Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Muneyuki Tanabu"'
Publikováno v:
Pediatrics International. 55:e67-e69
Skin hamartoma is an extremely rare disease on the hand in newborn infants. Reported herein is the case of a newborn infant who presented with a skin hamartoma on the hand. The patient was a girl born at 37 weeks of gestational age. The mass was seen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7aca60df29105ae4f2da0184e2509ce2
https://doi.org/10.1111/ped.12021
https://doi.org/10.1111/ped.12021
Autor:
Akimune, Kaga, Chieko, Itabashi, Susumu, Kanda, Yutaka, Suzuki, Muneyuki, Tanabu, Shigeo, Kure
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 55(3)
Skin hamartoma is an extremely rare disease on the hand in newborn infants. Reported herein is the case of a newborn infant who presented with a skin hamartoma on the hand. The patient was a girl born at 37 weeks of gestational age. The mass was seen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::21e2416ad668647213d1feb2fa1b16d5
https://pubmed.ncbi.nlm.nih.gov/23782383
https://pubmed.ncbi.nlm.nih.gov/23782383
Autor:
Mamiko Ishitobi, Akira Ohnuma, Kazuhiro Haginoya, Yajuan Zhao, Kazuie Iinuma, Masahiro Kikuchi, Jun Minato, Muneyuki Tanabu, Toshiro Yanagisawa
Publikováno v:
Neuroreport. 11(18)
The progression of muscular weakness of patients suffering from muscular dystrophies directly correlates with the progressive loss of myofibers, accompanied by fibrosis. Since transforming growth factor beta1 (TGF-beta1) promotes tissue fibrosis, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::486e902ea045c0fd8ec79426dda4c042
https://pubmed.ncbi.nlm.nih.gov/11192624
https://pubmed.ncbi.nlm.nih.gov/11192624
Publikováno v:
BMC Research Notes; 2012, Vol. 5 Issue 1, p481-484, 4p, 3 Black and White Photographs
Publikováno v:
The Tohoku Journal of Experimental Medicine. 116:53-55
In a hypouricemic and mentally retarded infant due to a defect of 5-phosphoribosylpyrophosphate synthetase, electroencephalograms were recorded at the age of 4, 7, 10 and 11 months. Hypsarrhythmia was first observed at the age of 10 months, and marke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5290b07b349d867818248d23e4c9aad0
https://doi.org/10.1620/tjem.116.53
https://doi.org/10.1620/tjem.116.53
Autor:
Toshio Yoshida, Tsuneo Arakawa, Yozo Yoshimura, Yoshiro Wada, Yasuhiro Nishimura, Muneyuki Tanabu, Kazuie Iinuma
Publikováno v:
The Tohoku journal of experimental medicine. 113(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::626da0b12c2721050348f8a39c551658
https://pubmed.ncbi.nlm.nih.gov/4373874
https://pubmed.ncbi.nlm.nih.gov/4373874
Publikováno v:
The Tohoku journal of experimental medicine. 112(2)
Out of 49 epileptic children treated with diphenylhydantoin and phenobarbital there were 36 cases with poor or partial control of seizures, among whom 20 cases had serum diphenylhydantoin levels below 5 γ/ml and 8 cases had serum phenobarbital level
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a39c896b392f2d3a711a16aa3ca85d48
https://pubmed.ncbi.nlm.nih.gov/4836029
https://pubmed.ncbi.nlm.nih.gov/4836029
Publikováno v:
The Tohoku journal of experimental medicine. 112(2)
In six epileptic children who had been treated with diphenylhydantoin, phenobarbital, and/or mysoline, a decrease in serum diphenylydantoin levels was found in five cases on the 23 rd to 35 th day of withdrawal of phenobarbital and mysoline, among wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be74862341689223170a7f258df00c21
https://pubmed.ncbi.nlm.nih.gov/4836028
https://pubmed.ncbi.nlm.nih.gov/4836028
Autor:
Yutaka Suzuki, Muneyuki Tanabu, Takuma Matsuki, Yo-hei Watanabe, Susumu Kanda, Akimune Kaga, Sachiko Saito, Yukimune Ohkubo, Shigeo Kure, Haruo Usuda
Publikováno v:
BMC Research Notes
Background Uridine diphosphate-glucuronosyltransferase (UGT) gene family is involved in the detoxification of biomaterials and drugs in the liver. Among the UGT gene family members, only UGT1A1 is involved in bilirubin conjugation. As a result, defic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94b32426c812b39f11ad65b35e42368e
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 5, Iss 1, p 481 (2012)
BMC Research Notes, Vol 5, Iss 1, p 481 (2012)
Background Intestinal malrotation is an incomplete rotation of the intestine. Failure to rotate leads to abnormalities in intestinal positioning and attachment that leave obstructing bands across the duodenum and a narrow pedicle for the midgut loop,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46cbc8ab6255f3d1c6b14ebf3735cb82