Works matching AU Saitoh, Shinji

Results: 127

Early-onset absence epilepsy at eight months of age.

Published in:

Epileptic Disorders, 2011, v. 13, n. 4, p. 417, doi. 10.1684/epd.2011.0477

By:

Kobayashi, Yu;
Akasaka, Noriyuki;
Ohashi, Tsukasa;
Saitoh, Shinji;
Tomonoh, Yuko;
Hirose, Shinichi;
Tohyama, Jun

Publication type:

Article

De novo CDKN1C variant in Beckwith–Wiedermann spectrum with atypical complications.

Published in:

Human Genome Variation, 2025, v. 12, n. 1, p. 1, doi. 10.1038/s41439-025-00316-0

By:

Moriura, Yuri;
Nishio, Yosuke;
Ichimura, Shintaro;
Noda, Haruka;
Tanahashi, Yoshihiro;
Yamamoto, Hikaru;
Nakazawa, Yuka;
Oso, Taichi;
Sato, Yoshiaki;
Takenouchi, Toshiki;
Saitoh, Shinji;
Muramatsu, Yukako;
Ogi, Tomoo

Publication type:

Article

A DYNC1H1 mutation causes a dominant spinal muscular atrophy with lower extremity predominance.

Published in:

Neurogenetics, 2012, v. 13, n. 4, p. 327, doi. 10.1007/s10048-012-0337-6

By:

Tsurusaki, Yoshinori;
Saitoh, Shinji;
Tomizawa, Kazuhiro;
Sudo, Akira;
Asahina, Naoko;
Shiraishi, Hideaki;
Ito, Jun-ichi;
Tanaka, Hajime;
Doi, Hiroshi;
Saitsu, Hirotomo;
Miyake, Noriko;
Matsumoto, Naomichi

Publication type:

Article

Visualization of the spatial positioning of the SNRPN, UBE3A, and GABRB3 genes in the normal human nucleus by three-color 3D fluorescence in situ hybridization.

Published in:

Chromosome Research, 2012, v. 20, n. 6, p. 659, doi. 10.1007/s10577-012-9300-5

By:

Kawamura, Rie;
Tanabe, Hideyuki;
Wada, Takahito;
Saitoh, Shinji;
Fukushima, Yoshimitsu;
Wakui, Keiko

Publication type:

Article

Near-infrared light scattering and water diffusion in newborn brains.

Published in:

Annals of Clinical & Translational Neurology, 2022, v. 9, n. 9, p. 1417, doi. 10.1002/acn3.51641

By:

Sachiko Iwata;
Reiji Katayama;
Kennosuke Tsuda;
Yung-Chieh Lin;
Tsuyoshi Kurata;
Masahiro Kinoshita;
Koya Kawase;
Takenori Kato;
Shin Kato;
Tadashi Hisano;
Motoki Oda;
Etsuko Ohmae;
Sachio Takashima;
Yuko Araki;
Shinji Saitoh;
Osuke Iwata

Publication type:

Article

Early phase 2 trial of TAS‐205 in patients with Duchenne muscular dystrophy.

Published in:

Annals of Clinical & Translational Neurology, 2020, v. 7, n. 2, p. 181, doi. 10.1002/acn3.50978

By:

Komaki, Hirofumi;
Maegaki, Yoshihiro;
Matsumura, Tsuyoshi;
Shiraishi, Kazuhiro;
Awano, Hiroyuki;
Nakamura, Akinori;
Kinoshita, Satoru;
Ogata, Katsuhisa;
Ishigaki, Keiko;
Saitoh, Shinji;
Funato, Michinori;
Kuru, Satoshi;
Nakayama, Takahiro;
Iwata, Yasuyuki;
Yajima, Hiroyuki;
Takeda, Shin'ichi

Publication type:

Article

Adverse pregnancy outcomes of cancer survivors and infectious disease in their infants: The Japan Environment and Children's Study.

Published in:

Oncology Letters, 2023, v. 25, n. 3, p. N.PAG, doi. 10.3892/ol.2023.13686

By:

Nishikawa, Ryutaro;
Sugiura-Ogasawara, Mayumi;
Ebara, Takeshi;
Matsuki, Taro;
Tamada, Hazuki;
Kato, Sayaka;
Kaneko, Kayo;
Saitoh, Shinji;
Kamijima, Michihiro

Publication type:

Article

Association of HLA-A*31:01 Screening With the Incidence of Carbamazepine-Induced Cutaneous Adverse Reactions in a Japanese Population.

