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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
1988 1
1990 1
1993 1
1995 1
1996 2
1997 4
1998 3
1999 4
2000 5
2001 3
2002 3
2003 3
2004 5
2005 5
2006 4
2007 10
2008 8
2009 9
2010 8
2011 13
2012 14
2013 14
2014 15
2015 12
2016 12
2017 21
2018 23
2019 30
2020 53
2021 52
2022 51
2023 12
2024 0

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Similar articles for PMID: 27126636

348 results

Results by year

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Page 1
Novel PHEX gene locus-specific database: Comprehensive characterization of vast number of variants associated with X-linked hypophosphatemia (XLH).
Sarafrazi S, Daugherty SC, Miller N, Boada P, Carpenter TO, Chunn L, Dill K, Econs MJ, Eisenbeis S, Imel EA, Johnson B, Kiel MJ, Krolczyk S, Ramesan P, Truty R, Sabbagh Y. Sarafrazi S, et al. Hum Mutat. 2022 Feb;43(2):143-157. doi: 10.1002/humu.24296. Epub 2021 Dec 5. Hum Mutat. 2022. PMID: 34806794 Free PMC article.
Genotype-phenotype analysis, and assessment of the importance of the zinc-binding site in PHEX in Japanese patients with X-linked hypophosphatemic rickets using 3D structure modeling.
Ishihara Y, Ohata Y, Takeyari S, Kitaoka T, Fujiwara M, Nakano Y, Yamamoto K, Yamada C, Yamamoto K, Michigami T, Mabe H, Yamaguchi T, Matsui K, Tamada I, Namba N, Yamamoto A, Etoh J, Kawaguchi A, Kosugi R, Ozono K, Kubota T. Ishihara Y, et al. Bone. 2021 Dec;153:116135. doi: 10.1016/j.bone.2021.116135. Epub 2021 Jul 30. Bone. 2021. PMID: 34333162 Free article.
Novel PHEX mutation associated with hypophosphatemic rickets.
Roetzer KM, Varga F, Zwettler E, Nawrot-Wawrzyniak K, Haller J, Forster E, Klaushofer K. Roetzer KM, et al. Nephron Physiol. 2007;106(1):p8-12. doi: 10.1159/000101487. Epub 2007 Apr 2. Nephron Physiol. 2007. PMID: 17406123
FGF23 and its role in X-linked hypophosphatemia-related morbidity.
Beck-Nielsen SS, Mughal Z, Haffner D, Nilsson O, Levtchenko E, Ariceta G, de Lucas Collantes C, Schnabel D, Jandhyala R, Mäkitie O. Beck-Nielsen SS, et al. Orphanet J Rare Dis. 2019 Feb 26;14(1):58. doi: 10.1186/s13023-019-1014-8. Orphanet J Rare Dis. 2019. PMID: 30808384 Free PMC article. Review.
348 results