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5 results on '"Schretlen ED"'

1. The IMP dehydrogenase catalysed reaction in erythrocytes of normal individuals and patients with hypoxanthine guanine phosphoribosyltransferase deficiency.

Author

Lommen EJ, de Abreu RA, Trijbels JM, and Schretlen ED

Subjects
Depression, Chemical, Diphosphoglyceric Acids administration & dosage, Dose-Response Relationship, Drug, Humans, Inosine Nucleotides, Ketone Oxidoreductases isolation & purification, Lesch-Nyhan Syndrome blood, Tritium, Diphosphoglyceric Acids pharmacology, Erythrocytes enzymology, Ketone Oxidoreductases blood, Lesch-Nyhan Syndrome enzymology
Published
1974
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2. Concentration of purine nucleotides in erythrocytes of patients with the Lesch-Nyhan syndrome before and during oral administration of adenine.

Author

Lommen EJ, Vogels GD, van der Zee SP, Trijbels JM, and Schretlen ED

Subjects
Chemical Precipitation, Child, Child, Preschool, Hematocrit, Humans, Intellectual Disability blood, Lesch-Nyhan Syndrome blood, Male, Purines biosynthesis, Purines metabolism, Self Mutilation blood, Adenine therapeutic use, Athetosis blood, Erythrocytes analysis, Nucleotides blood, Purine-Pyrimidine Metabolism, Inborn Errors blood
Published
1971
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3. L-asparaginase treatment of acute leukaemia in children.

Author

de Vaan GA, Bakkeren JA, Schretlen ED, and Reerink H

Subjects
Acute Disease, Afibrinogenemia chemically induced, Anaphylaxis chemically induced, Asparaginase adverse effects, Blood Cell Count, Bone Marrow Examination, Child, Child, Preschool, Humans, Asparaginase therapeutic use
Published
1971
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4. A patient with a deficiency of serum-carnosinase activity.

Author

van Heeswijk PJ, Trijbels JM, Schretlen ED, van Munster PJ, and Monnens LA

Subjects
Blood Transfusion, Child, Preschool, Consanguinity, Deficiency Diseases genetics, Deficiency Diseases therapy, Dipeptides blood, Electroencephalography, Humans, Male, Deficiency Diseases complications, Dipeptidases blood, Dipeptides urine, Intellectual Disability complications, Seizures complications
Published
1969
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5. The influence of adenine on the clinical features and purine metabolism in the Lesch-Nyhan syndrome.

Author

van der Zee SP, Lommen EJ, Trijbels JM, and Schretlen ED

Subjects
Allopurinol therapeutic use, Athetosis genetics, Bone Marrow pathology, Carbon Isotopes, Child, Child, Preschool, Chorea genetics, Compulsive Behavior, Diet Therapy, Erythrocytes analysis, Folic Acid therapeutic use, Glycine metabolism, Humans, Intellectual Disability complications, Male, Metabolism, Inborn Errors complications, Movement Disorders complications, Purines biosynthesis, Self Mutilation complications, Transferases blood, Uric Acid urine, Vitamin B 12 therapeutic use, Adenine therapeutic use, Metabolism, Inborn Errors drug therapy, Metabolism, Inborn Errors genetics, Purines metabolism, Uric Acid blood
Published
1970
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