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Annals of Neurology|September 11, 1999
Hippocampal N-methyl-D-aspartate receptor subunit mRNA levels in temporal lobe epilepsy patientsG W Mathern, J K Pretorius, D Mendoza, et al.Journal of Inherited Metabolic Disease|July 10, 2009
Danon disease: case report and detection of new mutationG Regelsberger, R Höftberger, W F Pickl, et al.Arquivos De Neuro-Psiquiatria|December 1, 1990
[Striated muscle in protein malnutrition: an experimental study in albino rats]O J Nascimento, K Madi, J B Guedes e Silva, et al.Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|April 6, 2013
Myosin Va is developmentally regulated and expressed in the human cerebellum from birth to old ageC C R Souza, T C D Dombroski, H R Machado, et al.Neurobiology of Disease|December 16, 1998
Altered hippocampal kainate-receptor mRNA levels in temporal lobe epilepsy patientsG W Mathern, J K Pretorius, H I Kornblum, et al.European Journal of Cancer (Oxford, England : 1990)|September 26, 2006
Histopathological prognostic factors in medulloblastoma: high expression of survivin is related to unfavourable outcomeC Haberler, I Slavc, T Czech, et al.Annals of Neurology|August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsP Parchi, A Giese, S Capellari, et al.Physics in Medicine and Biology|May 7, 2004
Advances in broad bandwidth light sources for ultrahigh resolution optical coherence tomographyA Unterhuber, B Povazay, K Bizheva, et al.Neurology|February 20, 1999
Hippocampal GABA and glutamate transporter immunoreactivity in patients with temporal lobe epilepsyG W Mathern, D Mendoza, A Lozada, et al.American Journal of Human Genetics|March 26, 1999
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob diseaseH S Lee, N Sambuughin, L Cervenakova, et al.Pageof 29