Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Mondo Kuroda"'
Autor:
Yuko Tasaki, Natsumi Inoue, Masaki Shimizu, Naotoshi Sugimoto, Sayaka Ishikawa, Mao Mizuta, Tadafumi Yokoyama, Mondo Kuroda, Kazuhide Ohta, Akihiro Yachie, Taizo Wada
Publikováno v:
Renal Failure, Vol 43, Iss 1, Pp 382-387 (2021)
Background Insulin-like growth factor-binding protein (IGFBP) 2 plays an important role in the regulation of cell adhesion, migration, growth, and apoptosis. This study aimed to investigate the clinical significance of serum IGFBP2 as a biomarker for
Externí odkaz:
https://doaj.org/article/488f71c1825b419594be9940245c659b
Autor:
Shuya Kaneko, Kiyoshi Hatasaki, Kazuyuki Ueno, Shuhei Fujita, Noboru Igarashi, Mondo Kuroda, Taizo Wada
Publikováno v:
Journal of Infection and Chemotherapy. 28:1682-1686
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b794adf823375053230c8c0e6e45a0c
https://doi.org/10.1016/j.jiac.2022.08.027
https://doi.org/10.1016/j.jiac.2022.08.027
Autor:
Tadafumi Yokoyama, Sayaka Ishikawa, Kazuhide Ohta, Yuko Tasaki, Masaki Shimizu, Natsumi Inoue, Mao Mizuta, Taizo Wada, Naotoshi Sugimoto, Mondo Kuroda, Akihiro Yachie
Publikováno v:
Renal Failure, Vol 43, Iss 1, Pp 382-387 (2021)
Renal Failure
article-version (VoR) Version of Record
Renal Failure
article-version (VoR) Version of Record
Background Insulin-like growth factor-binding protein (IGFBP) 2 plays an important role in the regulation of cell adhesion, migration, growth, and apoptosis. This study aimed to investigate the clinical significance of serum IGFBP2 as a biomarker for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2763e2d20e988abfce82e8078572b8c
https://doaj.org/article/488f71c1825b419594be9940245c659b
https://doaj.org/article/488f71c1825b419594be9940245c659b
Publikováno v:
Neuroophthalmology
Recurrent painful ophthalmoplegic neuropathy (RPON) is a rare disorder, which typically occurs in children, and causes headaches and unilateral oculomotor palsy. Early high-dose corticosteroid therapy is recommended to rapidly resolve acute episodes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28ee7840905e83d52fe983755875351f
https://doi.org/10.1080/01658107.2020.1791190
https://doi.org/10.1080/01658107.2020.1791190
Autor:
Toshihiro Fujiki, Ryosei Nishimura, Raita Araki, Mondo Kuroda, Yasuo Tohma, Hironori Fujisawa, Akihiro Yachie
Publikováno v:
Paediatrics and international child health. 42(1)
A subarachnoid pleural fistula - a connection between the pleural cavity and the subarachnoid space - generally presents after trauma or surgery. A 1-year 11-month-old girl without a history of trauma or surgery presented with fatigue, cyanosis and d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::847625628513951783c354d03d8a571c
https://pubmed.ncbi.nlm.nih.gov/35298889
https://pubmed.ncbi.nlm.nih.gov/35298889
Autor:
Akihiro Yachie, Hitoshi Irabu, Masaki Shimizu, Mondo Kuroda, Naotoshi Sugimoto, Maiko Takakura, Natsumi Inoue, Kazuhide Ohta, Hisashi Kaneda
Publikováno v:
Clinical and Experimental Nephrology. 21:1083-1087
To investigate the diagnostic value of serum ferritin levels as a marker of disease activity and the development of encephalopathy in hemolytic uremic syndrome (HUS) induced by enterohemorrhagic Escherichia coli. Twenty patients with HUS were studied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c47f5e421d4d8c99144242fecb90c9e1
https://doi.org/10.1007/s10157-017-1391-z
https://doi.org/10.1007/s10157-017-1391-z
Publikováno v:
Brain and Development. 38:674-677
Background Infantile neuronal ceroid lipofuscinosis (INCL) is an autosomal recessive disorder starting in infancy as early as 12-month-old, caused by PPT1 (palmitoyl-protein thioesterase 1) mutations, and characterized by progressive psychomotor dete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::084395d067b64afa2b7f3a512d7d307d
https://doi.org/10.1016/j.braindev.2016.01.004
https://doi.org/10.1016/j.braindev.2016.01.004
Publikováno v:
Congenital Anomalies. 57:86-88
The Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome (SBBYSS) (MIM# 603736) and genitopatellar syndrome (GPS) (MIM#606170) are allelic diseases caused by KAT6B mutation. Genotype-phenotype correlation is assumed, but a few patients manifes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80859d0b3d5f8f9238761fded594ce7f
https://doi.org/10.1111/cga.12196
https://doi.org/10.1111/cga.12196
Autor:
Natsumi Inoue, Shimpei Yamada, Akihiro Yachie, Mondo Kuroda, Masaki Shimizu, Naotoshi Sugimoto
Publikováno v:
Clinical and experimental nephrology. 23(4)
Interleukin (IL)-33 plays an important role in host defense, immune regulation, and inflammation. This study assessed IL-33’s role in the pathogenesis of severe hemolytic uremic syndrome (HUS) induced by enterohemorrhagic Escherichia coli (EHEC). W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb5f8653c37caa05f6bd9624aa2eaea0
https://pubmed.ncbi.nlm.nih.gov/30467800
https://pubmed.ncbi.nlm.nih.gov/30467800
Publikováno v:
Journal of Paediatrics and Child Health. 55:248-249
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::506d35e80551ec61d3df3e337f56e007
https://doi.org/10.1111/jpc.14343
https://doi.org/10.1111/jpc.14343