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JAMA Neurology
|
June 14, 2016
Nitric Oxide Deficiency Triggering Strokelike Episodes-Reply
Mary Kay Koenig
Pediatric Neurology
|
April 16, 2008
Presentation and diagnosis of mitochondrial disorders in children
Mary Kay Koenig
Clinical Case Reports
|
December 2, 2024
Expanded-Access Use of Elamipretide Improves Quality of Life in Patients With Rare Mitochondrial Disorders Characterized by Ophthalmic Symptoms: A Case Series
Sharique Ansari, Mary Kay Koenig
Journal of Child Neurology
|
January 14, 2012
Friedreich-like ataxia as an initial manifestation of mitochondrial DNA 8344A>G mutation
Justyna A Chevallier, Mary Kay Koenig
JIMD Reports
|
February 27, 2018
Metabolomics Profile in ABAT Deficiency Pre- and Post-treatment
Mary Kay Koenig, Penelope E Bonnen
Journal of Child Neurology
|
December 14, 2011
Glucose transporter type I deficiency causing mitochondrial dysfunction
Jeremy Lankford, Ian J Butler, Mary Kay Koenig
Journal of Child Neurology
|
April 2, 2010
Incidence of papilledema and obesity in children diagnosed with idiopathic ''benign'' intracranial hypertension: case series and review
Gabriel Faz, Ian J Butler, Mary Kay Koenig
Journal of Child Neurology
|
January 20, 2009
Rapamycin reduces seizure frequency in tuberous sclerosis complex
Jennifer Muncy, Ian J Butler, Mary Kay Koenig
Journal of Child Neurology
|
October 28, 2008
Regression of subependymal giant cell astrocytoma with rapamycin in tuberous sclerosis complex
Mary Kay Koenig, Ian J Butler, Hope Northrup
Archives of Neurology
|
February 29, 2012
Adult-onset cerebral folate deficiency
Zsila Sadighi, Ian J Butler, Mary Kay Koenig
Page
of 9
Search research articles
Search
Showing results (1-10 of 82) with videos related to
Sort By:
Page
of 9
JAMA Neurology
|
June 14, 2016
Nitric Oxide Deficiency Triggering Strokelike Episodes-Reply
Mary Kay Koenig
Pediatric Neurology
|
April 16, 2008
Presentation and diagnosis of mitochondrial disorders in children
Mary Kay Koenig
Clinical Case Reports
|
December 2, 2024
Expanded-Access Use of Elamipretide Improves Quality of Life in Patients With Rare Mitochondrial Disorders Characterized by Ophthalmic Symptoms: A Case Series
Sharique Ansari, Mary Kay Koenig
Journal of Child Neurology
|
January 14, 2012
Friedreich-like ataxia as an initial manifestation of mitochondrial DNA 8344A>G mutation
Justyna A Chevallier, Mary Kay Koenig
JIMD Reports
|
February 27, 2018
Metabolomics Profile in ABAT Deficiency Pre- and Post-treatment
Mary Kay Koenig, Penelope E Bonnen
Journal of Child Neurology
|
December 14, 2011
Glucose transporter type I deficiency causing mitochondrial dysfunction
Jeremy Lankford, Ian J Butler, Mary Kay Koenig
Journal of Child Neurology
|
April 2, 2010
Incidence of papilledema and obesity in children diagnosed with idiopathic ''benign'' intracranial hypertension: case series and review
Gabriel Faz, Ian J Butler, Mary Kay Koenig
Journal of Child Neurology
|
January 20, 2009
Rapamycin reduces seizure frequency in tuberous sclerosis complex
Jennifer Muncy, Ian J Butler, Mary Kay Koenig
Journal of Child Neurology
|
October 28, 2008
Regression of subependymal giant cell astrocytoma with rapamycin in tuberous sclerosis complex
Mary Kay Koenig, Ian J Butler, Hope Northrup
Archives of Neurology
|
February 29, 2012
Adult-onset cerebral folate deficiency
Zsila Sadighi, Ian J Butler, Mary Kay Koenig
Page
of 9