Published in:

JAMA Neurology, 2018, v. 75, n. 7, p. 842, doi. 10.1001/jamaneurol.2018.0278

By:

Mushiroda, Taisei;
Takahashi, Yukitoshi;
Onuma, Teiichi;
Yamamoto, Yoshiaki;
Kamei, Tetsumasa;
Hoshida, Tohru;
Takeuchi, Katsuya;
Otsuka, Kotaro;
Okazaki, Mitsutoshi;
Watanabe, Masako;
Kanemoto, Kosuke;
Oshima, Tomohiro;
Watanabe, Atsushi;
Minami, Shiro;
Saito, Kayoko;
Tanii, Hisashi;
Shimo, Yasushi;
Hara, Minoru;
Saitoh, Shinji;
Kinoshita, Toshihiko

Publication type:

Article

Estimation of elevated intracranial pressure in infants with hydroce-phalus by using transcranial Doppler velocimetry with fontanel compression.

Published in:

Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-30274-3

By:

Yoshizuka, Teiko;
Kinoshita, Masahiro;
Iwata, Sachiko;
Tsuda, Kennosuke;
Kato, Takenori;
Saikusa, Mamoru;
Shindou, Ryota;
Hara, Naoko;
Harada, Eimei;
Takashima, Sachio;
Takeshige, Nobuyuki;
Saitoh, Shinji;
Yamashita, Yushiro;
Iwata, Osuke

Publication type:

Article

Combination of Miller-Dieker syndrome and VACTERL association causes extremely severe clinical presentation.

Published in:

European Journal of Pediatrics, 2014, v. 173, n. 11, p. 1541, doi. 10.1007/s00431-013-2099-z

By:

Ueda, Hiroko;
Sugiura, Tokio;
Takeshita, Satoru;
Ito, Koichi;
Kakita, Hiroki;
Nagasaki, Rika;
Kurosawa, Kenji;
Saitoh, Shinji

Publication type:

Article

Reliability and validity of a Japanese version of the psychosocial assessment tool for families of children with cancer.

Published in:

Japanese Journal of Clinical Oncology, 2020, v. 50, n. 3, p. 296, doi. 10.1093/jjco/hyz181

By:

Tsumura, Akemi;
Okuyama, Toru;
Ito, Yoshinori;
Kondo, Masaki;
Saitoh, Shinji;
Kamei, Michi;
Sato, Iori;
Ishida, Yuji;
Kato, Yuka;
Takeda, Yoshimi;
Akechi, Tatsuo

Publication type:

Article

Antenatal Growth, Gestational Age, Birth, Enteral Feeding, and Blood Citrulline Levels in Very Low Birth Weight Infants.

Published in:

Nutrients, 2024, v. 16, n. 4, p. 476, doi. 10.3390/nu16040476

By:

Obayashi, Midori;
Iwata, Sachiko;
Okuda, Tomoya;
Mori, Ichita;
Nakane, Shigeharu;
Togawa, Yasuko;
Sugimoto, Mari;
Togawa, Takao;
Muramatsu, Kanji;
Saitoh, Shinji;
Sugiura, Takahiro;
Iwata, Osuke

Publication type:

Article

Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance.

Published in:

Clinical Epigenetics, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13148-024-01744-5

By:

Urakawa, Tatsuki;
Soejima, Hidenobu;
Yamoto, Kaori;
Hara-Isono, Kaori;
Nakamura, Akie;
Kawashima, Sayaka;
Narusawa, Hiromune;
Kosaki, Rika;
Nishimura, Yutaka;
Yamazawa, Kazuki;
Hattori, Tetsuo;
Muramatsu, Yukako;
Inoue, Takanobu;
Matsubara, Keiko;
Fukami, Maki;
Saitoh, Shinji;
Ogata, Tsutomu;
Kagami, Masayo

Publication type:

Article

Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 8, p. 1019, doi. 10.1038/ejhg.2008.90

By:

Hosoki, Kana;
Ogata, Tsutomu;
Kagami, Masayo;
Tanaka, Touju;
Saitoh, Shinji

Publication type:

Article

Intrauterine Inflammation, Excessive Fetal Growth and Respiratory Morbidities in Moderate-To-Late Preterm Neonates.

