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

Year Number of Results
1886 3
1887 5
1888 1
1892 1
1895 4
1897 2
1899 1
1907 1
1909 1
1910 2
1913 1
1915 1
1921 1
1933 3
1934 1
1937 2
1941 3
1942 1
1944 2
1945 2
1946 5
1947 12
1948 4
1949 6
1950 7
1951 6
1952 7
1953 7
1954 5
1955 3
1956 8
1957 6
1958 3
1959 8
1960 5
1961 5
1962 5
1963 8
1964 4
1965 5
1966 6
1967 4
1968 10
1969 4
1970 8
1971 15
1972 12
1973 19
1974 19
1975 10
1976 18
1977 18
1978 10
1979 31
1980 20
1981 18
1982 31
1983 32
1984 33
1985 17
1986 19
1987 17
1988 15
1989 14
1990 17
1991 17
1992 10
1993 13
1994 18
1995 16
1996 14
1997 16
1998 26
1999 18
2000 7
2001 19
2002 18
2003 25
2004 20
2005 32
2006 36
2007 19
2008 23
2009 34
2010 37
2011 27
2012 37
2013 30
2014 28
2015 28
2016 33
2017 46
2018 50
2019 54
2020 62
2021 68
2022 50
Text availability
Article attribute
Article type
Publication date

