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F J van Sprang

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Nederlands Tijdschrift Voor Geneeskunde|December 4, 1982
[Clinico-chemical diagnosis of hereditary metabolic disorders]S K Wadman, F J van Sprang, M Duran
Nederlands Tijdschrift Voor Geneeskunde|January 12, 1985
[Undetected phenylketonuria in a family]H J Dijkhuis, F J van Sprang, S K Wadman
Nederlands Tijdschrift Voor Geneeskunde|May 29, 1976
[Tyrosinosis]H D Bakker, F J van Sprang, S K Wadman
Journal of Inherited Metabolic Disease|January 1, 1986
A patient with sarcosinaemiaF J van Sprang, M Duran, H G Scholten, et al.
Pediatrics|May 1, 1974
Letter: Possible hazards of neomycin treatment in methylmalonic acidemiaM Duran, H D Bakker, S K Wadman, et al.
Lancet (London, England)|May 28, 1977
Low serum-tyrosine in patients with phenylketonuria on dietary treatmentM Brouwer, P K de Bree, F J van Sprang, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Novel storage products in human beta-mannosidosisC H Hokke, M Duran, L Dorland, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1974
Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis"H D Bakker, P K de Bree, F J van Sprang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 27, 1973
Dietary correction of histidinemia in older children possibleS K Wadman, P K de Bree, J P van Biervliet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 1, 1971
Automatic column chromatographic analysis of urinary and serum imidazoles in patients with histidinaemia and normalsS K Wadman, P K De Bree, C Van der Heiden, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Nederlands Tijdschrift Voor Geneeskunde|December 4, 1982
[Clinico-chemical diagnosis of hereditary metabolic disorders]S K Wadman, F J van Sprang, M Duran
Nederlands Tijdschrift Voor Geneeskunde|January 12, 1985
[Undetected phenylketonuria in a family]H J Dijkhuis, F J van Sprang, S K Wadman
Nederlands Tijdschrift Voor Geneeskunde|May 29, 1976
[Tyrosinosis]H D Bakker, F J van Sprang, S K Wadman
Journal of Inherited Metabolic Disease|January 1, 1986
A patient with sarcosinaemiaF J van Sprang, M Duran, H G Scholten, et al.
Pediatrics|May 1, 1974
Letter: Possible hazards of neomycin treatment in methylmalonic acidemiaM Duran, H D Bakker, S K Wadman, et al.
Lancet (London, England)|May 28, 1977
Low serum-tyrosine in patients with phenylketonuria on dietary treatmentM Brouwer, P K de Bree, F J van Sprang, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Novel storage products in human beta-mannosidosisC H Hokke, M Duran, L Dorland, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1974
Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis"H D Bakker, P K de Bree, F J van Sprang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 27, 1973
Dietary correction of histidinemia in older children possibleS K Wadman, P K de Bree, J P van Biervliet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 1, 1971
Automatic column chromatographic analysis of urinary and serum imidazoles in patients with histidinaemia and normalsS K Wadman, P K De Bree, C Van der Heiden, et al.
Pageof 3