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Results by year

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

Year Number of Results
1962 1
1963 1
1972 2
1973 1
1976 1
1978 1
1979 1
1980 3
1981 1
1982 2
1983 2
1984 2
1985 1
1987 1
1988 3
1989 1
1990 5
1991 2
1995 2
1996 2
1998 1
1999 4
2000 7
2001 4
2002 2
2003 2
2004 2
2005 2
2006 2
2007 1
2008 1
2009 2
2010 5
2011 3
2012 2
2013 6
2014 5
2015 5
2016 11
2017 14
2018 10
2019 10
2020 9
2021 12
2022 11
2023 4
2024 0

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Similar articles for PMID: 26783040

156 results

Results by year

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Page 1
Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene.
Baumgartner-Sigl S, Haberlandt E, Mumm S, Scholl-Bürgi S, Sergi C, Ryan L, Ericson KL, Whyte MP, Högler W. Baumgartner-Sigl S, et al. Bone. 2007 Jun;40(6):1655-61. doi: 10.1016/j.bone.2007.01.020. Epub 2007 Feb 14. Bone. 2007. PMID: 17395561
Pyridoxal 5'-phosphate and related metabolites in hypophosphatasia: Effects of enzyme replacement therapy.
Akiyama T, Kubota T, Ozono K, Michigami T, Kobayashi D, Takeyari S, Sugiyama Y, Noda M, Harada D, Namba N, Suzuki A, Utoyama M, Kitanaka S, Uematsu M, Mitani Y, Matsunami K, Takishima S, Ogawa E, Kobayashi K. Akiyama T, et al. Mol Genet Metab. 2018 Sep;125(1-2):174-180. doi: 10.1016/j.ymgme.2018.07.006. Epub 2018 Jul 17. Mol Genet Metab. 2018. PMID: 30049651
Clinical Significance of Hypophosphatasemia in Children.
Bayramli R, Cevlik T, Guran T, Atay Z, Bas S, Haklar G, Bereket A, Turan S. Bayramli R, et al. Calcif Tissue Int. 2020 Jun;106(6):608-615. doi: 10.1007/s00223-020-00677-4. Epub 2020 Feb 22. Calcif Tissue Int. 2020. PMID: 32088736
156 results