Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Yosuke Ichihashi"'
Autor:
Miho Iida, Hiroshi Asanuma, Yoshifumi Kasuga, Mariko Hida, Daigo Ochiai, Mamoru Tanaka, Toyohide Endo, Satoru Ikenoue, Tomohiro Ishii, Yosuke Ichihashi, Tomonobu Hasegawa, Takeshi Sato, Maki Oishi
Publikováno v:
Placenta. 130:53-59
Little is known about the association between hypospadias and small fetuses, as well as the pathological implications of fetal growth restriction (FGR). Thus, we aimed to investigate the association between hypospadias and small fetuses using a datab
Autor:
Yosuke Ichihashi, Satoshi Narumi, Naoki Umehara, Miwa Ozawa, Takeshi Sato, Tomonobu Hasegawa, Taiki Nozaki, Naoki Kanomata, Daisuke Hasegawa, Keigo Yada, S. Eguchi, Rintaro Ono
Publikováno v:
Medicine
Rationale: Paraganglioma (PGL), an extra-adrenal pheochromocytoma, is a rare tumor, especially in children. While hypersecretion of catecholamines causes the classic triad of headaches, palpitations, and profuse sweating, prompt diagnosis is still ch
Publikováno v:
Clinical Pediatric Endocrinology
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 64(1)
Autor:
Takeshi Sato, Tomohiro Ishii, Yu Yamaguchi, Yosuke Ichihashi, Daigo Ochiai, Hiroshi Asanuma, Tatsuo Kuroda, Tomonobu Hasegawa
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Frontiers in Pediatrics
Frontiers in Pediatrics
The occurrence of fetuses suspected of having ambiguous genitalia will likely increase in the future. Currently, the impact of prenatal genetic counseling on parents' understanding and psychological preparedness has not been addressed. We provided pr
Autor:
Gen Nishimura, Masaki Takagi, Tomonobu Hasegawa, Tomohiro Ishii, Yosuke Ichihashi, Kenji Watanabe
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 5, Iss 1, Pp 1-3 (2018)
Human Genome Variation, Vol 5, Iss 1, Pp 1-3 (2018)
Mutations in the cartilage oligomeric matrix protein (COMP) gene cause both pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED). Most mutations in COMP are located in the region encoding type 3 thrombospondin like domain (TSP3D). We
Publikováno v:
Global Pediatric Health
Global Pediatric Health, Vol 4 (2017)
Global Pediatric Health, Vol 4 (2017)
Child abuse is a major public health and social welfare problem in Western high-income countries such as the United Kingdom, the United States, Canada, and Australia. Also in Japan, recently, the number of child abuse cases reported to child guidance
Autor:
Yu Sato, Tadashi Matsumoto, Mamoru Tanaka, Toshimi Michigami, Yosuke Ichihashi, Yoshifumi Kasuga, Tomonobu Hasegawa, Kanako Tachikawa, Satoru Ikenoue, Tomohiro Ishii, Kei Miyakoshi, Gen Nishimura, Kazushige Ikeda, Daigo Ochiai, Yohei Akiba, Toshimitsu Otani, Yohei Matsuzaki
Publikováno v:
American journal of medical genetics. Part A. 176(1)
Hypophosphatasia (HPP) is an autosomal recessive metabolic disorder with impaired bone mineralization due to mutations in the ALPL gene. The genotype-phenotype correlation of this disorder has been widely described. Here, we present two affected sibl
Autor:
Yasuaki Kobayashi, Takahiro Tominaga, Yosuke Ichihashi, Takeshi Sato, Midori Awazu, Naoko Amano
Publikováno v:
CEN case reports. 6(1)
Type IV renal tubular acidosis is known to occur in obstructive uropathy with urinary tract infection. Fanconi syndrome, however, has not been described in these settings. We report two preterm infants who developed Fanconi syndrome associated with h
Autor:
Masatoshi Kohga, Yosuke Ichihashi
Publikováno v:
Pediatrics International. 14:17-17