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M Brunner-Krainz

Showing results (1-10 of 8) with videos related to

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Metabolic Brain Disease|May 29, 1999
Normal ascorbic acid in cerebrospinal fluid of patients with infantile neuronal ceroid-lipofuscinosisJ O Sass, D Skladal, M Brunner-Krainz
Journal of Inherited Metabolic Disease|June 21, 2006
Copper concentration of liver tissue under long-term copper-histidine therapy in a patient with Menkes diseaseT Kroepfl, E Mair, J Deutsch, et al.
Neuropediatrics|December 19, 2009
Epilepsy in patients with propionic acidemiaE Haberlandt, C Canestrini, M Brunner-Krainz, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 22, 2012
Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis opticaK Rostásy, S Mader, E M Hennes, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 27, 2016
Epileptic phenotypes, electroclinical features and clinical characteristics in 17 children with anti-NMDAR encephalitisE Haberlandt, M Ensslen, U Gruber-Sedlmayr, et al.
Journal of Neurology|November 29, 2017
Pompe disease in Austria: clinical, genetic and epidemiological aspectsW N Löscher, M Huemer, T M Stulnig, et al.
Journal of Inherited Metabolic Disease|December 3, 2011
Propionic acidemia: neonatal versus selective metabolic screeningS C Grünert, S Müllerleile, L de Silva, et al.
Journal of Inherited Metabolic Disease|October 29, 2011
Mutation analysis in 54 propionic acidemia patientsJ P Kraus, E Spector, S Venezia, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Metabolic Brain Disease|May 29, 1999
Normal ascorbic acid in cerebrospinal fluid of patients with infantile neuronal ceroid-lipofuscinosisJ O Sass, D Skladal, M Brunner-Krainz
Journal of Inherited Metabolic Disease|June 21, 2006
Copper concentration of liver tissue under long-term copper-histidine therapy in a patient with Menkes diseaseT Kroepfl, E Mair, J Deutsch, et al.
Neuropediatrics|December 19, 2009
Epilepsy in patients with propionic acidemiaE Haberlandt, C Canestrini, M Brunner-Krainz, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 22, 2012
Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis opticaK Rostásy, S Mader, E M Hennes, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 27, 2016
Epileptic phenotypes, electroclinical features and clinical characteristics in 17 children with anti-NMDAR encephalitisE Haberlandt, M Ensslen, U Gruber-Sedlmayr, et al.
Journal of Neurology|November 29, 2017
Pompe disease in Austria: clinical, genetic and epidemiological aspectsW N Löscher, M Huemer, T M Stulnig, et al.
Journal of Inherited Metabolic Disease|December 3, 2011
Propionic acidemia: neonatal versus selective metabolic screeningS C Grünert, S Müllerleile, L de Silva, et al.
Journal of Inherited Metabolic Disease|October 29, 2011
Mutation analysis in 54 propionic acidemia patientsJ P Kraus, E Spector, S Venezia, et al.
Pageof 1