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European Journal of Endocrinology|July 1, 1997
Variability of endocrinological dysfunction in 55 patients with X-linked adrenoleucodystrophy: clinical, laboratory and genetic findingsG C Korenke, C Roth, E Krasemann, et al.Neuropediatrics|November 12, 1998
Quantitative proton magnetic resonance spectroscopy of childhood adrenoleukodystrophyP J Pouwels, B Kruse, G C Korenke, et al.Zeitschrift Fur Geburtshilfe Und Neonatologie|August 31, 2007
[Maternal vitamin B12 deficiency: cause for neurological symptoms in infancy]T Lücke, G C Korenke, I Poggenburg, et al.Journal of Computer Assisted Tomography|May 1, 1992
Proton NMR spectroscopy of cerebral metabolic alterations in infantile peroxisomal disordersH Bruhn, B Kruse, G C Korenke, et al.Annals of Neurology|August 1, 1996
Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotypeG C Korenke, S Fuchs, E Krasemann, et al.Genes|December 23, 2022
Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L-Associated NeuropathyK Eggermann, R Meyer, M Begemann, et al.Journal of Inherited Metabolic Disease|March 1, 1997
Decreased platelet membrane anisotropy in patients with adrenoleukodystrophy treated with erucic acid (22:1)-rich triglyceridesS Stöckler, C Opper, A Greinacher, et al.European Journal of Pediatrics|July 12, 2012
Rational diagnostic strategies for Lyme borreliosis in children and adolescents: recommendations by the Committee for Infectious Diseases and Vaccinations of the German Academy for Pediatrics and Adolescent HealthH I Huppertz, P Bartmann, U Heininger, et al.Pediatric Research|December 1, 1992
Atypical (mild) forms of dihydropteridine reductase deficiency: neurochemical evaluation and mutation detectionN Blau, C W Heizmann, W Sperl, et al.Pediatric Neurology|September 1, 1996
Arrested cerebral adrenoleukodystrophy: a clinical and proton magnetic resonance spectroscopy study in three patientsG C Korenke, P J Pouwels, J Frahm, et al.Pageof 4