Aldesia Provenzano

Evidence of a four-hit mechanism involving<i>SMARCB1</i>and<i>NF2</i>in schwannomatosis-associated schwannomas

Roberta Sestini, Costanza Bacci, Aldesia Provenzano et al. · Human Mutation · 2007 · 179 citations

Neuro-oncology, Somatic Variant, Mendelian Disorder +15

The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis

Viviana Palazzo, Aldesia Provenzano, Francesca Becherucci et al. · Kidney International · 2017 · 120 citations · Full text

Hemodialysis, Urology, Renal Function +8

Human Urine-Derived Renal Progenitors for Personalized Modeling of Genetic Kidney Disorders

Elena Lazzeri, Elisa Ronconi, Maria Lucia Angelotti et al. · Journal of the American Society of Nephrology · 2015 · 103 citations · Full text

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

Costanza Bacci, Roberta Sestini, Aldesia Provenzano et al. · Neurogenetics · 2009 · 101 citations

Neuro-oncology, Familial Smarcb1 Mutation, Mendelian Disorder +6

Heterogeneous Genetic Alterations in Sporadic Nephrotic Syndrome Associate with Resistance to Immunosuppression

Sabrina Giglio, Aldesia Provenzano, Benedetta Mazzinghi et al. · Journal of the American Society of Nephrology · 2014 · 96 citations · Full text

Glomerular Disease, Genetics, Immunology +22