J. Bakkeren

发表

Urinary excretion of 2-methyl-2,3-butanediol and 2,3-pentanediol in patients with disorders of propionate and methylmalonate metabolism.

M. Durán, D. Ketting, S. K. Wadman, 1987, Clinica chimica acta; international journal of clinical chemistry.

Specificity of indexes of malnutrition when applied to apparently healthy people: the effect of age.

M. Katan, T. Naber, J. Bakkeren, 1997, The American journal of clinical nutrition.

Screening for microalbuminuria in patients with diabetes mellitus: frozen storage of urine samples decreases their albumin content.

P. V. VAN MUNSTER, L. Elving, M. Jansen, 1989, Clinical chemistry.

The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.

K. Gibson, D. Rabier, E. Christensen, 1997, Pediatrics.

Serum very long chain fatty acid pattern in Zellweger syndrome.

L. Monnens, J. Trijbels, J. Bakkeren, 1984, Clinica chimica acta; international journal of clinical chemistry.

High-performance liquid chromatographic assay for identification and quantitation of nucleotides in lymphocytes and malignant lymphoblasts.

R. D. De Abreu, J. V. van Baal, J. Bakkeren, 1982, Journal of chromatography.

Studies on (Na+-K+)-activated ATPase. XXI. Changes in (Na+-K+)-activated ATPase activity and ouabain-sensitive 86Rb+ uptake rate in regenerating rat liver.

S. L. Bonting, J. Bakkeren, 1968, Biochimica et biophysica acta.

Determination of Kappa and Lambda Light Chains in Serum Immunoglobulins G, A and M

T. D. de Boo, Á. Haraldsson, J. Bakkeren, 1991, Annals of clinical biochemistry.

An accurate and sensitive assay of [14C]octanoate oxidation and its application on tissue homogenates and fibroblasts.

J. Veerkamp, H. V. van Moerkerk, J. Bakkeren, 1986, Biochimica et biophysica acta.

Purine metabolism in childhood acute lymphoblastic leukemia: biochemical markers for diagnosis and chemotherapy.

G. Spierenburg, C. De Bruyn, S. Geerts, 1983, Leukemia research.

High-performance liquid chromatographic determination of purine and pyrimidine bases, ribonucleosides, deoxyribonucleosides and cyclic ribonucleotides in biological fluids.

R. D. De Abreu, J. V. van Baal, C. De Bruyn, 1982, Journal of chromatography.

Immunological studies in the hyper-immunoglobulin D syndrome

Á. Haraldsson, G. Stoelinga, J. Bakkeren, 1992, Journal of Clinical Immunology.

Role of bacteria in the pathogenesis of short bowel syndrome-associated D-lactic acidemia.

A. Naber, W. Sperl, J. Willems, 1997, Microbial pathogenesis.

Immune responses in four patients with Bloom syndrome.

B. T. ter Haar, C. Weemaes, P. V. VAN MUNSTER, 1979, Clinical immunology and immunopathology.

Breakdown of Various Serum Proteins by Periodontal Bacteria

J. S. Hoeven, J. Bakkeren, H. Jansen, 1994 .

Degradation of immunoglobulin G by periodontal bacteria.

J. S. van der Hoeven, J. Bakkeren, P. Camp, 1994, Oral microbiology and immunology.

Immunoglobulin G Cleaving Species in Serum-degrading Consortia of Periodontal Bacteria

J. S. Hoeven, P. F. Steeg, J. Bakkeren, 1989 .

DEFECT IN BILE ACID CONCENTRATING ABILITY OF THE GALLBLADDER IN CONGENITAL CHLORIDE DIARRHOEA

L. Monnens, J. Bakkeren, Cook Os, 1981, Acta paediatrica Scandinavica.

Dihydropyrimidine dehydrogenase deficiency Neurological aspects

F. Gabreëls, R. Sengers, J. Braakhekke, 1987, Journal of the Neurological Sciences.

Discrepancies in ribonucleotide concentrations in human lymphocytes isolated from heparinized and defibrinized blood.

G. Peters, R. D. De Abreu, J. Veerkamp, 1985, Clinica chimica acta; international journal of clinical chemistry.

Lactobacilli and acidosis in children with short small bowel.

R. Wevers, H. Willems, W. Sperl, 2000, Journal of pediatric gastroenterology and nutrition.

Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dihydrothymine dehydrogenase deficiency.

F. Gabreëls, R. D. De Abreu, R. Sengers, 1984, Clinica chimica acta; international journal of clinical chemistry.

Immunological studies in two children of a mother with IgA deficiency and anti-IgA antibodies.

