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

Year Number of Results
1949 1
1956 1
1957 1
1960 2
1961 2
1963 1
1964 1
1988 1
2006 2
2007 4
2008 3
2009 6
2010 7
2011 14
2012 7
2013 10
2014 11
2015 12
2016 6
2017 4
2018 8
2019 2
2020 3
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Article type
Publication date

Similar Articles for PMID: 29735534

97 results
Results by year
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Page 1
Rickets presenting as gross motor delay in twin girls.
Prasad C, Cummings E. Prasad C, et al. CMAJ. 2018 May 7;190(18):E565-E568. doi: 10.1503/cmaj.170962. CMAJ. 2018. PMID: 29735534 Free PMC article. No abstract available.
Hereditary vitamin D-resistant rickets presenting as alopecia.
Casey G, McPherson T, Kini U, Ryan F, Taibjee SM, Moss C, Burge S. Casey G, et al. Pediatr Dermatol. 2014 Jul-Aug;31(4):519-20. doi: 10.1111/pde.12327. Epub 2014 Jun 11. Pediatr Dermatol. 2014. PMID: 24917549
Discordance for X-linked hypophosphataemic rickets in identical twin girls.
Owen CJ, Habeb A, Pearce SH, Wright M, Ichikawa S, Sorenson AH, Econs MJ, Cheetham TD. Owen CJ, et al. Horm Res. 2009;71(4):237-44. doi: 10.1159/000201113. Epub 2009 Mar 4. Horm Res. 2009. PMID: 19258716
The nature of covariation between autistic traits and clumsiness: a twin study in a general population sample.
Moruzzi S, Ogliari A, Ronald A, Happé F, Battaglia M. Moruzzi S, et al. J Autism Dev Disord. 2011 Dec;41(12):1665-74. doi: 10.1007/s10803-011-1199-8. J Autism Dev Disord. 2011. PMID: 21347613
Hypophosphatemic rickets caused by a novel PHEX gene mutation in an Indian girl.
Dayal D, Sharda S, Attri SV, Kumar R. Dayal D, et al. J Pediatr Endocrinol Metab. 2014 Jul;27(7-8):787-9. doi: 10.1515/jpem-2013-0270. J Pediatr Endocrinol Metab. 2014. PMID: 24756041
[X-linked hypophosphatemic rickets].
Michigami T. Michigami T. Nihon Naika Gakkai Zasshi. 2007 Apr 10;96(4):725-30. doi: 10.2169/naika.96.725. Nihon Naika Gakkai Zasshi. 2007. PMID: 17506311 Review. Japanese. No abstract available.
Monozygotic twins concordant and discordant for DCD: two sides to the story.
Pearsall-Jones JG, Piek JP, Steed L, McDougall MR, Levy F. Pearsall-Jones JG, et al. Twin Res Hum Genet. 2011 Feb;14(1):79-87. doi: 10.1375/twin.14.1.79. Twin Res Hum Genet. 2011. PMID: 21314259
[X-linked hypophosphatemic rickets due to mutations in PHEX: Clinical and evolutionary variability].
Martos Moreno GÁ, Aparicio C, de Lucas C, Gil Peña H, Argente J. Martos Moreno GÁ, et al. An Pediatr (Barc). 2016 Jul;85(1):41-3. doi: 10.1016/j.anpedi.2016.04.012. Epub 2016 May 21. An Pediatr (Barc). 2016. PMID: 27221261 Free article. Spanish. No abstract available.
Mutational analysis of patients with FGF23-related hypophosphatemic rickets.
Kinoshita Y, Saito T, Shimizu Y, Hori M, Taguchi M, Igarashi T, Fukumoto S, Fujita T. Kinoshita Y, et al. Eur J Endocrinol. 2012 Aug;167(2):165-72. doi: 10.1530/EJE-12-0071. Epub 2012 May 10. Eur J Endocrinol. 2012. PMID: 22577109
Vitamin D receptor genotype in hypophosphatemic rickets as a predictor of growth and response to treatment.
Jehan F, Gaucher C, Nguyen TM, Walrant-Debray O, Lahlou N, Sinding C, Déchaux M, Garabédian M. Jehan F, et al. J Clin Endocrinol Metab. 2008 Dec;93(12):4672-82. doi: 10.1210/jc.2007-2553. Epub 2008 Sep 30. J Clin Endocrinol Metab. 2008. PMID: 18827005
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