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Research article

First published 2013-9

A Novel c.1135_1138delCTGT Mutation in CLN3 Leads to Juvenile Neuronal Ceroid Lipofuscinosis

Arlene V. Drack, Jake N. Miller, David A. Pearce

Journal of Child Neurology

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Research article

First published 1994-01

Klüver-Bucy Syndrome in Juvenile Neuronal Ceroid Lipofuscinosis

Douglas J. Lanska, Mary Jo Lanska

Journal of Child Neurology

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Research article

First published 2013-9

Neurobehavioral Features and Natural History of Juvenile Neuronal Ceroid Lipofuscinosis (Batten Disease)

Heather R. Adams, Jonathan W. Mink, University of Rochester Batten Center Study Group

Journal of Child Neurology

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Research article

First published 2017-7

ABCA4 Mutation in a Patient With Juvenile Neuronal Ceroid Lipofuscinosis

Daniela Reyes-Capó, Camila V. Ventura, Mustafa Tekin [...]

Journal of VitreoRetinal Diseases

Free access

Research article

First published 1994-1

Juvenile-onset Neuronal Ceroid-Lipofuscinosis in Rambouillet Sheep

J. F. Edwards, R. W. Storts, J. R. Joyce [...]

Veterinary Pathology

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Other

First published 1997-09

Somatosensory Evoked Magnetic Fields From Primary Sensorimotor Cortex in Juvenile Neuronal Ceroid Lipofuscinosis

Leena Lauronen, Erika Heikkilä, Taina Autti [...]

Journal of Child Neurology

Open access

Research article

First published 2026

Neurodevelopmental and Psychiatric Disorders and the Use of Psychotropic Medications in a National Sample of Individuals With Juvenile Neuronal Ceroid Lipofuscinosis

Beate Oerbeck, Ingrid B. Helland, Heather R. Adams [...]

Journal of Child Neurology

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Research article

First published 2016-3

Remote Assessment of Cognitive Function in Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)

Shayne N. Ragbeer, Erika F. Augustine, Jonathan W. Mink [...]

Journal of Child Neurology

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Research article

First published 2014-03

Partial Correction of the CNS Lysosomal Storage Defect in a Mouse Model of Juvenile Neuronal Ceroid Lipofuscinosis by Neonatal CNS Administration of an Adeno-Associated Virus Serotype rh.10 Vector Expressing the Human CLN3 Gene

Dolan Sondhi, Emma C. Scott, Alvin Chen [...]

Human Gene Therapy

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Other

First published 2004-1

Profound Infantile Neuroretinal Dysfunction in a Heterozygote for the CLN3 Genetic Defect

Emily de los Reyes, Paul Richard Dyken, Paul Phillips [...]

Journal of Child Neurology

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