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

Year Number of Results
1973 1
1981 1
1984 2
1986 2
1987 1
1988 2
1989 3
1991 4
1992 10
1993 5
1994 8
1995 10
1996 9
1997 15
1998 5
1999 16
2000 14
2001 13
2002 4
2003 12
2004 1
2013 1
2014 1
2020 1
2021 0
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140 results
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Page 1
Q-PINE: A quick to implant peripheral intraneural electrode.
Strauss I, Niederhoffer T, Giannotti A, Panarese AM, Bernini F, Gabisonia K, Ottaviani MM, Petrini FM, Recchia FA, Raspopovic S, Micera S. Strauss I, et al. Among authors: giannotti a. J Neural Eng. 2020 Nov 19;17(6). doi: 10.1088/1741-2552/abc52a. J Neural Eng. 2020. PMID: 33108764
Congenital heart defects in Kabuki syndrome.
Digilio MC, Marino B, Toscano A, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. Am J Med Genet. 2001 May 15;100(4):269-74. doi: 10.1002/ajmg.1265. Am J Med Genet. 2001. PMID: 11343317 Review.
Atrioventricular canal and 8p- syndrome.
Digilio MC, Giannotti A, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. Am J Med Genet. 1993 Sep 1;47(3):437-8. doi: 10.1002/ajmg.1320470331. Am J Med Genet. 1993. PMID: 8135296 Review. No abstract available.
Ext-mutation analysis in Italian sporadic and hereditary osteochondromas.
Gigante M, Matera MG, Seripa D, Izzo AM, Venanzi R, Giannotti A, Digilio MC, Gravina C, Lazzari M, Monteleone G, Monteleone M, Dallapiccola B, Fazio VM. Gigante M, et al. Among authors: giannotti a. Int J Cancer. 2001 Nov 20;95(6):378-83. doi: 10.1002/1097-0215(20011120)95:6<378::aid-ijc1067>3.0.co;2-f. Int J Cancer. 2001. PMID: 11668521 Free article.
Deletion 8p syndrome.
Digilio MC, Marino B, Guccione P, Giannotti A, Mingarelli R, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. Am J Med Genet. 1998 Feb 17;75(5):534-6. Am J Med Genet. 1998. PMID: 9489800 No abstract available.
Discrete subaortic stenosis.
Digilio MC, Marino B, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: giannotti a. Am Heart J. 1994 Jun;127(6):1665-6. doi: 10.1016/0002-8703(94)90417-0. Am Heart J. 1994. PMID: 8198010 No abstract available.
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.
Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, Voullaire L, Lerzo F, Rossi E, Dellavecchia C, Bonaglia MC, Digilio MC, Giannotti A, Marino B, Carrozzo R, Korenberg JR, Danesino C, Sujansky E, Dallapiccola B, Zuffardi O. Giglio S, et al. Among authors: giannotti a. Circulation. 2000 Jul 25;102(4):432-7. doi: 10.1161/01.cir.102.4.432. Circulation. 2000. PMID: 10908216
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