P. V. VAN MUNSTER, J. Bakkeren, C. Weemaes, 1982, Clinical immunology and immunopathology.

Deficiency of the α and β subunits of pyruvate dehydrogenase in a patient with lactic acidosis and unexpected sudden death

W. Sperl, R. Sengers, J. Guggenbichler, 1990, European Journal of Pediatrics.

IgG2 Deficiency in Young Children Treated with Continuous Ambulatory Peritoneal Dialysis (CAPD)

L. Monnens, C. Schröder, J. Bakkeren, 1989, Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.

Peritoneal Dialysis International, Vol

L. Monnens, C. Schröder, J. Bakkeren, 2006 .

Dihydropyrimidinase deficiency, a progressive neurological disorder?

R. D. De Abreu, R. Wevers, J. Rotteveel, 1997, Neuropediatrics.

Nephelometry of the kappa/lambda light-chain ratio in serum of normal and diseased children.

P. V. VAN MUNSTER, M. Jansen, J. Bakkeren, 1986, Clinical chemistry.

Organic aciduria in hypoxic premature newborns simulating an inborn error of metabolism

R. Sengers, J. Trijbels, J. Bakkeren, 1977, European Journal of Pediatrics.

Glutaric aciduria mediated by gut bacteria

G. Bongaerts, U. Wendel, J. Bakkeren, 1995, Journal of Inherited Metabolic Disease.

Prevalence of malnutrition in nonsurgical hospitalized patients and its association with disease complications.

M B Katan, M. Katan, T. Naber, 1997, The American journal of clinical nutrition.

D-lactic acidemia and aciduria in pediatric and adult patients with short bowel syndrome.

H. Willems, G. Bongaerts, T. Naber, 1995, Clinical chemistry.

Studies on (Na+-K+)-activated ATPase. XX. Properties of (Na+-K+)-activated ATPase in rat liver.

S. L. Bonting, J. Bakkeren, 1968, Biochimica et biophysica acta.

A Dysbalanced Immune System in Cryptogenic Lennox‐Gastaut Syndrome

G. Borm, B. Engelen, P. Strengers, 1995, Scandinavian journal of immunology.

Neonatal lethal mitochondrial trifunctional protein deficiency mimicking a respiratory chain defect

R. Wanders, U. Wendel, J. Bakkeren, 1997, Journal of Inherited Metabolic Disease.

Biochemical studies in the cerebro-hepato-renal syndrome of Zellweger: A disturbance in the metabolism of pipecolic acid

L. Monnens, J. Trijbels, J. Bakkeren, 1979, Journal of Inherited Metabolic Disease.

Disturbed very long chain (C24–C26) fatty acid pattern in fibroblasts of patients with Zellweger's syndrome

W. Kleijer, L. Monnens, L. Govaerts, 1985, Journal of Inherited Metabolic Disease.

A milder variant of Zellweger syndrome

H. Heymans, P. Barth, J. V. Moorsel, 1985, European Journal of Pediatrics.

Disturbances in bile acid metabolism of infants with the Zellweger (cerebro-hepato-renal) syndrome

G. Janssen, G. Parmentier, H. Eyssen, 2004, European Journal of Pediatrics.

R. Wanders, R. Schutgens, H. Heymans, 1986, Journal of Inherited Metabolic Disease.

Increased trihydroxycoprostanic acid in bile in familial intrahepatic biliary atresia.

G. Parmentier, H. Eyssen, J. Bakkeren, 1973, Padiatrie und Padologie.

Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency

H. Laak, R. Sengers, W. Ruitenbeek, 2004, European Journal of Pediatrics.

Daily rhythmic changes in sodium-potassium activated adenosine-triphosphatase activities in rat liver and kidney

S. L. Bonting, J. Bakkeren, J. V. D. Beek, 1971, Pflügers Archiv.

L-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retina.

A. Deutman, R. Sengers, J. Trijbels, 1977, Clinica chimica acta; international journal of clinical chemistry.

Linkage analysis in X-linked adrenoleukodystrophy and application in post-and prenatal diagnosis

H. Brunner, B. Hamel, H. Ropers, 1991, Human Genetics.

p-Nitrophenylglucuronide formation by homozygous adult Gunn rats.

J. Bakkeren, H. V. van Leusden, Zillikenf, 1962, Biochemical and biophysical research communications.

Dysmyelination and disturbed metabolism of pyruvate: a case report

H. Laak, R. Sengers, W. Ruitenbeek, 1983, European Journal of Pediatrics.

A NEW CHROMOSOMAL INSTABILITY DISORDER: THE NIJMEGEN BREAKAGE SYNDROME

R. Taalman, C. Weemaes, J. Scheres, 1981, Acta paediatrica Scandinavica.

Effects of 8‐Aminoguanosine on the Toxicity of Guanosine and Deoxyguanosine for Malignant and Normal Lymphoid Cells

R. D. De Abreu, P. M. Kraan, J. Bakkeren, 1988, Journal of leukocyte biology.

Inhibition of 3H-thymidine incorporation by adenosine and deoxyadenosine in human peripheral lymphocytes and malignant lymphoid cell lines.

