Noninvasive prenatal testing suggesting an abnormality in chromosome 15 confirmed to be a case of Prader–Willi syndrome caused by trisomy rescue in the neonatal period
Okuda, Tomohiro, Moroto, Masaharu, Yamamoto, Toshiyuki
Published in The journal of obstetrics and gynaecology research (01.08.2022)
Published in The journal of obstetrics and gynaecology research (01.08.2022)
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High-fat diet accelerates extreme obesity with hyperphagia in female heterozygous Mecp2-null mice
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Published in PloS one (04.01.2019)
Published in PloS one (04.01.2019)
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Published in Journal of medical genetics (01.06.2019)
Published in Journal of medical genetics (01.06.2019)
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Bilateral choroid plexus resection in a 9p hexasomy/tetrasomy mosaic patient
Takada, Rei, Tozawa, Takenori, Yamanaka, Takumi, Moroto, Masaharu, Iehara, Tomoko, Chiyonobu, Tomohiro
Published in Human genome variation (26.02.2024)
Published in Human genome variation (26.02.2024)
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Regional Difference in Myelination in Monocarboxylate Transporter 8 Deficiency: Case Reports and Literature Review of Cases in Japan
Iwayama, Hideyuki, Tanaka, Tatsushi, Aoyama, Kohei, Moroto, Masaharu, Adachi, Shinsuke, Fujisawa, Yasuko, Matsuura, Hiroki, Takano, Kyoko, Mizuno, Haruo, Okumura, Akihisa
Published in Frontiers in neurology (15.07.2021)
Published in Frontiers in neurology (15.07.2021)
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Effects of chemotherapy on the brain in childhood: diffusion tensor imaging of subtle white matter damage
Morioka, Shigemi, Morimoto, Masafumi, Yamada, Kei, Hasegawa, Tatsuji, Morita, Takashi, Moroto, Masaharu, Isoda, Kenichi, Chiyonobu, Tomohiro, Imamura, Toshihiko, Nishimura, Akira, Morimoto, Akira, Hosoi, Hajime
Published in Neuroradiology (01.10.2013)
Published in Neuroradiology (01.10.2013)
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Serial investigation of PTPN11 mutation in nonhematopoietic tissues in a patient with juvenile myelomonocytic leukemia who was treated with unrelated cord blood transplantation
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Published in International journal of hematology (01.12.2015)
Published in International journal of hematology (01.12.2015)
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Alternating cerebral edema and arterial dilations in M olybdenum cofactor deficiency type‐A
Matsuura, Amane, Tozawa, Takenori, Moroto, Masaharu, Miyamoto, Yosuke, Kawabe, Yasuhiro, Zuiki, Masashi, Hasegawa, Tatsuji, Kayaki, Taisei, Yano, Naoko, Yoshida, Takeshi, Chiyonobu, Tomohiro, Morimoto, Masafumi, Iehara, Tomoko
Published in Journal of inherited metabolic disease (01.09.2024)
Published in Journal of inherited metabolic disease (01.09.2024)
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Alternating cerebral edema and arterial dilations in Molybdenum cofactor deficiency type-A
Matsuura, Amane, Tozawa, Takenori, Moroto, Masaharu, Miyamoto, Yosuke, Kawabe, Yasuhiro, Zuiki, Masashi, Hasegawa, Tatsuji, Kayaki, Taisei, Yano, Naoko, Yoshida, Takeshi, Chiyonobu, Tomohiro, Morimoto, Masafumi, Iehara, Tomoko
Published in Journal of inherited metabolic disease (04.07.2024)
Published in Journal of inherited metabolic disease (04.07.2024)
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Low-grade intraventricular hemorrhage disrupts cerebellar white matter in preterm infants: evidence from diffusion tensor imaging
Morita, Takashi, Morimoto, Masafumi, Yamada, Kei, Hasegawa, Tatsuji, Morioka, Shigemi, Kidowaki, Satoshi, Moroto, Masaharu, Yamashita, Satoshi, Maeda, Hiroshi, Chiyonobu, Tomohiro, Tokuda, Sachiko, Hosoi, Hajime
Published in Neuroradiology (01.05.2015)
Published in Neuroradiology (01.05.2015)
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Journal Article
Noninvasive prenatal testing suggesting an abnormality in chromosome 15 confirmed to be a case of Prader-Willi syndrome caused by trisomy rescue in the neonatal period
Okuda, Tomohiro, Moroto, Masaharu, Yamamoto, Toshiyuki
Published in The journal of obstetrics and gynaecology research (01.08.2022)
Published in The journal of obstetrics and gynaecology research (01.08.2022)
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Regional Difference in Myelination in Monocarboxylate Transporter 8 Deficiency: Case Reports and Literature Review of Cases in Japan
Iwayama, Hideyuki, Tanaka, Tatsushi, Aoyama, Kohei, Moroto, Masaharu, Adachi, Shinsuke, Fujisawa, Yasuko, Matsuura, Hiroki, Takano, Kyoko, Mizuno, Haruo, Okumura, Akihisa
Published in Frontiers in neurology (01.01.2021)
Published in Frontiers in neurology (01.01.2021)
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