HaroldGeorgeMarksMD

Pediatrics • Philadelphia, PA

Neurodevelopmental Disabilities, Child Neurology

Professor, Pediatrics, Drexel College of Medicine/Hahnemann School of Medicine

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Office
St Christophers Hospital fo
Erie Avenue at Front Street
Philadelphia, PA 19134
Phone+1 215-427-5464

Fax+1 215-427-4393
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Summary

Dr. Harold Marks, MD is a board certified pediatrician in Philadelphia, Pennsylvania. He is currently licensed to practice medicine in Pennsylvania, New Jersey, and Florida. He is affiliated with St. Christopher's Hospital for Children and is a Professor at Drexel College of Medicine/Hahnemann School of Medicine.

Education & Training

Tower HealthFellowship, Child Neurology, 1978 - 1979
University of Michigan Health SystemFellowship, Child Neurology, 1975 - 1976
University of Michigan Health SystemResidency, Pediatrics, 1972 - 1975
University of Michigan Medical SchoolClass of 1972

Certifications & Licensure

MI State Medical License 1973 - Present
NJ State Medical License 2001 - 2023
PA State Medical License 1978 - 2016
FL State Medical License 1999 - 2014
DE State Medical License 1976 - 2003
American Board of Pediatrics Pediatrics
American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology

