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

Year Number of Results
1962 1
1964 2
1965 1
1978 1
1979 2
1982 1
1990 1
1991 2
1992 1
1993 1
1994 1
1995 2
1996 1
1997 2
1998 2
1999 5
2000 4
2001 1
2002 1
2003 6
2005 1
2006 5
2007 2
2008 5
2009 6
2010 4
2011 3
2012 2
2013 4
2014 3
2015 2
2016 7
2017 1
2018 7
2019 6
2020 1
Text availability
Article attribute
Article type
Publication date

Similar Articles for PMID: 30622207

95 results
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Page 1
The Role of Technology in Newborn Screening.
Millington DS. Millington DS. N C Med J. 2019 Jan-Feb;80(1):49-53. doi: 10.18043/ncm.80.1.49. N C Med J. 2019. PMID: 30622207 Free article.
Newborn screening of inherited metabolic diseases by tandem mass spectrometry.
Yu CL, Gu XF. Yu CL, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):103-6. Beijing Da Xue Xue Bao Yi Xue Ban. 2006. PMID: 16415979 Review.
Rapid diagnosis of phenylketonuria by quantitative analysis for phenylalanine and tyrosine in neonatal blood spots by tandem mass spectrometry.
Chace DH, Millington DS, Terada N, Kahler SG, Roe CR, Hofman LF. Chace DH, et al. Clin Chem. 1993 Jan;39(1):66-71. Clin Chem. 1993. PMID: 8419060
Neonatal screening of phenylketonuria and congenital hypothyroidism in China.
Fan GX, Jun Y, Rui-guan C. Fan GX, et al. Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:17-9. Southeast Asian J Trop Med Public Health. 1999. PMID: 11400761
Newborn screening of metabolic disorders.
Arélin M, Beblo S. Arélin M, et al. J Pediatr Endocrinol Metab. 2016 Jan;29(1):1-3. doi: 10.1515/jpem-2015-0456. J Pediatr Endocrinol Metab. 2016. PMID: 26756088 Free article. No abstract available.
An overview of newborn screening.
Levy PA. Levy PA. J Dev Behav Pediatr. 2010 Sep;31(7):622-31. doi: 10.1097/DBP.0b013e3181eedf01. J Dev Behav Pediatr. 2010. PMID: 20814260 Review.
Efficacy and outcome of expanded newborn screening for metabolic diseases--report of 10 years from South-West Germany.
Lindner M, Gramer G, Haege G, Fang-Hoffmann J, Schwab KO, Tacke U, Trefz FK, Mengel E, Wendel U, Leichsenring M, Burgard P, Hoffmann GF. Lindner M, et al. Orphanet J Rare Dis. 2011 Jun 20;6:44. doi: 10.1186/1750-1172-6-44. Orphanet J Rare Dis. 2011. PMID: 21689452 Free PMC article.
[Neonatal screening for phenylketonuria and hypothyroidism].
Maurin N, Sarles J. Maurin N, et al. Rev Prat. 2000 Oct 1;50(15):1728-31. Rev Prat. 2000. PMID: 11116617 French. No abstract available.
Fifty years of phenylketonuria newborn screening - A great success for many, but what about the rest?
Groselj U, Tansek MZ, Battelino T. Groselj U, et al. Mol Genet Metab. 2014 Sep-Oct;113(1-2):8-10. doi: 10.1016/j.ymgme.2014.07.019. Epub 2014 Jul 25. Mol Genet Metab. 2014. PMID: 25174964
Phenylketonuria screening in the Republic of Macedonia.
Kocova M, Anastasovska V. Kocova M, et al. Orphanet J Rare Dis. 2016 Aug 5;11(1):112. doi: 10.1186/s13023-016-0483-2. Orphanet J Rare Dis. 2016. PMID: 27496147 Free PMC article.
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