Rezultati - Nakamura, Natsuko

Recovery of Vision following Enzyme Replacement Therapy in a Patient with Mucopolysaccharidosis Type II, Hunter Syndrome od Yamanishi, Ryutaro, Nakamura, Natsuko, Tsunoda, Kazushige

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Surgical repair of orbital fat prolapse by conjunctival fixation to the sclera od Nakamura, Natsuko, Akiyama, Kunihiko, Shigeyasu, Chika, Yamada, Masakazu

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Evaluation of cone function by a handheld non-mydriatic flicker electroretinogram device od Nakamura, Natsuko, Fujinami, Kaoru, Mizuno, Yoshinobu, Noda, Toru, Tsunoda, Kazushige

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Effects of topical TGF-β1, TGF-β2, ATX, and LPA on IOP elevation and regulation of the conventional aqueous humor outflow pathway od Nakamura, Natsuko, Yamagishi, Reiko, Honjo, Megumi, Igarashi, Nozomi, Shimizu, Shota, Aihara, Makoto

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Effects of selective EP2 receptor agonist, omidenepag, on trabecular meshwork cells, Schlemm’s canal endothelial cells and ciliary muscle contraction od Nakamura, Natsuko, Honjo, Megumi, Yamagishi, Reiko, Igarashi, Nozomi, Sakata, Rei, Aihara, Makoto

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Automated specimen search in cryo-TEM observation with DIFF-defocus imaging od Nakamura, Natsuko, Shimizu, Yuko, Shinkawa, Takao, Nakata, Munetaka, Bammes, Benjamin, Zhang, Junjie, Chiu, Wah

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Time-lapse monitoring of fertilized human oocytes focused on the incidence of 0PN embryos in conventional in vitro fertilization cycles od Kobayashi, Tatsuya, Ishikawa, Hiroshi, Ishii, Kumiko, Sato, Asuka, Nakamura, Natsuko, Saito, Yoshiko, Hasegawa, Hisataka, Fujita, Maki, Mitsuhashi, Akira, Shozu, Makio

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Clinical Characteristics of Neuronal Intranuclear Inclusion Disease-Related Retinopathy With CGG Repeat Expansions in the NOTCH2NLC Gene od Nakamura, Natsuko, Tsunoda, Kazushige, Mitsutake, Akihiko, Shibata, Shota, Mano, Tatsuo, Nagashima, Yu, Ishiura, Hiroyuki, Iwata, Atsushi, Toda, Tatsushi, Tsuji, Shoji, Sawamura, Hiromasa

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JADAS: A Customizable Automated Data Acquisition System and its Application to Ice-embedded Single Particles od Zhang, Junjie, Nakamura, Natsuko, Shimizu, Yuko, Liang, Nathan, Liu, Xiangan, Jakana, Joanita, Marsh, Michael P., Booth, Christopher R., Shinkawa, Takao, Nakata, Munetaka, Chiu, Wah

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Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort od Maeda-Katahira, Akiko, Nakamura, Natsuko, Hayashi, Takaaki, Katagiri, Satoshi, Shimizu, Satoko, Ohde, Hisao, Matsunaga, Tatsuo, Kaga, Kimitaka, Nakano, Tadashi, Kameya, Shuhei, Matsuura, Tomokazu, Fujinami, Kaoru, Iwata, Takeshi, Tsunoda, Kazushige

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Molecular characteristics of four Japanese cases with KCNV2 retinopathy: Report of novel disease-causing variants od Fujinami, Kaoru, Tsunoda, Kazushige, Nakamura, Natsuko, Kato, Yu, Noda, Toru, Shinoda, Kei, Tomita, Kaoru, Hatase, Tetsuhisa, Usui, Tomoaki, Akahori, Masakazu, Itabashi, Takeshi, Iwata, Takeshi, Ozawa, Yoko, Tsubota, Kazuo, Miyake, Yozo

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Preoperative weight loss program involving a 20‐day very low‐calorie diet for obesity before laparoscopic gastrectomy for gastric cancer od Inoue, Kentaro, Yoshiuchi, Sawako, Yoshida, Mika, Nakamura, Natsuko, Nakajima, Sachiko, Kitamura, Akiko, Mouri, Keiko, Michiura, Taku, Mukaide, Hiromi, Ozaki, Takashi, Miki, Hirokazu, Yanagimoto, Hiroaki, Satoi, Sohei, Kaibori, Masaki, Hamada, Madoka, Kimura, Yutaka, Kon, Masanori

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Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3 od Ahn, Seong Joon, Yang, Lizhu, Tsunoda, Kazushige, Kondo, Mineo, Fujinami-Yokokawa, Yu, Nakamura, Natsuko, Iwata, Takeshi, Kim, Min Seok, Mun, Yongseok, Park, Jun Young, Joo, Kwangsic, Park, Kyu Hyung, Miyake, Yozo, Sui, Ruifang, Fujinami, Kaoru, Woo, Se Joon

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Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association od Fujinami-Yokokawa, Yu, Fujinami, Kaoru, Kuniyoshi, Kazuki, Hayashi, Takaaki, Ueno, Shinji, Mizota, Atsushi, Shinoda, Kei, Arno, Gavin, Pontikos, Nikolas, Yang, Lizhu, Liu, Xiao, Sakuramoto, Hiroyuki, Katagiri, Satoshi, Mizobuchi, Kei, Kominami, Taro, Terasaki, Hiroko, Nakamura, Natsuko, Kameya, Shuhei, Yoshitake, Kazutoshi, Miyake, Yozo, Kurihara, Toshihide, Tsubota, Kazuo, Miyata, Hiroaki, Iwata, Takeshi, Tsunoda, Kazushige

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Clinical and Genetic Characteristics of 15 Affected Patients From 12 Japanese Families with GUCY2D-Associated Retinal Disorder od Liu, Xiao, Fujinami, Kaoru, Kuniyoshi, Kazuki, Kondo, Mineo, Ueno, Shinji, Hayashi, Takaaki, Mochizuki, Kiyofumi, Kameya, Shuhei, Yang, Lizhu, Fujinami-Yokokawa, Yu, Arno, Gavin, Pontikos, Nikolas, Sakuramoto, Hiroyuki, Kominami, Taro, Terasaki, Hiroko, Katagiri, Satoshi, Mizobuchi, Kei, Nakamura, Natsuko, Yoshitake, Kazutoshi, Miyake, Yozo, Li, Shiying, Kurihara, Toshihide, Tsubota, Kazuo, Iwata, Takeshi, Tsunoda, Kazushige

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Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency od Yang, Lizhu, Fujinami, Kaoru, Ueno, Shinji, Kuniyoshi, Kazuki, Hayashi, Takaaki, Kondo, Mineo, Mizota, Atsushi, Naoi, Nobuhisa, Shinoda, Kei, Kameya, Shuhei, Fujinami-Yokokawa, Yu, Liu, Xiao, Arno, Gavin, Pontikos, Nikolas, Kominami, Taro, Terasaki, Hiroko, Sakuramoto, Hiroyuki, Katagiri, Satoshi, Mizobuchi, Kei, Nakamura, Natsuko, Mawatari, Go, Kurihara, Toshihide, Tsubota, Kazuo, Miyake, Yozo, Yoshitake, Kazutoshi, Iwata, Takeshi, Tsunoda, Kazushige

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