H. J. ter Laak - Concepedia

Author

H. J. ter Laak

Also Known As

H J Ter Laak, H J ter Laak, H. J. TER LAAK, H. J. Ter Laak, H. J. ter Laak, H.J ter Laak, H.J. Ter Laak, H.J. Ter Laak/, H.J. ter Laak, Henk J Ter Laak

Publications

3.4K

Citations

H-Index

119

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center University of Amsterdam Elisabeth-TweeSteden Ziekenhuis

About

H. J. ter Laak is an author at Radboud University Nijmegen specializing in medicine, physiology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	33	1.6K
2	Health Sciences	9	9	391
3	Engineering	2	2	121
4	Natural Sciences	1	1	129
5	Allergy	1	1	14

H. J. ter Laak

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Anti-signal recognition particle autoantibodies: marker of a necrotising myopathy G.J.D. Hengstman, H. J. ter Laak, W.T.M. Vree Egberts, Annals of the Rheumatic Diseases	2006	334
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
Complex regional pain syndrome type I (RSD) Lijckle van der Laan, H. J. ter Laak, Anneke Gabreëls-Festen, Neurology	1998	186
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
Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies. J. Van der Pas, G.J.D. Hengstman, H. J. ter Laak, PubMed	2004	146
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
A 4–base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome I.F.M. de Coo, W.O. Renier, W. Ruitenbeek, Annals of Neurology Mitochondrial Respiratory ChainNeurodegenerative DiseasesMendelian DisorderMitochondrial FunctionGenetic Disorder	1999	129
A 4-base pair deletion in the mitochondrial cytochromeb gene associated with parkinsonism/MELAS overlap syndrome I.F.M. de Coo, W.O. Renier, W. Ruitenbeek, Annals of Neurology MitophagyMitochondrial Cytochromeb GeneGeneticsGenetic EpidemiologyMolecular Biology	1999	128
Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders Paul J. Blijham, H. J. ter Laak, Helenius J. Schelhaas, Journal of Applied Physiology	2006	107
Fatigue in type I fiber predominance: A muscle force and surface EMG study on the relative role of type I and type II muscle fibers Wim H.J.P. Linssen, Dick F. Stegeman, E.M.G. Joosten, Muscle & Nerve Muscle FunctionEngineeringKinesiologyMuscle InjurySkeletal Muscle	1991	97

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