H S A Heymans


Ontology type: schema:Person     


Person Info

NAME

H S A

SURNAME

Heymans

Publications in SciGraph latest 50 shown

  • 2014-12 Psychosocial well-being in young adults with chronic illness since childhood: the role of illness cognitions in CHILD AND ADOLESCENT PSYCHIATRY AND MENTAL HEALTH
  • 2013-12 Health-related quality of life, anxiety and depression in young adults with disability benefits due to childhood-onset somatic conditions in CHILD AND ADOLESCENT PSYCHIATRY AND MENTAL HEALTH
  • 2011-12 The effectiviness of an innovative web-based application to monitor HRQOL problems in paediatric rheumatology clinical practice in PEDIATRIC RHEUMATOLOGY
  • 2011-10 Wajongers opgegroeid met een somatische aandoening in TIJDSCHRIFT VOOR KINDERGENEESKUNDE
  • 2010-12 Kwaliteit van Leven in Kaart (KLIK) in TIJDSCHRIFT VOOR KINDERGENEESKUNDE
  • 2009-12 A predictive model of Health Related Quality of life of parents of chronically ill children: the importance of care-dependency of their child and their support system in HEALTH AND QUALITY OF LIFE OUTCOMES
  • 2003-03 Cardiac disease in young adult patients with end-stage renal disease since childhood: A Dutch cohort study in KIDNEY INTERNATIONAL
  • 2002-02 Mortality and causes of death of end-stage renal disease in children: A Dutch cohort study in KIDNEY INTERNATIONAL
  • 2000-08 Heterozygosity for the Common LCHAD Mutation (1528G>C) Is Not a Major Cause of HELLP Syndrome and the Prevalence of the Mutation in the Dutch Population Is Low in PEDIATRIC RESEARCH
  • 2000-04 Ontwikkeling van allergische aandoeningen bij kinderen met koemelkallergie op de zuigelingenleeftijd in TIJDSCHRIFT VOOR KINDERGENEESKUNDE
  • 1999-04 Prenatal Exposure to Coumarins and Long Term Growth in PEDIATRIC RESEARCH
  • 1997-07 Immortalized human hepatocytes as a tool for the study of hepatocytic (de-)differentiation in CELL BIOLOGY AND TOXICOLOGY
  • 1997-04 Intestinal permeability in premature infants. † 1437 in PEDIATRIC RESEARCH
  • 1997-04 A critical appraisal of current management practices for infant regurgitation – recommendations of a working party in EUROPEAN JOURNAL OF PEDIATRICS
  • 1993-09 A proposition for the diagnosis and treatment of gastro-oesophageal reflux disease in children: A report from a working group on gastro-oesophageal reflux disease in EUROPEAN JOURNAL OF PEDIATRICS
  • 1993-06 Acyclovir for varicella in immunocompetent patients in JOURNAL OF MOLECULAR MEDICINE
  • 1989-03 Prenatal and perinatal diagnosis of peroxisomal disorders in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989 Tyrosinaemia Type I: Orthotopic Liver Transplantation as the Only Definitive Answer to a Metabolic as well as an Oncological Problem in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988-08 118: MULTIPLE PEROXISOMAL ENZYME DEFICIENCIES IN RHIZOMELIC CHONDRODYSPLASIA PUNCTATA in PEDIATRIC RESEARCH
  • 1987-07 Giardiasis in childhood: an unnecessarily expensive diagnosis in EUROPEAN JOURNAL OF PEDIATRICS
  • 1987-06 A genetic disorder due to the deficiency of the peroxisomal β-oxidation enzyme 3-oxoacyl-CoA thiolase in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987 Biochemical Analysis in Peroxisomal Disorders in PEROXISOMES IN BIOLOGY AND MEDICINE
  • 1986-12 Age-related differences in plasmalogen content of erythrocytes from patients with the cerebro-hepato-renal (Zellweger) syndrome: Implications for postnatal detection of the disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986-02 Hepatic artery embolisation; successful treatment of multinodular haemangiomatosis of the liver in EUROPEAN JOURNAL OF PEDIATRICS
  • 1986 Peroxisomal Abnormalities in Rhizomelic Chondrodysplasia Punctata in PRACTICAL DEVELOPMENTS IN INHERITED METABOLIC DISEASE: DNA ANALYSIS, PHENYLKETONURIA AND SCREENING FOR CONGENITAL ADRENAL HYPERPLASIA
  • 1986 Impaired Cholesterol Side Chain Cleavage Activity in Liver from Patients with the Cerebro-Hepato-Renal (Zellweger) Syndrome in Relation to the Accumulation of Di- and Trihydroxycoprostanoic Acid in Serum in PRACTICAL DEVELOPMENTS IN INHERITED METABOLIC DISEASE: DNA ANALYSIS, PHENYLKETONURIA AND SCREENING FOR CONGENITAL ADRENAL HYPERPLASIA
  • 1986 Deficiencies in Ether Glycerolipids and Their Biosynthesis in Inherited Peroxisomal Disorders in ENZYMES OF LIPID METABOLISM II
  • 1985-11 A milder variant of Zellweger syndrome in EUROPEAN JOURNAL OF PEDIATRICS
  • 1985-06 Prenatal diagnosis of the cerebro-hepato-renal (Zellweger) syndrome by detection of an impaired plasmalogen biosynthesis in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1985 Prenatal Diagnosis of the Cerebro-hepato-renal (Zellweger) Syndrome by Detection of an Impaired Plasmalogen Biosynthesis in INHERITED DISORDERS OF VITAMINS AND COFACTORS
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