Hereditary diffuse leukoencephalopathy with axonal spheroids caused by R782H mutation in CSF1R: Case report

Case report 3

Murray K. Dalinka, R. E. Brennan, Arthur S. Patchefsky · Skeletal Radiology · 1976 · 4.1K citations

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

Anne Joutel, Christophe Corpechot, Anne Ducros et al. · Nature · 1996 · 2.1K citations

Life Sciences, Genetics, Neurology +14

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

Rosa Rademakers, Matt Baker, Alexandra M. Nicholson et al. · Nature Genetics · 2011 · 579 citations · Full text

Life Sciences, Molecular Genetics, Neuroscience +5

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease

Kenju Hara, Atsushi Shiga, Toshio Fukutake et al. · New England Journal of Medicine · 2009 · 462 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

MRI hyperintensities of the temporal lobe and external capsule in patients with CADASIL

Michael O’Sullivan, J. Jarosz, Ruvie Martin et al. · Neurology · 2001 · 363 citations

Medicine, Neurology, Radiology +16