Martina Petracca

Università Cattolica del Sacro Cuore - Milano / Italy

Medical and Health Sciences / Neurology

AD Scientific Index ID: 1851465

Catholic University of the Sacred Heart

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Martina Petracca's MOST POPULAR ARTICLES

1-) The role of small intestinal bacterial overgrowth in Parkinson\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\'s diseaseA Fasano, F Bove, M Gabrielli, M Petracca, MA Zocco, E Ragazzoni, ...Movement Disorders 28 (9), 1241-1249, 20132802013

2-) GBA‐Related Parkinson\'s Disease: Dissection of Genotype–Phenotype Correlates in a Large Italian CohortS Petrucci, M Ginevrino, I Trezzi, E Monfrini, L Ricciardi, A Albanese, ...Movement Disorders 35 (11), 2106-2111, 20201202020

3-) Clinical differences between botulinum neurotoxin type A and BAR Bentivoglio, A Del Grande, M Petracca, T Ialongo, L RicciardiToxicon 107, 77-84, 2015912015

4-) Survival, Mortality, Causes and Places of Death in a European Huntington\'s Disease Prospective Cohort.FJJ Rodrigues FB, Abreu D, Damásio J, Goncalves N, Correia-Guedes L, Coelho MMovement Disorders Clinical Practice 4 (5), 737-742, 2017802017

5-) Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early‐onset levodopa‐responsive ParkinsonismA Guidubaldi, C Piano, FM Santorelli, G Silvestri, M Petracca, A Tessa, ...Movement Disorders 26 (3), 553-556, 2011772011

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