๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Three families with hereditary hemolytic anemia and pyrimidine 5/-nucleotidase deficiency: electrophoretic and kinetic studies

โœ Scribed by Hirono Akira; Fujii Hisaichi; Miyajima Hidetoshi; Kawakatsu Takeo; Hiyoshi Yasuhiko; Miwa Shiro


Book ID
115824259
Publisher
Elsevier Science
Year
1983
Tongue
English
Weight
543 KB
Volume
130
Category
Article
ISSN
0009-8981

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Three cases of hereditary hemolytic anem
โœ Shiro Miwa; Koji Nakashima; Hisaichi Fujii; Minoru Matsumoto; Koichiro Nomura ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› Springer ๐ŸŒ English โš– 174 KB

## Introduction. Erythrocyte pyrimidine 5'-nucleotidase (5"ribonucleotide phosphohydrolase EC 3.1.3.5, P5N) deficiency associated with hereditary nonspherocytic hemolytic anemia was first described by Valentine et al. (1974). We now report three female cases with this deficiency found in a Japanes

Electrophoretic and kinetic studies of h
โœ Raymonde Rosa; Henri Rochant; Bernard Dreyfus; Colette Valentin; Jean Rosa ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› Springer ๐ŸŒ English โš– 418 KB

A new case of a defect in red cell pyrimidine 5'-nucleotide (P5N) activity was found in a large family from Guadeloupe in the West Indies. The propositus presented a characteristic hemolytic anemia with red cell basophilic stippling, an increased GSH level, and a shift of the peak in absorbance of n

Kinetic and electrophoretic studies of h
โœ Kenji Shinohara; Kouichi R. Tanaka ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› Springer ๐ŸŒ English โš– 292 KB

The mutant enzyme of a patient with hereditary pyrimidine 5'-nucleotidase deficiency was analyzed biochemically. Partially purified by DEAE-Sephadex and concentrated by ultrafiltration, the enzyme had a high Km for the substrate uridine monophosphate. Utilization of the substrate cytidine monophosph

Glucose phosphate isomerase deficiency w
โœ Vives-Corrons, J. L. ;Rozman, C. ;Kahn, A. ;Carrera, A. ;Triginer, J. ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› Springer-Verlag โš– 348 KB

A new case of glucose phosphate isomerase deficiency associated with cogenital nonspherocytic hemolytic anemia is described in a 12-year-old girl of Spanish origin. The parents exhibited erythrocyte glucose phosphate isomerase activity between 50 and 60% of normal. The enzyme of the propositus had n