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Molecular Genetics and Metabolism
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March 19, 2011
Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation
Gary Fruhman, Megan L Landsverk, Timothy E Lotze, et al.
The Journal of Pediatrics
|
May 2, 2017
Lung Transplantation for FLNA-Associated Progressive Lung Disease
Lindsay C Burrage, R Paul Guillerman, Shailendra Das, et al.
Annals of Clinical and Translational Neurology
|
May 4, 2026
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, et al.
The Pediatric Infectious Disease Journal
|
September 14, 2022
Management of Extensive Central Nervous System Cladophialophora bantiana Infection in a 9-Year-Old Child
Juri Boguniewicz, Gail J Demmler-Harrison, Timothy E Lotze, et al.
Annals of Clinical and Translational Neurology
|
June 29, 2026
Reply to: A Lethal Progressive Neuroinflammation Disguised as MOGAD Revealing a Final Diagnosis of Griscelli Syndrome: Regarding: MOGAD is the Most Common Cause of Isolated Optic Neuritis in Children
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography
|
April 25, 2015
Feasibility and Reproducibility of Echocardiographic Measures in Children with Muscular Dystrophies
Christopher F Spurney, Francis M McCaffrey, Avital Cnaan, et al.
Pediatric Neurology
|
August 6, 2023
Fulminant Anti-Myelin Oligodendrocyte Glycoprotein-Associated Cerebral Cortical Encephalitis: Case Series of a Severe Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Phenotype
Varun Kannan, Alexander J Sandweiss, Timothy A Erickson, et al.
Pediatric Neurology
|
September 16, 2023
An International Pediatric-Onset Opsoclonus-Myoclonus Ataxia Syndrome Registry and Clinical Research Network: Development, Progress, and Vision
Lauren M Kerr, Morgan E Ryan, Ming Lim, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
April 11, 2017
Impact of an electronic monitoring device and behavioral feedback on adherence to multiple sclerosis therapies in youth: results of a randomized trial
E Ann Yeh, Stephanie A Grover, Victoria E Powell, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
December 24, 2017
Correction to: Impact of an electronic monitoring device and behavioural feedback on adherence to multiple sclerosis therapies in youth: results of a randomized trial
E Ann Yeh, Stephanie A Grover, Victoria E Powell, et al.
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Search research articles
Search
Showing results (31-40 of 59) with videos related to
Sort By:
Page
of 6
Molecular Genetics and Metabolism
|
March 19, 2011
Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation
Gary Fruhman, Megan L Landsverk, Timothy E Lotze, et al.
The Journal of Pediatrics
|
May 2, 2017
Lung Transplantation for FLNA-Associated Progressive Lung Disease
Lindsay C Burrage, R Paul Guillerman, Shailendra Das, et al.
Annals of Clinical and Translational Neurology
|
May 4, 2026
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, et al.
The Pediatric Infectious Disease Journal
|
September 14, 2022
Management of Extensive Central Nervous System Cladophialophora bantiana Infection in a 9-Year-Old Child
Juri Boguniewicz, Gail J Demmler-Harrison, Timothy E Lotze, et al.
Annals of Clinical and Translational Neurology
|
June 29, 2026
Reply to: A Lethal Progressive Neuroinflammation Disguised as MOGAD Revealing a Final Diagnosis of Griscelli Syndrome: Regarding: MOGAD is the Most Common Cause of Isolated Optic Neuritis in Children
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography
|
April 25, 2015
Feasibility and Reproducibility of Echocardiographic Measures in Children with Muscular Dystrophies
Christopher F Spurney, Francis M McCaffrey, Avital Cnaan, et al.
Pediatric Neurology
|
August 6, 2023
Fulminant Anti-Myelin Oligodendrocyte Glycoprotein-Associated Cerebral Cortical Encephalitis: Case Series of a Severe Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Phenotype
Varun Kannan, Alexander J Sandweiss, Timothy A Erickson, et al.
Pediatric Neurology
|
September 16, 2023
An International Pediatric-Onset Opsoclonus-Myoclonus Ataxia Syndrome Registry and Clinical Research Network: Development, Progress, and Vision
Lauren M Kerr, Morgan E Ryan, Ming Lim, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
April 11, 2017
Impact of an electronic monitoring device and behavioral feedback on adherence to multiple sclerosis therapies in youth: results of a randomized trial
E Ann Yeh, Stephanie A Grover, Victoria E Powell, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
December 24, 2017
Correction to: Impact of an electronic monitoring device and behavioural feedback on adherence to multiple sclerosis therapies in youth: results of a randomized trial
E Ann Yeh, Stephanie A Grover, Victoria E Powell, et al.
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of 6