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

Year Number of Results
2009 2
2015 4
2016 3
2017 2
2018 2
2019 6
2020 11
2021 1
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29 results
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Page 1
Newborn Screening for Pompe Disease: Pennsylvania Experience.
Ficicioglu C, Ahrens-Nicklas RC, Barch J, Cuddapah SR, DiBoscio BS, DiPerna JC, Gordon PL, Henderson N, Menello C, Luongo N, Ortiz D, Xiao R. Ficicioglu C, et al. Among authors: ahrens nicklas rc. Int J Neonatal Screen. 2020 Nov 13;6(4):89. doi: 10.3390/ijns6040089. Int J Neonatal Screen. 2020. PMID: 33202836 Free PMC article.
Clinical utility of exome sequencing in infantile heart failure.
Ritter A, Bedoukian E, Berger JH, Copenheaver D, Gray C, Krantz I, Izumi K, Juusola J, Leonard J, Lin K, Medne L, Santani A, Skraban C, Yang S, Ahrens-Nicklas RC. Ritter A, et al. Among authors: ahrens nicklas rc. Genet Med. 2020 Feb;22(2):423-426. doi: 10.1038/s41436-019-0654-3. Epub 2019 Sep 17. Genet Med. 2020. PMID: 31527676 Free PMC article.
Genetic variant burden and adverse outcomes in pediatric cardiomyopathy.
Burstein DS, Gaynor JW, Griffis H, Ritter A, OʼConnor MJ, Rossano JW, Lin KY, Ahrens-Nicklas RC. Burstein DS, et al. Among authors: ahrens nicklas rc. Pediatr Res. 2020 Aug 3. doi: 10.1038/s41390-020-1101-5. Online ahead of print. Pediatr Res. 2020. PMID: 32746448
Variants in NAA15 cause pediatric hypertrophic cardiomyopathy.
Ritter A, Berger JH, Deardorff M, Izumi K, Lin KY, Medne L, Ahrens-Nicklas RC. Ritter A, et al. Among authors: ahrens nicklas rc. Am J Med Genet A. 2021 Jan;185(1):228-233. doi: 10.1002/ajmg.a.61928. Epub 2020 Oct 26. Am J Med Genet A. 2021. PMID: 33103328
Case 2: Severe Hyperammonemia in a Neonate: An Alternate Ending.
Sheppard S, Herrick H, Ahrens-Nicklas RC, Cohen JL, Flibbotte J, Pyle LC. Sheppard S, et al. Among authors: ahrens nicklas rc. Neoreviews. 2019 Feb;20(2):e90-e92. doi: 10.1542/neo.20-2-e90. Neoreviews. 2019. PMID: 31261090 Free PMC article. No abstract available.
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