C. Ceuterick

Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia

G. Van Goethem, J.J. Martin, Bart Dermaut et al. · Neuromuscular Disorders · 2003 · 244 citations

Ocular Disease, Mendelian Disorder, Ophthalmology +10

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype

Peter De Jonghe, Vincent Timmerman, C. Ceuterick et al. · Brain · 1999 · 221 citations · Full text

Dense-Core Plaques in Tg2576 and PSAPP Mouse Models of Alzheimer's Disease Are Centered on Vessel Walls

Samir Kumar‐Singh, Daniel Pirici, Eileen McGowan et al. · American Journal Of Pathology · 2005 · 180 citations · Full text

Alzheimer's Disease, Vessel Walls, Dementia +12

Mutations in <i>GDAP1</i>

Eva Nelis, Peter Van den Bergh, Marie‐Claude Belpaire‐Dethiou et al. · Neurology · 2002 · 156 citations

Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype

Vincent Timmerman, Peter De Jonghe, C. Ceuterick et al. · Neurology · 1999 · 153 citations