A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects von Zhang, Jinglan, Lachance, Véronik, Schaffner, Adam, Li, Xianting, Fedick, Anastasia, Kaye, Lauren E, Liao, Jun, Rosenfeld, Jill, Yachelevich, Naomi, Chu, Mary-Lynn, Mitchell, Wendy G, Boles, Richard G, Moran, Ellen, Tokita, Mari, Gorman, Elizabeth, Bagley, Kaytee, Zhang, Wei, Xia, Fan, Leduc, Magalie, Yang, Yaping, Eng, Christine, Wong, Lee-Jun, Schiffmann, Raphael, Diaz, George A, Kornreich, Ruth, Thummel, Ryan, Wasserstein, Melissa, Yue, Zhenyu, Edelmann, Lisa

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The Limb–Girdle Muscular Dystrophies: Is Treatment on the Horizon? von Chu, Mary Lynn, Moran, Ellen

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Fidelity of Gamma-Glutamyl Transferase (GGT) in Differentiating Skeletal Muscle From Liver Damage von Rosales, Xiomara Q., Chu, Mary-Lynn, Shilling, Christopher, Wall, Cheryl, Pastores, Gregory M., Mendell, Jerry R.

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Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome von Rizvi, Midhat, Truong, Tina K, Zhou, Janet, Batta, Manav, Moran, Ellen S, Pappas, John, Chu, Mary Lynn, Caluseriu, Oana, Evrony, Gilad D, Leslie, Elaine M, Cordat, Emmanuelle

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Idiopathic toe-walking: a review von Sala, Debra A, Shulman, Lisa H, Kennedy, Rose F, Grant, Alfred D, Chu, Mary Lynn Y

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Accuracy of Activity Monitors for Measuring Ambulation in Children with Cerebral Palsy von Grissom, Helyn, Chu, Alice, Sala, Debra A., DelSole, Edward, Chu, Mary Lynn, Godfried, David, Bhattacharyya, Surjya, Karamitopoulos, Mara

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Measuring ambulation with wrist‐based and hip‐based activity trackers for children with cerebral palsy von Sala, Debra A, Grissom, Helyn E, Delsole, Edward M, Chu, Mary Lynn, Godfried, David H, Bhattacharyya, Surjya, Karamitopoulos, Mara S, Chu, Alice

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Six Month Results of Spinraza in Adults with Spinal Muscular Atrophy (SAS) Study (2446) von Zaidman, Craig M., Proud, Crystal M., Thonhoff, Jason R., Rad, Nassim, Swoboda, Kathryn J., Chu, Mary-Lynn, Ladha, Shafeeq, Crawford, Thomas O., Choi, Joseph M., Genge, Angela, Frey, Margaret R., Heatwole, Chad, Lew, Daphne, Wilkins, Heather

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Intrathecal baclofen in X-linked adrenoleukodystrophy von Chu, Mary Lynn Y, Sala, Debra A, Weiner, Howard L

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Kufor‐Rakeb Syndrome Due to a Novel ATP13A2 Mutation in 2 Chinese‐American Brothers von Noch, Evan, Henchcliffe, Claire, Hellmers, Natalie, Chu, Mary Lynn, Pappas, John, Moran, Ellen, Alcaraz, Wendy, Sarva, Harini

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Kufor‐Rakeb Syndrome Due to a Novel ATP 13A2 Mutation in 2 Chinese‐American Brothers von Noch, Evan, Henchcliffe, Claire, Hellmers, Natalie, Chu, Mary Lynn, Pappas, John, Moran, Ellen, Alcaraz, Wendy, Sarva, Harini

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The use of tiagabine in pediatric spasticity management von Chu, Mary Lynn, Sala, Debra A

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The use of tiagabine in pediatric spasticity management von Chu, Mary Lynn, Sala, Debra A

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Developmental implications of idiopathic toe walking von Shulman, Lisa H., Sala, Debra A., Chu, Mary Lynn Y., McCaul, Patricia R., Sandler, Bonnie J.

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Allgrove syndrome: Documenting cholinergic dysfunction by autonomic tests von Chu, Mary Lynn, Berlin, Dena, Axelrod, Felicia B.

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Demyelinating focal motor neuropathy of the ulnar nerve masquerading as compression in Guyon's canal: A case report von Dhillon, Manjit S., Chu, Mary Lynn, Posner, Martin A.

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Idiopathic toe‐walking: a review von Sala, Debra A, Shulman, Lisa H, Kennedy, Rose F, Grant, Alfred D, Chu, Mary Lynn Y

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Kufor-Rakeb Syndrome Due to a Novel ATP13A2 Mutation in 2 Chinese-American Brothers von Noch, Evan, Henchcliffe, Claire, Hellmers, Natalie, Chu, Mary Lynn, Pappas, John, Moran, Ellen, Alcaraz, Wendy, Sarva, Harini

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A new form of complicated hereditary spastic paraplegia with cataracts, atretic ear canals and hypopigmentation von Guillén-Navarro, Encarna, Wallerstein, Robert, Moran, Ellen, Chu, Mary Lynn, Grant, Alfred

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Cranial nerve palsies in Streptococcus pneumoniae meningitis von Chu, Mary Lynn Y., Litman, Nathan, Kaufman, David M., Shinnar, Shlomo

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