Sylvia Stöckler


Ontology type: schema:Person     


Person Info

NAME

Sylvia

SURNAME

Stöckler

Publications in SciGraph latest 50 shown

  • 1997-03 Decreased platelet membrane anisotropy in patients with adrenoleukodystrophy treated with erucic acid (22:1)-rich triglycerides in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1995-01 Glyceroltrioleate/glyceroltrierucate therapy in 16 patients with X-chromosomal adrenoleukodystrophy/adrenomyeloneuropathy: Effect on clinical, biochemical and neurophysiological parameters in EUROPEAN JOURNAL OF PEDIATRICS
  • 1995-01 Severely depressed natural killer cell activity of patients with adrenoleukodystrophy under treatment with Lorenzo's oil in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-09 Reduced stimulability of platelet surface adhesion molecules under treatment with Lorenzo's oil in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-09 Creatine Deficiency in the Brain: A New, Treatable Inborn Error of Metabolism in PEDIATRIC RESEARCH
  • 1993-12 Liposomal amphotericin-B (AmBisome) for treatment of cutaneous widespread candidosis in an infant with methylmalonic acidaemia in EUROPEAN JOURNAL OF PEDIATRICS
  • 1993-09 Mucopolysaccharidosis I and intracranial tumor in a patient with high-pressure hydrocephalus in PEDIATRIC RADIOLOGY
  • 1993-07 Physiology and pathophysiology of organic acids in cerebrospinal fluid in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1993-03 Cerebral blood flow velocities in the first minutes of life in EUROPEAN JOURNAL OF PEDIATRICS
  • 1992-12 Asymptomatic lesions of the basal ganglia in a patient with methylmalonic aciduria in EUROPEAN JOURNAL OF PEDIATRICS
  • 1992-03 Combined deficiencies of the pyruvate dehydrogenase complex and enzymes of the respiratory chain in mitochondrial myopathies in EUROPEAN JOURNAL OF PEDIATRICS
  • 1991 Perinatologisches Management von sofort Operationspflichtigen Fehlbildungen — Evaluierungsstudie Nr II/C des steirisehes Fehlbildungsregisters in GYNÄKOLOGIE UND GEBURTSHILFE 1990
  • 1990 Selektives Screening zur Erfassung peroxisomaler Erkrankungen in AKTUELLE NEUROPÄDIATRIE 1989
  • 1988-12 A simple concept for the screening of amino- and organic acidurias in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987-09 Ornithine transcarbamylase variant in a male patient in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1985-09 The Cerebrohepatorenal (Zellweger) Syndrome: An Improved Method for the Biochemical Diagnosis and its Potential Value for Prenatal Detection in PEDIATRIC RESEARCH
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