Rosana Hermínia Scola

Long-term effect of thymectomy plus prednisone versus prednisone alone in patients with non-thymomatous myasthenia gravis: 2-year extension of the MGTX randomised trial

Gil I. Wolfe, Henry J. Kaminski, Inmaculada Aban et al. · The Lancet Neurology · 2019 · 216 citations · Full text

Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes

Violeta Mihaylova, Juliane S. Müller, Juan J. Vílchez et al. · Brain · 2008 · 159 citations · Full text

Developmental Anomaly, Rare Diseases, Ache Deficiency +13

A missense mutation in the Kv1.1 voltage-gated potassium channel–encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia

Bob Glaudemans, Jenny van der Wijst, Rosana Hermínia Scola et al. · Journal of Clinical Investigation · 2009 · 156 citations · Full text

Electrolyte Disorder, Genetics, Blood Mg2+ Levels +22

A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome

Amina Chaouch, Juliane S. Müller, Velina Guergueltcheva et al. · Journal of Neurology · 2011 · 73 citations

Channelopathies, Retrospective Clinical Study, Pediatrics

Clinical follow-up of pregnancy in myasthenia gravis patients

Renata Dal‐Prá Ducci, Paulo José Lorenzoni, Cláudia Suemi Kamoi Kay et al. · Neuromuscular Disorders · 2017 · 63 citations

Maternal Complication, Myasthenia Gravis Patients, Gynecology +6