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Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7qL Notelet, F Chapon, S Khoury, et al.
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
Annals of Emergency Medicine|August 1, 1989
A community survey of the potential use of thrombolytic agents for acute myocardial infarctionM S Eisenberg, M T Ho, S Schaeffer, et al.
Oecologia|November 6, 2009
Population synchrony of a native fish across three Laurentian Great Lakes: evaluating the effects of dispersal and climateDavid B Bunnell, Jean V Adams, Owen T Gorman, et al.
Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
The Neuroradiology Journal|September 25, 2013
Five-Year Longitudinal MRI Follow-up and (1)H Single Voxel MRS in 14 patients with Gliomatosis Treated with Temodal, Radiotherapy and Antiangiogenic TherapyJ M Constans, S Collet, F Kauffmann, et al.
Der Nervenarzt|August 24, 2016
[Specialist Training in Psychiatry and Psychotherapy : Evaluation of the East Westphalia-Lippe Academy curriculum]M Driessen, B Hötger, K Kronmüller, et al.
European Neurology|January 1, 1997
New mutations in the X-linked form of Charcot-Marie-Tooth diseaseP Latour, A Fabreguette, C Ressot, et al.
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