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

Year Number of Results
1976 1
1979 2
1982 1
1983 1
1985 2
1986 1
1993 1
1994 1
1995 2
1996 2
1997 1
1998 2
1999 2
2001 2
2002 4
2003 4
2004 3
2007 3
2008 3
2009 7
2010 1
2011 3
2012 3
2013 2
2014 1
2015 2
2016 5
2017 1
2018 3
2019 2
2020 3
2021 3
2022 2
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Article attribute
Article type
Publication date

Search Results

71 results
Results by year
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Page 1
Amino acid disorders.
Aliu E, Kanungo S, Arnold GL. Aliu E, et al. Among authors: arnold gl. Ann Transl Med. 2018 Dec;6(24):471. doi: 10.21037/atm.2018.12.12. Ann Transl Med. 2018. PMID: 30740402 Free PMC article. Review.
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.
Lemke JR, Geider K, Helbig KL, Heyne HO, Schütz H, Hentschel J, Courage C, Depienne C, Nava C, Heron D, Møller RS, Hjalgrim H, Lal D, Neubauer BA, Nürnberg P, Thiele H, Kurlemann G, Arnold GL, Bhambhani V, Bartholdi D, Pedurupillay CR, Misceo D, Frengen E, Strømme P, Dlugos DJ, Doherty ES, Bijlsma EK, Ruivenkamp CA, Hoffer MJ, Goldstein A, Rajan DS, Narayanan V, Ramsey K, Belnap N, Schrauwen I, Richholt R, Koeleman BP, Sá J, Mendonça C, de Kovel CG, Weckhuysen S, Hardies K, De Jonghe P, De Meirleir L, Milh M, Badens C, Lebrun M, Busa T, Francannet C, Piton A, Riesch E, Biskup S, Vogt H, Dorn T, Helbig I, Michaud JL, Laube B, Syrbe S. Lemke JR, et al. Among authors: arnold gl. Neurology. 2016 Jun 7;86(23):2171-8. doi: 10.1212/WNL.0000000000002740. Epub 2016 May 6. Neurology. 2016. PMID: 27164704 Free PMC article.
Newborn screening for Krabbe disease in New York State: the first eight years' experience.
Orsini JJ, Kay DM, Saavedra-Matiz CA, Wenger DA, Duffner PK, Erbe RW, Biski C, Martin M, Krein LM, Nichols M, Kurtzberg J, Escolar ML, Adams DJ, Arnold GL, Iglesias A, Galvin-Parton P, Kronn DF, Kwon JM, Levy PA, Pellegrino JE, Shur N, Wasserstein MP, Caggana M; New York State Krabbe Disease Consortium. Orsini JJ, et al. Among authors: arnold gl. Genet Med. 2016 Mar;18(3):239-48. doi: 10.1038/gim.2015.211. Epub 2016 Jan 21. Genet Med. 2016. PMID: 26795590 Free article.
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Brunetti-Pierri N, Berg JS, Scaglia F, Belmont J, Bacino CA, Sahoo T, Lalani SR, Graham B, Lee B, Shinawi M, Shen J, Kang SH, Pursley A, Lotze T, Kennedy G, Lansky-Shafer S, Weaver C, Roeder ER, Grebe TA, Arnold GL, Hutchison T, Reimschisel T, Amato S, Geragthy MT, Innis JW, Obersztyn E, Nowakowska B, Rosengren SS, Bader PI, Grange DK, Naqvi S, Garnica AD, Bernes SM, Fong CT, Summers A, Walters WD, Lupski JR, Stankiewicz P, Cheung SW, Patel A. Brunetti-Pierri N, et al. Among authors: arnold gl. Nat Genet. 2008 Dec;40(12):1466-71. doi: 10.1038/ng.279. Nat Genet. 2008. PMID: 19029900 Free PMC article.
Successful orthotopic heart transplantation in CPTII deficiency.
Arnold GL, Yester J, McCracken E, Feingold BD, Vockley J. Arnold GL, et al. Mol Genet Metab. 2021 Jun;133(2):182-184. doi: 10.1016/j.ymgme.2021.04.005. Epub 2021 Apr 28. Mol Genet Metab. 2021. PMID: 34020866 Free PMC article.
Thoroughly modern medicine.
Arnold GL, Vockley J. Arnold GL, et al. Mol Genet Metab. 2011 Sep-Oct;104(1-2):1-2. doi: 10.1016/j.ymgme.2011.07.011. Epub 2011 Jul 20. Mol Genet Metab. 2011. PMID: 21807540
Metabolic providers in crisis - Burning out on the road to burnout?
Arnold GL, Kanungo S, Bush L; Wellness Committee of the Society for Inherited Metabolic Disorders. Arnold GL, et al. Mol Genet Metab. 2021 Dec;134(4):285-286. doi: 10.1016/j.ymgme.2021.11.007. Epub 2021 Nov 16. Mol Genet Metab. 2021. PMID: 34810068 No abstract available.
PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights.
Johnstone DL, Al-Shekaili HH, Tarailo-Graovac M, Wolf NI, Ivy AS, Demarest S, Roussel Y, Ciapaite J, van Roermund CWT, Kernohan KD, Kosuta C, Ban K, Ito Y, McBride S, Al-Thihli K, Abdelrahim RA, Koul R, Al Futaisi A, Haaxma CA, Olson H, Sigurdardottir LY, Arnold GL, Gerkes EH, Boon M, Heiner-Fokkema MR, Noble S, Bosma M, Jans J, Koolen DA, Kamsteeg EJ, Drögemöller B, Ross CJ, Majewski J, Cho MT, Begtrup A, Wasserman WW, Bui T, Brimble E, Violante S, Houten SM, Wevers RA, van Faassen M, Kema IP, Lepage N; Care4Rare Canada Consortium, Lines MA, Dyment DA, Wanders RJA, Verhoeven-Duif N, Ekker M, Boycott KM, Friedman JM, Pena IA, van Karnebeek CDM. Johnstone DL, et al. Among authors: arnold gl. Brain. 2019 Mar 1;142(3):542-559. doi: 10.1093/brain/awy346. Brain. 2019. PMID: 30668673 Free PMC article.
71 results