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The Israel Medical Association Journal : IMAJ
|
August 26, 2004
Sydenham's chorea--an entity in progress
Michael Rotstein, Shaul Harel
Journal of Inherited Metabolic Disease
|
March 5, 2009
Consideration of gene therapy for paediatric neurotransmitter diseases
Michael Rotstein, Un Jung Kang
Annals of Neurology
|
March 13, 2010
Childhood absence epilepsy as a manifestation of GLUT1 deficiency
Michael Rotstein, Darryl C De Vivo
Journal of Clinical Medicine
|
January 11, 2022
Acute and Long-Term Effects of an Internet-Based, Self-Help Comprehensive Behavioral Intervention for Children and Teens with Tic Disorders with Comorbid Attention Deficit Hyperactivity Disorder, or Obsessive Compulsive Disorder: A Reanalysis of Data from a Randomized Controlled Trial
Lilach Rachamim, Hila Mualem-Taylor, Osnat Rachamim, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
July 11, 2006
NAP enhances neurodevelopment of newborn apolipoprotein E-deficient mice subjected to hypoxia
Michael Rotstein, Haim Bassan, Naam Kariv, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 12, 2010
The spectrum of movement disorders in Glut-1 deficiency
Roser Pons, Abbie Collins, Michael Rotstein, et al.
European Child & Adolescent Psychiatry
|
June 13, 2022
Group comprehensive behavioral intervention for tics contribution to broader cognitive and emotion regulation in children
Noa Gur, Sharon Zimmerman-Brenner, Aviva Fattal-Valevski, et al.
European Child & Adolescent Psychiatry
|
November 24, 2020
Internet-based guided self-help comprehensive behavioral intervention for tics (ICBIT) for youth with tic disorders: a feasibility and effectiveness study with 6 month-follow-up
Lilach Rachamim, Sharon Zimmerman-Brenner, Osnat Rachamim, et al.
Movement Disorders Clinical Practice
|
February 5, 2019
Levodopa Responsive Parkinsonism in Two Patients With Phosphoglycerate Kinase Deficiency
Tuhin Virmani, Michael Rotstein, Ronen Spiegel, et al.
Annals of Neurology
|
August 6, 2010
Glut1 deficiency: inheritance pattern determined by haploinsufficiency
Michael Rotstein, Kristin Engelstad, Hong Yang, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
The Israel Medical Association Journal : IMAJ
|
August 26, 2004
Sydenham's chorea--an entity in progress
Michael Rotstein, Shaul Harel
Journal of Inherited Metabolic Disease
|
March 5, 2009
Consideration of gene therapy for paediatric neurotransmitter diseases
Michael Rotstein, Un Jung Kang
Annals of Neurology
|
March 13, 2010
Childhood absence epilepsy as a manifestation of GLUT1 deficiency
Michael Rotstein, Darryl C De Vivo
Journal of Clinical Medicine
|
January 11, 2022
Acute and Long-Term Effects of an Internet-Based, Self-Help Comprehensive Behavioral Intervention for Children and Teens with Tic Disorders with Comorbid Attention Deficit Hyperactivity Disorder, or Obsessive Compulsive Disorder: A Reanalysis of Data from a Randomized Controlled Trial
Lilach Rachamim, Hila Mualem-Taylor, Osnat Rachamim, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
July 11, 2006
NAP enhances neurodevelopment of newborn apolipoprotein E-deficient mice subjected to hypoxia
Michael Rotstein, Haim Bassan, Naam Kariv, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 12, 2010
The spectrum of movement disorders in Glut-1 deficiency
Roser Pons, Abbie Collins, Michael Rotstein, et al.
European Child & Adolescent Psychiatry
|
June 13, 2022
Group comprehensive behavioral intervention for tics contribution to broader cognitive and emotion regulation in children
Noa Gur, Sharon Zimmerman-Brenner, Aviva Fattal-Valevski, et al.
European Child & Adolescent Psychiatry
|
November 24, 2020
Internet-based guided self-help comprehensive behavioral intervention for tics (ICBIT) for youth with tic disorders: a feasibility and effectiveness study with 6 month-follow-up
Lilach Rachamim, Sharon Zimmerman-Brenner, Osnat Rachamim, et al.
Movement Disorders Clinical Practice
|
February 5, 2019
Levodopa Responsive Parkinsonism in Two Patients With Phosphoglycerate Kinase Deficiency
Tuhin Virmani, Michael Rotstein, Ronen Spiegel, et al.
Annals of Neurology
|
August 6, 2010
Glut1 deficiency: inheritance pattern determined by haploinsufficiency
Michael Rotstein, Kristin Engelstad, Hong Yang, et al.
Page
of 2