Michaela Brunner‐Krainz

Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients

Sarah C. Grünert, S. Müllerleile, Linda De Silva et al. · Orphanet Journal of Rare Diseases · 2013 · 185 citations · Full text

Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis optica

Kevin Rostásy, Simone Mader, EM Hennes et al. · Multiple Sclerosis Journal · 2012 · 151 citations

Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice

Sebene Mayorandan, Uta Meyer, Gülden Gökçay et al. · Orphanet Journal of Rare Diseases · 2014 · 135 citations · Full text

Propionic acidemia: neonatal versus selective metabolic screening

Sarah C. Grünert, S. Müllerleile, L. de Silva et al. · Journal of Inherited Metabolic Disease · 2011 · 90 citations · Full text

Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1

Alleene V. Strickland, Maria Schabhüttl, H. Offenbacher et al. · Journal of Neurology · 2015 · 69 citations · Full text

Genome Instability, Engineering, Somatic Variant +8