Search Results - "Takanori Yamagata" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Diagnostic accuracy of a novel severe acute respiratory syndrome coronavirus 2 rapid antigen test and usefulness of specimens collected from the anterior nasal cavity

Diagnostic accuracy of a novel severe acute respiratory syndrome coronavirus 2 rapid antigen test and usefulness of specimens collected from the anterior nasal cavity

by Tamura, Daisuke, Yamagishi, Hirokazu, Morisawa, Yuji, Mato, Takashi, Nunomiya, Shin, Maehara, Yuta, Ochiai, Yasushi, Okuyama, Shinya, Ohmika, Narumi, Yamagata, Takanori, Osaka, Hitoshi
Published in International journal of infectious diseases (17.09.2022)

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WDR45 variants cause ferrous iron loss due to impaired ferritinophagy associated with nuclear receptor coactivator 4 and WD repeat domain phosphoinositide interacting protein 4 reduction

WDR45 variants cause ferrous iron loss due to impaired ferritinophagy associated with nuclear receptor coactivator 4 and WD repeat domain phosphoinositide interacting protein 4 reduction

by Tsukida, Kiwako, Muramatsu, Shin-Ichi, Osaka, Hitoshi, Yamagata, Takanori, Muramatsu, Kazuhiro
Published in Brain communications (2022)

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Praxis‐induced reflex seizures in two Japanese cases with ring chromosome 20 syndrome

Praxis‐induced reflex seizures in two Japanese cases with ring chromosome 20 syndrome

by Yamagishi, Hirokazu, Goto, Masahide, Osaka, Hitoshi, Kuwajima, Mari, Muramatsu, Kazuhiro, Yamagata, Takanori
Published in Epileptic disorders (01.04.2020)

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Early distribution of18 F‐labeled AAV9 vectors in the cerebrospinal fluid after intracerebroventricular or intracisternal magna infusion in non‐human primates

Early distribution of18 F‐labeled AAV9 vectors in the cerebrospinal fluid after intracerebroventricular or intracisternal magna infusion in non‐human primates

by Kumagai, Shinichi, Nakajima, Takeshi, Shimazaki, Kuniko, Kakiuchi, Takeharu, Harada, Norihiro, Ohba, Hiroyuki, Onuki, Yoshiyuki, Takino, Naomi, Ito, Mika, Sato, Makoto, Nakamura, Sachie, Osaka, Hitoshi, Yamagata, Takanori, Kawai, Kensuke, Muramatsu, Shin‐ichi
Published in The journal of gene medicine (01.01.2023)

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Early distribution of 18 F-labeled AAV9 vectors in the cerebrospinal fluid after intracerebroventricular or intracisternal magna infusion in non-human primates

Early distribution of 18 F-labeled AAV9 vectors in the cerebrospinal fluid after intracerebroventricular or intracisternal magna infusion in non-human primates

by Kumagai, Shinichi, Nakajima, Takeshi, Shimazaki, Kuniko, Kakiuchi, Takeharu, Harada, Norihiro, Ohba, Hiroyuki, Onuki, Yoshiyuki, Takino, Naomi, Ito, Mika, Sato, Makoto, Nakamura, Sachie, Osaka, Hitoshi, Yamagata, Takanori, Kawai, Kensuke, Muramatsu, Shin-Ichi
Published in The journal of gene medicine (01.01.2023)

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A Patient-Specific Hollow Three-Dimensional Model for Simulating Percutaneous Occlusion of Patent Ductus Arteriosus: Its Clinical Usefulness

A Patient-Specific Hollow Three-Dimensional Model for Simulating Percutaneous Occlusion of Patent Ductus Arteriosus: Its Clinical Usefulness

by Matsubara, Daisuke, Kataoka, Koichi, Takahashi, Hironori, Minami, Takaomi, Yamagata, Takanori
Published in International Heart Journal (2019)

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Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A

by Kosho, Tomoki, Okamoto, Nobuhiko
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.09.2014)

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Predictive score for early diagnosis of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD)

Predictive score for early diagnosis of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD)

by Tada, Hiroko, Takanashi, Jun-ichi, Okuno, Hideo, Kubota, Masaya, Yamagata, Takanori, Kawano, Gou, Shiihara, Takashi, Hamano, Shin-ichiro, Hirose, Shinichi, Hayashi, Takuya, Osaka, Hitoshi, Mizuguchi, Masashi
Published in Journal of the neurological sciences (15.11.2015)

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Glucocorticoid effects on bone strength in children with renal diseases

Glucocorticoid effects on bone strength in children with renal diseases

by Aoyagi, Jun, Kanai, Takahiro, Ito, Takane, Odaka, Jun, Saito, Takashi, Betsui, Hiroyuki, Kurosaki, Masanori, Maru, Tomomi, Yamagata, Takanori
Published in Nephrology (Carlton, Vic.) (01.02.2021)

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Dominant-Negative Mutations in α-II Spectrin Cause West Syndrome with Severe Cerebral Hypomyelination, Spastic Quadriplegia, and Developmental Delay

