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

Year Number of Results
2002 1
2003 5
2004 6
2005 5
2006 7
2007 3
2008 4
2009 6
2010 4
2011 5
2012 1
2013 1
2014 2
2015 9
2016 4
2017 3
2018 2
2019 3
2021 3
2022 2
2023 2
2024 1

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75 results

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Page 1
Key European guidelines for the diagnosis and management of patients with phenylketonuria.
van Spronsen FJ, van Wegberg AM, Ahring K, Bélanger-Quintana A, Blau N, Bosch AM, Burlina A, Campistol J, Feillet F, Giżewska M, Huijbregts SC, Kearney S, Leuzzi V, Maillot F, Muntau AC, Trefz FK, van Rijn M, Walter JH, MacDonald A. van Spronsen FJ, et al. Among authors: walter jh. Lancet Diabetes Endocrinol. 2017 Sep;5(9):743-756. doi: 10.1016/S2213-8587(16)30320-5. Epub 2017 Jan 10. Lancet Diabetes Endocrinol. 2017. PMID: 28082082 Review.
Newborn screening for homocystinuria.
Walter JH, Jahnke N, Remmington T. Walter JH, et al. Cochrane Database Syst Rev. 2015 Oct 1;2015(10):CD008840. doi: 10.1002/14651858.CD008840.pub4. Cochrane Database Syst Rev. 2015. PMID: 26423208 Free PMC article. Review.
IEMs in adults.
Walter J. Walter J. J Inherit Metab Dis. 2007 Oct;30(5):627. doi: 10.1007/s10545-007-9983-5. J Inherit Metab Dis. 2007. PMID: 17891476 No abstract available.
Vitamin B12 deficiency and phenylketonuria.
Walter JH. Walter JH. Mol Genet Metab. 2011;104 Suppl:S52-4. doi: 10.1016/j.ymgme.2011.07.020. Epub 2011 Jul 22. Mol Genet Metab. 2011. PMID: 21824796 Review.
Newborn screening for homocystinuria.
Walter JH, Jahnke N, Remmington T. Walter JH, et al. Cochrane Database Syst Rev. 2013 Aug 1;(8):CD008840. doi: 10.1002/14651858.CD008840.pub3. Cochrane Database Syst Rev. 2013. PMID: 23908001 Updated. Review.
Newborn screening for homocystinuria.
Walter JH, Jahnke N, Remmington T. Walter JH, et al. Cochrane Database Syst Rev. 2011 Aug 10;(8):CD008840. doi: 10.1002/14651858.CD008840.pub2. Cochrane Database Syst Rev. 2011. PMID: 21833972 Updated. Review.
Swallowed partial dentures.
Hashmi S, Walter J, Smith W, Latis S. Hashmi S, et al. Among authors: walter j. J R Soc Med. 2004 Feb;97(2):72-5. doi: 10.1177/014107680409700206. J R Soc Med. 2004. PMID: 14749401 Free PMC article. Review.
An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study.
Steenweg ME, Jakobs C, Errami A, van Dooren SJ, Adeva Bartolomé MT, Aerssens P, Augoustides-Savvapoulou P, Baric I, Baumann M, Bonafé L, Chabrol B, Clarke JT, Clayton P, Coker M, Cooper S, Falik-Zaccai T, Gorman M, Hahn A, Hasanoglu A, King MD, de Klerk HB, Korman SH, Lee C, Meldgaard Lund A, Mejaski-Bosnjak V, Pascual-Castroviejo I, Raadhyaksha A, Rootwelt T, Roubertie A, Ruiz-Falco ML, Scalais E, Schimmel U, Seijo-Martinez M, Suri M, Sykut-Cegielska J, Trefz FK, Uziel G, Valayannopoulos V, Vianey-Saban C, Vlaho S, Vodopiutz J, Wajner M, Walter J, Walter-Derbort C, Yapici Z, Zafeiriou DI, Spreeuwenberg MD, Celli J, den Dunnen JT, van der Knaap MS, Salomons GS. Steenweg ME, et al. Among authors: walter j. Hum Mutat. 2010 Apr;31(4):380-90. doi: 10.1002/humu.21197. Hum Mutat. 2010. PMID: 20052767 Review.
Obturators for acquired palatal defects.
Walter J. Walter J. Dent Update. 2005 Jun;32(5):277-80, 283-4. doi: 10.12968/denu.2005.32.5.277. Dent Update. 2005. PMID: 15977722 Review.
75 results