Хайлтын үр дүнгүүд - Nakamura, Natsuko

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

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

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Evaluation of cone function by a handheld non-mydriatic flicker electroretinogram device -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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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