Edith Müller

Clinical Course, Early Diagnosis, Treatment, and Prevention of Disease in Glutaryl-CoA Dehydrogenase Deficiency

G. F. Hoffmann, S. Athanassopoulos, A Burlina et al. · Neuropediatrics · 1996 · 227 citations

Life Sciences, Neurology, Nutrition +15

Guideline for the diagnosis and management of glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria type I)

S. Kölker, E. Christensen, James V. Leonard et al. · Journal of Inherited Metabolic Disease · 2007 · 146 citations

Life Sciences, Biochemistry, Pediatrics +6

Assignment of genes for immunoglobulin kappa and heavy chains to chromosomes 6 and 12 in mouse.

Hans Hengartner, T Meo, Edith Müller · Proceedings of the National Academy of Sciences · 1978 · 134 citations · Full text

Life Sciences, Cell Biology, Genetics +17

Decline of Acute Encephalopathic Crises in Children with Glutaryl-CoA Dehydrogenase Deficiency Identified by Newborn Screening in Germany

Stefan Kölker, Sven F. Garbade, Nikolas Boy et al. · Pediatric Research · 2007 · 111 citations

Medicine, Neurology, Pediatrics +10

Phylloides tumor: findings on mammography, sonography, and aspiration cytology in 10 cases.

W. Buchberger, K Strasser, K. Heim et al. · American Journal of Roentgenology · 1991 · 91 citations

Medicine, Oncology, Pathology +17