F.J.M. Gabreëls - Concepedia

Author

F.J.M. Gabreëls

Also Known As

F J Gabreels, F J Gabreëls, F J M Gabreëls, F. J. Gabreels, F. J. Gabreëls, F. J. M. GABREELS, F. J. M. GABREËLS, F. J. M. Gabreels, F. J. M. Gabreéls, F. J. M. Gabreëls

245

Publications

8.4K

Citations

H-Index

198

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center

About

F.J.M. Gabreëls is an author at Radboud University Nijmegen specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	31	77	3.5K
2	Health Sciences	13	15	696
3	Engineering	1	1	35
4	Management	1	1	35
5	Natural Sciences	1	1	31

F.J.M. Gabreëls

134

Publications

Citations

H-Index

Page 1

	Year	Citations
A new leukoencephalopathy with vanishing white matter Marjo S. van der Knaap, P. G. Barth, F.J.M. Gabreëls, Neurology Neurological DisorderWhite MatterClinical NeurologyDiagnosisPathology	1997	390
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome D. Daniëlle de Vries, Baziel G.M. van Engelen, F.J.M. Gabreëls, Annals of Neurology	1993	262
Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis Aad Verrips, Lies H. Hoefsloot, Gerry Steenbergen, Brain	2000	247
Effect of Botulinum Toxin in the Treatment of Drooling: A Controlled Clinical Trial Peter H. Jongerius, Frank J. A. van den Hoogen, Jacques van Limbeek, PEDIATRICS	2004	201
Cerebrotendinous Xanthomatosis: The Spectrum of Imaging Findings and the Correlation with Neuropathologic Findings Frederik Barkhof, Aad Verrips, Pieter Wesseling, Radiology	2000	184
A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q Johan Fischer, W. Ruitenbeek, F.J.M. Gabreëls, European Journal of Pediatrics Mitochondrial MyopathyMitochondrial FunctionBiochemistryPhysiologyDegenerative Disease	1986	166
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
Two divergent types of nerve pathology in patients with different P sub 0 mutations in Charcot-Marie-Tooth disease Anneke Gabreëls-Festen, Jessica E. Hoogendijk, P.H.S. Meijerink, Neurology	1996	149
Congenital muscular dystrophy Q.H. Leyten, F.J.M. Gabreëls, W.O. Renier, The Journal of Pediatrics PediatricsDegenerative DiseaseNeuromuscular DisordersNeuromusculoskeletal DisorderCongenital Muscular Dystrophy	1989	146
The Clinical Phenotype of Succinic Semialdehyde Dehydrogenase Deficiency (4-Hydroxybutyric Aciduria): Case Reports of 23 New Patients K. Michael Gibson, Ernst Christensen, Cornelis Jakobs, PEDIATRICS	1997	142

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