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Acta Neurologica Scandinavica
|
May 12, 2018
Exercise testing-based algorithms to diagnose McArdle disease and MAD defects
J-B Noury, F Zagnoli, J-L Carré, et al.
Revue Neurologique
|
September 10, 2013
[Exercise-induced muscle pain due to phosphofrutokinase deficiency: Diagnostic contribution of metabolic explorations (exercise tests, 31P-nuclear magnetic resonance spectroscopy)]
A Drouet, F Zagnoli, T Fassier, et al.
La Revue De Medecine Interne
|
June 20, 2003
[Disseminated and central nervous system Histoplasma capsulatum infection mimicking neoplasm: difficulties in diagnosis, failure in management]
X Nicolas, H Granier, J-P Laborde, et al.
Revue Neurologique
|
October 2, 2021
Cost-utility of oral methylprednisolone in the treatment of multiple sclerosis relapses: Results from the COPOUSEP trial
M Michel, E Le Page, D A Laplaud, et al.
Annales De Cardiologie Et D'Angeiologie
|
February 18, 2014
[Systematic implementation of transthoracic echocardiography, transesophageal echocardiography and 24-hour Holter ECG for the detection of cardiac sources of embolism in patients with stroke or transient ischemic attack. A retrospective study of 220 patients]
U Vinsonneau, A Leblanc, J-F Buchet, et al.
Annales De Cardiologie Et D'Angeiologie
|
February 11, 2011
[Cannabis and myocardial infarction without angiographic stenosis in young patient: guilty or not guilty? A case report]
A Leblanc, A Tirel-Badets, N Paleiron, et al.
Neuroepidemiology
|
March 26, 2014
High completeness of the brest stroke registry evidenced by analysis of sources and capture-recapture method
S Timsit, E Nowak, F Rouhart, et al.
Revue Neurologique
|
September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease
P Laforêt, K Laloui, B Granger, et al.
Journal of Neurology
|
December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
A Ben Ammar, F Petit, N Alexandri, et al.
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of 3
Search research articles
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Showing results (21-30 of 29) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 29 results.
Acta Neurologica Scandinavica
|
May 12, 2018
Exercise testing-based algorithms to diagnose McArdle disease and MAD defects
J-B Noury, F Zagnoli, J-L Carré, et al.
Revue Neurologique
|
September 10, 2013
[Exercise-induced muscle pain due to phosphofrutokinase deficiency: Diagnostic contribution of metabolic explorations (exercise tests, 31P-nuclear magnetic resonance spectroscopy)]
A Drouet, F Zagnoli, T Fassier, et al.
La Revue De Medecine Interne
|
June 20, 2003
[Disseminated and central nervous system Histoplasma capsulatum infection mimicking neoplasm: difficulties in diagnosis, failure in management]
X Nicolas, H Granier, J-P Laborde, et al.
Revue Neurologique
|
October 2, 2021
Cost-utility of oral methylprednisolone in the treatment of multiple sclerosis relapses: Results from the COPOUSEP trial
M Michel, E Le Page, D A Laplaud, et al.
Annales De Cardiologie Et D'Angeiologie
|
February 18, 2014
[Systematic implementation of transthoracic echocardiography, transesophageal echocardiography and 24-hour Holter ECG for the detection of cardiac sources of embolism in patients with stroke or transient ischemic attack. A retrospective study of 220 patients]
U Vinsonneau, A Leblanc, J-F Buchet, et al.
Annales De Cardiologie Et D'Angeiologie
|
February 11, 2011
[Cannabis and myocardial infarction without angiographic stenosis in young patient: guilty or not guilty? A case report]
A Leblanc, A Tirel-Badets, N Paleiron, et al.
Neuroepidemiology
|
March 26, 2014
High completeness of the brest stroke registry evidenced by analysis of sources and capture-recapture method
S Timsit, E Nowak, F Rouhart, et al.
Revue Neurologique
|
September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease
P Laforêt, K Laloui, B Granger, et al.
Journal of Neurology
|
December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
A Ben Ammar, F Petit, N Alexandri, et al.
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of 3