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Research article

First published 2025

Clinical and Genetic Landscape of Children With Congenital Muscular Dystrophies From North India

Anirban Basu, Renu Suthar, Abhishek Pandey [...]

Journal of Child Neurology

Open access

Research article

First published 2023-07-04

Brain MRI Abnormalities,Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy – a Genotype/Phenotype Correlation

Clara Gontijo Camelo, Mariana Cunha Artilheiro, Cristiane Araújo Martins Moreno [...]

Journal of Neuromuscular Diseases

Open access

Research article

First published 2024-11

An international retrospective early natural history study of LAMA2-related dystrophies

Lauren Hinkley, Rotem Orbach, Justin Park [...]

Journal of Neuromuscular Diseases

Open access

Review article

First published 2017

Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy

Raffaella Willmann, Heather Gordish-Dressman, Sarina Meinen [...]

Journal of Neuromuscular Diseases

Open access

Research article

First published 2024

A Multicenter Cross-Sectional Study of the Swiss Cohort of LAMA2-Related Muscular Dystrophy

Cornelia Enzmann, Leonie Steiner, Katarzyna Pospieszny [...]

Journal of Neuromuscular Diseases

Free access

Case report

First published 2023-1-3

LAMA2 -Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMD

Tanya Stojkovic, Marion Masingue, Corinne Métay [...]

Journal of Neuromuscular Diseases

Open access

Case report

First published 2025

Broadening the paradigm of laminin α2-related muscular dystrophy: A case of partial merosin deficiency with compound heterozygous variants

Azita Tavasoli, Shayan Eghdami, Maryam Kachuei [...]

Sage Open Medical Case Reports

Search results

Clinical and Genetic Landscape of Children With Congenital Muscular Dystrophies From North India

Brain MRI Abnormalities,Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy – a Genotype/Phenotype Correlation

An international retrospective early natural history study of LAMA2-related dystrophies

Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy

A Multicenter Cross-Sectional Study of the Swiss Cohort of LAMA2-Related Muscular Dystrophy

LAMA2 -Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMD

Broadening the paradigm of laminin α2-related muscular dystrophy: A case of partial merosin deficiency with compound heterozygous variants