摘要:

SummaryWith respect to 4 cases of Waldenström’s macroglobulinemia, the main problems of the disease are reviewed.Biological, cytological and histological documents illustrate the observations.The modern technics for proteins exploration are exposed, and unusual chromosomial abnormalities are commented.

ISSN:1784-3286    

DOI:10.1080/17843286.1968.11716670

出版商:Taylor&Francis    

年代:1968

数据来源: Taylor

摘要:

SummaryRubella vaccine, prepared with the attenuated strain Cendehill 51, was injected to 33 children and 5 adults belonging to a closed community. Seroconversions were obtained in all children (21) who did not possess any antibody before vaccination, as detected by the inhibition of hemagglutination test. Among the 17 individuals who possessed a residual level of antibodies, due to previous natural immunization, 7 showed a rise in antibody titre following vaccination.

ISSN:1784-3286    

DOI:10.1080/17843286.1968.11716671

出版商:Taylor&Francis    

年代:1968

数据来源: Taylor

摘要:

SummaryThe effect of a new piperazine derivative, piposulfan or Ancyte, was studied in 21 patients suffering from leukemias and malignant lymphomas and in 51 patients with solid tumors.Remissions were observed in about 50 % of the cases of Hodgkin’s disease, effects also were observed in polycythemia vera and in chronic myeloid leukemia.A remission of 15 months was obtained in one case of breast cancer resistant to androgens and estrogens.Other cases did not respond to treatment.Blood toxicity was moderate and, in most cases, reversible. The mean daily dose should not exceed 140 mg.

ISSN:1784-3286    

DOI:10.1080/17843286.1968.11716672

出版商:Taylor&Francis    

年代:1968

数据来源: Taylor

摘要:

SummaryThe authors relate their experience of 36 cases of porphyria : 14 cases of acute intermittent porphyria, 4 cases of mixed porphyria and 18 cases of pure cutaneous porphyria. They review the main clinical, biochemical and biological characteristics of these groups of patients. The factors inducing porphyria and the evolution of the disease are also discussed. Two unusual forms of porphyria are presented in the group of pure cutaneous porphyria : a melanodermic form and a sclerodermic form with mutilations. Reflections on the biochemical diagnosis of the different forms of porphyrias, on the main causes of error in the detection of porphobilinogen by the Watson-Schwartz reaction and a survey of the different possibilities of therapy end this review of clinical cases.

ISSN:1784-3286    

DOI:10.1080/17843286.1968.11716673

出版商:Taylor&Francis    

年代:1968

数据来源: Taylor

ISSN:1784-3286    

DOI:10.1080/17843286.1968.11716674

出版商:Taylor&Francis    

年代:1968

数据来源: Taylor