Wolf Endres


Ontology type: schema:Person     


Person Info

NAME

Wolf

SURNAME

Endres

Publications in SciGraph latest 50 shown

  • 1993-08 Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria in EUROPEAN JOURNAL OF PEDIATRICS
  • 1992-12 Hartnup syndrome, progressive encephalopathy and allo-albuminaemia in EUROPEAN JOURNAL OF PEDIATRICS
  • 1992-05 Screening for tetrahydrobiopterin deficiency in newborns using dried urine on filter paper in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1991-07 Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies in VIRCHOWS ARCHIV A PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY
  • 1991-05 Purification ofα andβ subunits of phosphorylase-b-kinase in human liver and cardiac muscle by affinity chromatography and immunodetection in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1991-04 Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuria in EUROPEAN JOURNAL OF PEDIATRICS
  • 1991-03 Bone marrow transplantation in Lesch-Nyhan disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990-09 96 DIFFERENTIAL DIAGNOSIS OF HYPERPHENYLALANI N-AEMIA (HPA) AND FOLLOW UP OF SEVEN PATIENTS WITH TETRAHYDROBIOPTERIN (BH4) DEFICIENCY in PEDIATRIC RESEARCH
  • 1990-07 Plasma polyol levels in patients with cataract in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990-07 Cataract and metabolic disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990-05 Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotype in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990 Plasma Polyol Levels in Patients with Cataract in CARBOHYDRATE AND GLYCOPROTEIN METABOLISM; MATERNAL PHENYLKETONURIA
  • 1989-04 First Trimester Diagnosis of Glycogen Storage Disease Type II and Type III in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989 First Trimester Diagnosis of Glycogen Storage Disease Type II and Type III in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988-12 Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency in EUROPEAN JOURNAL OF PEDIATRICS
  • 1988-05 Elevated plasma galactitol levels in patients with congenital cataracts without apparent enzyme defect in EUROPEAN JOURNAL OF PEDIATRICS
  • 1987-10 Priapism in Fabry's disease during testosterone treatment in JOURNAL OF MOLECULAR MEDICINE
  • 1987-08 SORBITOL DEHYDROGENASE IN HUMAN LENS: STUDY OF THE ENZYME IN VARIOUS HUMAN TISSUES in PEDIATRIC RESEARCH
  • 1987-06 Radioisotopic methods for assay of the enzymes in the urea cycle: First trimester diagnostic possibilities for urea cycle disorders using chorionic villi sampling in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987-05 “Peripheral” tetrahydrobiopterin deficiency with hyperphenylalaninaemia due to incomplete 6-pyruvoyl tetrahydropterin synthase deficiency or heterozygosity in EUROPEAN JOURNAL OF PEDIATRICS
  • 1986-10 146 GLYCOGEN METABOLISM IN CHORIONIC VILLOUS SAMPLINGS: POSSIBILITIES FOR PRENATAL DIAGNOSIS OF GLYCOGEN STORAGE DISEASES in PEDIATRIC RESEARCH
  • 1985-10 METABOLITE PATTERNS AND CLINICAL EXPRESSIONS OF URIDINE DIPHOSPHOGALACTOSE EPIMERASE DEFICIENCY in PEDIATRIC RESEARCH
  • 1985-10 HBAlab, A POSSIBLE MEANS OF METABOLIC CONTROL IN HEREDITARY FRUCTOSE INTOLERANCE (HFI) AND GALACTOSEMIA (G) in PEDIATRIC RESEARCH
  • 1984-08 D-Thyroxine Treatment in Glycogen Storage Disease Type VIa in PEDIATRIC RESEARCH
  • 1984-03 Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1984 Sorbitol Dehydrogenase Deficiency in a Family with Congenital Cataracts in ORGANIC ACIDURIAS
  • 1983-06 A simple method for histidase assay and an alteration in the affinity of skin histidase for histidine in histidinaemia in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1982-01 Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine in VIRCHOWS ARCHIV A PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY
  • 1981-12 A new enzymatic method for pyridoxal-5-phosphate determination in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1981-09 Zur Morphologie und Diagnostik des Zellweger Syndroms in VIRCHOWS ARCHIV A PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY
  • 1981-06 D-penicillamine in pregnancy — to ban or not to ban? in JOURNAL OF MOLECULAR MEDICINE
  • 1981 New aspects in biopterin biosyntheses in FUNCTION AND REGULATION OF MONOAMINE ENZYMES: BASIC AND CLINICAL ASPECTS
  • 1977-02 Cataract in a fetus at risk for oculo-cerebro-renal syndrome (lowe) in JOURNAL OF MOLECULAR MEDICINE
  • 1971-03 Sekundäre Cystathioninurie in EUROPEAN JOURNAL OF PEDIATRICS
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