Helena Maier

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)

Katherine Dick, Matthias Eckhardt, Coro Paisán‐Ruíz et al. · Human Mutation · 2010 · 197 citations

Life Sciences, Genetics, Neurology +17

Increasing Sulfatide Synthesis in Myelin-Forming Cells of Arylsulfatase A-Deficient Mice Causes Demyelination and Neurological Symptoms Reminiscent of Human Metachromatic Leukodystrophy

Hariharasubramanian Ramakrishnan, Kerstin Khalaj Hedayati, Renate Lüllmann‐Rauch et al. · Journal of Neuroscience · 2007 · 77 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

Ceramide synthase 4 deficiency in mice causes lipid alterations in sebum and results in alopecia

Philipp Ebel, Silke Imgrund, Katharina vom Dorp et al. · Biochemical Journal · 2014 · 71 citations

Medicine, Biochemistry, Dermatology +14

<i>N</i>-Acetylaspartate Synthase Deficiency Corrects the Myelin Phenotype in a Canavan Disease Mouse Model But Does Not Affect Survival Time

Helena Maier, Lihua Wang‐Eckhardt, Dieter Hartmann et al. · Journal of Neuroscience · 2015 · 52 citations · Full text

Life Sciences, Neuroscience, Pathology +17

Normal Fur Development and Sebum Production Depends on Fatty Acid 2-Hydroxylase Expression in Sebaceous Glands

Helena Maier, Marion Meixner, Dieter Hartmann et al. · Journal of Biological Chemistry · 2011 · 45 citations · Full text

Life Sciences, Biochemistry, Dermatology +17