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Neonatology
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December 8, 2021
Bronchopulmonary Dysplasia and Risk of Developmental Delay: An EPIPAGE-2 Cohort Study
Ludovic Tréluyer, Pierre-Henri Jarreau, Laetitia Marchand-Martin, et al.
Journal of Attention Disorders
|
January 15, 2014
Effects of Methylphenidate on Default-Mode Network/Task-Positive Network Synchronization in Children With ADHD
Laurent Querne, Sidy Fall, Anne-Gaëlle Le Moing, et al.
Seizure
|
June 18, 2023
Retrospective chart review study of use of cannabidiol (CBD) independent of concomitant clobazam use in patients with Lennox-Gastaut syndrome or Dravet syndrome
Rima Nabbout, Alexis Arzimanoglou, Stéphane Auvin, et al.
Plant Direct
|
June 11, 2025
BdNRT2A and BdNRT3.2 Are the Major Components of the High-Affinity Nitrate Transport System in <i>Brachypodium distachyon</i>
Laure C David, Mathilde Grégoire, Patrick Berquin, et al.
European Child & Adolescent Psychiatry
|
October 11, 2017
A double-blind placebo-controlled randomised trial of omega-3 supplementation in children with moderate ADHD symptoms
Catherine Cornu, Catherine Mercier, Tiphanie Ginhoux, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
August 19, 2010
Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome
Jacques Rochette, Patrice Roll, Ying-Hui Fu, et al.
Epilepsia
|
May 31, 2016
ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate
Sylvain Rheims, Vania Herbillon, Nathalie Villeneuve, et al.
Epilepsia Open
|
January 4, 2024
Phosphatidylserine enriched with polyunsaturated n-3 fatty acid supplementation for attention-deficit hyperactivity disorder in children and adolescents with epilepsy: A randomized placebo-controlled trial
Sylvain Rheims, Vania Herbillon, Ségolène Gaillard, et al.
American Journal of Human Genetics
|
May 13, 2014
Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness
Isabelle Perrault, Fadi F Hamdan, Marlène Rio, et al.
Plos Genetics
|
February 14, 2009
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females
Christel Depienne, Delphine Bouteiller, Boris Keren, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
Neonatology
|
December 8, 2021
Bronchopulmonary Dysplasia and Risk of Developmental Delay: An EPIPAGE-2 Cohort Study
Ludovic Tréluyer, Pierre-Henri Jarreau, Laetitia Marchand-Martin, et al.
Journal of Attention Disorders
|
January 15, 2014
Effects of Methylphenidate on Default-Mode Network/Task-Positive Network Synchronization in Children With ADHD
Laurent Querne, Sidy Fall, Anne-Gaëlle Le Moing, et al.
Seizure
|
June 18, 2023
Retrospective chart review study of use of cannabidiol (CBD) independent of concomitant clobazam use in patients with Lennox-Gastaut syndrome or Dravet syndrome
Rima Nabbout, Alexis Arzimanoglou, Stéphane Auvin, et al.
Plant Direct
|
June 11, 2025
BdNRT2A and BdNRT3.2 Are the Major Components of the High-Affinity Nitrate Transport System in <i>Brachypodium distachyon</i>
Laure C David, Mathilde Grégoire, Patrick Berquin, et al.
European Child & Adolescent Psychiatry
|
October 11, 2017
A double-blind placebo-controlled randomised trial of omega-3 supplementation in children with moderate ADHD symptoms
Catherine Cornu, Catherine Mercier, Tiphanie Ginhoux, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
August 19, 2010
Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome
Jacques Rochette, Patrice Roll, Ying-Hui Fu, et al.
Epilepsia
|
May 31, 2016
ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate
Sylvain Rheims, Vania Herbillon, Nathalie Villeneuve, et al.
Epilepsia Open
|
January 4, 2024
Phosphatidylserine enriched with polyunsaturated n-3 fatty acid supplementation for attention-deficit hyperactivity disorder in children and adolescents with epilepsy: A randomized placebo-controlled trial
Sylvain Rheims, Vania Herbillon, Ségolène Gaillard, et al.
American Journal of Human Genetics
|
May 13, 2014
Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness
Isabelle Perrault, Fadi F Hamdan, Marlène Rio, et al.
Plos Genetics
|
February 14, 2009
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females
Christel Depienne, Delphine Bouteiller, Boris Keren, et al.
Page
of 5