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La Radiologia Medica
|
January 13, 2011
CT and MRI of Wernicke's encephalopathy
A Cerase, E Rubenni, A Rufa, et al.
Journal of Chemical Theory and Computation
|
July 14, 2023
Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex
Ivy Zhang, Dominic A Rufa, Iván Pulido, et al.
Journal of Chemical Theory and Computation
|
January 2, 2024
Correction to Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex
Ivy Zhang, Dominic A Rufa, Iván Pulido, et al.
Biorxiv : the Preprint Server for Biology
|
March 22, 2023
Identifying and overcoming the sampling challenges in relative binding free energy calculations of a model protein:protein complex
Ivy Zhang, Dominic A Rufa, Iván Pulido, et al.
European Journal of Neurology
|
September 23, 2008
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
G Piccirillo, D Magrì, M Mitra, et al.
Journal of Submicroscopic Cytology and Pathology
|
July 1, 1997
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case
K Plewnia, M T Dotti, A Malandrini, et al.
Clinical Genetics
|
July 13, 2011
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy
G N Gallus, E Cardaioli, A Rufa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 17, 2002
Genetic leukoencephalopathies with unknown metabolic pathogenesis
A Federico, A Rufa, C Battisti, et al.
Acta Neurologica Scandinavica
|
May 12, 2018
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases
I Taglia, I Di Donato, S Bianchi, et al.
Neurology
|
January 30, 2008
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene
M Szlago, G N Gallus, A Schenone, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 4
La Radiologia Medica
|
January 13, 2011
CT and MRI of Wernicke's encephalopathy
A Cerase, E Rubenni, A Rufa, et al.
Journal of Chemical Theory and Computation
|
July 14, 2023
Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex
Ivy Zhang, Dominic A Rufa, Iván Pulido, et al.
Journal of Chemical Theory and Computation
|
January 2, 2024
Correction to Identifying and Overcoming the Sampling Challenges in Relative Binding Free Energy Calculations of a Model Protein:Protein Complex
Ivy Zhang, Dominic A Rufa, Iván Pulido, et al.
Biorxiv : the Preprint Server for Biology
|
March 22, 2023
Identifying and overcoming the sampling challenges in relative binding free energy calculations of a model protein:protein complex
Ivy Zhang, Dominic A Rufa, Iván Pulido, et al.
European Journal of Neurology
|
September 23, 2008
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
G Piccirillo, D Magrì, M Mitra, et al.
Journal of Submicroscopic Cytology and Pathology
|
July 1, 1997
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case
K Plewnia, M T Dotti, A Malandrini, et al.
Clinical Genetics
|
July 13, 2011
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy
G N Gallus, E Cardaioli, A Rufa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 17, 2002
Genetic leukoencephalopathies with unknown metabolic pathogenesis
A Federico, A Rufa, C Battisti, et al.
Acta Neurologica Scandinavica
|
May 12, 2018
AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases
I Taglia, I Di Donato, S Bianchi, et al.
Neurology
|
January 30, 2008
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene
M Szlago, G N Gallus, A Schenone, et al.
Page
of 4