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A.A.W.M. Gabreëls‐Festen | Researchclopedia

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A.A.W.M. Gabreëls‐Festen

Radboud University Nijmegen

65

Works

2,696

Citations

31

h-index

47

i10-index

Research Topics

Hereditary Neurological Disorders Neurological diseases and metabolism Neurogenetic and Muscular Disorders Research

Affiliations

Radboud University Nijmegen1973–2007

University of Antwerp1997–2002

Inserm1999–1999

Radboud University Medical Center2000–2007

Nijmegen Institute for Scientist Practitioners in Addiction1991–1991

Top Works

Neuromuscular complications in patients given pavulon/sr (pancuronium bromide) during artificial ventilation

A.A.W. Op de Coul,P.C.L.A. Lambregts,et al.

1985217 citations

Genetic Neurodegenerative Diseases

Lysosomal Storage Disorders Research

De-novo mutation in hereditary motor and sensory neuropathy type I

Jessica E. Hoogendijk,Gerard W. Hensels,et al.

1992162 citations

Mutations in <i>GDAP1</i>

Eva Nelis,Sevim Erdem‐Özdamar,et al.

2002156 citations

Macrophage clustering as a diagnostic marker in sural nerve biopsies of patients with CIDP

Claudia Sommer,Stefan Koch,et al.

2005129 citations

Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22.

Donatella D’Urso,Reinhard Prior,et al.

1998117 citations

Spine deformities in Charcot-Marie-Tooth 4C caused by <i>SH3TC2</i> gene mutations

Hamid Azzedine,N. Ravisé,et al.

2006105 citations

Hereditary neuropathy with liability to pressure palsies: A clinical, electroneurophysiological and morphological study

W. I. M. Verhagen,A.A.W.M. Gabreëls‐Festen,et al.

1993101 citations

Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I)

A.A.W.M. Gabreëls‐Festen,E.M.G. Joosten,et al.

199296 citations

Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A*

Andrea Robertson,Javier Perea,et al.

200292 citations