Search Results - "Schretlen, E D"

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    Morphology and incidence of the "posttherapeutic lymphoid cell" in the bone marrow of children with acute lymphoblastic leukemia by Schuurmans Stekhoven, JH, Langenhuysen, CA, Bakkeren, JA, Holland, R, Holler, I, De Vaan, GA, Schretlen, ED

    Published in The American journal of pathology (01-07-1986)
    “…In the posttherapeutic bone marrow of a group of 30 children with acute lymphoblastic leukemia (ALL), small numbers of a particular lymphoid cell with a…”
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    6-Mercaptopurine: high-dose 24-h infusions in goats by SCHOUTEN, T. J, DE ABREU, R. A, SCHRETLEN, E. D. A. M, VANBAAL, J. M, VAN LEEUWEN, M. B, DEVAAN, G. A. M

    “…In vitro investigations have indicated the need for both prolonged exposure to 6-mercaptopurine (6MP) and the use of high concentrations to achieve maximal…”
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    Citrullinaemia with Rapidly Fatal Neonatal Course by Van Der Zee, S. P. M., Trijbels, J. M. F., Monnens, L. A. H., Hommes, F. A., Schretlen, E. D. A. M.

    Published in Archives of disease in childhood (01-12-1971)
    “…An infant with a deficiency of argininosuccinate synthetase in liver and brain developed rapidly increasing apathy, respiratory insufficiency, and convulsions…”
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    6-Mercaptopurine: total body autoradiograms and plasma concentration-time curves of 6MP and metabolites from marmoset monkeys by Schouten, T J, De Abreu, R A, Schretlen, E D, de Vaan, G A, van der Kleijn, E

    Published in Pediatric hematology and oncology (1986)
    “…To study the body distribution of 6-mercaptopurine (6MP), [8-14C]6MP was given by infusion to 2 marmoset monkeys at a dose rate of 5 mg/kg body weight/h for 1…”
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    Effects of methotrexate on purine and pyrimidine metabolism and cell-kinetic parameters in human malignant lymphoblasts of different lineages by Bökkerink, J P, De Abreu, R A, Bakker, M A, Hulscher, T W, van Baal, J M, Schretlen, E D, De Bruijn, C H

    Published in Biochemical pharmacology (15-06-1988)
    “…MOLT-4 (T-), RAJI (B-), and KM-3 (non-B-non-T-, common ALL) malignant lymphoblasts demonstrated significant differences in their activities of purine de novo…”
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    Sideroblastic anaemia. A review of seven paediatric cases by Hamel, B C, Schretlen, E D

    Published in European journal of pediatrics (01-03-1982)
    “…Sideroblastic Anaemias are characterised by a) chronic hypochromic anemia, b) ringed sideroblasts in the bone marrow, c) an increase in total body iron, d)…”
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    Purine metabolism in childhood acute lymphoblastic leukemia: biochemical markers for diagnosis and chemotherapy by van Laarhoven, J P, Spierenburg, G T, Bakkeren, J A, Schouten, T J, De Bruyn, C H, Geerts, S J, Schretlen, E D

    Published in Leukemia research (1983)
    “…Adenosine deaminase (ADA), purine nucleoside phosphorylase (PNP), 5'nucleotidase (5'NT), ecto-5'NT, hypoxanthine-guanine phosphoribosyltransferase(HGPRT),…”
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    Haemolytic-uraemic syndrome. Epidemiological and clinical study by van Wieringen, P M, Monnens, L A, Schretlen, E D

    Published in Archives of disease in childhood (01-06-1974)
    “…Between January 1965 and December 1970, 212 patients with the haemolytic-uraemic syndrome in the Netherlands were analysed in an epidemiological and clinical…”
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    6-thioguanine: high-dose 2-H infusions in goats by SCHOUTEN, T. J, DE ABREU, R. A, SCHRETLEN, E. D. A. M, VAN LEEUWEN, M. B, VAN BAAL, J. M, DE VAAN, G. A. M

    “…6-Thioguanine (6TG) is poorly absorbed after oral administration. Bolus injections of 6TG result in high peak concentrations with relatively short-lived plasma…”
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    Haemolytic-uraemic syndrome by van Wieringen, P. M. V., Monnens, L. A. H., Schretlen, E. D. A. M.

    Published in Archives of disease in childhood (01-06-1974)
    “…Between January 1965 and December 1970, 212 patients with the haemolytic-uraemic syndrome in the Netherlands were analysed in an epidemiological and clinical…”
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    Glucosephosphate isomerase deficiency, a new variant in a Dutch family. Case report by Rotteveel, J J, de Vaan, G A, Staal, G E, van Biervliet, J P, Schretlen, E D

    Published in European journal of pediatrics (26-04-1977)
    “…The clinical course and the biochemical findings are reported from a patient suffering from glucosephosphate isomerase (G.P.I EC 5.3.1.9) deficiency type…”
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