Published in:

Neonatology (16617800), 2024, v. 121, n. 2, p. 258, doi. 10.1159/000534163

By:

Yokoi, Kyoko;
Iwata, Osuke;
Kobayashi, Satoru;
Jinnou, Hideo;
Kato, Shin;
Saitoh, Shinji;
Goto, Haruo

Publication type:

Article

Diclofenac Enhances Proinflammatory Cytokine-Induced Aquaporin-4 Expression in Cultured Astrocyte.

Published in:

Cellular & Molecular Neurobiology, 2013, v. 33, n. 3, p. 393, doi. 10.1007/s10571-013-9905-z

By:

Asai, Hayato;
Kakita, Hiroki;
Aoyama, Mineyoshi;
Nagaya, Yoshiaki;
Saitoh, Shinji;
Asai, Kiyofumi

Publication type:

Article

Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome.

Published in:

2017

By:

Ohashi, Kei;
Togawa, Takao;
Sugiura, Tokio;
Ito, Koichi;
Endo, Takeshi;
Aoyama, Kohei;
Negishi, Yutaka;
Kudo, Toyoichiro;
Ito, Reiko;
Saitoh, Shinji

Publication type:

journal article

Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy.

Published in:

2019

By:

Negishi, Yutaka;
Ieda, Daisuke;
Hori, Ikumi;
Nozaki, Yasuyuki;
Yamagata, Takanori;
Komaki, Hirofumi;
Tohyama, Jun;
Nagasaki, Keisuke;
Tada, Hiroko;
Saitoh, Shinji

Publication type:

journal article

A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.

Published in:

Nature Genetics, 2001, v. 28, n. 1, p. 19, doi. 10.1038/88209

By:

Meguro, Makiko;
Kashiwagi, Akiko;
Mitsuya, Kohzoh;
Nakao, Mitsuyoshi;
Kondo, Ikuko;
Saitoh, Shinji;
Oshimura, Mitsuo

Publication type:

Article

Multicenter study of paroxysmal dyskinesias in Japan-Clinical and pedigree analysis.

Published in:

Movement Disorders, 1999, v. 14, n. 4, p. 658, doi. 10.1002/1531-8257(199907)14:4<658::AID-MDS1016>3.0.CO;2-7

By:

Nagamitsu, Shinichiro;
Matsuishi, Toyojiro;
Hashimoto, Kiyoshi;
Yamashita, Yushiro;
Aihara, Masao;
Shimizu, Katsunori;
Mizuguchi, Masashi;
Iwamoto, Hiroko;
Saitoh, Shinji;
Hirano, Yukiko;
Kato, Hirohisa;
Fukuyama, Yukio;
Shimada, Morimi

Publication type:

Article

Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7.

Published in:

Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0503-6

By:

Ishii, Jun;
Suzuki, Atsushi;
Kimura, Toru;
Tateyama, Michihiro;
Tanaka, Tatsushi;
Yazawa, Takuya;
Arimasu, Yu;
Chen, I-Shan;
Aoyama, Kohei;
Kubo, Yoshihiro;
Saitoh, Shinji;
Mizuno, Haruo;
Kamma, Hiroshi

Publication type:

Article

Novel SPEG variants in a neonate with severe dilated cardiomyopathy and relatively mild hypotonia.

Published in:

Human Genome Variation, 2023, v. 10, n. 1, p. 1, doi. 10.1038/s41439-023-00253-w

By:

Fujimoto, Hana Milena;
Fujimoto, Masanori;
Sugiura, Takahiro;
Nakane, Shigeharu;
Wakano, Yasuhiro;
Sato, Emi;
Oshita, Hironori;
Togawa, Yasuko;
Sugimoto, Mari;
Kato, Takenori;
Yasuda, Kazushi;
Muramatsu, Kanji;
Saitoh, Shinji

Publication type:

Article

Novel SPEG variants in a neonate with severe dilated cardiomyopathy and relatively mild hypotonia.

