Early Mitochondrial Dysfunction in an Infant With Alexander Disease

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

Michael Brenner, Odile Boespflug‐Tanguy, Diana Rodriguez et al. · Nature Genetics · 2001 · 686 citations

Life Sciences, Genetics, Neuroscience +10

Alexander disease: diagnosis with MR imaging.

Marjo S. van der Knaap, Sakkubai Naidu, Steven N. Breiter et al. · PubMed · 2001 · 340 citations · Full text

Medicine, Neurology, Radiology +17

Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease

Rong Li, Gajja S. Salomons, James E. Goldman et al. · Annals of Neurology · 2005 · 271 citations

Medicine, Neurology, Pathology +15

Mitochondrial dysfunction in neurodegenerative disorders

Anthony H.V. Schapira · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 1998 · 207 citations

Life Sciences, Cell Biology, Neuroscience +14

Metabolic and destructive brain disorders in children: findings with localized proton MR spectroscopy.

Wolfgang Grodd, Ingeborg Krägeloh‐Mann, Uwe Klose et al. · Radiology · 1991 · 172 citations

Medicine, Neurology, Radiology +17