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

Year Number of Results
1969 1
1970 1
1971 1
2003 1
2004 6
2005 1
2006 6
2008 5
2009 8
2010 6
2011 7
2012 1
2013 6
2014 4
2015 1
2017 9
2018 2
2019 5
2020 1
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Search Results

65 results
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Page 1
Testing for Respiratory Viruses in Children: To Swab or Not to Swab.
Gill PJ, Richardson SE, Ostrow O, Friedman JN. Gill PJ, et al. Among authors: Friedman JN. JAMA Pediatr. 2017 Aug 1;171(8):798-804. doi: 10.1001/jamapediatrics.2017.0786. JAMA Pediatr. 2017. PMID: 28672402 Review.
CHARGE syndrome gastrointestinal involvement: from mouth to anus.
Hudson A, Macdonald M, Friedman JN, Blake K. Hudson A, et al. Among authors: Friedman JN. Clin Genet. 2017 Jul;92(1):10-17. doi: 10.1111/cge.12892. Epub 2017 Feb 2. Clin Genet. 2017. PMID: 28155231 Review.
Making it easier to 'choose wisely'.
Friedman JN, Mahant S. Friedman JN, et al. Paediatr Child Health. 2017 May;22(2):66-67. doi: 10.1093/pch/pxx027. Epub 2017 Apr 17. Paediatr Child Health. 2017. PMID: 29479182 Free PMC article.
Saying Yes to the Less: Making It Easier to Choose Wisely.
Friedman JN. Friedman JN. J Pediatr. 2017 May;184:4-5.e1. doi: 10.1016/j.jpeds.2017.01.062. Epub 2017 Feb 21. J Pediatr. 2017. PMID: 28233541 No abstract available.
A 7-year-old girl with acute onset esotropia.
Erdle SC, Friedman JN. Erdle SC, et al. Among authors: Friedman JN. Paediatr Child Health. 2017 Aug;22(5):245-246. doi: 10.1093/pch/pxx082. Epub 2017 May 31. Paediatr Child Health. 2017. PMID: 29479226 Free PMC article. No abstract available.
Vision loss in a child with autism spectrum disorder.
Kinlin LM, Vresk L, Friedman JN. Kinlin LM, et al. Among authors: Friedman JN. Paediatr Child Health. 2019 Jun;24(3):148-150. doi: 10.1093/pch/pxy058. Epub 2018 Jun 1. Paediatr Child Health. 2019. PMID: 31110453 No abstract available.
Planning for effective hospital discharge.
Apkon M, Friedman JN. Apkon M, et al. Among authors: Friedman JN. JAMA Pediatr. 2014 Oct;168(10):890-1. doi: 10.1001/jamapediatrics.2014.1028. JAMA Pediatr. 2014. PMID: 25154591 No abstract available.
A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay.
Schoch K, Meng L, Szelinger S, Bearden DR, Stray-Pedersen A, Busk OL, Stong N, Liston E, Cohn RD, Scaglia F, Rosenfeld JA, Tarpinian J, Skraban CM, Deardorff MA, Friedman JN, Akdemir ZC, Walley N, Mikati MA, Kranz PG, Jasien J, McConkie-Rosell A, McDonald M, Wechsler SB, Freemark M, Kansagra S, Freedman S, Bali D, Millan F, Bale S, Nelson SF, Lee H, Dorrani N; UCLA Clinical Genomics Center; Undiagnosed Diseases Network, Goldstein DB, Xiao R, Yang Y, Posey JE, Martinez-Agosto JA, Lupski JR, Wangler MF, Shashi V. Schoch K, et al. Among authors: Friedman JN. Am J Hum Genet. 2017 Feb 2;100(2):343-351. doi: 10.1016/j.ajhg.2016.12.013. Epub 2017 Jan 26. Am J Hum Genet. 2017. PMID: 28132692 Free PMC article.
General paediatric inpatient deaths over a 15-year period.
Roth A, Rapoport A, Widger K, Friedman JN. Roth A, et al. Among authors: Friedman JN. Paediatr Child Health. 2017 May;22(2):80-83. doi: 10.1093/pch/pxx005. Epub 2017 Apr 17. Paediatr Child Health. 2017. PMID: 29479186 Free PMC article.
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