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

Year Number of Results
1947 1
1948 1
1949 3
1952 1
1953 4
1954 4
1955 3
1956 3
1958 1
1959 3
1960 3
1961 1
1962 2
1963 2
1964 3
1965 1
1966 4
1967 2
1968 4
1969 3
1970 3
1971 5
1972 4
1973 4
1974 12
1975 9
1976 6
1977 3
1978 8
1979 3
1980 7
1981 9
1982 7
1983 9
1984 14
1985 11
1986 8
1987 5
1988 2
1989 1
1990 3
1992 2
1993 5
1994 3
1995 2
1996 4
1997 5
1998 4
1999 11
2000 8
2001 11
2002 8
2003 8
2004 2
2005 9
2006 7
2007 4
2008 5
2009 7
2010 8
2011 9
2012 11
2013 8
2014 9
2015 6
2016 5
2017 9
2018 11
2019 8
2020 4
2021 6
2022 8
2023 10
2024 9

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384 results

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Page 1
What is new in migraine management in children and young people?
Loh NR, Whitehouse WP, Howells R. Loh NR, et al. Among authors: whitehouse wp. Arch Dis Child. 2022 Dec;107(12):1067-1072. doi: 10.1136/archdischild-2021-322373. Epub 2022 Feb 21. Arch Dis Child. 2022. PMID: 35190383 Review.
Genotype, extrapyramidal features, and severity of variant ataxia-telangiectasia.
Schon K, van Os NJH, Oscroft N, Baxendale H, Scoffings D, Ray J, Suri M, Whitehouse WP, Mehta PR, Everett N, Bottolo L, van de Warrenburg BP, Byrd PJ, Weemaes C, Willemsen MA, Tischkowitz M, Taylor AM, Hensiek AE. Schon K, et al. Among authors: whitehouse wp. Ann Neurol. 2019 Feb;85(2):170-180. doi: 10.1002/ana.25394. Ann Neurol. 2019. PMID: 30549301 Free PMC article.
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
Crow YJ, Chase DS, Lowenstein Schmidt J, Szynkiewicz M, Forte GM, Gornall HL, Oojageer A, Anderson B, Pizzino A, Helman G, Abdel-Hamid MS, Abdel-Salam GM, Ackroyd S, Aeby A, Agosta G, Albin C, Allon-Shalev S, Arellano M, Ariaudo G, Aswani V, Babul-Hirji R, Baildam EM, Bahi-Buisson N, Bailey KM, Barnerias C, Barth M, Battini R, Beresford MW, Bernard G, Bianchi M, Billette de Villemeur T, Blair EM, Bloom M, Burlina AB, Carpanelli ML, Carvalho DR, Castro-Gago M, Cavallini A, Cereda C, Chandler KE, Chitayat DA, Collins AE, Sierra Corcoles C, Cordeiro NJ, Crichiutti G, Dabydeen L, Dale RC, D'Arrigo S, De Goede CG, De Laet C, De Waele LM, Denzler I, Desguerre I, Devriendt K, Di Rocco M, Fahey MC, Fazzi E, Ferrie CD, Figueiredo A, Gener B, Goizet C, Gowrinathan NR, Gowrishankar K, Hanrahan D, Isidor B, Kara B, Khan N, King MD, Kirk EP, Kumar R, Lagae L, Landrieu P, Lauffer H, Laugel V, La Piana R, Lim MJ, Lin JP, Linnankivi T, Mackay MT, Marom DR, Marques Lourenço C, McKee SA, Moroni I, Morton JE, Moutard ML, Murray K, Nabbout R, Nampoothiri S, Nunez-Enamorado N, Oades PJ, Olivieri I, Ostergaard JR, Pérez-Dueñas B, Prendiville JS, Ramesh V, Rasmussen M, Régal L, Ricci F, Rio M, Rodriguez… See abstract for full author list ➔ Crow YJ, et al. Among authors: whitehouse wp. Am J Med Genet A. 2015 Feb;167A(2):296-312. doi: 10.1002/ajmg.a.36887. Epub 2015 Jan 16. Am J Med Genet A. 2015. PMID: 25604658 Free PMC article.
Investigating ataxia in childhood.
Petley E, Prasad M, Ojha S, Whitehouse WP. Petley E, et al. Among authors: whitehouse wp. Arch Dis Child Educ Pract Ed. 2020 Aug;105(4):214-221. doi: 10.1136/archdischild-2018-315893. Epub 2019 Oct 23. Arch Dis Child Educ Pract Ed. 2020. PMID: 31645356 Review.
Paediatric coma scales.
Kirkham FJ, Newton CR, Whitehouse W. Kirkham FJ, et al. Among authors: whitehouse w. Dev Med Child Neurol. 2008 Apr;50(4):267-74. doi: 10.1111/j.1469-8749.2008.02042.x. Epub 2008 Feb 27. Dev Med Child Neurol. 2008. PMID: 18312424 Free article. Review.
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.
Rice GI, Forte GM, Szynkiewicz M, Chase DS, Aeby A, Abdel-Hamid MS, Ackroyd S, Allcock R, Bailey KM, Balottin U, Barnerias C, Bernard G, Bodemer C, Botella MP, Cereda C, Chandler KE, Dabydeen L, Dale RC, De Laet C, De Goede CG, Del Toro M, Effat L, Enamorado NN, Fazzi E, Gener B, Haldre M, Lin JP, Livingston JH, Lourenco CM, Marques W Jr, Oades P, Peterson P, Rasmussen M, Roubertie A, Schmidt JL, Shalev SA, Simon R, Spiegel R, Swoboda KJ, Temtamy SA, Vassallo G, Vilain CN, Vogt J, Wermenbol V, Whitehouse WP, Soler D, Olivieri I, Orcesi S, Aglan MS, Zaki MS, Abdel-Salam GM, Vanderver A, Kisand K, Rozenberg F, Lebon P, Crow YJ. Rice GI, et al. Among authors: whitehouse wp. Lancet Neurol. 2013 Dec;12(12):1159-69. doi: 10.1016/S1474-4422(13)70258-8. Epub 2013 Oct 30. Lancet Neurol. 2013. PMID: 24183309 Free PMC article.
SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy.
Roshandel D, Sanders EJ, Shakeshaft A, Panjwani N, Lin F, Collingwood A, Hall A, Keenan K, Deneubourg C, Mirabella F, Topp S, Zarubova J, Thomas RH, Talvik I, Syvertsen M, Striano P, Smith AB, Selmer KK, Rubboli G, Orsini A, Ng CC, Møller RS, Lim KS, Hamandi K, Greenberg DA, Gesche J, Gardella E, Fong CY, Beier CP, Andrade DM, Jungbluth H, Richardson MP, Pastore A, Fanto M, Pal DK, Strug LJ; BIOJUME Consortium. Roshandel D, et al. NPJ Genom Med. 2023 Sep 28;8(1):28. doi: 10.1038/s41525-023-00370-z. NPJ Genom Med. 2023. PMID: 37770509 Free PMC article.
Fifteen minute consultation: tremor in children.
Prasad M, Ong MT, Whitehouse WP. Prasad M, et al. Among authors: whitehouse wp. Arch Dis Child Educ Pract Ed. 2014 Aug;99(4):130-4. doi: 10.1136/archdischild-2013-305410. Epub 2014 Jan 29. Arch Dis Child Educ Pract Ed. 2014. PMID: 24477580 Review.
384 results