Brunhilde Molzer

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice

Sonja Forss-Petter, Hauke Werner, Johannes Berger et al. · Journal of Neuroscience Research · 1997 · 217 citations

Life Sciences, Molecular Genetics, Neurobiology +17

Adrenoleukodystrophy-Related Protein Can Compensate Functionally for Adrenoleukodystrophy Protein Deficiency (X-ALD): Implications for Therapy

Angela Netik, Sonja Forss‐Petter, Andreas Holzinger et al. · Human Molecular Genetics · 1999 · 155 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

X-Linked Adrenoleukodystrophy (ALD): A Novel Mutation of the ALD Gene in 6 Members of a Family Presenting with 5 Different Phenotypes

Johannes Berger, Brunhilde Molzer, Ingrid Faé et al. · Biochemical and Biophysical Research Communications · 1994 · 129 citations

Medicine, Genetics, Molecular Genetics +10

Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy

Johannes Berger, Beate Löschl, H. Bernheimer et al. · American Journal of Medical Genetics · 1997 · 86 citations

Life Sciences, Genetics, Molecular Genetics +14

The Cerebrohepatorenal (Zellweger) Syndrome: An Improved Method for the Biochemical Diagnosis and its Potential Value for Prenatal Detection

Adelbert A. Roscher, Brunhilde Molzer, Hans Bernheimer et al. · Pediatric Research · 1985 · 84 citations

Medicine, Obstetrics, Maternal-fetal Medicine +13