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Research article

First published 2012-2

Childhood Ataxia with Cerebral Hypomyelination Syndrome: A Variant of Patient with Early Childhood Onset Related to EIF 2 B 3 Mutation

F. Perfetto, L.P. Stoppino, A. Calì [...]

The Neuroradiology Journal

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Review article

First published 2012-4

A New Tyrosine Hydroxylase Genotype Associated With Early-Onset Severe Encephalopathy

Teresa Giovanniello, Dianella Claps, Carla Carducci [...]

Journal of Child Neurology

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Review article

First published 2011-12

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Vinodh Narayanan, Stephen G. Rice, Shannon S. Olfers [...]

Journal of Child Neurology

Open access

Review article

First published 2022

A Practical Approach to Early-Onset Parkinsonism

Giulietta M. Riboldi, Emanuele Frattini, Edoardo Monfrini [...]

Journal of Parkinson’s Disease

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Research article

First published 2009-8

Typical Radiological Findings of Lipoid Proteinosis of Urbach and Wiethe

K.G. Srinivasan, S. Ramprabananth, S. Srividya [...]

The Neuroradiology Journal

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Other

First published 2006-6

Pontobulbar Palsy and Neurosensory Deafness (Brown-Vialetto-van Laere Syndrome) With Hyperintense Brainstem Nuclei on Magnetic Resonance Imaging: New Finding in Three Siblings

Roshan Koul, Rajeev Jain, Alexander Chacko [...]

Journal of Child Neurology

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Other

First published 2000-01

Hallervorden-spatz Disease: Two New Early Childhood Onset Cases

Joaquin A. Pena, Omaira Molina, Jose Cardozo

Journal of Child Neurology

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Other

First published 2008-08

Ataxia With Oculomotor Apraxia Type 1 (AOA1): Clinical and Neuropsychological Features in 2 New Patients and Differential Diagnosis

Stefano D'Arrigo, Daria Riva, Sara Bulgheroni [...]

Journal of Child Neurology

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Research article

First published 2013-3

Alstrom syndrome – a diagnosis revisited

Bharati Vusirikala, Veena Rajkumar, Maitrayee Choudhary [...]

The British Journal of Diabetes & Vascular Disease

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Case report

First published 2019-4

Recessive congenital methemoglobinemia type II: Hypoplastic basal ganglia in two siblings with a novel mutation of the cytochrome b5 reductase gene

Manal Nicolas-Jilwan

The Neuroradiology Journal

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