Gianna Berti

Identification and characterization of three novel mutations in the<i>CASQ1</i>gene in four patients with tubular aggregate myopathy

Virginia Barone, Valeria Del Re, Alessandra Gamberucci et al. · Human Mutation · 2017 · 72 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +16

<i>PAX6</i> mutation in a family with aniridia, congenital ptosis, and mental retardation

Alessandro Malandrini, Francesca Mari, Silvia Palmeri et al. · Clinical Genetics · 2001 · 59 citations

Life Sciences, Genetics, Molecular Genetics +17

Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 cases.

Alex Malandrini, Marcello Villanova, Gianna Berti et al. · PubMed · 2000 · 54 citations

Medicine, Neurology, Pathology +15

Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family

Alessandro Malandrini, Gian Maria Fabrizi, Fabio Truschi et al. · Journal of the Neurological Sciences · 1994 · 44 citations

Medicine, Cardiology, Neurology +10

Muscle Biopsy and In Vitro  Contracture Test in Subjects with Idiopathic HyperCKemia

Alessandro Malandrini, Alfredo Orrico, Carmen Gaudiano et al. · Anesthesiology · 2008 · 39 citations · Full text

Medicine, Pathology, Histopathology +13