Sage Journals: Discover world-class research

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First published 2006-11

Childhood-Onset Spastic Paraplegia With NIPA1 Gene Mutation

Ricardo Bien-Willner, Nyamkhishig Sambuughin, Heather Holley [...]

Journal of Child Neurology

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Research article

First published 2014-06

Genes Related to Antiviral Activity,Cell Migration,and Lysis Are Differentially Expressed in CD4 + T Cells in Human T Cell Leukemia Virus Type 1-Associated Myelopathy/Tropical Spastic Paraparesis Patients

Mariana Tomazini Pinto, Tathiane Maistro Malta, Evandra Strazza Rodrigues [...]

AIDS Research and Human Retroviruses

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Research article

First published 2000-11

Hypoxanthine-Guanine Phosphoribosyltransferase Reporter Gene Mutation for Analysis of in Vivo Clonal Amplification in Patients with HTLV Type 1-Associated Myelopathy/Tropical Spastic Paraparesis

Richard J. Albertini, Stephanie K. Ardell, Steven A. Judice [...]

AIDS Research and Human Retroviruses

Free access

Research article

First published 2017

Postnatal Development of Spasticity Following Transgene Insertion in the Mouse βIV Spectrin Gene (SPTBN4)

Eva Kichkin, Archunan Visvanathan, Frank J. Lovicu [...]

Journal of Neuromuscular Diseases

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

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First published 2008-03

Hereditary spastic paraplegia,bipolar affective disorder and intellectual disability

Marie Whitty, Fionnuala Kelly, Louis Ramsay

Journal of Intellectual Disabilities

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Review article

First published 2001-10

A Mutation in the Rett Syndrome Gene,MECP2,Causes X-linked Mental Retardation and Progressive Spasticity in Males

Irwin A. Schafer

Clinical Pediatrics

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Research article

First published 2012-10

Very Early Onset and Severe Complicated Phenotype Caused by a New Spastic Paraplegia 3A Gene Mutation

Carlo Fusco, Daniele Frattini, Enrico Farnetti [...]

Journal of Child Neurology

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Other

First published 2000-04

Novel Missense Mutation in the L1 Gene in a Child With Corpus Callosum Agenesis,Retardation,Adducted Thumbs,Spastic Paraparesis,and Hydrocephalus

László Sztriha, Philippe Frossard, Robert M.W. Hofstra [...]

Journal of Child Neurology

Open access

Case report

First published 2025

Novel SPAST Deletion Mutation in an American Family With Hereditary Spastic Paraplegia: A Case Report

Sydney B. Bhopatkar, Juebin Huang

Journal of Investigative Medicine High Impact Case Reports

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