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Pheochromocytoma complicated by cyanotic congenital heart disease: a case report.
Yamamoto K, Namba N, Kubota T, Usui T, Takahashi K, Kitaoka T, Fujiwara M, Hori Y, Kogaki S, Oue T, Morii E, Ozono K. Yamamoto K, et al. Clin Pediatr Endocrinol. 2016 Apr;25(2):59-65. doi: 10.1297/cpe.25.59. Epub 2016 Apr 28. Clin Pediatr Endocrinol. 2016. PMID: 27212797 Free PMC article.
Intestinal clock system regulates skeletal homeostasis.
Kawai M, Kinoshita S, Yamazaki M, Yamamoto K, Rosen CJ, Shimba S, Ozono K, Michigami T. Kawai M, et al. Among authors: yamamoto k. JCI Insight. 2019 Mar 7;4(5):e121798. doi: 10.1172/jci.insight.121798. eCollection 2019 Mar 7. JCI Insight. 2019. PMID: 30730853 Free PMC article.
Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta.
Ohata Y, Takeyari S, Nakano Y, Kitaoka T, Nakayama H, Bizaoui V, Yamamoto K, Miyata K, Yamamoto K, Fujiwara M, Kubota T, Michigami T, Yamamoto K, Yamamoto T, Namba N, Ebina K, Yoshikawa H, Ozono K. Ohata Y, et al. Among authors: yamamoto k, yamamoto t. Osteoporos Int. 2020 Jun;31(6):1185. doi: 10.1007/s00198-020-05396-y. Osteoporos Int. 2020. PMID: 32246166 Free PMC article.
Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array.
Tamura M, Isojima T, Kawashima M, Yoshida H, Yamamoto K, Kitaoka T, Namba N, Oka A, Ozono K, Tokunaga K, Kitanaka S. Tamura M, et al. Among authors: yamamoto k. PLoS One. 2015 Jul 8;10(7):e0131157. doi: 10.1371/journal.pone.0131157. eCollection 2015. PLoS One. 2015. PMID: 26153892 Free PMC article.
15,643 results
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