T. L. Oei

Radboud University Nijmegen — Netherlands

Biochemistry, Genetics and Molecular Biology · Life Sciences

14h-index550citations45works0.02yr avg
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Research Topics

Biochemical and Molecular Research(29), Cytomegalovirus and herpesvirus research(15), Adenosine and Purinergic Signaling(9), Metabolism and Genetic Disorders(7), Porphyrin Metabolism and Disorders(5)

Publications45 total

The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK
Human Genetics·1988· 63 cited
Myoadenylate deaminase deficiency: A clinical, genetic, and biochemical study in nine families
Muscle & Nerve·1988· 32 cited
Effect of Yag-laser anterior capsulotomy on the biochemical content of aqueous humor.
PubMed·1988
AMP deaminase deficiency: Study of the human skeletal muscle purine metabolism during ischaemic isometric exercise
Clinical Science·1987· 32 cited
Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine
Clinical Science·1986· 20 cited
The relation between blood lactate and ammonia in ischemic handgrip exercise
Muscle & Nerve·1985· 29 cited
Clinical chemistry and the diagnosis of muscular disease; the ischemic forearm excercise test
Clinical Neurology and Neurosurgery·1984· 2 cited
Myoadenylate Deaminase Deficiency: An Enzyme Defect in Search of a Disease
Advances in experimental medicine and biology·1984· 9 cited
Hypoxanthine and inosine release induced by ischemic forearm exercise in McArdle's disease and myoadenylate deaminase deficiency
Clinical Neurology and Neurosurgery·1984
The influence of bilirubin, alcohol and certain drugs on the kinetics of 99mTC-diethyl IDA (EHIDA) in humans
European Journal of Nuclear Medicine and Molecular Imaging·1983· 14 cited
Heterozygote detection in Fabry's disease using mailed hair roots
British Journal of Dermatology·1980· 8 cited
Phosphoribosylpyrophosphate and enzymes of purine metabolism in erythrocytes from young hyperuricemic males
Biochemical Medicine·1980· 4 cited
Adenosine Deaminase and Purine Nucleoside Phosphorylase Activities during Culturing of Fibrolasts
Advances in experimental medicine and biology·1980
Heterozygote detection in glucose‐6‐phosphate dehydrogenase deficiency: limitation of hair follicle analysis
Clinical Genetics·1979· 4 cited
INBORN ERRORS OF METABOLISM: SCREENING FOR HETEROZYGOTES USING HAIR ROOTS
British Journal of Dermatology·1979· 7 cited
Glucose-6-phosphate Dehydrogenase Deficiency: Biochemical and Histochemical Studies on Hair Roots for Carrier Detection
Clinical Chemistry and Laboratory Medicine (CCLM)·1979· 7 citedOpen Access
Molecular and tissue-specific heterogeneity in HPRT deficiency
Biochemical Genetics·1978· 11 cited
Fluctuating adenosine deaminase activities in cultured fibroblasts
Biochemical Medicine·1978· 11 cited
Fabry's disease: biochemical and histochemical studies on hair roots for carrier detection
British Journal of Dermatology·1978· 17 cited
A new ultramicrochemical assay for purine nucleoside phosphorylase
Analytical Biochemistry·1978· 15 cited
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Frequent Co-authors

C. H. M. M. de Bruyn(30), P. Hösli(10), Coen A. M. van Bennekom(8), M.P. Uitendaal(8), E.M.G. Joosten(6), Ron A. Wevers(6), S. P. T. Sinkeler(5), R. A. Binkhorst(5), A.J.M. Vermorken(5), Frank Oerlemans(4), M. Coerwinkel(3), R. A. Geerdink(3), G. Th. Spierenburg(3), S.J. Geerts(3), Peter Wirtz(2), J.M. Coenegracht(2), J. M. F. Trijbels(2), Annette Wensing(2), Han G. Brunner(1), Cor A. van Bennekom(1)