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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 4, 2018
Transient regional cerebral hypoperfusion during a paroxysmal hemiplegic event in GLUT1 deficiency syndrome
Mohamed Almuqbil, Michael J Rivkin, Masanori Takeoka, et al.
Pediatric Emergency Care
|
November 3, 2017
Acute Illness Protocol for Maple Syrup Urine Disease
Lance H Rodan, Saud H Aldubayan, Gerard T Berry, et al.
Pediatric Emergency Care
|
February 1, 2017
Acute Illness Protocol for Organic Acidemias: Methylmalonic Acidemia and Propionic Acidemia
Saud H Aldubayan, Lance H Rodan, Gerard T Berry, et al.
Pediatric Emergency Care
|
November 15, 2017
Acute Illness Protocol for Urea Cycle Disorders
Lance H Rodan, Saud H Aldubayan, Gerard T Berry, et al.
Neurology. Genetics
|
April 12, 2016
Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome
Lance H Rodan, Maria Zak, James Stavropoulos, et al.
Plos One
|
May 21, 2015
L-Arginine Affects Aerobic Capacity and Muscle Metabolism in MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes) Syndrome
Lance H Rodan, Greg D Wells, Laura Banks, et al.
Plos One
|
September 4, 2020
L-arginine effects on cerebrovascular reactivity, perfusion and neurovascular coupling in MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes) syndrome
Lance H Rodan, Julien Poublanc, Joseph A Fisher, et al.
Movement Disorders Clinical Practice
|
June 23, 2018
The Spectrum of Movement Disorders in Childhood-Onset Lysosomal Storage Diseases
Darius Ebrahimi-Fakhari, Clara Hildebrandt, Peter E Davis, et al.
European Journal of Human Genetics : EJHG
|
November 12, 2016
A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene
Lance H Rodan, Julie Cohen, Ali Fatemi, et al.
The Journal of Rheumatology
|
August 4, 2012
Reversible splenial lesion syndrome in pediatric systemic lupus erythematosus
Gordon S Soon, Lance H Rodan, Suzanne Laughlin, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 76) with videos related to
Sort By:
Page
of 8
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 4, 2018
Transient regional cerebral hypoperfusion during a paroxysmal hemiplegic event in GLUT1 deficiency syndrome
Mohamed Almuqbil, Michael J Rivkin, Masanori Takeoka, et al.
Pediatric Emergency Care
|
November 3, 2017
Acute Illness Protocol for Maple Syrup Urine Disease
Lance H Rodan, Saud H Aldubayan, Gerard T Berry, et al.
Pediatric Emergency Care
|
February 1, 2017
Acute Illness Protocol for Organic Acidemias: Methylmalonic Acidemia and Propionic Acidemia
Saud H Aldubayan, Lance H Rodan, Gerard T Berry, et al.
Pediatric Emergency Care
|
November 15, 2017
Acute Illness Protocol for Urea Cycle Disorders
Lance H Rodan, Saud H Aldubayan, Gerard T Berry, et al.
Neurology. Genetics
|
April 12, 2016
Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome
Lance H Rodan, Maria Zak, James Stavropoulos, et al.
Plos One
|
May 21, 2015
L-Arginine Affects Aerobic Capacity and Muscle Metabolism in MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes) Syndrome
Lance H Rodan, Greg D Wells, Laura Banks, et al.
Plos One
|
September 4, 2020
L-arginine effects on cerebrovascular reactivity, perfusion and neurovascular coupling in MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes) syndrome
Lance H Rodan, Julien Poublanc, Joseph A Fisher, et al.
Movement Disorders Clinical Practice
|
June 23, 2018
The Spectrum of Movement Disorders in Childhood-Onset Lysosomal Storage Diseases
Darius Ebrahimi-Fakhari, Clara Hildebrandt, Peter E Davis, et al.
European Journal of Human Genetics : EJHG
|
November 12, 2016
A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene
Lance H Rodan, Julie Cohen, Ali Fatemi, et al.
The Journal of Rheumatology
|
August 4, 2012
Reversible splenial lesion syndrome in pediatric systemic lupus erythematosus
Gordon S Soon, Lance H Rodan, Suzanne Laughlin, et al.
Page
of 8