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

Year Number of Results
1978 1
1979 1
1980 1
1981 2
1983 2
1984 2
1988 1
1994 1
1997 1
1999 1
2010 1
2014 1
2017 1
2018 1
2019 1
2021 1
2023 0

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18 results

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Page 1
SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome.
Shima H, Tokuhiro E, Okamoto S, Nagamori M, Ogata T, Narumi S, Nakamura A, Izumi Y, Jinno T, Suzuki E, Fukami M. Shima H, et al. Among authors: tokuhiro e. J Endocr Soc. 2021 Mar 30;5(7):bvab056. doi: 10.1210/jendso/bvab056. eCollection 2021 Jul 1. J Endocr Soc. 2021. PMID: 34095692 Free PMC article.
A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.
Isojima T, Doi K, Mitsui J, Oda Y, Tokuhiro E, Yasoda A, Yorifuji T, Horikawa R, Yoshimura J, Ishiura H, Morishita S, Tsuji S, Kitanaka S. Isojima T, et al. Among authors: tokuhiro e. J Bone Miner Res. 2014 Apr;29(4):992-8. doi: 10.1002/jbmr.2091. J Bone Miner Res. 2014. PMID: 23996431 Free article.
Human T cell lymphotropic virus type I associated uveitis in a child.
Katakura S, Iijima Y, Imagawa T, Tokuhiro E, Nakamura S, Yabuki K, Yonemoto J, Ohno S, Yokota S. Katakura S, et al. Among authors: tokuhiro e. Br J Ophthalmol. 1997 Nov;81(11):1016. doi: 10.1136/bjo.81.11.1016. Br J Ophthalmol. 1997. PMID: 9505829 Free PMC article. No abstract available.
18 results