Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Shinobu, Higami"'
Autor:
Masahide, Minoda, Masaharu, Nishikawa, Shougo, Murata, Kensuke, Nakamura, Kazuhiro, Okahara, Takeshi, Okahara, Tamaki, Fujita, Yoshitane, Tamai, Shinobu, Higami
Publikováno v:
Gan to kagaku ryoho. Cancerchemotherapy. 35(8)
There is a growing need for home medicine in our graying society. New efforts are thus required to provide better treatment in the home. The Sakai Medical Association has established a new medical information system which uses the internet to increas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::08481048d7b9c9ed36c1b31d8cf39412
https://pubmed.ncbi.nlm.nih.gov/18701847
https://pubmed.ncbi.nlm.nih.gov/18701847
Autor:
Gen Isshiki, Tomoyuki Kawamura, Tsuneo Tsuruhara, Shinobu Higami, Kayo Nishimoto, Akira Ookita
Publikováno v:
Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases. 72(3)
An outbreak of Escherichia coli O157:H7 infection occurred in July 1996 in Sakai City. About 5000 children were infected, 122 of whom developed hemolytic uremic syndrome (HUS). In this outbreak, almost all patients were administrated some type of ant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83d2806bcf50857bacbed3b717a609af
https://pubmed.ncbi.nlm.nih.gov/9643979
https://pubmed.ncbi.nlm.nih.gov/9643979
Autor:
Kiyoshi Omura, Nobuko Yamanaka, Shinobu Higami, Osamu Matsuoka, Akie Fujimoto, Gen Issiki, Keiya Tada
Publikováno v:
Pediatrics. 57:102-105
A 21-month-old girl with physical and mental retardation is described. She excreted an increased amount of lysine in urine but no excessive quantities of arginine, ornithine, or cystine. Serum level of lysine was found to be low but the levels of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfbe416b08b66f8407b263d3706bf4a6
https://doi.org/10.1542/peds.57.1.102
https://doi.org/10.1542/peds.57.1.102
Publikováno v:
The Tohoku Journal of Experimental Medicine. 111:87-91
Prenatal diagnosis was successfully accomplished by investigating mucopolysaccharide pattern in amniotic fluid for two women who had previously borne children affected with the Hurler syndrome. Amniotic fluid obtained at the 20 th week of gestation f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce9f833bed8f199a3edc362b2de88ee6
https://doi.org/10.1620/tjem.111.87
https://doi.org/10.1620/tjem.111.87
Publikováno v:
European Journal of Pediatrics. 122:103-105
The activity of alpha-L-iduronidase was determined in leukocytes from two patients with the Hurler syndrome, five obligatory heterozygotes, one patient with the Hunter syndrome, and ten normal individuals. It was found that the determination of alpha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5fae3923e35719eb39162af27af3e56
https://doi.org/10.1007/bf00466268
https://doi.org/10.1007/bf00466268
Publikováno v:
Pediatric Cardiology ISBN: 9781461386001
The mucopolysaccharoidoses (MPS) are a group of inherited metabolic disorders characterized by the accumulation of various glycosaminoglycans due to deficiency or absence of the specific lysosomal enzymes. Cardiovascular involvement has been well doc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7adf96c0308c84976f333bee3040d16
https://doi.org/10.1007/978-1-4613-8598-1_275
https://doi.org/10.1007/978-1-4613-8598-1_275
Free amino acid levels in amniotic fluid of fetuses affected with Lowe's syndrome or Phenylketonuria
Publikováno v:
The Tohoku journal of experimental medicine. 113(2)
Amniotic fluid obtained at 34th week of gestation of the fetus, which was proved to be affected with Lowe's syndrome after delivery, revealed elevated levels of most of free amino acids. This suggests a possibility of antenatal diagnosis of Lowe's sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5734da9efe3c8db67b91d9667caa223
https://pubmed.ncbi.nlm.nih.gov/4439401
https://pubmed.ncbi.nlm.nih.gov/4439401
Publikováno v:
British Journal of Dermatology. 104:581-581
SUMMARY A skin biopsy from a 6-year-old girl was examined by electron microscopy and the diagnosis of ceroid-lipofuscinosis (CL) was confirmed. This has not been reported in the dermatology literature, because of the absence of specific skin manifest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1f3da6145dcf8c4938c0d645df05c18
https://doi.org/10.1111/j.1365-2133.1981.tb08176.x
https://doi.org/10.1111/j.1365-2133.1981.tb08176.x