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

Year Number of Results
1915 1
1918 1
1929 1
1935 1
1941 1
1945 1
1949 1
1954 1
1965 1
1966 1
1967 1
1976 1
1979 1
1983 2
1985 2
1986 5
1987 2
1988 4
1989 1
1990 4
1991 5
1992 6
1993 6
1994 5
1995 4
1996 6
1997 3
1998 11
1999 2
2000 9
2001 7
2002 7
2003 3
2004 7
2005 4
2006 3
2007 9
2008 5
2009 3
2010 6
2011 10
2012 12
2013 14
2014 13
2015 16
2016 17
2017 15
2018 8
2019 18
2020 9
2021 3
2022 10
2023 9
2024 9

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288 results

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Page 1
Diagnostic criteria for nonviable pregnancy early in the first trimester.
Doubilet PM, Benson CB, Bourne T, Blaivas M; Society of Radiologists in Ultrasound Multispecialty Panel on Early First Trimester Diagnosis of Miscarriage and Exclusion of a Viable Intrauterine Pregnancy; Barnhart KT, Benacerraf BR, Brown DL, Filly RA, Fox JC, Goldstein SR, Kendall JL, Lyons EA, Porter MB, Pretorius DH, Timor-Tritsch IE. Doubilet PM, et al. Among authors: fox jc. N Engl J Med. 2013 Oct 10;369(15):1443-51. doi: 10.1056/NEJMra1302417. N Engl J Med. 2013. PMID: 24106937 Review. No abstract available.
Efficacy and Safety of Acoramidis in Transthyretin Amyloid Cardiomyopathy.
Gillmore JD, Judge DP, Cappelli F, Fontana M, Garcia-Pavia P, Gibbs S, Grogan M, Hanna M, Hoffman J, Masri A, Maurer MS, Nativi-Nicolau J, Obici L, Poulsen SH, Rockhold F, Shah KB, Soman P, Garg J, Chiswell K, Xu H, Cao X, Lystig T, Sinha U, Fox JC; ATTRibute-CM Investigators. Gillmore JD, et al. Among authors: fox jc. N Engl J Med. 2024 Jan 11;390(2):132-142. doi: 10.1056/NEJMoa2305434. N Engl J Med. 2024. PMID: 38197816 Clinical Trial.
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
Carss KJ, Arno G, Erwood M, Stephens J, Sanchis-Juan A, Hull S, Megy K, Grozeva D, Dewhurst E, Malka S, Plagnol V, Penkett C, Stirrups K, Rizzo R, Wright G, Josifova D, Bitner-Glindzicz M, Scott RH, Clement E, Allen L, Armstrong R, Brady AF, Carmichael J, Chitre M, Henderson RHH, Hurst J, MacLaren RE, Murphy E, Paterson J, Rosser E, Thompson DA, Wakeling E, Ouwehand WH, Michaelides M, Moore AT; NIHR-BioResource Rare Diseases Consortium; Webster AR, Raymond FL. Carss KJ, et al. Am J Hum Genet. 2017 Jan 5;100(1):75-90. doi: 10.1016/j.ajhg.2016.12.003. Epub 2016 Dec 29. Am J Hum Genet. 2017. PMID: 28041643 Free PMC article.
Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe).
Ho CY, Day SM, Ashley EA, Michels M, Pereira AC, Jacoby D, Cirino AL, Fox JC, Lakdawala NK, Ware JS, Caleshu CA, Helms AS, Colan SD, Girolami F, Cecchi F, Seidman CE, Sajeev G, Signorovitch J, Green EM, Olivotto I. Ho CY, et al. Among authors: fox jc. Circulation. 2018 Oct 2;138(14):1387-1398. doi: 10.1161/CIRCULATIONAHA.117.033200. Epub 2018 Aug 23. Circulation. 2018. PMID: 30297972 Free PMC article.
Reply.
Fox JC, Lahham S, Maldonado G, Klaus S, Aish B, Sylwanowicz LV, Yanuck J, Wilson SP, Shieh M, Anderson CL, English C, Mayer R, Mohan UR. Fox JC, et al. J Ultrasound Med. 2018 Jun;37(6):1576. doi: 10.1002/jum.14441. Epub 2017 Oct 9. J Ultrasound Med. 2018. PMID: 28990214 No abstract available.
Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
Thaventhiran JED, Lango Allen H, Burren OS, Rae W, Greene D, Staples E, Zhang Z, Farmery JHR, Simeoni I, Rivers E, Maimaris J, Penkett CJ, Stephens J, Deevi SVV, Sanchis-Juan A, Gleadall NS, Thomas MJ, Sargur RB, Gordins P, Baxendale HE, Brown M, Tuijnenburg P, Worth A, Hanson S, Linger RJ, Buckland MS, Rayner-Matthews PJ, Gilmour KC, Samarghitean C, Seneviratne SL, Sansom DM, Lynch AG, Megy K, Ellinghaus E, Ellinghaus D, Jorgensen SF, Karlsen TH, Stirrups KE, Cutler AJ, Kumararatne DS, Chandra A, Edgar JDM, Herwadkar A, Cooper N, Grigoriadou S, Huissoon AP, Goddard S, Jolles S, Schuetz C, Boschann F; Primary Immunodeficiency Consortium for the NIHR Bioresource; Lyons PA, Hurles ME, Savic S, Burns SO, Kuijpers TW, Turro E, Ouwehand WH, Thrasher AJ, Smith KGC. Thaventhiran JED, et al. Nature. 2020 Jul;583(7814):90-95. doi: 10.1038/s41586-020-2265-1. Epub 2020 May 6. Nature. 2020. PMID: 32499645 Free PMC article.
Efficacy and Safety of Encaleret in Autosomal Dominant Hypocalcemia Type 1.
Gafni RI, Hartley IR, Roszko KL, Nemeth EF, Pozo KA, Lombardi E, Sridhar AV, Roberts MS, Fox JC, Collins MT. Gafni RI, et al. Among authors: fox jc. N Engl J Med. 2023 Sep 28;389(13):1245-1247. doi: 10.1056/NEJMc2302708. N Engl J Med. 2023. PMID: 37754292 Free PMC article. No abstract available.
Transthyretin Stabilization by AG10 in Symptomatic Transthyretin Amyloid Cardiomyopathy.
Judge DP, Heitner SB, Falk RH, Maurer MS, Shah SJ, Witteles RM, Grogan M, Selby VN, Jacoby D, Hanna M, Nativi-Nicolau J, Patel J, Rao S, Sinha U, Turtle CW, Fox JC. Judge DP, et al. Among authors: fox jc. J Am Coll Cardiol. 2019 Jul 23;74(3):285-295. doi: 10.1016/j.jacc.2019.03.012. Epub 2019 Mar 15. J Am Coll Cardiol. 2019. PMID: 30885685 Free article. Clinical Trial.
Erdheim-Chester disease.
Liotta EM, Jhaveri MD, Fox JC, Parameswaran V, Lewis SL. Liotta EM, et al. Among authors: fox jc. Arch Neurol. 2012 Nov;69(11):1514-5. doi: 10.1001/archneurol.2012.180. Arch Neurol. 2012. PMID: 22925950 No abstract available.
Schizophrenia.
Fox JC, Kane CF. Fox JC, et al. Annu Rev Nurs Res. 1998;16:287-322. Annu Rev Nurs Res. 1998. PMID: 9695895 Review.
288 results