Showing results (91-100 of 144) with videos related to
Sort By:
Pageof 15
Neurosurgery|February 1, 1997
The in vivo metabolic pattern of low-grade brain gliomas: a positron emission tomographic study using 18F-fluorodeoxyglucose and 11C-L-methylmethionineJ M Derlon, M C Petit-Taboué, F Chapon, et al.Human Mutation|January 1, 1995
Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1BP Latour, F Blanquet, E Nelis, et al.European Journal of Human Genetics : EJHG|January 1, 1994
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutationsE Plassart, J Reboul, C S Rime, et al.European Journal of Neurology|November 29, 2013
Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generationsF Degoul, M Diry, F Viader, et al.Mutagenesis|August 18, 2005
Screening of TP53 mutations by DHPLC and sequencing in brain tumours from patients with an occupational exposure to pesticides or organic solventsV Loyant, A Jaffré, J Breton, et al.AJNR. American Journal of Neuroradiology|July 16, 2011
Is brain maturation comparable in fetuses and premature neonates at term equivalent age?A Viola, S Confort-Gouny, J F Schneider, et al.Archives of Neurology|March 31, 1998
Paraneoplastic cerebellar syndrome and optic neuritis with anti-CV2 antibodies: clinical response to excision of the primary tumorV de la Sayette, F Bertran, J Honnorat, et al.Revue Neurologique|April 1, 1997
[Multiple and unilateral paralysis of the cranial nerves revealing 2 cerebellar infarctions]L Dubuc, F Bertran, P Busson, et al.Journal of Orthopaedic Surgery and Research|November 19, 2025
Life after bone infection: a retrospective comparison of quality of life in patients with periprosthetic joint infection and fracture-related infectionsJ Frese, L Schwake, A-P Schulz, et al.American Journal of Physiology. Cell Physiology|July 3, 2009
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubesS Sacconi, D Simkin, N Arrighi, et al.Pageof 15