B. Wuyts

发表

Reevaluation of formulas for predicting creatinine clearance in adults and children, using compensated creatinine methods.

R. Vanholder, N. Van Den Noortgate, J. Delanghe, 2003, Clinical chemistry.

Molecular and clinical characterization of a Moroccan Cog7 deficient patient.

H. Freeze, B. G. Ng, M. Durán, 2007, Molecular genetics and metabolism.

Methods for a prompt and reliable laboratory diagnosis of Pompe disease: report from an international consensus meeting.

H. Mandel, A. Reuser, D. Bali, 2008, Molecular genetics and metabolism.

Sex Steroids Affect Triglyceride Handling, Glucose-Dependent Insulinotropic Polypeptide, and Insulin Sensitivity

J. Holst, J. Kaufman, L. T. ’t Hart, 2010, Diabetes Care.

Creatine supplementation does not affect kidney function in an animal model with pre-existing renal failure.

J. van de Voorde, N. Lameire, J. Delanghe, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Determination of carbohydrate-deficient transferrin using capillary zone electrophoresis.

H. Neels, J. Delanghe, I. Kasvosve, 2001, Clinical chemistry.

Highly viscous guar gum shifts dietary amino acids from metabolic use to fermentation substrate in domestic cats

L. Vanhaecke, M. Hesta, G. Janssens, 2012, British Journal of Nutrition.

Oligofructose and inulin modulate glucose and amino acid metabolism through propionate production in normal-weight and obese cats

J. Buyse, S. Daminet, M. Hesta, 2009, British Journal of Nutrition.

Novel Haptoglobin Insertion/Deletion Polymorphism Is Associated with the Lipid Profile and C-Reactive Protein (CRP) Concentration

B. Grandchamp, G. Hetet, J. Delanghe, 2002, Clinical chemistry and laboratory medicine.

Citrulline levels in a paediatric age group: does measurement on dried blood spots have additional value?

L. Goossens, G. van Maele, B. Wuyts, 2011, Clinica chimica acta; international journal of clinical chemistry.

Critical sample pretreatment in monitoring dried blood spot citrulline.

L. Goossens, V. Stove, B. Wuyts, 2007, Clinica chimica acta; international journal of clinical chemistry.

The use of dried blood spot samples in the diagnosis of lysosomal storage disorders--current status and perspectives.

W. Hwu, Kate Zhang, Z. Lukacs, 2011, Molecular genetics and metabolism.

Compensating for the influence of total serum protein in the Schwartz formula

V. Stove, J. Walle, M. Speeckaert, 2012, Clinical chemistry and laboratory medicine.

Intestinal fermentation modulates postprandial acylcarnitine profile and nitrogen metabolism in a true carnivore: the domestic cat (Felis catus)

J. Buyse, L. Vanhaecke, S. Daminet, 2010, British Journal of Nutrition.

The Analysis of Carbohydrate-Deficient Transferrin, Marker of Chronic Alcoholism, Using Capillary Electrophoresis

J. Delanghe, B. Wuyts, 2003, Clinical chemistry and laboratory medicine.

Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis population.

R. Vanholder, K. Claes, B. Maes, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Two-tier approach for the detection of alpha-galactosidase A deficiency in kidney transplant recipients.

R. Vanholder, K. Claes, B. Maes, 2008, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Quantitative measurement of ketone bodies in urine using reflectometry

T. Fiers, J. Delanghe, M. Giri, 2005, Clinical chemistry and laboratory medicine.

Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q

G. Dacremont, P. Jorens, N. Van Regenmortel, 2015, Anesthesiology.

Choline supplementation restores substrate balance and alleviates complications of Pcyt2 deficiency.

M. Bakovic, Junzeng Zhang, L. Schenkel, 2015, The Journal of nutritional biochemistry.

Effect of Haptoglobin Phenotypes on Growth of Streptococcus pyogenes

M. Buyzere, G. Claeys, J. Delanghe, 1998, Clinical chemistry and laboratory medicine.

Dietary supplementation of propionylated starch to domestic cats provides propionic acid as gluconeogenic substrate potentially sparing the amino acid valine

L. Vanhaecke, T. Lockett, J. Clarke, 2014, Journal of nutritional science.

Microheterogeneity of serum β-hexosaminidase in chronic alcohol abusers in a driver's license regranting program.

H. Van Vlierberghe, M. D. De Buyzere, J. Delanghe, 2013, Alcoholism, clinical and experimental research.

A new Method for Fast Haptoglobin Phenotyping and Hemoglobin Binding Capacity Calculation Based on Capillary Zone Electrophoresis

M. Buyzere, J. Delanghe, M. Langlois, 2000, Clinical chemistry and laboratory medicine.

Transferrin polymorphism influences iron status in blacks.

J. Delanghe, I. Kasvosve, J. Boelaert, 2000, Clinical chemistry.

Prohepcidin accumulates in renal insufficiency

J. Delanghe, Y. Taes, J. Boelaert, 2004, Clinical chemistry and laboratory medicine.

The impact of metrological traceability on the validity of creatinine measurement as an index of renal function

R. Vanholder, J. Walle, J. Delanghe, 2004 .

Trueness verification of actual creatinine assays in the European market demonstrates a disappointing variability that needs substantial improvement. An international study in the framework of the EC4 creatinine standardization working group

R. Jansen, M. Galteau, M. Panteghini, 2008, Clinical chemistry and laboratory medicine.

Carbohydrate-Deficient Transferrin and Chronic Alcohol Ingestion in Subjects with Transferrin CD-Variants

V. Gordeuk, J. Delanghe, I. Kasvosve, 2001, Clinical chemistry and laboratory medicine.

Performance of Urinary Flow Cytometry in Predicting Outcome of Urine Cultures

M. D. De Buyzere, J. Delanghe, M. Langlois, 2002, Journal of Clinical Microbiology.

Conflicting results between electrophoresis methods of serum M‐proteins

G. Verhoef, N. Blanckaert, X. Bossuyt, 2004, Electrophoresis.

Angiotensin I-converting enzyme insertion/deletion polymorphism: clinical implications.

M. D. De Buyzere, J. Delanghe, B. Wuyts, 1997, Acta clinica Belgica.

Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q

G. Dacremont, P. Jorens, N. Van Regenmortel, 2015, Anesthesiology.

Choline supplementation restores substrate balance and alleviates complications of Pcyt2 deficiency.

M. Bakovic, Junzeng Zhang, L. Schenkel, 2015, The Journal of nutritional biochemistry.