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T. Lian Oei

Observed names: T L OEI, T L Oei, T Li An Oei, T. L. OEI, T. L. Oei, T. L.OEI, T. Oei, T.L. Oei
OpenAlex ID: A5110113495
The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK
1988 · Han G. Brunner, Cor A. van Bennekom, et al. · Human Genetics · 62
Phosphorylase Activity in Leucocytes From Patients With Glycogen-storage Disease
1961 · W.C. Hülsmann, T.L. Oei, et al. · The Lancet · 58
AMP deaminase deficiency: Study of the human skeletal muscle purine metabolism during ischaemic isometric exercise
1987 · S. P. T. Sinkeler, R. A. Binkhorst, et al. · Clinical Science · 34
Myoadenylate deaminase deficiency: A clinical, genetic, and biochemical study in nine families
1988 · Sietze P. T. Sinkeler, M. G. Joosten, et al. · Muscle & Nerve · 32
The relation between blood lactate and ammonia in ischemic handgrip exercise
1985 · Sytze P. T. Sinkeler, Hein A. M. Daanen, et al. · Muscle & Nerve · 29
Studies on hair roots for carrier detection in hypoxanthine‐guanine phosphoribosyl transferase deficiency
1974 · C. H. M. M. de Bruyn, T. L. Oei, et al. · Clinical Genetics · 28
Quantitative radiochemical enzyme assays in single cells: Purine phosphoribosyl transferase activities in cultured fibroblasts
1976 · C.H.M.M. de Bruyn, T.L. Oei, et al. · Biochemical and Biophysical Research Communications · 22
Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine
1986 · S. P. T. Sinkeler, E. M. G. Joosten, et al. · Clinical Science · 20
An atypical case of hypoxanthine‐guanine phosphoribosyltransferase deficiency (Lesch‐Nyhan syndrome)
1973 · R. A. Geerdink, W. H. M. de Vries, et al. · Clinical Genetics · 19
Fabry's disease: biochemical and histochemical studies on hair roots for carrier detection
1978 · A. J. M. VERMORKEN, P. J. J. M. WETERINGS, et al. · British Journal of Dermatology · 17
Hexose monophosphate, pyruvate and lactate In the peripheral blood in glycogen-storage disease Type I
1962 · T.L. Oei · Clinica Chimica Acta · 17
A new ultramicrochemical assay for purine nucleoside phosphorylase
1978 · M.P. Uitendaal, C.H.M.M. de Bruyn, et al. · Analytical Biochemistry · 15
The influence of bilirubin, alcohol and certain drugs on the kinetics of 99mTC-diethyl IDA (EHIDA) in humans
1983 · J. M. Coenegracht, T. L. Oei, et al. · European Journal of Nuclear Medicine and Molecular Imaging · 14
Incorporation of Purine Bases by Intact Red Blood Cells
1977 · C. H. M. M. de Bruyn, T. L. Oei · Advances in experimental medicine and biology · 14
Purine Metabolism in Intact Erythrocytes from Controls and HG-PRT Deficient Individuals
1974 · C. H. M. M. de Bruyn, T. L. Oei · Advances in experimental medicine and biology · 14
An atypical case of hypoxanthine‐guanine phosphoribosyltransferase deficiency (Lesch‐Nyhan syndrome)
1973 · C. H. M. M. DE Bruyn, T. L. Oei, et al. · Clinical Genetics · 14
Molecular and tissue-specific heterogeneity in HPRT deficiency
1978 · M. P. Uitendaal, C. H. M. M. de Bruyn, et al. · Biochemical Genetics · 11
Fluctuating adenosine deaminase activities in cultured fibroblasts
1978 · M.P. Uitendaal, C.H.M.M. de Bruyn, et al. · Biochemical Medicine · 11
Development of a Micro HG-PRT Activity Assay: Preliminary Complementation Studies with Lesch — Nyhan Cell Strains
1974 · P. Hösli, C. H. M. M. de Bruyn, et al. · Advances in experimental medicine and biology · 10
Myoadenylate Deaminase Deficiency: An Enzyme Defect in Search of a Disease
1984 · E. Joosten, C. van Bennekom, et al. · Advances in experimental medicine and biology · 9
Characterisation of Purine Nucleoside Phosphorylase from Fibroblasts Using Ultra-Microchemical Methods
1978 · M.P. Uitendaal, C.H.M.M. de Bruyn, et al. · Human Heredity · 9
Heterozygote detection in Fabry's disease using mailed hair roots
1980 · A.J.M. Vermorken, C.A. van Bennekom, et al. · British Journal of Dermatology · 8
Metabolic cooperation studied by a quantitative enzyme assay of single cells
1976 · M.P. Uitendaal, T.L. Oei, et al. · Biochemical and Biophysical Research Communications · 8
Lesch-Nyhan syndrome: Incorporation of hypoxanthine in stimulated lymphocytes
1973 · C.H.M.M. De Bruyn, T.L. Oei · Experimental Cell Research · 8
Inborn Errors of Metabolism: Screening for Heterozygotes Using Hair Roots
1979 · C.H.M.M. Bruyn, A.J.M. Vermorken, et al. · British Journal of Dermatology · 7
Works count: 47
Citation count: 555
H-index: 14
I10-index: 19
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