Jean Louis Dhondt


Ontology type: schema:Person     


Person Info

NAME

Jean Louis

SURNAME

Dhondt

Publications in SciGraph latest 50 shown

  • 2007-08 Neonatal screening: from the ‘Guthrie age’ to the ‘genetic age’ in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2007-08 First ISNS Reference Preparation for Neonatal Screening for thyrotropin, phenylalanine and 17α-hydroxyprogesterone in blood spots in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2003-12 Neonatal screening for cystic fibrosis: France rises to the challenge in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1998-12 Measuring dobutamine (Db) clearance during continuous hemofiltration (CHF) in CRITICAL CARE
  • 1997-04 NEWBORN SCREENING FOR SICLE CELL DISEASE IN FRANCE. 523 in PEDIATRIC RESEARCH
  • 1996-01 International database of tetrahydrobiopterin deficiencies in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1995-03 Physical growth in patients with phenylketonuria in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1995-02 Changes of Cerebral Biopterin and Biogenic Amine Metabolism in Leukemic Children Receiving 5 g/m2 Intravenous Methotrexate in PEDIATRIC RESEARCH
  • 1993 Tetrahydrobiopterin Deficiency and an International Database of Patients in CHEMISTRY AND BIOLOGY OF PTERIDINES AND FOLATES
  • 1991-12 99 CEREBRAL FLUID NEOPTERIN LEVELS IN CHILDREN WITH MENINGEAL RELAPSE OF MALIGNANT HEMOPATHY in PEDIATRIC RESEARCH
  • 1991-07 Economic evaluation of cost-benefit ratio of neonatal screening procedure for phenylketonuria and hypothyroidism in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1991-03 Strategy for the screening of tetrahydrobiopterin deficiency among hyperphenylalaninaemic patients: 15-Years experience in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1991 Economic Evaluation of Cost-Benefit Ratio of Neonatal Screening Procedure for Phenylketonuria and Hypothyroidism in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990-11 Pterins analysis in amniotic fluid for the prenatal diagnosis of GTP cyclohydrolase deficiency in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989-04 Primapterinuria: A New Variant of Atypical Phenylketonuria in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989 Intellectual Outcome in Hypothyroid Children Screened at Birth in RESEARCH IN CONGENITAL HYPOTHYROIDISM
  • 1989 Primapterinuria: A New Variant of Atypical Phenylketonuria in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988-11 New variant of hyperphenylalaninaemia with excretion of 7-substituted pterins in EUROPEAN JOURNAL OF PEDIATRICS
  • 1988-08 32 INTESTINAL ABSORPTION OF PTERIDINES IN CHILDHOOD in PEDIATRIC RESEARCH
  • 1988-02 Neonatal hyperphenylalaninaemia presumably caused by a new variant of biopterin synthetase defieiency in EUROPEAN JOURNAL OF PEDIATRICS
  • 1987-01 Atypical cases of phenylketonuria in EUROPEAN JOURNAL OF PEDIATRICS
  • 1986-06 Hepatic phenylalanine hydroxylase and dietary tolerance in hyperphenylalaninaemic patients in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986-03 Neonatal screening for congenital adrenal hyperplasia: a pilot study in France in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986 Neonatal Screening for Congenital Adrenal Hyperplasia: a Pilot Study in France in PRACTICAL DEVELOPMENTS IN INHERITED METABOLIC DISEASE: DNA ANALYSIS, PHENYLKETONURIA AND SCREENING FOR CONGENITAL ADRENAL HYPERPLASIA
  • 1986 Hepatic Phenylalanine Hydroxylase and Dietary Tolerance in Hyperphenylalaninaemic Patients in PRACTICAL DEVELOPMENTS IN INHERITED METABOLIC DISEASE: DNA ANALYSIS, PHENYLKETONURIA AND SCREENING FOR CONGENITAL ADRENAL HYPERPLASIA
  • 1985-03 Clinical diagnosis of a new case of ceramidase deficiency (Farber's disease) in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1983-12 Dihydrobiopterin biosynthesis deficiency in EUROPEAN JOURNAL OF PEDIATRICS
  • 1982-03 Lactobionic acid: a pitfall in screening for oligosaccharidurias in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1982-03 Plasmapheresis in type IIa hypercholesterolaemia in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1982-01 Apolipoprotein B measurement in blood spotted on paper in INTERNATIONAL JOURNAL OF CLINICAL AND LABORATORY RESEARCH
  • 1981-12 Pterin metabolism in normal subjects and hyperphenylalaninaemic patients in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1981-12 Hepatic phenylalanine hydroxylase activity in hyperphenylalaninaemia in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1981-12 Antenatal diagnosis of propionic acidaemia by methylcitrate determination in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1980-02 Portacaval shunt (PCS) in type IIa hypercholesterolemia; results from three cases: 21 in PEDIATRIC RESEARCH
  • 1980-02 Reduction of serum phenylalanine levels in PKU rats with intestinal absorption inhibitors of phenylalanine (PHE): 61 in PEDIATRIC RESEARCH
  • 1980-02 Congenital Thyroid Binding Globulin (TBG) deficiency. Its incidence on a screening program for neonatal hypothyroidism: 92 in PEDIATRIC RESEARCH
  • 1978-06 Radiological signs of mucolipidosis II or I-cell disease A study of nine cases in PEDIATRIC RADIOLOGY
  • 1976-05 Type I Hyperprolinemia: A Study of the Intestinal Absorption of Proline, Hydroxyproline, and Glycine in PEDIATRIC RESEARCH
  • 1974-09 Hyperammonemia through deficiency of ornithine carbamyl transferase in EUROPEAN JOURNAL OF PEDIATRICS
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