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Acta Oto-Laryngologica|March 25, 2014
A Japanese family showing high-frequency hearing loss with KCNQ4 and TECTA mutationsKotaro Ishikawa, Takehiko Naito, Shin-Ya Nishio, et al.
International Journal of Hematology|December 2, 2022
Splenectomy as an effective treatment for macrothrombocytopenia in Takenouchi-Kosaki syndromeShio Yamano, Akihiro Iguchi, Kotaro Ishikawa, et al.
Nihon Shokakibyo Gakkai Zasshi = the Japanese Journal of Gastro-Enterology|December 10, 2020
[A case of autoimmune hepatitis with tuberculosis caused by prednisolone from undeterminable enzyme-linked immunospot assay]Kotaro Ishikawa, Osamu Kimura, Akio Ubukata, et al.
The Laryngoscope|November 1, 2006
Temporal bone histopathologic abnormalities associated with mitochondrial mutation T7511CKotaro Ishikawa, Yuya Tamagawa, Katsumasa Takahashi, et al.
Biochemical and Biophysical Research Communications|January 27, 2005
Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese familyRonghua Li, Kotaro Ishikawa, Jian-Hong Deng, et al.
Neuron|July 23, 2013
TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner earBifeng Pan, Gwenaelle S Géléoc, Yukako Asai, et al.
Auris, Nasus, Larynx|December 15, 2015
Guidelines for the evaluation of hearing aid fitting (2010)Kazuoki Kodera, Hiroshi Hosoi, Makito Okamoto, et al.
Plos One|March 13, 2014
Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1Hidekane Yoshimura, Satoshi Iwasaki, Shin-Ya Nishio, et al.
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