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Klinische Padiatrie|May 1, 1992
[Effect of psychotherapeutic interventions on weight reduction and personality development of a 13-year-old boy with Prader-Willi syndrome]E Wurst, D Möslinger, K WidhalmIndian Pediatrics|February 10, 2012
Venovenous hemodiafiltration and hypothermia for treatment of cerebral edema associated with hyperammonemiaR Vargha, D Möslinger, O Wagner, et al.Zeitschrift Fur Geburtshilfe Und Neonatologie|December 29, 2000
[Maternal phenylketonuria: dietary treatment of a 2 generation illness]D Möslinger, S Scheibenreiter, E Spoula, et al.Acta Medica Austriaca|January 1, 1997
[Neonatal screening for congenital hypothyroidism]D Möslinger, H Frisch, W Strobl, et al.European Journal of Human Genetics : EJHG|April 21, 2001
Molecular characterisation of 34 patients with biotinidase deficiency ascertained by newborn screening and family investigationA Mühl, D Möslinger, C B Item, et al.Journal of Inherited Metabolic Disease|July 14, 2007
Growth and body composition in children with classical phenylketonuria: results in 34 patients and review of the literatureM Huemer, C Huemer, D Möslinger, et al.Wiener Klinische Wochenschrift|January 1, 1995
[Meconium peritonitis: intrauterine follow-up--postnatal outcome]D Möslinger, K Chalubinski, M Radner, et al.Journal of Inherited Metabolic Disease|February 1, 2012
Free asymmetric dimethylarginine (ADMA) is low in children and adolescents with classical phenylketonuria (PKU)M Huemer, B Simma, D Mayr, et al.Acta Paediatrica (Oslo, Norway : 1992)|July 4, 2003
Reversibility of cirrhotic regenerative liver nodules upon NTBC treatment in a child with tyrosinaemia type IJ Crone, D Möslinger, O A Bodamer, et al.Neuropediatrics|December 19, 2009
Epilepsy in patients with propionic acidemiaE Haberlandt, C Canestrini, M Brunner-Krainz, et al.Pageof 2