Spinocerebellar ataxia type 7 mimicking Kearns–Sayre syndrome: A clinical diagnosis is desirable von Gupta, Surya N, Marks, Harold G

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

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Microarray Analysis in Children With Developmental Disorder or Epilepsy von Ezugha, Herbert, MD, Anderson, Carol E., MD, Marks, Harold G., MD, Khurana, Divya, MD, Legido, Agustín, MD, Valencia, Ignacio, MD

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Efficacy and Tolerability of Topiramate in Pediatric Migraine von Cruz, Marcos J., MD, Valencia, Ignacio, MD, Legido, Agustín, MD, PhD, Kothare, Sanjeev V., MD, Khurana, Divya S., MD, Yum, Sabrina, MD, Hardison, Huntley H., MD, Melvin, Joseph J., MD, Marks, Harold G., MD

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The CNS phenotype of X-linked Charcot-Marie-Tooth disease: More than a peripheral problem von TAYLOR, Robert A, SIMON, Erin M, MARKS, Harold G, SCHERER, Steven S

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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 von Fernández, Cristina, Legido, Agustín, Jethva, Reena, Marks, Harold G.

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Idiopathic pulmonary fibrosis von Richeldi, Luca, Prof, Collard, Harold R, MD, Jones, Mark G, PhD

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Magnetic resonance imaging and computed tomography in Pelizaeus-Merzbacher disease von Caro, Pilar A., Marks, Harold G.

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Molecular genetics of familial spastic paraplegia: a multitude of responsible genes von Kobayashi, Hisashi, Garcia, Carlos A., Alfonso, Gishlaine, Marks, Harold G., Hoffman, Eric P.

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Oxcarbazepine Monotherapy in Children and Adolescents: A Single-Center Clinical Experience von Kothare, Sanjeev V., Khurana, Divya S., Mostofi, Navid, Melvin, Joseph J., Marks, Harold G., Valencia, Ignacio, Legido, Agustin

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Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 ( PMP22 ) gene von Roa, Benjamin B, Dyck, Peter J, Marks, Harold G, Chance, Phillip F, Lupski, James R

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

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The rumpshaker mutation in spastic paraplegia von Kobayashi, Hisashi, Hoffman, Eric P, Marks, Harold G

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Hip Dysplasia Associated with Charcot-Marie-Tooth Disease in the Older Child and Adolescent von Kumar, S Jay, Marks, Harold G, Bowen, J Richard, MacEwen, G Dean

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Effect of Triplet Repeat Expansion on Chromatin Structure and Expression of DMPK and Neighboring Genes, SIX5 and DMWD, in Myotonic Dystrophy von Frisch, Richard, Singleton, Kenneth R., Moses, Priscilla A., Gonzalez, Iris L., Carango, Paul, Marks, Harold G., Funanage, Vicky L.

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MR Imaging Findings in Children with Merosin-Deficient Congenital Muscular Dystrophy von Caro, Pilar A, Scavina, Mena, Hoffman, Eric, Pegoraro, Elena, Marks, Harold G

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A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease von Hobson, Grace M., Stabley, Deborah L., Funanage, Vicky L., Marks, Harold G.

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Intraspinal Tumors in Children Presenting Primarily with Hip Symptoms: A Report of Three Cases von Kumar, S Jay, Marks, Harold G, Ghiragossian, Jorge D, MacEwen, G Dean, Longnecker, Steven

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A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection ofPLP1 gene duplication in Pelizaeus-Merzbacher disease von Hobson, Grace M., Stabley, Deborah L., Funanage, Vicky L., Marks, Harold G.

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Delayed cervical central cord syndrome after trivial trauma von RIVIELLO, JAMES J, MARKS, HAROLD G, FAERBER, ERIC N, STEG, NINA L

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