Zobrazeno 1 - 10
of 53
pro vyhledávání: '"S. K. Wadman"'
Autor:
S. K. Wadman, H. J. Backer
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 68:595-603
Une nouvelle synthese, au moyen de la reaction de la p-nitrophenyl-sulfonylcyanamide sur des amines aromatiques, au sein d'acide acetique, nous rend aisement accessibles les aryl-p-nitrophenylsulfonylguanidines, dont la decomposition, en solution alc
Publikováno v:
Neuropediatrics. 20:3-11
Kinetics of catecholamine biosynthesis and metabolism have been examined in patients with hereditary progressive dystonia with marked diurnal fluctuation of symptoms (HPD, Segawa's disease). Three patients and a healthy control received an oral load
Publikováno v:
The Journal of Immunology. 132:2311-2317
The effect of deoxyguanosine on mitogen- and antigen-induced proliferation of peripheral blood lymphocytes from healthy donors was studied. Deoxyguanosine was found to inhibit the proliferative response to mitogens and antigens. Concentrations of deo
Autor:
S. K. Wadman, J. H. P. Jonxis
Publikováno v:
Nature. 169:884-886
THE existence of two forms of haemoglobin is well known. The fœtal form is found in the fœtus and in the new-born mammal, the other occurring in the older individual. It is remarkable that whereas the character of the haemoglobin depends on genetic
Publikováno v:
Advances in experimental medicine and biology.
Publikováno v:
Journal of inherited metabolic disease. 7(2)
Publikováno v:
Ciba Foundation symposium. 87
More than twenty-five inherited organic acidurias have been identified during the last fifteen years. This remarkable development is due mainly to the introduction of gas chromatography, and gas chromatography combined with mass spectrometry, in paed
Publikováno v:
The Netherlands journal of medicine. 21(1)
Autor:
M. Duran, S. K. Wadman
Publikováno v:
Inherited Disorders of Vitamins and Cofactors ISBN: 9789401180214
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd8e53da4c457381d154d2ce73127dea
https://doi.org/10.1007/978-94-011-8019-1_13
https://doi.org/10.1007/978-94-011-8019-1_13
Publikováno v:
Archives francaises de pediatrie. 34(4)
The absence of aryl sulphatase B (Maroteaux-Lamy syndrome) has been confirmed in a five month old child. The estimation of urine mucopolysaccharides and enzyme studies on cultured fibroblasts were performed at an early stage.