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

Year Number of Results
1969 1
1971 2
1985 1
1991 2
1992 1
1993 4
1995 2
1996 1
1998 1
1999 8
2000 4
2001 5
2002 5
2003 8
2004 12
2005 7
2006 10
2007 8
2008 6
2009 12
2010 15
2011 16
2012 21
2013 19
2014 26
2015 17
2016 17
2017 12
2018 17
2019 23
2020 16
2021 30
2022 15
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Article type
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Search Results

311 results
Results by year
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Page 1
Williams syndrome.
Kozel BA, Barak B, Kim CA, Mervis CB, Osborne LR, Porter M, Pober BR. Kozel BA, et al. Among authors: kim ca. Nat Rev Dis Primers. 2021 Jun 17;7(1):42. doi: 10.1038/s41572-021-00276-z. Nat Rev Dis Primers. 2021. PMID: 34140529 Review.
Frailty in Older Adults Undergoing Aortic Valve Replacement: The FRAILTY-AVR Study.
Afilalo J, Lauck S, Kim DH, Lefèvre T, Piazza N, Lachapelle K, Martucci G, Lamy A, Labinaz M, Peterson MD, Arora RC, Noiseux N, Rassi A, Palacios IF, Généreux P, Lindman BR, Asgar AW, Kim CA, Trnkus A, Morais JA, Langlois Y, Rudski LG, Morin JF, Popma JJ, Webb JG, Perrault LP. Afilalo J, et al. Among authors: kim ca. J Am Coll Cardiol. 2017 Aug 8;70(6):689-700. doi: 10.1016/j.jacc.2017.06.024. Epub 2017 Jul 7. J Am Coll Cardiol. 2017. PMID: 28693934 Free article. Clinical Trial.
Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.
Quaio CRDC, Moreira CM, Novo-Filho GM, Sacramento-Bobotis PR, Groenner Penna M, Perazzio SF, Dutra AP, da Silva RA, Santos MNP, de Arruda VYN, Freitas VG, Pereira VC, Pintao MC, Fornari ARDS, Buzolin AL, Oku AY, Burger M, Ramalho RF, Marco Antonio DS, E Ferreira EN, Pereira OJE, Cantagalli VD, Trindade ACG, de Sousa RRF, Reys Furuzawa C, Verzini F, Matalhana SD, Romano N, Paixão D, Olivati C, Spolador GM, Maciel GAR, Rocha VZ, Miguelez J, de Carvalho MHB, de Souza AWS, Andrade LEC, Chauffaille ML, Perazzio ADSB, Catelani ALPM, Mitne-Neto M, Kim CA, Baratela WADR. Quaio CRDC, et al. Among authors: kim ca. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):955-964. doi: 10.1002/ajmg.c.31860. Epub 2020 Nov 30. Am J Med Genet C Semin Med Genet. 2020. PMID: 33258288
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome.
Yamamoto GL, Aguena M, Gos M, Hung C, Pilch J, Fahiminiya S, Abramowicz A, Cristian I, Buscarilli M, Naslavsky MS, Malaquias AC, Zatz M, Bodamer O, Majewski J, Jorge AA, Pereira AC, Kim CA, Passos-Bueno MR, Bertola DR. Yamamoto GL, et al. Among authors: kim ca. J Med Genet. 2015 Jun;52(6):413-21. doi: 10.1136/jmedgenet-2015-103018. Epub 2015 Mar 20. J Med Genet. 2015. PMID: 25795793
Maximizing TADF via Conformational Optimization.
Kim CA, Van Voorhis T. Kim CA, et al. J Phys Chem A. 2021 Sep 9;125(35):7644-7654. doi: 10.1021/acs.jpca.1c05104. Epub 2021 Aug 25. J Phys Chem A. 2021. PMID: 34432438
Auditory hypersensitivity in Williams syndrome.
Silva LAF, Kawahira RSH, Kim CA, Matas CG. Silva LAF, et al. Among authors: kim ca. Int J Pediatr Otorhinolaryngol. 2021 Jul;146:110740. doi: 10.1016/j.ijporl.2021.110740. Epub 2021 Apr 28. Int J Pediatr Otorhinolaryngol. 2021. PMID: 33965724
Mucopolysaccharidosis VII in Brazil: natural history and clinical findings.
Giugliani R, Barth AL, Dumas MRC, da Silva Franco JF, de Rosso Giuliani L, Grangeiro CHP, Horovitz DDG, Kim CA, de Araújo Leão EKE, de Medeiros PFV, Miguel DSCG, Moreira MESA, Dos Santos HMGP, da Silva LCS, da Silva LR, de Souza IN, Nalin T, Garcia D. Giugliani R, et al. Among authors: kim ca. Orphanet J Rare Dis. 2021 May 22;16(1):238. doi: 10.1186/s13023-021-01870-w. Orphanet J Rare Dis. 2021. PMID: 34022924 Free PMC article. Review.
Targeted massively parallel sequencing for congenital generalized lipodystrophy.
Costa-Riquetto AD, Santana LS, Caetano LA, Lerário AM, Correia-Deur JEM, Bertola DR, Kim CA, Nery M, Jorge AAL, Teles MG. Costa-Riquetto AD, et al. Among authors: kim ca. Arch Endocrinol Metab. 2021 May 18;64(5):559-566. doi: 10.20945/2359-3997000000278. Arch Endocrinol Metab. 2021. PMID: 34033296
Abnormal auditory event-related potentials in Williams syndrome.
Fagundes Silva LA, Honjo Kawahira RS, Kim CA, Matas CG. Fagundes Silva LA, et al. Among authors: kim ca. Eur J Med Genet. 2021 Mar;64(3):104163. doi: 10.1016/j.ejmg.2021.104163. Epub 2021 Feb 9. Eur J Med Genet. 2021. PMID: 33571693 Free article.
311 results