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Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects.
Published in:
Clinical Epigenetics, 2017, v. 9, p. 1, doi. 10.1186/s13148-017-0350-6
By:
- Takanobu Inoue;
- Akie Nakamura;
- Tomoko Fuke;
- Kazuki Yamazawa;
- Shinichiro Sano;
- Keiko Matsubara;
- Seiji Mizuno;
- Yoshika Matsukura;
- Chie Harashima;
- Tatsuji Hasegawa;
- Hisakazu Nakajima;
- Kumi Tsumura6;
- Zenro Kizaki;
- Akira Oka;
- Tsutomu Ogata;
- Maki Fukami;
- Masayo Kagami
Publication type:
Article
Cerebellar peduncle damage in Langerhans cell histiocytosis-associated neurodegenerative disease revealed by diffusion tensor imaging.
Published in:
Neuroradiology, 2024, v. 66, n. 1, p. 43, doi. 10.1007/s00234-023-03249-z
By:
- Imai, Tomohiko;
- Sakamoto, Kenichi;
- Hasegawa, Tatsuji;
- Shioda, Yoko;
- Tsutsumi, Yoshiyuki;
- Sakaue, Satoshi;
- Imamura, Toshihiko;
- Morimoto, Akira;
- Iehara, Tomoko
Publication type:
Article
Low-grade intraventricular hemorrhage disrupts cerebellar white matter in preterm infants: evidence from diffusion tensor imaging.
Published in:
Neuroradiology, 2015, v. 57, n. 5, p. 507, doi. 10.1007/s00234-015-1487-7
By:
- Morita, Takashi;
- Morimoto, Masafumi;
- Yamada, Kei;
- Hasegawa, Tatsuji;
- Morioka, Shigemi;
- Kidowaki, Satoshi;
- Moroto, Masaharu;
- Yamashita, Satoshi;
- Maeda, Hiroshi;
- Chiyonobu, Tomohiro;
- Tokuda, Sachiko;
- Hosoi, Hajime
Publication type:
Article
Effects of chemotherapy on the brain in childhood: diffusion tensor imaging of subtle white matter damage.
Published in:
Neuroradiology, 2013, v. 55, n. 10, p. 1251, doi. 10.1007/s00234-013-1245-7
By:
- Morioka, Shigemi;
- Morimoto, Masafumi;
- Yamada, Kei;
- Hasegawa, Tatsuji;
- Morita, Takashi;
- Moroto, Masaharu;
- Isoda, Kenichi;
- Chiyonobu, Tomohiro;
- Imamura, Toshihiko;
- Nishimura, Akira;
- Morimoto, Akira;
- Hosoi, Hajime
Publication type:
Article
Low‐grade IVH in preterm infants causes cerebellar damage, motor, and cognitive impairment.
Published in:
Pediatrics International, 2021, v. 63, n. 11, p. 1327, doi. 10.1111/ped.14691
By:
- Sakaue, Satoshi;
- Hasegawa, Tatsuji;
- Sakai, Koji;
- Zen, Yui;
- Tozawa, Takenori;
- Chiyonobu, Tomohiro;
- Yamada, Kei;
- Morimoto, Masafumi;
- Hosoi, Hajime
Publication type:
Article
Validity of stress assessment using heart‐rate variability in newborns.
Published in:
Pediatrics International, 2020, v. 62, n. 6, p. 694, doi. 10.1111/ped.14149
By:
- Hashiguchi, Kanae;
- Kuriyama, Nagato;
- Koyama, Teruhide;
- Matsui, Daisuke;
- Ozaki, Etsuko;
- Hasegawa, Tatsuji;
- Tokuda, Sachiko;
- Niwa, Fumitoshi;
- Iwasa, Koichi;
- Watanabe, Isao;
- Teramukai, Satoshi;
- Kitawaki, Jo;
- Watanabe, Yoshiyuki;
- Uehara, Ritei;
- Hosoi, Hajime
Publication type:
Article
A Case of Fetal Tachycardia after Electroconvulsive Therapy: A Possible Effect of Maternal Hypoxia and Uterine Contractions.
Published in:
Case Reports in Psychiatry, 2019, p. 1, doi. 10.1155/2019/3709612
By:
- Watanabe, Anri;
- Ayani, Nobutaka;
- Waratani, Miyoko;
- Hasegawa, Tatsuji;
- Ishii, Maki;
- Matsuoka, Teruyuki;
- Narumoto, Jin
Publication type:
Article
The prediction of estimated cerebral perfusion pressure with trans-systolic time in preterm and term infants.
Published in:
European Journal of Pediatrics, 2024, v. 183, n. 6, p. 2587, doi. 10.1007/s00431-024-05511-9
By:
- Zuiki, Masashi;
- Ohta, Mikito;
- Fujita, Naoe;
- Uda, Daisuke;
- Uesugi, Madoka;
- Yamano, Akio;
- Ichise, Eisuke;
- Morimoto, Hidechika;
- Hashiguchi, Kanae;
- Kinoshita, Daisuke;
- Hasegawa, Tatsuji;
- Iehara, Tomoko
Publication type:
Article
Effectiveness of cardiac palliative surgery for trisomy 18 patients with increased pulmonary blood flow.
Published in:
American Journal of Medical Genetics. Part A, 2023, v. 191, n. 11, p. 2703, doi. 10.1002/ajmg.a.63401
By:
- Takai, Akari;
- Yamagishi, Masaaki;
- Ikeda, Kazuyuki;
- Sugimoto, Atsuya;
- Ichise, Eisuke;
- Maeda, Yoshinobu;
- Teramukai, Satoshi;
- Hasegawa, Tatsuji;
- Oda, Shinichiro;
- Iehara, Tomoko
Publication type:
Article
Early manifestations of BPAN in a pediatric patient.
Published in:
American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 12, p. 3095, doi. 10.1002/ajmg.a.36779
By:
- Okamoto, Nobuhiko;
- Ikeda, Tae;
- Hasegawa, Tatsuji;
- Yamamoto, Yuto;
- Kawato, Kazumi;
- Komoto, Tomohiro;
- Imoto, Issei
Publication type:
Article
Thyroid hypogenesis is associated with a novel AKT3 germline variant that causes megalencephaly and cortical malformation.
Published in:
Human Genome Variation, 2022, v. 9, n. 1, p. 1, doi. 10.1038/s41439-022-00197-7
By:
- Mori, Jun;
- Hasegawa, Tatsuji;
- Miyamoto, Yosuke;
- Kitamura, Kazumasa;
- Morimoto, Hidechika;
- Tozawa, Takenori;
- Pooh, Ritsuko Kimata;
- Chiyonobu, Tomohiro
Publication type:
Article
De novo IGF2 mutation on the paternal allele in a patient with Silver-Russell syndrome and ectrodactyly.
Published in:
Human Mutation, 2017, v. 38, n. 8, p. 953, doi. 10.1002/humu.23253
By:
- Yamoto, Kaori;
- Saitsu, Hirotomo;
- Nakagawa, Norio;
- Nakajima, Hisakazu;
- Hasegawa, Tatsuji;
- Fujisawa, Yasuko;
- Kagami, Masayo;
- Fukami, Maki;
- Ogata, Tsutomu
Publication type:
Article

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