F. J. M. Gabre�ls

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

Botulinum toxin A: a new option for treatment of drooling in children with cerebral palsy. Presentation of a case series

Peter H. Jongerius, Jan J. Rotteveel, F.H.J. van den Hoogen et al. · European Journal of Pediatrics · 2001 · 113 citations

Medicine, Neurology, Pediatrics +8

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

Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain

P.M.M. van Erven, F. J. M. Gabre�ls, W. Ruitenbeek et al. · Journal of Neurology · 1987 · 26 citations

Life Sciences, Genetics, Neuroscience +12

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