Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
K. E. Niezen-Koning

Veröffentlichungen von K. E. Niezen-Koning zu Niezen-Koning, K. E.. ->
weitere Veröffentlichungen von K. E. Niezen-Koning:
Neutropenia and neutrophil dysfunction in glycogen storage disease type 1c (1998)
Determination of medium chain acyl-CoA dehydrogenase activity in cultured skin fibroblasts using mass spectrometry (1991)
Argininosuccinic Aciduria: Clinical and Biochemical Findings in Three Children with the Late Onset Form, with Special Emphasis on Cerebrospinal Fluid Findings of Amino Acids and Pyrimidines (1993)
A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MS (1992)
Measurement of short-chain acyl-CoA dehydrogenase (SCAD) in cultured skin fibroblasts with hexanoyl-CoA as a competitive inhibitor to eliminate the contribution of medium-chain acyl-CoA dehydrogenase (1994)
The frequency of lysosomal storage diseases in The Netherlands (1999)
A patient with lethal cardiomyopathy and a carnitine — acylcarnitine translocase deficiency (1995)
Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature (1997)
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency (1999)
Veröffentlichungen zu Niezen-Koning, K. E..
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Visser, G., Herwig, J., ... Neutropenia and neutrophil dysfunction in glycogen storage disease type 1c
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (3. 1998), p. 227-231
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
2
Niezen-Koning, K.E., Chapman, T.E., ... Determination of medium chain acyl-CoA dehydrogenase activity in cultured skin fibroblasts using mass spectrometry
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 199, No. 2 (1991), p. 173-184
Zugang: zum Volltext
ähnliche Vorschläge
1991
zeige Details
3
Gerrits, G.P. J. M.. Argininosuccinic Aciduria: Clinical and Biochemical Findings in Three Children with the Late Onset Form, with Special Emphasis on Cerebrospinal Fluid Findings of Amino Acids and...
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 24, No. 01 (2. 1993), p. 15-18
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
4
Niezen-Koning, K.E., Wanders, R.J.A., ... A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MS
in: Biochimica et Biophysica Acta (BBA)/Molecular Basis of Disease, in: Biochimica et Biophysica Acta (BBA)/Molecular Basis of Disease . - Amsterdam : Elsevier, ISSN 0925-4439, ZDB-ID 2209528-7 Vol. 1180, No. 1 (1992), p. 28-32
Zugang: zum Volltext
ähnliche Vorschläge
1992
zeige Details
5
Niezen-Koning, K.E., Wanders, R.J.A., ... Measurement of short-chain acyl-CoA dehydrogenase (SCAD) in cultured skin fibroblasts with hexanoyl-CoA as a competitive inhibitor to eliminate the contribution of medium-chain...
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 229, No. 1-2 (1994), p. 99-106
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
6
Poorthuis, B.J.H.M., Wevers, R.A., ... The frequency of lysosomal storage diseases in The Netherlands
in: Human genetics , ISSN 1432-1203, Vol. 105 (1/2. 1999), p. 151-156
Zugang: zum Volltext
ähnliche Vorschläge
1999
zeige Details
7
Niezen-Koning, K. E., Spronsen, F. J., ... A patient with lethal cardiomyopathy and a carnitine — acylcarnitine translocase deficiency
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 18 (2. 1995), p. 230-232
Zugang: zum Volltext
ähnliche Vorschläge
1995
Copyright: Copyright 1995 Society for the Study of Inborn Errors of Metabolism and Kluwer Academic Publishers mehr
beteiligte Personen: Niezen-Koning, K. E. , Spronsen, F. J. , Ijlst, L. , Wanders, R. J. A. , Brivet, M. , Duran, M. , Reijngoud, D. J. , Heymans, H. S. A. , Smit, G. P. A.
Erschienen: 1995.
Serie: Springer Online Journal Archives 1860-2000 [Dig. Serial]
Schlagwörter:
URL: http://dx.doi.org/10.1007/BF00711775
zeige Details
8
Niezen-Koning, K. E., Wanders, R. J. A., ... Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature
in: European journal of pediatrics , ISSN 1432-1076, Vol. 156 (11. 1997), p. 870-873
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
9
Van Kuilenburg, A. B. P., Vreken, P., ... Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency
in: Human genetics , ISSN 1432-1203, Vol. 104 (1. 1999), p. 1-9
Zugang: zum Volltext
ähnliche Vorschläge
1999