Publications by authors named "Harold Marks"

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Mitochondrial enzyme dysfunction in autism spectrum disorders; a novel biomarker revealed from buccal swab analysis.
Michael J Goldenthal, Shirish Damle, Sudip Sheth, Nidhi Shah, Joseph Melvin, Harold Marks

Biomark Med· August 2016

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Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27.
Takeshi Tsuda, Kristi Fitzgerald, Mena Scavena, Samuel Gidding, Mary O Cox, Harold Marks

J Hum Genet· March 2015

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Recessive TTN truncating mutations define novel forms of core myopathy with heart disease.
Claire Chauveau, Carsten G Bonnemann, Cedric Julien, Ay Lin Kho, Harold Marks

Hum Mol Genet· February 2014

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Correction of a short cardiac PR interval in a 12-year-old girl with late-onset Pompe disease following enzyme replacement therapy.
Cristina Fernández, Agustín Legido, Reena Jethva, Harold G Marks

Genet Med· August 2012

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Non-invasive evaluation of buccal respiratory chain enzyme dysfunction in mitochondrial disease: comparison with studies in muscle biopsy.
Michael J Goldenthal, Teddy Kuruvilla, Shirish Damle, Leon Salganicoff, Sudip Sheth, Harold Marks

Mol Genet Metab· March 2012

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Microarray analysis in children with developmental disorder or epilepsy.
Herbert Ezugha, Carol E Anderson, Harold G Marks, Divya Khurana, Agustín Legido

Pediatr Neurol· December 2010

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5q14.3 deletion manifesting as mitochondrial disease and autism: case report.
Herbert Ezugha, Michael Goldenthal, Ignacio Valencia, Carol E Anderson, Agustin Legido, Harold Marks

J Child Neurol· October 2010

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Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.
Rita Horvath, John P Kemp, Helen A L Tuppen, Gavin Hudson, Anders Oldfors, Harold M Marks

Brain· November 2009

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Efficacy and tolerability of topiramate in pediatric migraine.
Marcos J Cruz, Ignacio Valencia, Agustín Legido, Sanjeev V Kothare, Divya S Khurana, Harold G Marks

Pediatr Neurol· September 2009

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Subacute sclerosing panencephalitis (SSPE) presenting as acute disseminated encephalomyelitis in a child.
Jatinder Goraya, Harold Marks, Divya Khurana, Agustin Legido, Joseph Melvin

J Child Neurol· July 2009

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Efficacy and safety of lamotrigine monotherapy in children and adolescents with epilepsy.
Ignacio Valencia, Gerard Piñol-Ripoll, Divya S Khurana, Huntley H Hardison, Sanjeev V Kothare, Harold G Marks

Eur J Paediatr Neurol· March 2009

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Sleep study abnormalities in children with attention deficit hyperactivity disorder.
Jatinder S Goraya, Marcos Cruz, Ignacio Valencia, Joseph Kaleyias, Divya S Khurana, Harold Marks

Pediatr Neurol· January 2009

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Epilepsy and respiratory chain defects in children with mitochondrial encephalopathies.
Divya Khurana, Leon Salganicoff, Joseph Melvin, Elizabeth Hobdell, Ignacio Valencia, Harold Marks

Epilepsia· November 2008

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Spinocerebellar ataxia type 7 mimicking Kearns-Sayre syndrome: a clinical diagnosis is desirable.
Surya N Gupta, Harold G Marks

J Neurol Sci· January 2008

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Treatment of drop attacks in Coffin-Lowry syndrome with the use of sodium oxybate.
Navasuma Havaligi, Chandra Matadeen-Ali, Divya S Khurana, Harold Marks, Sanjeev V Kothare

Pediatr Neurol· November 2007

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Oxcarbazepine monotherapy in children and adolescents: a single-center clinical experience.
Sanjeev V Kothare, Divya S Khurana, Navid Mostofi, Joseph J Melvin, Harold G Marks

Pediatr Neurol· October 2006

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The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem.
Robert A Taylor, Erin M Simon, Harold G Marks, Steven S Scherer

Neurology· December 2003

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A PLP splicing abnormality is associated with an unusual presentation of PMD.
Grace M Hobson, Zhong Huang, Karen Sperle, Deborah L Stabley, Harold G Marks

Ann Neurol· October 2002

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