Paulo José Lorenzoni

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

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

Molecular characterisation of congenital myasthenic syndromes in Southern Brazil

Violeta Mihaylova, Rosana Hermínia Scola, Bianca Lamas Gervini et al. · Journal of Neurology Neurosurgery & Psychiatry · 2010 · 62 citations

Salbutamol therapy in congenital myasthenic syndrome due to DOK7 mutation

Paulo José Lorenzoni, Rosana Hermínia Scola, Cláudia Suemi Kamoi Kay et al. · Journal of the Neurological Sciences · 2013 · 51 citations

Medicine, Salbutamol Therapy, Pediatrics

Novel synaptobrevin‐1 mutation causes fatal congenital myasthenic syndrome

Xin‐Ming Shen, Rosana Hermínia Scola, Paulo José Lorenzoni et al. · Annals of Clinical and Translational Neurology · 2017 · 45 citations · Full text