A.A.W.M. Gabreëls‐Festen

Author

Also Known As

A A Gabreels-Festen, A A Gabreëls-Festen, A A. W. M Gabreëls-Festen, A Gabreëls-Festen, A. A. Gabreëls-Festen, A. A. Gabreëls‐Festen, A. A. Gabreëls–Festen, A. A. W. Gabreëls-Festen, A. A. W. M. GABREËLS-FESTEN, A. A. W. M. Gabreels-Festen

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Amsterdam UMC Location University of Amsterdam University of Antwerp

About

A.A.W.M. Gabreëls‐Festen is an author at Radboud University Nijmegen specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	21	1.2K
2	Health Sciences	2	2	122
3	Anatomy	2	2	45
4	Social Sciences	1	1	33
5	Anesthesia	1	1	216

A.A.W.M. Gabreëls‐Festen

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Neuromuscular complications in patients given pavulon/sr (pancuronium bromide) during artificial ventilation A.A.W. Op de Coul, P.C.L.A. Lambregts, J. Koeman, Clinical Neurology and Neurosurgery Spinal Cord InjuryMedicineVentilationArtificial VentilationNeuromuscular Complications	1985	216
De-novo mutation in hereditary motor and sensory neuropathy type I Jessica E. Hoogendijk, Gerard W. Hensels, Emiel A. M. Janssen, The Lancet Rare DiseasesHereditary MotorMendelian DisorderGenetic DisorderMedicine	1992	161
Mutations in <i>GDAP1</i> Eva Nelis, Peter Van den Bergh, Marie‐Claude Belpaire‐Dethiou, Neurology	2002	156
Macrophage clustering as a diagnostic marker in sural nerve biopsies of patients with CIDP Claudia Sommer, Stefan Koch, Martin Lammens, Neurology	2005	128
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, Regine Greiner–Petter, PubMed ImmunologyPeripheral NervesCellular NeurobiologyCellular PhysiologyTrj Point Mutation	1998	117
Spine deformities in Charcot-Marie-Tooth 4C caused by <i>SH3TC2</i> gene mutations Hamid Azzedine, N. Ravisé, Christophe Verny, Neurology	2006	104
Hereditary neuropathy with liability to pressure palsies: A clinical, electroneurophysiological and morphological study W. I. M. Verhagen, A.A.W.M. Gabreëls‐Festen, P.J.M. van Wensen, Journal of the Neurological Sciences Hereditary NeuropathyPeripheral NervesMorphological StudyNeurologyCerebral Palsy	1993	101
Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I) A.A.W.M. Gabreëls‐Festen, E.M.G. Joosten, F.J.M. Gabreëls, Journal of the Neurological Sciences Health SciencesNeurological DisorderNeuroanatomyNeuromotor DisordersMedicine	1992	96
Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33 A.A.W.M. Gabreëls‐Festen, Sylvia E. C. van Beersum, L. Eshuis, Journal of Neurology Neurosurgery & Psychiatry	1999	85
CONGENITAL DEMYELINATING MOTOR AND SENSORY NEUROPATHY WITH FOCALLY FOLDED MYELIN SHEATHS A.A.W.M. Gabreëls‐Festen, E.M.G. Joosten, F.J.M. Gabreëls, Brain Neurological DisorderPeripheral NerveCommon Neurological DisordersOptic NerveHmsn Type Iii	1990	70

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