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A Baruzzi

Showing results (141-150 of 149) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 28, 2010
Autonomic innervation in multiple system atrophy and pure autonomic failureV Donadio, P Cortelli, M Elam, et al.
Journal of Medical Genetics|July 4, 2006
The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotypeM L Valentino, P Barboni, C Rengo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 16, 2009
Agrypnia Excitata: a microneurographic study of muscle sympathetic nerve activityV Donadio, P Montagna, M Pennisi, et al.
Brain : a Journal of Neurology|April 20, 2004
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic casesF Bisulli, P Tinuper, P Avoni, et al.
European Journal of Neurology|March 23, 2012
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?C La Morgia, P Barboni, G Rizzo, et al.
Endothelium : Journal of Endothelial Cell Research|March 15, 2005
Endothelial function is preserved in Chagas' heart disease patients without heart failureFernanda M Consolim-Colombo, Heno F Lopes, Eliana A Rosetto, et al.
Leukemia|September 18, 2009
Different isoforms of the B-cell mutator activation-induced cytidine deaminase are aberrantly expressed in BCR-ABL1-positive acute lymphoblastic leukemia patientsI Iacobucci, A Lonetti, F Messa, et al.
Neurology|November 29, 2008
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndromeA Di Fonzo, M C J Dekker, P Montagna, et al.
Neuro-Oncology Practice|June 3, 2015
Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center?Alba A Brandes, Enrico Franceschi, Mario Ermani, et al.
Pageof 15

Showing results (141-150 of 149) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 149 results.
Journal of Neurology, Neurosurgery, and Psychiatry|July 28, 2010
Autonomic innervation in multiple system atrophy and pure autonomic failureV Donadio, P Cortelli, M Elam, et al.
Journal of Medical Genetics|July 4, 2006
The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotypeM L Valentino, P Barboni, C Rengo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 16, 2009
Agrypnia Excitata: a microneurographic study of muscle sympathetic nerve activityV Donadio, P Montagna, M Pennisi, et al.
Brain : a Journal of Neurology|April 20, 2004
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic casesF Bisulli, P Tinuper, P Avoni, et al.
European Journal of Neurology|March 23, 2012
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?C La Morgia, P Barboni, G Rizzo, et al.
Endothelium : Journal of Endothelial Cell Research|March 15, 2005
Endothelial function is preserved in Chagas' heart disease patients without heart failureFernanda M Consolim-Colombo, Heno F Lopes, Eliana A Rosetto, et al.
Leukemia|September 18, 2009
Different isoforms of the B-cell mutator activation-induced cytidine deaminase are aberrantly expressed in BCR-ABL1-positive acute lymphoblastic leukemia patientsI Iacobucci, A Lonetti, F Messa, et al.
Neurology|November 29, 2008
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndromeA Di Fonzo, M C J Dekker, P Montagna, et al.
Neuro-Oncology Practice|June 3, 2015
Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center?Alba A Brandes, Enrico Franceschi, Mario Ermani, et al.
Pageof 15