Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Shinji Saitoh"'
Autor:
Hana Milena Fujimoto, Masanori Fujimoto, Takahiro Sugiura, Shigeharu Nakane, Yasuhiro Wakano, Emi Sato, Hironori Oshita, Yasuko Togawa, Mari Sugimoto, Takenori Kato, Kazushi Yasuda, Kanji Muramatsu, Shinji Saitoh
Publikováno v:
Human Genome Variation, Vol 10, Iss 1, Pp 1-4 (2023)
Abstract Striated muscle preferentially expressed protein kinase (SPEG) variants have been reported to cause centronuclear myopathy associated with cardiac diseases. The severity of skeletal muscle symptoms and cardiac symptoms are presumably related
Externí odkaz:
https://doaj.org/article/d7182805ebe743dfb5db97479f0f5f34
Autor:
Kennosuke Tsuda, Seiichi Morokuma, Masahiro Kinoshita, Fumie Fujita, Mitsuaki Unno, Sachiko Iwata, Takashi Horinouchi, Shinji Saitoh, Osuke Iwata
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Scientific Reports
Scientific Reports
Peripartum depression is a common, serious complication in mothers. To assess the influence of infant care, sleep and growth on the risk of peripartum depression, 1,271 mothers of healthy one-month-old infants completed comprehensive questionnaires i
Autor:
Shinji Saitoh, Akie Nakamura, Reiko Horikawa, Maki Fukami, Tohru Yorifuji, Rika Kosaki, Keisuke Nagasaki, Tsutomu Ogata, Keiko Matsubara, Seiji Mizuno, Chikahiko Numakura, Masayo Kagami, Yasuhiro Naiki, Toshihiro Tajima
Publikováno v:
Genetics in Medicine
Purpose Temple syndrome (TS14) is a rare imprinting disorder caused by aberrations at the 14q32.2 imprinted region. Here, we report comprehensive molecular and clinical findings in 32 Japanese patients with TS14. Methods We performed molecular studie
Autor:
Mami Yamasaki, Kenjiro Kosaki, Shinji Saitoh, Fuyuki Miya, Ikumi Hori, Mitsuhiro Kato, Tatsuhiko Tsunoda, Yutaka Negishi, Yonehiro Kanemura, Naoki Ando, Ayako Hattori, Nobuhiko Okamoto, Kentaro Mizuno
Publikováno v:
Human Genome Variation
Chromosome 1p32-p31 deletion syndrome involving the Nuclear factor I/A (NFIA) gene is characterized by corpus callosum hypoplasia or defects and urinary tract defects. Herein we report on a case resembling the 1p32-p31 deletion syndrome carrying a de