Published in:

Human Genome Variation, 2023, v. 10, n. 1, p. 1, doi. 10.1038/s41439-023-00253-w

By:

Fujimoto, Hana Milena;
Fujimoto, Masanori;
Sugiura, Takahiro;
Nakane, Shigeharu;
Wakano, Yasuhiro;
Sato, Emi;
Oshita, Hironori;
Togawa, Yasuko;
Sugimoto, Mari;
Kato, Takenori;
Yasuda, Kazushi;
Muramatsu, Kanji;
Saitoh, Shinji

Publication type:

Article

De novo 2q36.3q37.1 deletion encompassing TRIP12 and NPPC yields distinct phenotypes.

Published in:

2020

By:

Kondo, Yuto;
Aoyama, Kohei;
Suzuki, Hisato;
Hattori, Ayako;
Hori, Ikumi;
Ito, Koichi;
Yoshida, Aya;
Koroki, Mari;
Ueda, Kentaro;
Kosaki, Kenjiro;
Saitoh, Shinji

Publication type:

Case Study

A novel CUL4B splice site variant in a young male exhibiting less pronounced features.

Published in:

Human Genome Variation, 2019, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41439-019-0074-6

By:

Nakamura, Yuji;
Okuno, Yusuke;
Muramatsu, Hideki;
Kawai, Tomoko;
Satou, Kazuhito;
Ieda, Daisuke;
Hori, Ikumi;
Ohashi, Kei;
Negishi, Yutaka;
Hattori, Ayako;
Takahashi, Yoshiyuki;
Kojima, Seiji;
Saitoh, Shinji

Publication type:

Article

A novel splicing mutation in SLC9A6 in a boy with Christianson syndrome.

Published in:

Human Genome Variation, 2019, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41439-019-0046-x

By:

Ieda, Daisuke;
Hori, Ikumi;
Nakamura, Yuji;
Ohashi, Kei;
Negishi, Yutaka;
Hattori, Ayako;
Arisaka, Atsuko;
Hasegawa, Setsuko;
Saitoh, Shinji

Publication type:

Article

Effect of swimming initiation period and continuation frequency on motor competence development in children aged up to 3 years: the Japan environment and children's study.

Published in:

BMC Sports Science, Medicine & Rehabilitation, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13102-024-00980-9

By:

Kano, Hirohisa;
Ebara, Takeshi;
Matsuki, Taro;
Tamada, Hazuki;
Yamada, Yasuyuki;
Kato, Sayaka;
Kaneko, Kayo;
Matsuzaki, Kazuki;
Sato, Hirotaka;
Minato, Kyoko;
Sugiura-Ogasawara, Mayumi;
Saitoh, Shinji;
Kamijima, Michihiro

Publication type:

Article

Influence of mothers' nighttime responses on the sleep–wake rhythm of 1-month-old infants.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-03717-7

By:

Kuroda, Momoka;
Suetsugu, Yoshiko;
Iwata, Sachiko;
Kinoshita, Masahiro;
Fujita, Fumie;
Sato, Yoko;
Saitoh, Shinji;
Iwata, Osuke;
Morokuma, Seiichi

Publication type:

Article

Evidence of both foetal inflammation and hypoxia–ischaemia is associated with meconium aspiration syndrome.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-96275-x

By:

Yokoi, Kyoko;
Iwata, Osuke;
Kobayashi, Satoru;
Kobayashi, Mizuho;
Saitoh, Shinji;
Goto, Haruo

Publication type:

Article

Increased Protein Stability of CDKN1C Causes a Gain-of-Function Phenotype in Patients with IMAGe Syndrome.

Published in:

PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0075137

By:

Hamajima, Naoki;
Johmura, Yoshikazu;
Suzuki, Satoshi;
Nakanishi, Makoto;
Saitoh, Shinji

Publication type:

Article

House dust mite SLIT-tablet is well tolerated in pediatric patients with controlled asthma.

Published in:

Asian Pacific Journal of Allergy & Immunology, 2024, v. 42, n. 4, p. 368, doi. 10.12932/ap-051220-1009

By:

Hisashi Tanida;
Takayasu Nomura;
Yuto Kondo;
Yasutaka Hirabayashi;
Jun Wakatsuki;
Shinji Saitoh

Publication type:

Article

Control variables of serum ferritin concentrations in hospitalized newborn infants: an observational study.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-35404-0

By:

Hisano, Tadashi;
Okada, Junichiro;
Tsuda, Kennosuke;
Iwata, Sachiko;
Saitoh, Shinji;
Iwata, Osuke

Publication type:

Article

MYCN in human development and diseases.