Dominant-Negative Mutations in α-II Spectrin Cause West Syndrome with Severe Cerebral Hypomyelination, Spastic Quadriplegia, and Developmental Delay

by Saitsu, Hirotomo, Tohyama, Jun, Kumada, Tatsuro, Egawa, Kiyoshi, Hamada, Keisuke, Okada, Ippei, Mizuguchi, Takeshi, Osaka, Hitoshi, Miyata, Rie, Furukawa, Tomonori, Haginoya, Kazuhiro, Hoshino, Hideki, Goto, Tomohide, Hachiya, Yasuo, Yamagata, Takanori, Saitoh, Shinji, Nagai, Toshiro, Nishiyama, Kiyomi, Nishimura, Akira, Miyake, Noriko, Komada, Masayuki, Hayashi, Kenji, Hirai, Syu-ichi, Ogata, Kazuhiro, Kato, Mitsuhiro, Fukuda, Atsuo, Matsumoto, Naomichi
Published in American journal of human genetics (11.06.2010)

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Panipenem-betamipron and decreases in serum valproic acid concentration

Panipenem-betamipron and decreases in serum valproic acid concentration

by Yamagata, T, Momoi, M Y, Murai, K, Ikematsu, K, Suwa, K, Sakamoto, K, Fujimura, A
Published in Therapeutic drug monitoring (01.08.1998)

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Functional analysis of PAX8 variants identified in patients with congenital hypothyroidism in situ

Functional analysis of PAX8 variants identified in patients with congenital hypothyroidism in situ

by Batjargal, Khishigjargal, Tajima, Toshihiro, Fujita-Jimbo, Eriko, Yamaguchi, Takeshi, Nakamura, Akie, Yamagata, Takanori
Published in Clinical Pediatric Endocrinology (2022)

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Gene therapy for Glut1‐deficient mouse using an adeno‐associated virus vector with the human intrinsic GLUT1 promoter

Gene therapy for Glut1‐deficient mouse using an adeno‐associated virus vector with the human intrinsic GLUT1 promoter

by Nakamura, Sachie, Muramatsu, Shin‐ichi, Takino, Naomi, Ito, Mika, Jimbo, Eriko F., Shimazaki, Kuniko, Onaka, Tatsushi, Ohtsuki, Sumio, Terasaki, Tetsuya, Yamagata, Takanori, Osaka, Hitoshi
Published in The journal of gene medicine (01.04.2018)

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Surfactant Protein D for Pathological Evaluation of Infant Acute Respiratory Distress Syndrome Caused by Respiratory Syncytial Virus Infection

Surfactant Protein D for Pathological Evaluation of Infant Acute Respiratory Distress Syndrome Caused by Respiratory Syncytial Virus Infection

by Tamura, Daisuke, Inoue, Shun, Oishi, Takatoshi, Ozaki, Ayafumi, Yamagata, Takanori
Published in Open journal of pediatrics (2020)

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The neural basis underlying impaired recognition of angry expression in ADHD children measured by near-infrared spectroscopy

The neural basis underlying impaired recognition of angry expression in ADHD children measured by near-infrared spectroscopy

by Kobayashi, Megumi, Nagashima, Masako, Tokuda, Tatsuya, Ikeda, Takahiro, Monden, Yukifumi, Kanazawa, So, Yamaguchi, Masami K, Sakuta, Ryoichi, Yamagata, Takanori, Dan, Ippeita
Published in Journal of vision (Charlottesville, Va.) (06.09.2019)

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A New Method for Measuring the Speed of Sound in Rat Liver ex Vivo Using an Ultrasound System: Correlation of Sound Speed with Fat Deposition

A New Method for Measuring the Speed of Sound in Rat Liver ex Vivo Using an Ultrasound System: Correlation of Sound Speed with Fat Deposition

by Kumagai, Hideki, Yokoyama, Koji, Katsuyama, Kimito, Hara, Shoji, Yamamoto, Hiroaki, Yamagata, Takanori, Taniguchi, Nobuyuki, Hirota, Norio, Itoh, Kouichi
Published in Ultrasound in medicine & biology (01.10.2014)

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Treatment of a patient with Kawasaki disease associated with selective IgA deficiency by continuous infusion of cyclosporine A without intravenous immunoglobulin

Treatment of a patient with Kawasaki disease associated with selective IgA deficiency by continuous infusion of cyclosporine A without intravenous immunoglobulin

by Anzai, Tatsuya, Minami, Takaomi, Sato, Tomoyuki, Furui, Sadahiro, Yamagata, Takanori
Published in Turkish journal of pediatrics (01.11.2016)

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Genome Organization of Human 48-kDa Oligosaccharyltransferase (DDOST)

Genome Organization of Human 48-kDa Oligosaccharyltransferase (DDOST)

by Yamagata, Takanori, Tsuru, Tomohiko, Momoi, Mariko Y., Suwa, Kiyotaka, Nozaki, Yasuyuki, Mukasa, Takeshi, Ohashi, Hirofumi, Fukushima, Yoshimitsu, Momoi, Takashi
Published in Genomics (San Diego, Calif.) (01.11.1997)

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Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boy

Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boy

by Suwa, Kiyotaka, Yamagata, Takanori, Momoi, Mariko Y., Kawakami, Akio, Kikuchi, Yutaka, Miyao, Masutomo, Hirokawa, Hideaki, Oikawa, Tadao
Published in Brain & development (Tokyo. 1979) (01.12.1999)

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Surges in proteinuria are associated with plasma GL-3 elevations in a young patient with classic Fabry disease

Surges in proteinuria are associated with plasma GL-3 elevations in a young patient with classic Fabry disease

by Kanai, Takahiro, Ito, Takane, Odaka, Jun, Saito, Takashi, Aoyagi, Jun, Betsui, Hiroyuki, Yamagata, Takanori
Published in European journal of pediatrics (01.03.2016)

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