C.S.M. Straathof - Concepedia

Author

C.S.M. Straathof

Also Known As

C. S. M. Straathof, C. S. Straathof, C. Straathof, C.S.M Straathof, C.S.M. Straathof, Chiara S M Straathof, Chiara S Straathof, Chiara S. M. Straathof, Chiara S. Straathof, Chiara S.M. Straathof

Publications

Citations

H-Index

Concepts

All Affiliations

Leiden University Medical Center Radboud University Nijmegen Radboud University Medical Center Santhera Pharmaceuticals (Switzerland)Erasmus University Rotterdam

About

C.S.M. Straathof is an author at Leiden University Medical Center specializing in medicine, neurology, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	819
2	Health Sciences	2	2	216
3	Applied Physiology	1	1	34
4	Biostatistics	1	1	148
5	Molecular Biology	1	1	148

C.S.M. Straathof

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
The diagnostic accuracy of magnetic resonance imaging and cerebrospinal fluid cytology in leptomeningeal metastasis C.S.M. Straathof, Hein G. de Bruin, Diederik W.J. Dippel, Journal of Neurology Neuro-oncologyCerebrospinal FluidHistopathologyDiagnosisPathology	1999	249
Long-term effect of thymectomy plus prednisone versus prednisone alone in patients with non-thymomatous myasthenia gravis: 2-year extension of the MGTX randomised trial Gil I. Wolfe, Henry J. Kaminski, Inmaculada Aban, The Lancet Neurology	2019	216
Efficacy of idebenone on respiratory function in patients with Duchenne muscular dystrophy not using glucocorticoids (DELOS): a double-blind randomised placebo-controlled phase 3 trial Gunnar Buyse, Thomas Voït, Ulrike Schara, The Lancet Placebo-controlled Phase 3Respiratory FunctionExerciseDuchenne Muscular DystrophyClinical Trials	2015	182
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials Karen Anthony, Sebahattin Çirak, Silvia Torelli, Brain GeneticsBecker Muscular DystrophyDystrophin QuantificationMolecular BiologyMolecular Genetics	2011	148
<i><scp>RYR</scp>1</i>‐related myopathies: a wide spectrum of phenotypes throughout life Marc Snoeck, Baziel G.M. van Engelen, Benno Küsters, European Journal of Neurology	2015	138
Reduced cerebral gray matter and altered white matter in boys with <scp>D</scp>uchenne muscular dystrophy N. Doorenweerd, C.S.M. Straathof, Eve M. Dumas, Annals of Neurology	2014	119
Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy Craig M. McDonald, Thomas Meier, Thomas Voït, Neuromuscular Disorders	2016	63
Predicting Outcome in Guillain-Barré Syndrome Alex Y. Doets, Hester F. Lingsma, Christa Walgaard, Neurology	2021	61
Autosomal recessive limb‐girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients Leroy ten Dam, Wendy S. Frankhuizen, Wim H.J.P. Linssen, Clinical Genetics	2019	60
Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients A.T.J.M. Helderman-van den Enden, C.S.M. Straathof, Annemieke Aartsma‐Rus, Neuromuscular Disorders Duchenne PatientsPromising OutlookMedicineDegenerative DiseaseRehabilitation	2010	57

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