A. A. W. M. Gabre�ls-Festen

Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutations

A. A. W. M. Gabre�ls-Festen, Pieter A. Bolhuis, Jessica E. Hoogendijk et al. · Acta Neuropathologica · 1995 · 123 citations

Life Sciences, Genetics, Molecular Genetics +12

Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy?

A. A. W. M. Gabre�ls-Festen, F. J. M. Gabre�ls, Jessica E. Hoogendijk et al. · Acta Neuropathologica · 1993 · 35 citations

Medicine, Neurology, Neuroscience +16

The neuropathy of Cockayne syndrome

A. Vos, A. A. W. M. Gabre�ls-Festen, E.M.G. Joosten et al. · Acta Neuropathologica · 1983 · 25 citations

Medicine, Neurology, Neuroscience +5

Electron microscopic investigation of inclusion material in a case of adult metachromatic leukodystrophy; Observations on kidney biopsy, peripheral nerve and cerebral white matter

E.M.G. Joosten, M.J.A.J.M. Hoes, A. A. W. M. Gabre�ls-Festen et al. · Acta Neuropathologica · 1975 · 20 citations

Medicine, Nephrology, Pathology +14

Major histocompatibility complex class II expression and macrophage responses in genetically proven Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies

Guido Stoll, A. A. W. M. Gabre�ls-Festen, Sebastian Jander et al. · Muscle & Nerve · 1998 · 16 citations

Medicine, Neurology, Pathology +14