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Research in Developmental Disabilities
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March 17, 2018
Feedforward motor control in developmental dyslexia and developmental coordination disorder: Does comorbidity matter?
Fabien Cignetti, Marianne Vaugoyeau, Aurelie Fontan, et al.
AIDS (London, England)
|
August 2, 2003
Persistent mitochondrial dysfunction in HIV-1-exposed but uninfected infants: clinical screening in a large prospective cohort
Béatrice Barret, Marc Tardieu, Pierre Rustin, et al.
European Journal of Human Genetics : EJHG
|
August 5, 2010
Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype
Pierre Cacciagli, Marie-Reine Haddad, Cécile Mignon-Ravix, et al.
Journal of Neurology
|
March 18, 2016
Normalisation of brain spectroscopy findings in Niemann-Pick disease type C patients treated with miglustat
Frédéric Sedel, Brigitte Chabrol, Bertrand Audoin, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology
|
June 2, 2022
Reduced plantar-flexors extensibility but improved selective motor control associated with age in young children with unilateral cerebral palsy and equinovalgus gait
Christophe Boulay, Morgan Sangeux, Guillaume Authier, et al.
Muscle & Nerve
|
October 9, 2009
Non-lethal neonatal neuromuscular variant of glycogenosis type IV with novel GBE1 mutations
Carla Fernandez, Cécile Halbert, André Maues De Paula, et al.
Journal of Palliative Medicine
|
February 14, 2024
Continuous Deep Sedation Until Death of Children at the End of Life: French Physicians' Opinions
Carole-Anne Pisa, Pierre Le Coz, Marie-Ange Einaudi, et al.
Molecular Genetics and Metabolism
|
February 7, 2012
Atypical pyridoxine-dependent epilepsy due to a pseudoexon in ALDH7A1
Mathieu Milh, Ana Pop, Warsha Kanhai, et al.
Pediatric Neurology
|
February 27, 2023
Improved Gait and Radiological Measurements After injection of Botulinum Toxin Into Peroneus Longus in Young Children With USCP and Equinovalgus Gait
Christophe Boulay, Morgan Sangeux, Guillaume Authier, et al.
Journal of Medical Genetics
|
July 29, 2009
Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia
Cécile Mignon-Ravix, Pierre Cacciagli, Bilal El-Waly, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 147) with videos related to
Sort By:
Page
of 15
Research in Developmental Disabilities
|
March 17, 2018
Feedforward motor control in developmental dyslexia and developmental coordination disorder: Does comorbidity matter?
Fabien Cignetti, Marianne Vaugoyeau, Aurelie Fontan, et al.
AIDS (London, England)
|
August 2, 2003
Persistent mitochondrial dysfunction in HIV-1-exposed but uninfected infants: clinical screening in a large prospective cohort
Béatrice Barret, Marc Tardieu, Pierre Rustin, et al.
European Journal of Human Genetics : EJHG
|
August 5, 2010
Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype
Pierre Cacciagli, Marie-Reine Haddad, Cécile Mignon-Ravix, et al.
Journal of Neurology
|
March 18, 2016
Normalisation of brain spectroscopy findings in Niemann-Pick disease type C patients treated with miglustat
Frédéric Sedel, Brigitte Chabrol, Bertrand Audoin, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology
|
June 2, 2022
Reduced plantar-flexors extensibility but improved selective motor control associated with age in young children with unilateral cerebral palsy and equinovalgus gait
Christophe Boulay, Morgan Sangeux, Guillaume Authier, et al.
Muscle & Nerve
|
October 9, 2009
Non-lethal neonatal neuromuscular variant of glycogenosis type IV with novel GBE1 mutations
Carla Fernandez, Cécile Halbert, André Maues De Paula, et al.
Journal of Palliative Medicine
|
February 14, 2024
Continuous Deep Sedation Until Death of Children at the End of Life: French Physicians' Opinions
Carole-Anne Pisa, Pierre Le Coz, Marie-Ange Einaudi, et al.
Molecular Genetics and Metabolism
|
February 7, 2012
Atypical pyridoxine-dependent epilepsy due to a pseudoexon in ALDH7A1
Mathieu Milh, Ana Pop, Warsha Kanhai, et al.
Pediatric Neurology
|
February 27, 2023
Improved Gait and Radiological Measurements After injection of Botulinum Toxin Into Peroneus Longus in Young Children With USCP and Equinovalgus Gait
Christophe Boulay, Morgan Sangeux, Guillaume Authier, et al.
Journal of Medical Genetics
|
July 29, 2009
Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia
Cécile Mignon-Ravix, Pierre Cacciagli, Bilal El-Waly, et al.
Page
of 15