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Retricted access

Research article

First published 2013-4

Homozygous Survival Motor Neuron 2 Gene Deletion and Sporadic Lower Motor Neuron Disease in Children

Lu Liping, Ma Hongwei, Wang Lin

Journal of Child Neurology

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Research article

First published 2004-3

Congenital Club Foot with Survival of Motor Neuron 1,Telomeric ( SMN1 ) Gene Deletion

Bernard Echenne, François Rivier, Agathe Roubertie [...]

Journal of Child Neurology

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Research article

First published 2022-11

Survival Motor Neuron Enhances Pluripotent Gene Expression and Facilitates Cell Reprogramming

Wei-Fang Chang, Tzu-Ying Lin, Min Peng [...]

Stem Cells and Development

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Research article

First published 2015-3

Association of Copy Numbers of Survival Motor Neuron Gene 2 and Neuronal Apoptosis Inhibitory Protein Gene With the Natural History in a Chinese Spinal Muscular Atrophy Cohort

Yu-jin Qu, Xiu-shan Ge, Jin-li Bai [...]

Journal of Child Neurology

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Other

First published 2003-01

Development of a Gene Therapy Strategy for the Restoration of Survival Motor Neuron Protein Expression: Implications for Spinal Muscular Atrophy Therapy

Christine J. DiDonato, Robin J. Parks, Rashmi Kothary

Human Gene Therapy

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Brief report

First published 2003-12

Survival Motor Neuron ( SMN ) Genes for Molecular Allele-Specific Amplification of Exon 7 in the Diagnosis of Spinal Muscular Atrophy

Mehmet Simsek, Talal Al-Bulushi, Muralitharan Shanmugakonar [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2013-11

Diabetic Ketoacidosis in an Adult Patient With Spinal Muscular Atrophy Type II

Nicole Holuba LaMarca, Lauren Golden, Rita Marie John [...]

Journal of Child Neurology

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Other

First published 1997-08

Gene Deletions in Arab Patients With Spinal Muscular Atrophy

Mohammad Z. Haider, Allie Moosa

Journal of Child Neurology

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Other

First published 2007-08

Animal Models of Spinal Muscular Atrophy

Aloicia Schmid, Christine J. DiDonato

Journal of Child Neurology

Open access

Research article

First published 2020

Infants Diagnosed with Spinal Muscular Atrophy and 4 SMN2 Copies through Newborn Screening – Opportunity or Burden? 1

Wolfgang Müller-Felber, Katharina Vill, Oliver Schwartz [...]

Journal of Neuromuscular Diseases

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