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

Year Number of Results
1950 1
1951 1
1952 2
1953 2
1956 3
1957 1
1960 1
1962 1
1963 5
1964 1
1965 1
1966 2
1967 1
1968 1
1979 1
1980 1
1987 1
1989 1
1993 2
1994 1
1995 1
1996 1
1998 2
1999 2
2000 2
2001 2
2003 1
2012 3
2013 2
2014 5
2015 7
2016 6
2017 3
2018 4
2019 1
2020 3
2021 3
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72 results
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Page 1
International meeting on Wolf-Hirschhorn syndrome: Update on the nosology and new insights on the pathogenic mechanisms for seizures and growth delay.
Nevado J, Ho KS, Zollino M, Blanco R, Cobaleda C, Golzio C, Beaudry-Bellefeuille I, Berrocoso S, Limeres J, Barrúz P, Serrano-Martín C, Cafiero C, Málaga I, Marangi G, Campos-Sánchez E, Moriyón-Iglesias T, Márquez S, Markham L, Twede H, Lortz A, Olson L, Sheng X, Weng C, Wassman ER 3rd, Newcomb T, Wassman ER, Carey JC, Battaglia A, López-Granados E; Wolf-Hirschhorn Spain's Working Group, Douglas D, Lapunzina P. Nevado J, et al. Among authors: newcomb t. Am J Med Genet A. 2020 Jan;182(1):257-267. doi: 10.1002/ajmg.a.61406. Epub 2019 Nov 25. Am J Med Genet A. 2020. PMID: 31769173
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.
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.
Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy.
Ostrander BEP, Butterfield RJ, Pedersen BS, Farrell AJ, Layer RM, Ward A, Miller C, DiSera T, Filloux FM, Candee MS, Newcomb T, Bonkowsky JL, Marth GT, Quinlan AR. Ostrander BEP, et al. Among authors: newcomb t. NPJ Genom Med. 2018 Aug 13;3:22. doi: 10.1038/s41525-018-0061-8. eCollection 2018. NPJ Genom Med. 2018. PMID: 30109124 Free PMC article.
Human platelet respiration.
Kitchens CS, Newcomb TF. Kitchens CS, et al. Among authors: newcomb tf. J Appl Physiol. 1968 Nov;25(5):581-5. doi: 10.1152/jappl.1968.25.5.581. J Appl Physiol. 1968. PMID: 4972032 No abstract available.
72 results
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