Sage Journals: Discover world-class research

Open access

Research article

First published 2024-01-02

Gene Distribution in Pediatric-Onset Inherited Peripheral Neuropathy: A Single Tertiary Center in Thailand

Pimchanok Kulsirichawaroj, Yanin Suksangkharn, Da Eun Nam [...]

Journal of Neuromuscular Diseases

Open access

Review article

First published 2021

Targeted Therapies for Hereditary Peripheral Neuropathies: Systematic Review and Steps Towards a ‘treatabolome’

Matthew J. Jennings, Angela Lochmüller, Antonio Atalaia [...]

Journal of Neuromuscular Diseases

Open access

Review article

First published 2019

Defects in Axonal Transport in Inherited Neuropathies

Danique Beijer, Angela Sisto, Jonas Van Lent [...]

Journal of Neuromuscular Diseases

Retricted access

Other

First published 2008-02

Mitochondrial Dynamics and Peripheral Neuropathy

Robert H. Baloh

The Neuroscientist

Retricted access

Other

First published 1995-11

Genetic Heterogeneity of Hereditary Motor and Sensory Neuropathy Type VI

Elly F. Ippel, Dienke Wittebol-Post, Frans G.I. Jennekens [...]

Journal of Child Neurology

Open access

Case report

First published 2022

Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay due to Novel Mutations in the SACS Gene

Rohan Sharma, Akilandeswari Aravindhan, Clara Puente [...]

Journal of Investigative Medicine High Impact Case Reports

Free access

Research article

First published 2016

Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 Locus

Delphine Bouhy, Thomas Geuens, Vicky De Winter [...]

Journal of Neuromuscular Diseases

Retricted access

Other

First published 2005-06

Familial Cognitive Impairment With Ataxia With Oculomotor Apraxia

Muhammad Mahajnah, Lina Basel-Vanagaite, Dov Inbar [...]

Journal of Child Neurology

Retricted access

Other

First published 2005-06

Familial Cognitive Impairment With Ataxia With Oculomotor Apraxia

Muhammad Mahajnah, Lina Basel-Vanagaite, Dov Inbar [...]

Journal of Child Neurology

Open access

Research article

First published 2014

Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene

Angela Pyle, Venkateswaran Ramesh, Marina Bartsakoulia [...]

Journal of Neuromuscular Diseases

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