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

Year Number of Results
1950 1
1952 1
1953 2
1957 1
1963 1
1966 1
1998 1
2001 1
2012 2
2013 1
2014 4
2015 3
2016 2
2018 1
2022 0
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20 results
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Page 1
Reassessing carrier status for dystrophinopathies.
Newcomb TM, Flanigan KM. Newcomb TM, et al. Neurol Genet. 2016 Oct 5;2(5):e108. doi: 10.1212/NXG.0000000000000108. eCollection 2016 Oct. Neurol Genet. 2016. PMID: 27761523 Free PMC article.
New therapeutic approaches to spinal muscular atrophy.
Lewelt A, Newcomb TM, Swoboda KJ. Lewelt A, et al. Among authors: newcomb tm. Curr Neurol Neurosci Rep. 2012 Feb;12(1):42-53. doi: 10.1007/s11910-011-0240-9. Curr Neurol Neurosci Rep. 2012. PMID: 22134788 Free PMC article. Review.
Social psychology and group processes.
NEWCOMB TM. NEWCOMB TM. Annu Rev Psychol. 1953;4:183-214. doi: 10.1146/annurev.ps.04.020153.001151. Annu Rev Psychol. 1953. PMID: 13125313 No abstract available.
Novel PLP1 Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical Phenotypes.
Margraf RL, Durtschi J, Krock B, Newcomb TM, Bonkowsky JL, Voelkerding KV, Bayrak-Toydemir P, Lutz RE, Swoboda KJ. Margraf RL, et al. Among authors: newcomb tm. Child Neurol Open. 2018 Jul 23;5:2329048X18789282. doi: 10.1177/2329048X18789282. eCollection 2018. Child Neurol Open. 2018. PMID: 30046645 Free PMC article.
Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis.
Butterfield RJ, Stevenson TJ, Xing L, Newcomb TM, Nelson B, Zeng W, Li X, Lu HM, Lu H, Farwell Gonzalez KD, Wei JP, Chao EC, Prior TW, Snyder PJ, Bonkowsky JL, Swoboda KJ. Butterfield RJ, et al. Among authors: newcomb tm. Neurology. 2014 Apr 15;82(15):1322-30. doi: 10.1212/WNL.0000000000000305. Epub 2014 Mar 19. Neurology. 2014. PMID: 24647030 Free PMC article.
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Heinzen EL, Swoboda KJ, Hitomi Y, Gurrieri F, Nicole S, de Vries B, Tiziano FD, Fontaine B, Walley NM, Heavin S, Panagiotakaki E; European Alternating Hemiplegia of Childhood (AHC) Genetics Consortium; Biobanca e Registro Clinico per l'Emiplegia Alternante (I.B.AHC) Consortium; European Network for Research on Alternating Hemiplegia (ENRAH) for Small and Medium-sized Enterpriese (SMEs) Consortium, Fiori S, Abiusi E, Di Pietro L, Sweney MT, Newcomb TM, Viollet L, Huff C, Jorde LB, Reyna SP, Murphy KJ, Shianna KV, Gumbs CE, Little L, Silver K, Ptáček LJ, Haan J, Ferrari MD, Bye AM, Herkes GK, Whitelaw CM, Webb D, Lynch BJ, Uldall P, King MD, Scheffer IE, Neri G, Arzimanoglou A, van den Maagdenberg AM, Sisodiya SM, Mikati MA, Goldstein DB. Heinzen EL, et al. Among authors: newcomb tm. Nat Genet. 2012 Sep;44(9):1030-4. doi: 10.1038/ng.2358. Epub 2012 Jul 29. Nat Genet. 2012. PMID: 22842232 Free PMC article.
20 results