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

Year Number of Results
1984 1
1986 3
1987 8
1988 1
1991 1
1992 4
1995 4
1997 1
1998 1
1999 1
2000 1
2001 1
2002 2
2003 5
2004 2
2006 4
2007 6
2008 4
2009 3
2010 1
2011 2
2012 1
2013 2
2014 3
2015 2
2016 2
2017 1
2018 2
2019 2
2020 1
2022 1
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66 results
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Page 1
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.
Flanigan KM, Dunn DM, von Niederhausern A, Soltanzadeh P, Gappmaier E, Howard MT, Sampson JB, Mendell JR, Wall C, King WM, Pestronk A, Florence JM, Connolly AM, Mathews KD, Stephan CM, Laubenthal KS, Wong BL, Morehart PJ, Meyer A, Finkel RS, Bonnemann CG, Medne L, Day JW, Dalton JC, Margolis MK, Hinton VJ; United Dystrophinopathy Project Consortium, Weiss RB. Flanigan KM, et al. Among authors: hinton vj. Hum Mutat. 2009 Dec;30(12):1657-66. doi: 10.1002/humu.21114. Hum Mutat. 2009. PMID: 19937601 Free PMC article.
Duchenne muscular dystrophy: a cerebellar disorder?
Cyrulnik SE, Hinton VJ. Cyrulnik SE, et al. Among authors: hinton vj. Neurosci Biobehav Rev. 2008;32(3):486-96. doi: 10.1016/j.neubiorev.2007.09.001. Epub 2007 Oct 4. Neurosci Biobehav Rev. 2008. PMID: 18022230 Review.
Visual memory failure presages conversion to MELAS phenotype.
Leaffer EB, De Vivo DC, Engelstad K, Fryer RH, Gu Y, Shungu DC, Hirano M, DiMauro S, Hinton VJ. Leaffer EB, et al. Among authors: hinton vj. Ann Clin Transl Neurol. 2022 Jun;9(6):841-852. doi: 10.1002/acn3.51564. Epub 2022 May 6. Ann Clin Transl Neurol. 2022. PMID: 35522125 Free PMC article.
Zika Virus-Associated Cognitive Impairment in Adolescent, 2016.
Zucker J, Neu N, Chiriboga CA, Hinton VJ, Leonardo M, Sheikh A, Thakur K. Zucker J, et al. Among authors: hinton vj. Emerg Infect Dis. 2017 Jun;23(6):1047-1048. doi: 10.3201/eid2306.162029. Emerg Infect Dis. 2017. PMID: 28518023 Free PMC article.
Longitudinal changes in clinical outcome measures in COL6-related dystrophies and LAMA2-related dystrophies.
Jain MS, Meilleur K, Kim E, Norato G, Waite M, Nelson L, McGuire M, Duong T, Keller K, Lott DJ, Glanzman A, Rose K, Main M, Fiorini C, Chrismer I, Linton M, Punjabi M, Elliott J, Tounkara F, Vasavada R, Logaraj R, Winkert J, Donkervoort S, Leach M, Dastgir J, Hynan L, Nichols C, Hartnett E, Averion GM, Collins JC, Kim ES, Kokkinis A, Schindler A, Zukosky K, Fee R, Hinton V, Mohassel P, Bharucha-Goebel D, Vuillerot C, McGraw P, Barton M, Fontana J, Rutkowski A, Foley AR, Bönnemann CG. Jain MS, et al. Among authors: hinton v. Neurology. 2019 Nov 19;93(21):e1932-e1943. doi: 10.1212/WNL.0000000000008517. Epub 2019 Oct 25. Neurology. 2019. PMID: 31653707 Free PMC article.
Long-term clinical course of Glut1 deficiency syndrome.
Alter AS, Engelstad K, Hinton VJ, Montes J, Pearson TS, Akman CI, De Vivo DC. Alter AS, et al. Among authors: hinton vj. J Child Neurol. 2015 Feb;30(2):160-9. doi: 10.1177/0883073814531822. Epub 2014 Apr 30. J Child Neurol. 2015. PMID: 24789115
66 results