Search Results

1,427 results
Results by year
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Page 1
Congenital Heart Disease.
Puri K, Allen HD, Qureshi AM. Puri K, et al. Among authors: allen hd. Pediatr Rev. 2017 Oct;38(10):471-486. doi: 10.1542/pir.2017-0032. Pediatr Rev. 2017. PMID: 28972050 Review. No abstract available.
Whole-genome sequencing of patients with rare diseases in a national health system.
Turro E, Astle WJ, Megy K, Gräf S, Greene D, Shamardina O, Allen HL, Sanchis-Juan A, Frontini M, Thys C, Stephens J, Mapeta R, Burren OS, Downes K, Haimel M, Tuna S, Deevi SVV, Aitman TJ, Bennett DL, Calleja P, Carss K, Caulfield MJ, Chinnery PF, Dixon PH, Gale DP, James R, Koziell A, Laffan MA, Levine AP, Maher ER, Markus HS, Morales J, Morrell NW, Mumford AD, Ormondroyd E, Rankin S, Rendon A, Richardson S, Roberts I, Roy NBA, Saleem MA, Smith KGC, Stark H, Tan RYY, Themistocleous AC, Thrasher AJ, Watkins H, Webster AR, Wilkins MR, Williamson C, Whitworth J, Humphray S, Bentley DR; NIHR BioResource for the 100,000 Genomes Project, Kingston N, Walker N, Bradley JR, Ashford S, Penkett CJ, Freson K, Stirrups KE, Raymond FL, Ouwehand WH. Turro E, et al. Among authors: allen hl. Nature. 2020 Jul;583(7814):96-102. doi: 10.1038/s41586-020-2434-2. Epub 2020 Jun 24. Nature. 2020. PMID: 32581362 Free PMC article.
Eteplirsen for the treatment of Duchenne muscular dystrophy.
Mendell JR, Rodino-Klapac LR, Sahenk Z, Roush K, Bird L, Lowes LP, Alfano L, Gomez AM, Lewis S, Kota J, Malik V, Shontz K, Walker CM, Flanigan KM, Corridore M, Kean JR, Allen HD, Shilling C, Melia KR, Sazani P, Saoud JB, Kaye EM; Eteplirsen Study Group. Mendell JR, et al. Among authors: allen hd. Ann Neurol. 2013 Nov;74(5):637-47. doi: 10.1002/ana.23982. Epub 2013 Sep 10. Ann Neurol. 2013. PMID: 23907995 Free article. Clinical Trial.
Patent Ductus Arteriosus.
Eilers LF, Kyle WB, Allen HD, Qureshi AM. Eilers LF, et al. Among authors: allen hd. Pediatr Rev. 2021 Nov;42(11):632-634. doi: 10.1542/pir.2020-004564. Pediatr Rev. 2021. PMID: 34725225 No abstract available.
Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma.
Grande BM, Gerhard DS, Jiang A, Griner NB, Abramson JS, Alexander TB, Allen H, Ayers LW, Bethony JM, Bhatia K, Bowen J, Casper C, Choi JK, Culibrk L, Davidsen TM, Dyer MA, Gastier-Foster JM, Gesuwan P, Greiner TC, Gross TG, Hanf B, Harris NL, He Y, Irvin JD, Jaffe ES, Jones SJM, Kerchan P, Knoetze N, Leal FE, Lichtenberg TM, Ma Y, Martin JP, Martin MR, Mbulaiteye SM, Mullighan CG, Mungall AJ, Namirembe C, Novik K, Noy A, Ogwang MD, Omoding A, Orem J, Reynolds SJ, Rushton CK, Sandlund JT, Schmitz R, Taylor C, Wilson WH, Wright GW, Zhao EY, Marra MA, Morin RD, Staudt LM. Grande BM, et al. Among authors: allen h. Blood. 2019 Mar 21;133(12):1313-1324. doi: 10.1182/blood-2018-09-871418. Epub 2019 Jan 7. Blood. 2019. PMID: 30617194 Free PMC article.
Early Enteral Nutrition Is Associated With Improved Clinical Outcomes in Critically Ill Children: A Secondary Analysis of Nutrition Support in the Heart and Lung Failure-Pediatric Insulin Titration Trial.
Srinivasan V, Hasbani NR, Mehta NM, Irving SY, Kandil SB, Allen HC, Typpo KV, Cvijanovich NZ, Faustino EVS, Wypij D, Agus MSD, Nadkarni VM; Heart and Lung Failure-Pediatric Insulin Titration (HALF-PINT) Study Investigators. Srinivasan V, et al. Among authors: allen hc. Pediatr Crit Care Med. 2020 Mar;21(3):213-221. doi: 10.1097/PCC.0000000000002135. Pediatr Crit Care Med. 2020. PMID: 31577692 Free PMC article. Clinical Trial.
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
Lorenzini T, Fliegauf M, Klammer N, Frede N, Proietti M, Bulashevska A, Camacho-Ordonez N, Varjosalo M, Kinnunen M, de Vries E, van der Meer JWM, Ameratunga R, Roifman CM, Schejter YD, Kobbe R, Hautala T, Atschekzei F, Schmidt RE, Schröder C, Stepensky P, Shadur B, Pedroza LA, van der Flier M, Martínez-Gallo M, Gonzalez-Granado LI, Allende LM, Shcherbina A, Kuzmenko N, Zakharova V, Neves JF, Svec P, Fischer U, Ip W, Bartsch O, Barış S, Klein C, Geha R, Chou J, Alosaimi M, Weintraub L, Boztug K, Hirschmugl T, Dos Santos Vilela MM, Holzinger D, Seidl M, Lougaris V, Plebani A, Alsina L, Piquer-Gibert M, Deyà-Martínez A, Slade CA, Aghamohammadi A, Abolhassani H, Hammarström L, Kuismin O, Helminen M, Allen HL, Thaventhiran JE, Freeman AF, Cook M, Bakhtiar S, Christiansen M, Cunningham-Rundles C, Patel NC, Rae W, Niehues T, Brauer N, Syrjänen J, Seppänen MRJ, Burns SO, Tuijnenburg P, Kuijpers TW; NIHR BioResource, Warnatz K, Grimbacher B; NIHR BioResource. Lorenzini T, et al. Among authors: allen hl. J Allergy Clin Immunol. 2020 Oct;146(4):901-911. doi: 10.1016/j.jaci.2019.11.051. Epub 2020 Apr 9. J Allergy Clin Immunol. 2020. PMID: 32278790 Free PMC article.
Forty Years' Experience.
Zenel JA, Allen HD. Zenel JA, et al. Among authors: allen hd. Pediatr Rev. 2019 Oct;40(Suppl 1):40. doi: 10.1542/pir.2019-40S40. Epub 2019 Oct 1. Pediatr Rev. 2019. PMID: 32106074 No abstract available.
1,427 results