Publications & Presentations

PubMed

30 citations
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 J. Melvin, Reena Jethva, H. Huntley Hardison, Harold Marks, Agustin Legido> ;Biomarkers in Medicine. 2015 Oct 6
16 citations
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 K Fitzgerald, Mena Scavena, Samuel S. Gidding, Mary O. Cox, Harold G. Marks, Kevin M. Flanigan, Steven A. Moore> ;Journal of Human Genetics. 2015 Mar 1
7 citations
Correction of a short cardiac PR interval in a 12-year-old girl with late-onset Pompe disease following enzyme replacement therapy.
Cristina Fernández, Agustin Legido, Reena Jethva, Harold Marks> ;Genetics in Medicine. 2012 Aug 1
26 citations
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, Nidhi Shah, Harold Marks, Divya S. Khurana, Ignacio Valencia, Agustin Legido> ;Molecular Genetics and Metabolism. 2012 Mar 1
16 citations
Microarray analysis in children with developmental disorder or epilepsy.
Herbert Ezugha, Carol E. Anderson, Harold Marks, Divya S. Khurana, Agustin Legido, Ignacio Valencia> ;Pediatric Neurology. 2010 Dec 1
33 citations
5q14.3 Deletion Manifesting as Mitochondrial Disease and Autism: Case Report
Herbert Ezugha, Michael J. Goldenthal, Ignacio Valencia, Carol E. Anderson, Agustin Legido, Harold Marks> ;Journal of Child Neurology. 2010 Feb 22
17 citations
Efficacy and tolerability of topiramate in pediatric migraine.
Marcos Cruz, Ignacio Valencia, Agustin Legido, Sanjeev V. Kothare, Divya S. Khurana, Sabrina W. Yum, H. Huntley Hardison, Joseph J. Melvin, Harold Marks> ;Pediatric Neurology. 2009 Sep 1
12 citations
Efficacy and safety of lamotrigine monotherapy in children and adolescents with epilepsy
Ignacio Valencia, Gerard Piñol-Ripoll, Divya S. Khurana, H. Huntley Hardison, Sanjeev V. Kothare, Joseph J. Melvin, Harold Marks, Agustin Legido> ;European Journal of Paediatric Neurology. 2009 Mar 1
11 citations
Subacute sclerosing panencephalitis (SSPE) presenting as acute disseminated encephalomyelitis in a child.
Jatinder S. Goraya, Harold Marks, Divya S. Khurana, Agustin Legido, Joseph J. Melvin> ;Journal of Child Neurology. 2009 Feb 9
23 citations
Sleep Study Abnormalities in Children With Attention Deficit Hyperactivity Disorder
Jatinder S. Goraya, Marcos Cruz, Ignacio Valencia, Joseph Kaleyias, Divya S. Khurana, H. Huntley Hardison, Harold Marks, Agustin Legido, Sanjeev V. Kothare> ;Pediatric Neurology. 2009 Jan 1
7 citations
Epilepsy and respiratory chain defects in children with mitochondrial encephalopathies.
Divya S. Khurana, Leon Salganicoff, Joseph J. Melvin, Elizabeth F. Hobdell, Ignacio Valencia, H. Huntley Hardison, Harold Marks, Warren D. Grover, Agustin Legido> ;Epilepsia. 2008 Nov 1
51 citations
Epilepsy and respiratory chain defects in children with mitochondrial encephalopathies.
Divya S. Khurana, Leon Salganicoff, Joseph J. Melvin, Elizabeth F. Hobdell, Ignacio Valencia, H. Huntley Hardison, Harold Marks, Warren D. Grover, Agustin Legido> ;Neuropediatrics. 2008 Feb 1
6 citations
Spinocerebellar ataxia type 7 mimicking Kearns-Sayre syndrome: a clinical diagnosis is desirable.
Surya N. Gupta, Harold Marks> ;Journal of the Neurological Sciences. 2008 Jan 15
8 citations
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> ;Pediatric Neurology. 2007 Nov 1
19 citations
Oxcarbazepine monotherapy in children and adolescents: a single-center clinical experience.
Sanjeev V. Kothare, Divya S. Khurana, Navid Mostofi, Joseph J. Melvin, Harold Marks, Ignacio Valencia, Agustin Legido> ;Pediatric Neurology. 2006 Oct 1
123 citations
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. 2003 Dec 9
43 citations
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, Franca Cambi> ;Annals of Neurology. 2002 Oct 1
25 citations
Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy.
Richard Frisch, Kenneth R. Singleton, Priscilla A. Moses, Iris L. Gonzalez, Paul Carango, Harold G. Marks, Vicky L. Funanage> ;Molecular Genetics and Metabolism. 2001 Sep 1
3 citations
A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease.
Grace M. Hobson, Deborah L. Stabley, Vicky L. Funanage, Harold G. Marks> ;Human Mutation. 2001 Feb 1
42 citations
Mutations in noncoding regions of the proteolipid protein gene in Pelizaeus-Merzbacher disease.
Grace M. Hobson, A. P. Davis, N. C. Stowell, Edwin H. Kolodny, Erik A. Sistermans, I.F.M. de Coo, Vicky L. Funanage, Harold G. Marks> ;Neurology. 2000 Oct 24
25 citations
MR imaging findings in children with merosin-deficient congenital muscular dystrophy.
Pilar A. Caro, Mena Scavina, Eric P. Hoffman, Elena Pegoraro, Harold G. Marks> ;AJNR. American Journal of Neuroradiology. 1999 Feb 1
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.
Pegoraro E, Marks H, Garcia CA, Crawford T, Mancias P, Connolly AM, Fanin M, Martinello F, Trevisan CP, Angelini C, Stella A, Scavina M, Munk RL, Servidei S, Bönnemann...> ;Neurology. 1998-07-01
18 citations
Krabbe's disease presenting as a peripheral neuropathy.
Harold G. Marks, Mena Scavina, Edwin H. Kolodny, Michael J. Palmieri, Judith Childs> ;Muscle & Nerve. 1997 Aug 1
Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy.
Pegoraro E, Mancias P, Swerdlow SH, Raikow RB, Garcia C, Marks H, Crawford T, Carver V, Di Cianno B, Hoffman EP> ;Ann. Neurol.. 1996-11-01
47 citations
Myotonia and the muscle chloride channel: Dominant mutations show variable penetrance and founder effect
Patrick P. Koty, Elena Pegoraro, Grace M. Hobson, Harold G. Marks, A. P. Turel, D. Flagler, M. Cadaldini, Corrado Angelini, Eric P. Hoffman> ;Neurology. 1996 Oct 1
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Hospital Affiliations

St. Christopher's Hospital for ChildrenPhiladelphia, Pennsylvania