Results 111 to 120 of about 3,643 (133)

LAMA2 Retrospective Natural History Study

Case Medical Research, 2020
openaire   +1 more source

Current Insights Into LAMA2 Disease

2022
openaire   +1 more source

VP427 The Swiss cohort of LAMA2-related muscular dystrophy patients

Neuromuscular Disorders, 2023
Enzmann, C., Klein, A., Fluss, J., Henzi, B., Lötscher, N., Jacquier, D., Ripellino, P., Stettner, G., Baumann, D., Steiner, L.   +9 more
openaire   +2 more sources

Cardiac involvement in two rare neuromuscular diseases: LAMA2-related muscular dystrophy and SELENON-related myopathy

Neuromuscular Disorders, 2022
Nicol Voermans, Corrie E Erasmus
exaly  

LAMA2-Related Dystrophies: Clinical Phenotypes, Disease Biomarkers, and Clinical Trial Readiness

Frontiers in Molecular Neuroscience, 2020
Carsten Bönnemann, Alberto A Zambon, Francesco Muntoni   +2 more
exaly  

Muscle magnetic resonance imaging in patients with LAMA2-related muscular dystrophy

Neuromuscular Disorders, 2021
Dandan Tan, Aijie Liu, Hui Xiong
exaly  

Epilepsy in LAMA2‐related muscular dystrophy: An electro‐clinico‐radiological characterization

Epilepsia, 2020
Daniel Natera-De Benito, Pia Gallano, Cecilia Jimenez-Mallebrera   +2 more
exaly  

LAMA2gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes

Human Mutation, 2018
Mario DE SOUSA, JOSÉ Vieira, Ana Gonçalves   +2 more
exaly  

Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant

Neuromuscular Disorders, 2020
Alice Abdel Aleem, Ömer Kuzu, Omar Osman   +2 more
exaly  

LAMA2‐related myopathy: Frequency among congenital and limb‐girdle muscular dystrophies

Muscle and Nerve, 2015
John Vissing, Nicoline Løkken
exaly