C. Ceuterick
Publications by Year
Research Areas
Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases, Neurological diseases and metabolism, Lysosomal Storage Disorders Research, Alzheimer's disease research and treatments
Most-Cited Works
- → Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia(2003)245 cited
- → The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype(1999)221 cited
- → Dense-Core Plaques in Tg2576 and PSAPP Mouse Models of Alzheimer's Disease Are Centered on Vessel Walls(2005)180 cited
- → Mutations in GDAP1(2002)156 cited
- → Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype(1999)153 cited
- → Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10(2003)118 cited
- → Periaxin mutations cause a broad spectrum of demyelinating neuropathies(2002)115 cited
- → Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala→Gly mutation(1998)112 cited
- → Dense-Core Senile Plaques in the Flemish Variant of Alzheimer's Disease Are Vasocentric(2002)110 cited
- → Behavioral Disturbances without Amyloid Deposits in Mice Overexpressing Human Amyloid Precursor Protein with Flemish (A692G) or Dutch (E693Q) Mutation(2000)105 cited