. 2020 Oct 1;383(14):1317-1327. doi: 10.1056/NEJMoa2019910. Epub 2020 Aug 29. N Engl J Med. 2020. PMID: 32865373 Clinical Trial.
KBG syndrome: Common and uncommon clinical features based on 31 new patients.
Gnazzo M, Lepri FR, Dentici ML, Capolino R, Pisaneschi E, Agolini E, Rinelli M, Alesi V, Versacci P, Genovese S, Cesario C, Sinibaldi L, Baban A, Bartuli A, Marino B, Cappa M, Dallapiccola B, Novelli A, Digilio MC. Gnazzo M, et al. Among authors: bartuli a. Am J Med Genet A. 2020 May;182(5):1073-1083. doi: 10.1002/ajmg.a.61524. Epub 2020 Mar 3. Am J Med Genet A. 2020. PMID: 32124548
Deciphering the Invdupdel(8p) Genotype-Phenotype Correlation: Our Opinion.
Lo Bianco M, Vecchio D, Timpanaro TA, Arena A, Macchiaiolo M, Bartuli A, Sciuto L, Presti S, Sciuto S, Sapuppo A, Fiumara A, Marino L, Messina G, Pavone P. Lo Bianco M, et al. Among authors: bartuli a. Brain Sci. 2020 Jul 15;10(7):451. doi: 10.3390/brainsci10070451. Brain Sci. 2020. PMID: 32679641 Free PMC article.
Dissecting the mechanisms of bone loss in Gorham-Stout disease.
Rossi M, Buonuomo PS, Battafarano G, Conforti A, Mariani E, Algeri M, Pelle S, D'Agostini M, Macchiaiolo M, De Vito R, Gonfiantini MV, Jenkner A, Rana I, Bartuli A, Del Fattore A. Rossi M, et al. Among authors: bartuli a. Bone. 2020 Jan;130:115068. doi: 10.1016/j.bone.2019.115068. Epub 2019 Sep 13. Bone. 2020. PMID: 31525474
Infantile myofibromatosis: a rare cause of subcutaneous nodules in an infant.
Mastrogiorgio G, Buonuomo PS, Rana I, Macchiaiolo M, Marchetti P, De Peppo F, Rinelli M, Gonfiantini MV, Novelli A, Bartuli A. Mastrogiorgio G, et al. Among authors: bartuli a. Arch Dis Child. 2020 Jun 23:archdischild-2020-319229. doi: 10.1136/archdischild-2020-319229. Online ahead of print. Arch Dis Child. 2020. PMID: 32576562 No abstract available.
Expanding the clinical spectrum associated with PACS2 mutations.
Dentici ML, Barresi S, Niceta M, Ciolfi A, Trivisano M, Bartuli A, Digilio MC, Specchio N, Dallapiccola B, Tartaglia M. Dentici ML, et al. Among authors: bartuli a. Clin Genet. 2019 Apr;95(4):525-531. doi: 10.1111/cge.13516. Epub 2019 Feb 28. Clin Genet. 2019. PMID: 30684285 Review.
Atherogenic dyslipidemia and cardiovascular risk factors in obese children.
D'Adamo E, Guardamagna O, Chiarelli F, Bartuli A, Liccardo D, Ferrari F, Nobili V. D'Adamo E, et al. Among authors: bartuli a. Int J Endocrinol. 2015;2015:912047. doi: 10.1155/2015/912047. Epub 2015 Jan 12. Int J Endocrinol. 2015. PMID: 25663838 Free PMC article. Review.
Langerhans cell histiocytosis in a young patient with Pitt-Hopkins syndrome.
Macchiaiolo M, Panfili FM, Gonfiantini MV, Mastrogiorgio G, Buonuomo PS, Gaspari S, Longo D, Zollino M, Bartuli A. Macchiaiolo M, et al. Among authors: bartuli a. Am J Med Genet A. 2020 Nov;182(11):2746-2750. doi: 10.1002/ajmg.a.61840. Epub 2020 Sep 18. Am J Med Genet A. 2020. PMID: 32945094
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