Published in:

Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2024.1417607

By:

Yosuke Nishio;
Kohji Kato;
Hisashi Oishi;
Yoshiyuki Takahashi;
Shinji Saitoh

Publication type:

Article

KIF1A mutation in a patient with progressive neurodegeneration.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 11, p. 639, doi. 10.1038/jhg.2014.80

By:

Okamoto, Nobuhiko;
Miya, Fuyuki;
Tsunoda, Tatsuhiko;
Yanagihara, Keiko;
Kato, Mitsuhiro;
Saitoh, Shinji;
Yamasaki, Mami;
Kanemura, Yonehiro;
Kosaki, Kenjiro

Publication type:

Article

Homoplasmy of a mitochondrial 3697G>A mutation causes Leigh syndrome.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 7, p. 405, doi. 10.1038/jhg.2014.41

By:

Negishi, Yutaka;
Hattori, Ayako;
Takeshita, Eri;
Sakai, Chika;
Ando, Naoki;
Ito, Tetsuya;
Goto, Yu-ichi;
Saitoh, Shinji

Publication type:

Article

Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 2, p. 110, doi. 10.1038/jhg.2010.129

By:

Hayashi, Shin;
Imoto, Issei;
Aizu, Yoshinori;
Okamoto, Nobuhiko;
Mizuno, Seiji;
Kurosawa, Kenji;
Okamoto, Nana;
Honda, Shozo;
Araki, Satoshi;
Mizutani, Shuki;
Numabe, Hironao;
Saitoh, Shinji;
Kosho, Tomoki;
Fukushima, Yoshimitsu;
Mitsubuchi, Hiroshi;
Endo, Fumio;
Chinen, Yasutsugu;
Kosaki, Rika;
Okuyama, Torayuki;
Ohki, Hirotaka

Publication type:

Article

Three KINSSHIP syndrome patients with mosaic and germline AFF3 variants.

Published in:

Clinical Genetics, 2023, v. 103, n. 5, p. 590, doi. 10.1111/cge.14292

By:

Inoue, Yuta;
Tsuchida, Naomi;
Okamoto, Nobuhiko;
Shuichi, Shimakawa;
Ohashi, Kei;
Saitoh, Shinji;
Ogawa, Atsushi;
Hamada, Keisuke;
Sakamoto, Masamune;
Miyake, Noriko;
Hamanaka, Kohei;
Fujita, Atsushi;
Koshimizu, Eriko;
Miyatake, Satoko;
Mizuguchi, Takeshi;
Ogata, Kazuhiro;
Uchiyama, Yuri;
Matsumoto, Naomichi

Publication type:

Article

A case of early‐onset epileptic encephalopathy with a homozygous TBC1D24 variant caused by uniparental isodisomy.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 4, p. 645, doi. 10.1002/ajmg.a.61056

By:

Nakashima, Mitsuko;
Negishi, Yutaka;
Hori, Ikumi;
Hattori, Ayako;
Saitoh, Shinji;
Saitsu, Hirotomo

Publication type:

Article

A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology.

Published in:

American Journal of Medical Genetics. Part A, 2017, v. 173, n. 10, p. 2690, doi. 10.1002/ajmg.a.38391

By:

Okamoto, Nobuhiko;
Tsuchiya, Yuki;
Miya, Fuyuki;
Tsunoda, Tatsuhiko;
Yamashita, Kumiko;
Boroevich, Keith A.;
Kato, Mitsuhiro;
Saitoh, Shinji;
Yamasaki, Mami;
Kanemura, Yonehiro;
Kosaki, Kenjiro;
Kitagawa, Daiju

Publication type:

Article

Novel MCA/ID syndrome with ASH1L mutation.

Published in:

American Journal of Medical Genetics. Part A, 2017, v. 173, n. 6, p. 1644, doi. 10.1002/ajmg.a.38193

By:

Okamoto, Nobuhiko;
Miya, Fuyuki;
Tsunoda, Tatsuhiko;
Kato, Mitsuhiro;
Saitoh, Shinji;
Yamasaki, Mami;
Kanemura, Yonehiro;
Kosaki, Kenjiro

Publication type:

Article

Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 7, p. 1863, doi. 10.1002/ajmg.a.37653

By:

