Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Hidehiko Maruyama"'
Autor:
Yohji Uehara, Yuka Sano Wada, Yuka Iwasaki, Kota Yoneda, Yasuhisa Ikuta, Shoichiro Amari, Hidehiko Maruyama, Keiko Tsukamoto, Tetsuya Isayama, Kenichi Sakamoto, Yoko Shioda, Osamu Miyazaki, Rie Irie, Takako Yoshioka, Naoko Mochimaru, Kazue Yoshida, Yushi Ito
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Systemic juvenile xanthogranuloma is a very rare disease typically presents as skin lesions with yellow papules or nodules and is sometimes fatal. We report a case of congenital neonatal systemic juvenile xanthogranuloma with atyp
Externí odkaz:
https://doaj.org/article/9f3e758b318c4b8a9add3412e2ee1ecd
Autor:
Ayano Tanzawa, Jumpei Saito, Kensuke Shoji, Yuka Kojo, Takanori Funaki, Hidehiko Maruyama, Tetsuya Isayama, Yushi Ito, Hidefumi Nakamura, Akimasa Yamatani
Publikováno v:
Microbiology Spectrum, Vol 10, Iss 2 (2022)
ABSTRACT A prospective single-center study was conducted to characterize the pharmacokinetics (PK) of fluconazole (FLCZ) in extremely low-birth-weight infants (ELBWIs) who received fosfluconazole (F-FLCZ). Intravenous F-FLCZ was administered at a dos
Externí odkaz:
https://doaj.org/article/94c29d1fa00b439b9d7be0a3c2dcda9f
Autor:
Jumpei Saito, Ayano Tanzawa, Yuka Kojo, Hidehiko Maruyama, Tetsuya Isayama, Kensuke Shoji, Yushi Ito, Akimasa Yamatani
Publikováno v:
Journal of Pharmaceutical Health Care and Sciences, Vol 6, Iss 1, Pp 1-7 (2020)
Abstract Background The need for a large volume of serum sample significantly reduces the feasibility of neonatal pharmacokinetic studies in daily practice, which must often rely on scavenged or opportunistic sampling. This problem is most apparent i
Externí odkaz:
https://doaj.org/article/e9cbffb5afb8462f9fe7bc14cba08966
Publikováno v:
American Journal of Perinatology Reports, Vol 10, Iss 04, Pp e403-e407 (2020)
Introduction Congenital complete atrioventricular block (CCAVB) associated with congenital chylothorax is a rare finding that has been reported in only one case in the literature. We report here the case of an infant with CCAVB complicated by congeni
Externí odkaz:
https://doaj.org/article/11a28dd94636447d911d805a5f9c2838
Autor:
Hidehiko Maruyama, Yuichi Hasegawa, Rika Sugibayashi, Yuka Iwasaki, Shuhei Fujino, Shoichiro Amari, Junko Nagasawa, Yuka Wada, Hideshi Fujinaga, Keiko Tsukamoto, Kazunori Tahara, Takako Yoshioka, Yushi Ito, Haruhiko Sago
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 34, Iss C, Pp 54-57 (2018)
Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital visceral myopathy. We experienced a case of an infant with MMIHS with prune belly syndrome (PBS). A pregnant woman was transferred at 16 gestational weeks for a cy
Externí odkaz:
https://doaj.org/article/498ef4eefaef4476a34c05809010d530
Autor:
Yuka Shibata, Hidehiko Maruyama, Taiyu Hayashi, Hiroshi Ono, Yuka Wada, Hideshi Fujinaga, Shuhei Fujino, Junko Nagasawa, Shoichiro Amari, Keiko Tsukamoto, Yushi Ito
Publikováno v:
American Journal of Perinatology Reports, Vol 09, Iss 03, Pp e213-e217 (2019)
Most cardiac rhabdomyomas with tuberous sclerosis (TS) are asymptomatic and spontaneously regress. However, some cases require surgical intervention due to arrhythmia and severe obstruction of cardiac inflow or outflow. We report herein a neonatal ca
Externí odkaz:
https://doaj.org/article/e7bd1d47fbce4548951ad5593f752496
Publikováno v:
American Journal of Perinatology Reports, Vol 03, Iss 01, Pp 025-028 (2013)
Abstract An infant with pancytopenia was born to a mother who used the common immunosuppressant azathioprine (AZA). Maternal and neonatal blood levels of 6-thioguanine nucleotides (6TGN; metabolite of AZA) were 1890 and 1480 pmol/8 × 108 red blood c
Externí odkaz:
https://doaj.org/article/b133f054367e4f8bb44959de5acb5a8c
Autor:
Hidehiko Maruyama, Yoko Shinno, Kaori Fujiwara, Akie Nakamura, Toshihiro Tajima, Makoto Nakamura, Misao Kageyama
Publikováno v:
American Journal of Perinatology Reports, Vol 03, Iss 01, Pp 021-024 (2013)
Abstract Neonatal Bartter syndrome (NBS) is an inherited renal tubular disorder associated with hypokalemic alkalosis. Here we report a case of genetically diagnosed NBS. Polyhydramnios was noted at 26 weeks. A boy was born at 31 weeks and 1 day, wei
Externí odkaz:
https://doaj.org/article/8ee7011e618a434b87972a5b22fb9cc0
Autor:
Hidehiko Maruyama, Takeshi Inagaki, Yusei Nakata, Akane Kanazawa, Yuka Iwasaki, Kiyoshi Sasaki, Ryuhei Nagai, Hiromi Kinoshita, Jun Iwata, Kiyoshi Kikkawa
Publikováno v:
American Journal of Perinatology Reports, Vol 05, Iss 02, Pp e124-e128 (2015)
Abstract Introduction This report will discuss a case of minimally conjoined omphalopagus twins (MCOTs) with a body stalk anomaly (BSA). Case Report We experienced monochorionic diamniotic (MD) twins born at 31 weeks. One infant was suspicious of
Externí odkaz:
https://doaj.org/article/fce7cb782d3f492086a9cdc990de4ad3
Autor:
Hidehiko Maruyama, Naohiro Yonemoto, Yumi Kono, Satoshi Kusuda, Masanori Fujimura, Neonatal Research Network of Japan
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0139014 (2015)
This study aimed to assess whether weight growth velocity (WGV) predicts neurodevelopmental outcomes in extremely low birth weight infants (ELBWIs).Subjects were infants who weighed 501-1000 g at birth and were included in the cohort of the Neonatal
Externí odkaz:
https://doaj.org/article/e747a95d184c4d2184767d00f759564a