Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Noboru Shiroma"'
Autor:
Kiyotake Hirayama, Yoshinori Izumikawa, Yoshinobu Goya, Kenji Naritomi, M. Gushiken, Noboru Shiroma
Publikováno v:
Clinical Genetics. 35:293-298
A girl with partial trisomy 9q is reported. She was characterized by dolichomorphism, abnormalities of the digits, a cardiac defect and craniofacial dysmorphism. A high-resolution analysis revealed the karyotype to be: 46,XX,-3,+ der(3)t(3;9)(q29;q13
Autor:
Katsuhiko Noguchi, Matao Sakanashi, Toshihiro Matsuzaki, Noboru Shiroma, Yoshihiko Ojiri, Mayuko Sakanashi
Publikováno v:
Clinical and Experimental Pharmacology and Physiology. 29:53-59
SUMMARY 1. Responses of splenic diameter measured by sonomicrometry to α- and β-adrenoceptor stimulants were estimated together with simultaneously measured systemic arterial and splenic venous concentrations of red blood cells (RBC), white blood c
Publikováno v:
British Journal of Pharmacology. 118:941-950
1. Platelet-activating factor (PAF) is a phospholipid mediator with potent cardiovascular and haematological actions. But its mechanisms of action in vivo have not been fully elucidated, probably due to difficulties arising from previous findings tha
Autor:
Toshihiro Matsuzaki, Yoshihiko Ojiri, Noboru Shiroma, Katsuhiko Noguchi, Matao Sakanashi, Kiyotake Hirayama
Publikováno v:
Toxicon : official journal of the International Society on Toxinology. 32(10)
This study was designed to examine haemodynamic and haematologic effects of the crown-of-thorns starfish venom ( Acanthaster planci venom: APV) in dogs. Severe systemic hypotension, thrombocytopenia and leukopenia were induced by APV (1.0 mg protein/
Publikováno v:
American journal of medical genetics. 49(3)
We present a 6-month-old boy with agenesis of the corpus callosum, hypertonicity, severe growth and psychomotor retardation, microcephaly, large prominent ears, and delayed bone age. Similarity of his manifestations to these in 3 sibs described by da
Publikováno v:
The Japanese journal of human genetics. 38(3)
A 3-year-old boy with Costello syndrome is reported. He had typical clinical features of the syndrome including severe postnatal growth retardation, poor sucking, mild developmental delay, a coarse characteristic facies, thick and loose skin of the h
Publikováno v:
Japanese Journal of Pharmacology. 64:192
Autor:
K. Sameshima, Kenji Naritomi, S. Ohdo, Yoshinori Izumikawa, Kiyotake Hirayama, Noboru Shiroma
Publikováno v:
Clinical genetics. 33(5)
A 1-year-old girl with an interstitial deletion of the long arm of chromosome 16 is reported. She was characterized by a distinct craniofacial dysmorphism, meningoencephalocele, mild hydrocephalus, short neck, broad great toes and abnormally position