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

Year Number of Results
1962 2
1970 1
1971 2
1972 1
1973 1
1976 1
2002 1
2003 2
2004 1
2007 2
2008 2
2009 4
2010 1
2013 3
2014 3
2015 7
2016 2
2017 7
2018 3
2019 11
2020 12
2021 15
2022 7
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79 results
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Page 1
Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients.
Bryant L, Li D, Cox SG, Marchione D, Joiner EF, Wilson K, Janssen K, Lee P, March ME, Nair D, Sherr E, Fregeau B, Wierenga KJ, Wadley A, Mancini GMS, Powell-Hamilton N, van de Kamp J, Grebe T, Dean J, Ross A, Crawford HP, Powis Z, Cho MT, Willing MC, Manwaring L, Schot R, Nava C, Afenjar A, Lessel D, Wagner M, Klopstock T, Winkelmann J, Catarino CB, Retterer K, Schuette JL, Innis JW, Pizzino A, Lüttgen S, Denecke J, Strom TM, Monaghan KG; DDD Study, Yuan ZF, Dubbs H, Bend R, Lee JA, Lyons MJ, Hoefele J, Günthner R, Reutter H, Keren B, Radtke K, Sherbini O, Mrokse C, Helbig KL, Odent S, Cogne B, Mercier S, Bezieau S, Besnard T, Kury S, Redon R, Reinson K, Wojcik MH, Õunap K, Ilves P, Innes AM, Kernohan KD; Care4Rare Canada Consortium, Costain G, Meyn MS, Chitayat D, Zackai E, Lehman A, Kitson H; CAUSES Study, Martin MG, Martinez-Agosto JA; Undiagnosed Diseases Network, Nelson SF, Palmer CGS, Papp JC, Parker NH, Sinsheimer JS, Vilain E, Wan J, Yoon AJ, Zheng A, Brimble E, Ferrero GB, Radio FC, Carli D, Barresi S, Brusco A, Tartaglia M, Thomas JM, Umana L, Weiss MM, Gotway G, Stuurman KE, Thompson ML, McWalter K, Stumpel CTRM, Stevens SJC, Stegmann APA, Tveten K, Vøllo A, Prescott T, Fagerberg C, Laulund LW, Larsen MJ, Byler M, Lebel RR, Hurst AC, Dean J, Schrier Vergano SA, Norman J, Mercimek-Andrews S, Neira J, Van Allen MI, Longo N, Sellars E, Louie RJ, Cathey SS, Brokamp E, Heron D, Snyder M, Vanderver A, Simon C, de la Cruz X, Padilla N, Crump JG, Chung W, Garcia B, Hakonarson HH, Bhoj EJ. Bryant L, et al. Among authors: carli d. Sci Adv. 2020 Dec 2;6(49):eabc9207. doi: 10.1126/sciadv.abc9207. Print 2020 Dec. Sci Adv. 2020. PMID: 33268356 Free PMC article.
Lateralized and Segmental Overgrowth in Children.
Mussa A, Carli D, Cardaropoli S, Ferrero GB, Resta N. Mussa A, et al. Among authors: carli d. Cancers (Basel). 2021 Dec 7;13(24):6166. doi: 10.3390/cancers13246166. Cancers (Basel). 2021. PMID: 34944785 Free PMC article. Review.
Bowel loop sign in a newborn.
Garofalo S, Guanà R, Schleef J, Cortese MG, Carli D, Suteu L, Ferrero GB, Gennari F. Garofalo S, et al. Among authors: carli d. Arch Dis Child Fetal Neonatal Ed. 2021 May;106(3):1-2. doi: 10.1136/archdischild-2020-318939. Epub 2020 Jul 6. Arch Dis Child Fetal Neonatal Ed. 2021. PMID: 32631848 No abstract available.
Esophageal duplication cyst in newborn.
Garofalo S, Schleef J, Guanà R, Suteu L, Cortese MG, Carli D, Ferrero GB, Gennari F. Garofalo S, et al. Among authors: carli d. Pediatr Neonatol. 2020 Feb;61(1):121-122. doi: 10.1016/j.pedneo.2019.08.007. Epub 2019 Sep 5. Pediatr Neonatol. 2020. PMID: 31558381 Free article. No abstract available.
Syndromic Disorders Caused by Disturbed Human Imprinting.
Carli D, Riberi E, Ferrero GB, Mussa A. Carli D, et al. J Clin Res Pediatr Endocrinol. 2020 Mar 19;12(1):1-16. doi: 10.4274/jcrpe.galenos.2019.2018.0249. Epub 2019 Apr 10. J Clin Res Pediatr Endocrinol. 2020. PMID: 30968677 Free PMC article. Review.
79 results