Valentina Codemo

Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort

Michela Catteruccia, Fabiana Fattori, Valentina Codemo et al. · Neuromuscular Disorders · 2013 · 62 citations · Full text

Mitochondrial Myopathy, Mendelian Disorder, Medicine +8

Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort

Fabiana Fattori, Lorenzo Maggi, Claudio Bruno et al. · Journal of Neurology · 2015 · 60 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers

Valeria Guglielmi, Gaetano Vattemi, Francesca Gualandi et al. · Molecular Genetics and Metabolism · 2013 · 38 citations

Mendelian Disorder, Genetic Disorder, Medicine +7

Neurological complications in hyperemesis gravidarum

Gabriella Zara, Valentina Codemo, Arianna Palmieri et al. · Neurological Sciences · 2011 · 26 citations

Spinal Cord Injury, Neurological Disorder, Clinical Neurology +6

Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study

Aurora Fusto, Denise Cassandrini, Chiara Fiorillo et al. · Acta Neuropathologica Communications · 2022 · 15 citations · Full text