Sage Journals: Discover world-class research

Retricted access

Other

First published 1998-07

Axonal Neuropathy and Predominance of Type II Myofibers in Infantile Spinal Muscular Atrophy

Heymut Omran, Uwe-Peter Ketelsen, Florian Heinen [...]

Journal of Child Neurology

Retricted access

Other

First published 2000-12

Fatal Infantile X-Linked Neuropathy

Elizabeth Sekul, James E. Carroll, Farivar Yaghmai [...]

Journal of Child Neurology

Retricted access

Other

First published 2011-6

Leber’s Hereditary Optic Neuropathy Mutations Associated With Infantile-Onset Myoclonic Epilepsy

Richard E. Frye

Journal of Child Neurology

Retricted access

Other

First published 2011-5

Optic Nerve Enlargement in Krabbe Disease: A Pathophysiologic and Clinical Perspective

Syed A. Hussain, Holly H. Zimmerman, Omar A. Abdul-Rahman [...]

Journal of Child Neurology

Retricted access

Research article

First published 1993-07

Unique Hereditary Serisory and Autonomic Neuropathy With Growth Hormone Deficiency

Ruth M. Liberfarb, Anthony H. Jackson, Roland D. Eavey [...]

Journal of Child Neurology

Retricted access

Research article

First published 2015-3

A Case of Infantile Neuroaxonal Dystrophy of Neonatal Onset

Carlo Fusco, Daniele Frattini, Celeste Panteghini [...]

Journal of Child Neurology

Retricted access

Other

First published 2000-08

Progressive Infantile Axonal Polyneuropathy

Thomas J. Geller, Anne M. Connolly, Suresh Kotagal [...]

Journal of Child Neurology

Retricted access

Research article

First published 1994-01

Leigh Syndrome: Pyruvate Dehydrogenase Defect. A Case With Peripheral Neuropathy

B. Chabrol, J. Mancini, C. Benelli [...]

Journal of Child Neurology

Retricted access

Case report

First published 2026-2

Early-Onset Sensorimotor Axonal Neuropathy as Sole Manifestation of HADHA -Related Disorder/ Mitochondrial Trifunctional Protein Defect

Giulia Balletto, Giulia Barbagallo, Matteo Cataldi [...]

Journal of Child Neurology

Retricted access

Research article

First published 1990-10

Late-Onset Globoid Cell Leukodystrophy: Unusual Ultrastructural Pathology and Subtotal β-Galactocerebrosidase Deficiency

H.H. Goebel, K. Harzer, J.P. Ernst [...]

Journal of Child Neurology

Search results