J. Bakkeren, J. V. Laarhoven, P. M. Zandvoort, 1986 .

Griscelli disease with cerebral involvement

R. Happle, Á. Haraldsson, J. Bakkeren, 1991, European Journal of Pediatrics.

Iatrogenic IgG2 deficiency in a leukaemic child

J. Bakkeren, C. Weemaes, A. W. Boer, 1992, European Journal of Pediatrics.

Antibody responses in vivo in chromosome instability syndromes with immunodeficiency.

T. The, P. V. VAN MUNSTER, J. Bakkeren, 1984, Clinical and experimental immunology.

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach

R. Sengers, W. Ruitenbeek, J. Trijbels, 1988, European Journal of Pediatrics.

Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism

B. Otten, Á. Haraldsson, G. Stoelinga, 1993, European Journal of Pediatrics.

Immunological studies in Bloom's syndrome. A follow-up report.

D. Smeets, Á. Haraldsson, J. Bakkeren, 1991, Annales de genetique.

Familial selective IgA deficiency with circulating anti-IgA antibodies: a distinct group of patients?

P. V. VAN MUNSTER, G. Stoelinga, J. Bakkeren, 1991, Clinical immunology and immunopathology.

Light chain ratios and concentrations of serum immunoglobulins in children with epilepsy

B. Engelen, W. Renier, C. Weemaes, 1992, Epilepsy Research.

Immunoglobulin G, A and M Light Chain Ratio in Children

T. D. de Boo, Á. Haraldsson, G. Stoelinga, 1992, Annals of clinical biochemistry.

Immunoglobulin Levels during Follow‐up of Children with Selective IgA Deficiency

J. Bakkeren, C. Weemaes, P. Laat, 1992, Scandinavian journal of immunology.

Clinical Manifestations in Selective IgA Deficiency in Childhood; A Follow‐up Report

G. Stoelinga, J. Bakkeren, C. Weemaes, 1991, Acta paediatrica Scandinavica.

The importance of immunoglobulin-breakdown supporting the growth of bacteria in oral abscesses.

J. S. van der Hoeven, S. Walji, J. Bakkeren, 1996, Journal of clinical periodontology.

3-methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism

R. Largo, R. Sengers, W. Ruitenbeek, 1992, European Journal of Pediatrics.

Altered immunoglobulin concentrations and light chain ratios in juvenile onset mixed connective tissue disease

H. Tiddens, Á. Haraldsson, J. Bakkeren, 2005, Clinical Rheumatology.

Pyruvate carboxylase activity is not abnormal in fibroblasts of patients with Friedreich's ataxia

F. Gabreëls, E. Joosten, W. Ruitenbeek, 1984, Annals of neurology.

Dihydropyrimidinase deficiency: Confirmation of the enzyme defect in dihydropyrimidinuria

P. Vreken, A. V. van Kuilenburg, H. van Lenthe, 1997, Journal of Inherited Metabolic Disease.

Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology

T. Suormala, R. Wevers, O. Diggelen, 1995, Journal of Inherited Metabolic Disease.

CELLULAR IMMUNITY IN CEREBROHEPATORENAL SYNDROME OF ZELLWEGER

L. Monnens, J. Bakkeren, I. Carpay, 1976, The Lancet.

[Isovaleric acidemia: identical biochemical picture in 3 patients with variable clinical manifestations].

R. Sengers, M. Houben, W. Ruitenbeek, 1982, Tijdschrift voor kindergeneeskunde.

Deficiency of the alpha and beta subunits of pyruvate dehydrogenase in a patient with lactic acidosis and unexpected sudden death.

W. Sperl, R. Sengers, J. Guggenbichler, 1990, European Journal of Pediatrics.

Yeast mediates lactic acidosis suppression after antibiotic cocktail treatment in short small bowel?

W. Sperl, G. Bongaerts, R. Severijnen, 2005, Scandinavian journal of gastroenterology.

Prenatal diagnosis of cytochrome c oxidase deficiency by biopsy of chorionic villi.

R. Sengers, F. Trijbels, W. Ruitenbeek, 1988, The New England journal of medicine.

Light chain ratios and concentrations of immunoglobulins G, A, and M in childhood common acute lymphoblastic leukemia.

W. J. van Dijk, Á. Haraldsson, J. Bakkeren, 1994, Pediatric hematology and oncology.

Canavan disease: value of N-acetylaspartic aciduria?

F. Gabreëls, J. Bakkeren, I. D. Coo, 1991, Neuropediatrics.

Propionic acid, an artefact which can leave methylmalonic acidemia undiscovered.

M. Durán, D. Ketting, S. K. Wadman, 1973, Clinica chimica acta; international journal of clinical chemistry.

Successful carnitine treatment in a non-carnitine-deficient lipid storage myopathy

H. Laak, R. Sengers, J. Trijbels, 1980, European Journal of Pediatrics.