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

Year Number of Results
1964 1
1966 2
1976 1
1982 1
1985 1
1987 1
1988 1
1989 2
1990 2
1992 3
1993 1
1994 2
1995 1
1997 3
2000 6
2001 3
2002 3
2003 2
2004 2
2005 1
2006 2
2007 4
2008 2
2009 3
2010 5
2011 3
2012 3
2013 1
2014 2
2015 1
2016 2
2017 2
2018 1
2019 1
2020 1
2021 1
2022 0
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69 results
Results by year
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Page 1
Pediatric functional neurologic symptoms.
Grattan-Smith PJ, Dale RC. Grattan-Smith PJ, et al. Handb Clin Neurol. 2016;139:489-498. doi: 10.1016/B978-0-12-801772-2.00040-0. Handb Clin Neurol. 2016. PMID: 27719866 Review.
Movement disorder emergencies.
Kipps CM, Fung VS, Grattan-Smith P, de Moore GM, Morris JG. Kipps CM, et al. Among authors: grattan smith p. Mov Disord. 2005 Mar;20(3):322-34. doi: 10.1002/mds.20325. Mov Disord. 2005. PMID: 15584031 Review.
Misleading title.
Grattan-Smith PJ. Grattan-Smith PJ. Med J Aust. 2006 Dec 4-18;185(11-12):674; author reply 674-5. doi: 10.5694/j.1326-5377.2006.tb00757.x. Med J Aust. 2006. PMID: 17181527 No abstract available.
Psychiatric comorbidity is common in dystonia and other movement disorders.
Lorentzos MS, Heyman I, Baig BJ, Coughtrey AE, McWilliams A, Dossetor DR, Waugh MC, Evans RA, Hollywood J, Burns J, Menezes MP, Mohammad SS, Grattan-Smith P, Gorman KM, Crowe BHA, Goodman R, Kurian MA, Dale RC. Lorentzos MS, et al. Among authors: grattan smith p. Arch Dis Child. 2021 Jan;106(1):62-67. doi: 10.1136/archdischild-2020-319541. Epub 2020 Jul 24. Arch Dis Child. 2021. PMID: 32709686
Spinal muscular atrophy: molecular mechanisms.
Farrar MA, Johnston HM, Grattan-Smith P, Turner A, Kiernan MC. Farrar MA, et al. Among authors: grattan smith p. Curr Mol Med. 2009 Sep;9(7):851-62. doi: 10.2174/156652409789105516. Curr Mol Med. 2009. PMID: 19860664 Review.
Phenotypic insights into ADCY5-associated disease.
Chang FC, Westenberger A, Dale RC, Smith M, Pall HS, Perez-Dueñas B, Grattan-Smith P, Ouvrier RA, Mahant N, Hanna BC, Hunter M, Lawson JA, Max C, Sachdev R, Meyer E, Crimmins D, Pryor D, Morris JG, Münchau A, Grozeva D, Carss KJ, Raymond L, Kurian MA, Klein C, Fung VS. Chang FC, et al. Among authors: grattan smith p. Mov Disord. 2016 Jul;31(7):1033-40. doi: 10.1002/mds.26598. Epub 2016 Apr 8. Mov Disord. 2016. PMID: 27061943 Free PMC article.
Mitochondrial dysfunction in a novel form of autosomal recessive ataxia.
Murad NA, Cullen JK, McKenzie M, Ryan MT, Thorburn D, Gueven N, Kobayashi J, Birrell G, Yang J, Dörk T, Becherel O, Grattan-Smith P, Lavin MF. Murad NA, et al. Among authors: grattan smith p. Mitochondrion. 2013 May;13(3):235-45. doi: 10.1016/j.mito.2012.11.006. Epub 2012 Nov 22. Mitochondrion. 2013. PMID: 23178371 Review.
Genetic epilepsy with febrile seizures plus: Refining the spectrum.
Zhang YH, Burgess R, Malone JP, Glubb GC, Helbig KL, Vadlamudi L, Kivity S, Afawi Z, Bleasel A, Grattan-Smith P, Grinton BE, Bellows ST, Vears DF, Damiano JA, Goldberg-Stern H, Korczyn AD, Dibbens LM, Ruzzo EK, Hildebrand MS, Berkovic SF, Scheffer IE. Zhang YH, et al. Among authors: grattan smith p. Neurology. 2017 Sep 19;89(12):1210-1219. doi: 10.1212/WNL.0000000000004384. Epub 2017 Aug 25. Neurology. 2017. PMID: 28842445
Migrating partial seizures in infancy: two new cases.
Wilmshurst JM, Appleton DB, Grattan-Smith PJ. Wilmshurst JM, et al. Among authors: grattan smith pj. J Child Neurol. 2000 Nov;15(11):717-22. doi: 10.1177/088307380001501102. J Child Neurol. 2000. PMID: 11108504 Review.
69 results