Nicoline Løkken

Loss-of-function mutations in<i>SCN4A</i>cause severe foetal hypokinesia or ‘classical’ congenital myopathy

Irina Zaharieva, Michael G. Thor, Emily C. Oates et al. · Brain · 2015 · 126 citations · Full text

Medicine, Genetics, Molecular Genetics +17

New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy

Jorge Alonso‐Pérez, Lidia González‐Quereda, Luca Bello et al. · Brain · 2020 · 76 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

MRI in sarcoglycanopathies: a large international cohort study

Giorgio Tasca, Mauro Monforte, Jordi Díaz‐Manera et al. · Journal of Neurology Neurosurgery & Psychiatry · 2017 · 72 citations

Medicine, Neurology, Radiology +14

<i>LAMA2</i>‐related myopathy: Frequency among congenital and limb‐girdle muscular dystrophies

Nicoline Løkken, Alfred Peter Born, John Vissing · Muscle & Nerve · 2015 · 63 citations

Medicine, Genetics, Molecular Genetics +16

European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A)

Andrea Barp, Pascal Laforêt, Luca Bello et al. · Journal of Neurology · 2019 · 62 citations · Full text

Medicine, Anatomy, Radiology +12