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Studies in Health Technology and Informatics
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June 24, 2020
Toward a Harmonized WHO Family of International Classifications Content Model
Samson W Tu, Csongor I Nyulas, Tania Tudorache, et al.
Orphanet Journal of Rare Diseases
|
October 15, 2020
Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)
Tomàs Pinós, Antoni L Andreu, Claudio Bruno, et al.
Plos One
|
April 15, 2016
Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study
Andrea Martinuzzi, Domenico Montanaro, Marinela Vavla, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
April 5, 2020
Psychosocial impact of sport activity in neuromuscular disorders
Gian Luca Vita, Claudia Stancanelli, Stefania La Foresta, et al.
European Journal of Physical and Rehabilitation Medicine
|
September 1, 2016
Assessing and treating pain associated with stroke, multiple sclerosis, cerebral palsy, spinal cord injury and spasticity. Evidence and recommendations from the Italian Consensus Conference on Pain in Neurorehabilitation
Stefano Paolucci, Andrea Martinuzzi, Giorgio Scivoletto, et al.
International Journal of Methods in Psychiatric Research
|
May 9, 2006
The Italian preadolescent mental health project (PrISMA): rationale and methods
Alessandra Frigerio, Laura Vanzin, Valentina Pastore, et al.
European Child & Adolescent Psychiatry
|
January 24, 2009
Prevalence and correlates of mental disorders among adolescents in Italy: the PrISMA study
Alessandra Frigerio, Paola Rucci, Robert Goodman, et al.
Biochimica Et Biophysica Acta
|
December 19, 2012
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions
Leonardo Caporali, Anna Maria Ghelli, Luisa Iommarini, et al.
Human Mutation
|
May 28, 2014
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance
Valeria Carossa, Anna Ghelli, Concetta Valentina Tropeano, et al.
Plos Genetics
|
February 15, 2018
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy
Leonardo Caporali, Luisa Iommarini, Chiara La Morgia, et al.
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of 17
Search research articles
Search
Showing results (131-140 of 163) with videos related to
Sort By:
Page
of 17
Studies in Health Technology and Informatics
|
June 24, 2020
Toward a Harmonized WHO Family of International Classifications Content Model
Samson W Tu, Csongor I Nyulas, Tania Tudorache, et al.
Orphanet Journal of Rare Diseases
|
October 15, 2020
Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)
Tomàs Pinós, Antoni L Andreu, Claudio Bruno, et al.
Plos One
|
April 15, 2016
Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study
Andrea Martinuzzi, Domenico Montanaro, Marinela Vavla, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
April 5, 2020
Psychosocial impact of sport activity in neuromuscular disorders
Gian Luca Vita, Claudia Stancanelli, Stefania La Foresta, et al.
European Journal of Physical and Rehabilitation Medicine
|
September 1, 2016
Assessing and treating pain associated with stroke, multiple sclerosis, cerebral palsy, spinal cord injury and spasticity. Evidence and recommendations from the Italian Consensus Conference on Pain in Neurorehabilitation
Stefano Paolucci, Andrea Martinuzzi, Giorgio Scivoletto, et al.
International Journal of Methods in Psychiatric Research
|
May 9, 2006
The Italian preadolescent mental health project (PrISMA): rationale and methods
Alessandra Frigerio, Laura Vanzin, Valentina Pastore, et al.
European Child & Adolescent Psychiatry
|
January 24, 2009
Prevalence and correlates of mental disorders among adolescents in Italy: the PrISMA study
Alessandra Frigerio, Paola Rucci, Robert Goodman, et al.
Biochimica Et Biophysica Acta
|
December 19, 2012
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions
Leonardo Caporali, Anna Maria Ghelli, Luisa Iommarini, et al.
Human Mutation
|
May 28, 2014
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance
Valeria Carossa, Anna Ghelli, Concetta Valentina Tropeano, et al.
Plos Genetics
|
February 15, 2018
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy
Leonardo Caporali, Luisa Iommarini, Chiara La Morgia, et al.
Page
of 17