Hori, Ikumi;
Miya, Fuyuki;
Ohashi, Kei;
Negishi, Yutaka;
Hattori, Ayako;
Ando, Naoki;
Okamoto, Nobuhiko;
Kato, Mitsuhiro;
Tsunoda, Tatsuhiko;
Yamasaki, Mami;
Kanemura, Yonehiro;
Kosaki, Kenjiro;
Saitoh, Shinji

Publication type:

Article

Tissue-limited ring chromosome 18 mosaicism as a cause of Pitt-Hopkins syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 10, p. 2621, doi. 10.1002/ajmg.a.35230

By:

Takenouchi, Toshiki;
Yagihashi, Tatsuhiko;
Tsuchiya, Hiroyuki;
Torii, Chiharu;
Hayashi, Kumiko;
Kosaki, Rika;
Saitoh, Shinji;
Takahashi, Takao;
Kosaki, Kenjiro

Publication type:

Article

Clinical phenotype and candidate genes for the 5q31.3 microdeletion syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 8, p. 1891, doi. 10.1002/ajmg.a.35439

By:

Hosoki, Kana;
Ohta, Tohru;
Natsume, Jun;
Imai, Sumiko;
Okumura, Akihisa;
Matsui, Takeshi;
Harada, Naoki;
Bacino, Carlos A.;
Scaglia, Fernando;
Jones, Jeremy Y.;
Niikawa, Norio;
Saitoh, Shinji

Publication type:

Article

Medical records as screening tools for child death review in Japan.

Published in:

Pediatrics International, 2023, v. 65, n. 1, p. 1, doi. 10.1111/ped.15692

By:

Numaguchi, Atsushi;
Ishii, Akira;
Natsume, Jun;
Saitoh, Shinji;
Aoki, Yasuhiro;
Yoshikawa, Tetsushi;
Isobe, Ichiro;
Okumura, Akihisa;
Seno, Hiroshi;
Takahashi, Yoshiyuki

Publication type:

Article

Two case reports of extended‐release guanfacine overdose in children.

Published in:

2023

By:

Shimozato, Asuka;
Ohashi, Kei;
Saitoh, Shinji

Publication type:

Case Study

Utility of breakpoint‐specific nested polymerase chain reaction for the diagnosis of Emanuel syndrome.

Published in:

Pediatrics International, 2021, v. 63, n. 12, p. 1534, doi. 10.1111/ped.14644

By:

Hayakawa, Kozue;
Kawase, Koya;
Fujimoto, Masanori;
Nakamura, Yuji;
Saitoh, Shinji

Publication type:

Article

A case of tricuspid atresia with Prader‐Willi syndrome.

Published in:

2020

By:

Abe, Jiro;
Takeda, Atsuhito;
Saitoh, Shinji

Publication type:

Case Study

Respiratory illness and acute flaccid myelitis in the Tokai district in 2018.

Published in:

Pediatrics International, 2020, v. 62, n. 3, p. 337, doi. 10.1111/ped.14128

By:

Okumura, Akihisa;
Numoto, Shingo;
Iwayama, Hideyuki;
Kurahashi, Hirokazu;
Natsume, Jun;
Saitoh, Shinji;
Yoshikawa, Tetsushi;
Fukao, Toshiyuki;
Hirayama, Masahiro;
Takahashi, Yoshiyuki

Publication type:

Article

Delayed recognition of childhood arterial ischemic stroke.

Published in:

Pediatrics International, 2019, v. 61, n. 9, p. 895, doi. 10.1111/ped.13966

By:

Hori, Ikumi;
Tsuji, Takeshi;
Miyake, Misa;
Ueda, Kazuto;
Kataoka, Erina;
Suzuki, Michio;
Kobayashi, Satoru;
Kurahashi, Hirokazu;
Takahashi, Yoshiyuki;
Okumura, Akihisa;
Yoshikawa, Tetsushi;
Saitoh, Shinji;
Natsume, Jun

Publication type:

Article

Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants.

Published in:

Pediatrics International, 2016, v. 58, n. 6, p. 461, doi. 10.1111/ped.12861

By:

Kawase, Koya;
Sugiura, Tokio;
Nagaya, Yoshiaki;
Yamada, Takaharu;
Sugimoto, Mari;
Ito, Koichi;
Togawa, Takao;
Nagasaki, Rika;
Kato, Takenori;
Kouwaki, Masanori;
Koyama, Norihisa;
Saitoh, Shinji

Publication type:

Article