Search research articles
Contact Us
Filters
Showing results (201-210 of 272) with videos related to
Page
of 28
Sort By:
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
March 6, 2012
Electrophysiological characteristics in four patients from Brazil with stiff person syndrome
Paulo J Lorenzoni, Rosana H Scola, Cláudia S K Kay, et al.
Journal of the Neurological Sciences
|
April 1, 2008
Cerebellar ataxia in non-paraneoplastic Lambert-Eaton myasthenic syndrome
Paulo J Lorenzoni, Rosana H Scola, Bethan Lang, et al.
Cell Biology International
|
October 27, 2018
Hyperbaric oxygen affects endothelial progenitor cells proliferation in vitro
Julia C Benincasa, Luiz H de Freitas Filho, Giane D Carneiro, et al.
Arquivos De Neuro-Psiquiatria
|
September 19, 2007
Chronic inflammatory demyelinating polyradiculoneuropathy in chronic graft-versus-host disease following allogeneic hematopoietic stem cell transplantation: case report
Paulo José Lorenzoni, Rosana Herminia Scola, Ana Lucila Moreira Carsten, et al.
Experimental Parasitology
|
November 23, 2017
Trypanosoma cruzi tryparedoxin II interacts with different peroxiredoxins under physiological and oxidative stress conditions
L Dias, E F Peloso, A F P Leme, et al.
Arquivos De Neuro-Psiquiatria
|
February 6, 2004
Myopathy of distal lower limbs: the clinical variant of Miyoshi
Cristiane N Soares, Marcos R G de Freitas, Osvaldo J M Nascimento, et al.
The Journal of Biological Chemistry
|
July 16, 2008
Deficiency in microfibril-associated glycoprotein-1 leads to complex phenotypes in multiple organ systems
Justin S Weinbaum, Thomas J Broekelmann, Richard A Pierce, et al.
Arquivos De Neuro-Psiquiatria
|
June 18, 2002
Hemimasticatory spasm treated with botulinum toxin: case report
Hélio A G Teive, Elcio J Piovesan, Francisco M B Germiniani, et al.
The New England Journal of Medicine
|
May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
C T Moraes, S DiMauro, M Zeviani, et al.
Annals of Clinical and Translational Neurology
|
February 8, 2017
Novel synaptobrevin-1 mutation causes fatal congenital myasthenic syndrome
Xin-Ming Shen, Rosana H Scola, Paulo J Lorenzoni, et al.
Page
of 28
Search research articles
Search
Showing results (201-210 of 272) with videos related to
Sort By:
Page
of 28
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
March 6, 2012
Electrophysiological characteristics in four patients from Brazil with stiff person syndrome
Paulo J Lorenzoni, Rosana H Scola, Cláudia S K Kay, et al.
Journal of the Neurological Sciences
|
April 1, 2008
Cerebellar ataxia in non-paraneoplastic Lambert-Eaton myasthenic syndrome
Paulo J Lorenzoni, Rosana H Scola, Bethan Lang, et al.
Cell Biology International
|
October 27, 2018
Hyperbaric oxygen affects endothelial progenitor cells proliferation in vitro
Julia C Benincasa, Luiz H de Freitas Filho, Giane D Carneiro, et al.
Arquivos De Neuro-Psiquiatria
|
September 19, 2007
Chronic inflammatory demyelinating polyradiculoneuropathy in chronic graft-versus-host disease following allogeneic hematopoietic stem cell transplantation: case report
Paulo José Lorenzoni, Rosana Herminia Scola, Ana Lucila Moreira Carsten, et al.
Experimental Parasitology
|
November 23, 2017
Trypanosoma cruzi tryparedoxin II interacts with different peroxiredoxins under physiological and oxidative stress conditions
L Dias, E F Peloso, A F P Leme, et al.
Arquivos De Neuro-Psiquiatria
|
February 6, 2004
Myopathy of distal lower limbs: the clinical variant of Miyoshi
Cristiane N Soares, Marcos R G de Freitas, Osvaldo J M Nascimento, et al.
The Journal of Biological Chemistry
|
July 16, 2008
Deficiency in microfibril-associated glycoprotein-1 leads to complex phenotypes in multiple organ systems
Justin S Weinbaum, Thomas J Broekelmann, Richard A Pierce, et al.
Arquivos De Neuro-Psiquiatria
|
June 18, 2002
Hemimasticatory spasm treated with botulinum toxin: case report
Hélio A G Teive, Elcio J Piovesan, Francisco M B Germiniani, et al.
The New England Journal of Medicine
|
May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
C T Moraes, S DiMauro, M Zeviani, et al.
Annals of Clinical and Translational Neurology
|
February 8, 2017
Novel synaptobrevin-1 mutation causes fatal congenital myasthenic syndrome
Xin-Ming Shen, Rosana H Scola, Paulo J Lorenzoni, et al.
Page
of 28