Hydrops fetalis associated with red cell pyruvate kinase deficiency

Autor: Hennekam, R. C. M., Beemer, F. A., Cats, B. P., Gerrit Jansen, Staal, G. E. J.

Publikováno v: Hennekam, R C, Beemer, F A, Cats, B P, Jansen, G & Staal, G E 1990, ' Hydrops fetalis associated with red cell pyruvate kinase deficiency ', Genetic Counseling, vol. 1, no. 1, pp. 75-9 .
Genetic Counseling, 1(1), 75-9. Editions Medecine et Hygiene
Scopus-Elsevier
Genetic counseling (Geneva, Switzerland), 1(1), 75-79. Editions Medecine et Hygiene

A hydrops fetalis and multicystic encephalomalacia were diagnosed in a neonate who was one of twins. The co-twin had died 5 weeks prior to delivery. The most likely explantation for both hydrops and multicystic encephalomalacia was fetal anemia cause

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::319776ada713074f54f7c8cc27e00cf9
https://research.vumc.nl/en/publications/02325fff-2475-467d-8dfe-ca00a419a12d

Fucosidosis – I. Clinical and Enzymological Studies.

Autor: Troost, J., Staal, G. E. J., Willemse, J., van der Heijden, M. C. M.

Publikováno v: Neuropädiatrie; 1977, Vol. 8 Issue 2, p155-162, 8p

Neuroectodermal tumors of childhood.

Autor: Beemer, F. A., Staal, G. E. J.

Publikováno v: Ophthalmic Paediatrics & Genetics; 1983, Vol. 3 Issue 2, p117-120, 4p

Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysis.

Autor: Vermorken, A. J. M., Spierenburg, G. Th., Bennekom, C. A. van, Bruyn, C. H. M. M. de, Oei, T. L., Staal, G. E. J., Geerdink, R. A.

Publikováno v: Clinical Genetics; Nov1979, Vol. 16 Issue 5, p353-356, 4p

Tyrosine protein kinase activity in normal and leukaemic human blood cells.

Autor: Punt, C. J. A., Rijksen, G., Vlug, A. M. C., Dekker, A. W., Staal, G. E. J.

Publikováno v: British Journal of Haematology; Sep1989, Vol. 73 Issue 1, p51-56, 6p