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Year Number of Results
1971 1
1972 1
1973 1
1978 1
1981 1
1982 1
1983 1
1985 2
1986 1
1987 1
1989 7
1990 9
1991 1
1992 7
1993 1
1994 8
1995 7
1996 4
1997 4
1998 3
1999 3
2000 3
2001 5
2002 2
2003 3
2004 7
2005 1
2006 6
2008 5
2009 5
2011 3
2012 1
2013 2
2014 1
2015 6
2016 4
2017 3
2018 2
2021 1
2024 0

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123 results

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Page 1
The complete European guidelines on phenylketonuria: diagnosis and treatment.
van Wegberg AMJ, MacDonald A, 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, van Rijn M, Trefz F, Walter JH, van Spronsen FJ. van Wegberg AMJ, et al. Among authors: walter jh. Orphanet J Rare Dis. 2017 Oct 12;12(1):162. doi: 10.1186/s13023-017-0685-2. Orphanet J Rare Dis. 2017. PMID: 29025426 Free PMC article. Review.
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.
L-Carnitine.
Walter JH. Walter JH. Arch Dis Child. 1996 Jun;74(6):475-8. doi: 10.1136/adc.74.6.475. Arch Dis Child. 1996. PMID: 8758120 Free PMC article. Review. No abstract available.
Amniotic band syndrome.
Walter JH Jr, Goss LR, Lazzara AT. Walter JH Jr, et al. J Foot Ankle Surg. 1998 Jul-Aug;37(4):325-33. doi: 10.1016/s1067-2516(98)80070-7. J Foot Ankle Surg. 1998. PMID: 9710786 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.
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.
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency.
Walter JH, Clayton PT, Leonard JV. Walter JH, et al. J Inherit Metab Dis. 1986;9(3):287-8. doi: 10.1007/BF01799665. J Inherit Metab Dis. 1986. PMID: 3099075 No abstract available.
Temporomandibular disorders. 2. Non-surgical treatment.
Dimitroulis G, Gremillion HA, Dolwick MF, Walter JH. Dimitroulis G, et al. Among authors: walter jh. Aust Dent J. 1995 Dec;40(6):372-6. doi: 10.1111/j.1834-7819.1995.tb04835.x. Aust Dent J. 1995. PMID: 8615742 Review.
Inborn errors of metabolism and pregnancy.
Walter JH. Walter JH. J Inherit Metab Dis. 2000 May;23(3):229-36. doi: 10.1023/a:1005679928521. J Inherit Metab Dis. 2000. PMID: 10863939 Review.
123 results