Publications by authors named "Alessandra Patitucci"

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From Hippocrates to Italian traditional medicine: Ethnopharmacological evidence for a potential pharmacological perspective in the management of polycystic ovary syndrome.
Rosalucia Mazzei, Alessandra Patitucci, Angela Magariello, Giampiero Russo, Giuseppe Tagarelli

J Ethnopharmacol· January 2026

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Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches.
Rosalucia Mazzei, Claudia Genovese, Angela Magariello, Alessandra Patitucci, Giampiero Russo

Plants (Basel)· February 2024

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A review of the antimicrobial potential of herbal drugs used in popular Italian medicine (1850s-1950s) to treat bacterial skin diseases.
Rosalucia Mazzei, Marco Leonti, Santo Spadafora, Alessandra Patitucci, Giuseppe Tagarelli

J Ethnopharmacol· March 2020

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: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders.
Valentina La Cognata, Giovanna Morello, Giulia Gentile, Francesca Cavalcanti, Rita Cittadella, Alessandra Patitucci

Curr Genomics· September 2018

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A rare association between multiple sclerosis and Charcot-Marie-Tooth type 1B.
Rosa Cortese, Stefano Zoccolella, Maria Muglia, Alessandra Patitucci, Antonio Scarafino

Brain Behav· December 2016

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Normal immunofluorescence pattern of skin basement membranes in a family with porencephaly due to COL4A1 G749S mutation.
Sara Gasparini, Antonio Qualtieri, Edoardo Ferlazzo, Vittoria Cianci, Alessandra Patitucci

Neurol Sci· March 2016

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Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis.
Francesca L Conforti, Rossella Spataro, William Sproviero, Rosalucia Mazzei, Francesca Cavalcanti, Alessandra Patitucci

Neurology· December 2012

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The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia.
Angela Magariello, Carla Tortorella, Luigi Citrigno, Alessandra Patitucci, Rosanna Tortelli

Muscle Nerve· June 2012

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SMN1 gene copy number analyses for SMA healthy carriers in Italian population.
Alessandra Patitucci, Angela Magariello, Carmine Ungaro, Maria Muglia, Francesca L Conforti

J Pediatr Genet· June 2012

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FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis.
William Sproviero, Vincenzo La Bella, Rosalucia Mazzei, Paola Valentino, Carmelo Rodolico, Alessandra Patitucci

Neurobiol Aging· April 2012

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An axon regeneration signature in a Charcot-Marie-Tooth disease type 2 patient.
Francesca Cavalcanti, Thomas Kidd, Alessandra Patitucci, Paola Valentino, Francesco Bono

J Neurogenet· December 2011

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A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy.
Maria Muglia, Giovanni Vazza, Alessandra Patitucci, Micaela Milani, Davide Pareyson

BMJ Case Rep· November 2011

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A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1.
Anna Lia Gabriele, Martino Ruggieri, Alessandra Patitucci, Angela Magariello, Francesca Luisa Conforti

Childs Nerv Syst· April 2011

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Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia.
Angela Magariello, Maria Muglia, Alessandra Patitucci, Carmine Ungaro, Rosalucia Mazzei

J Neurol Sci· January 2010

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Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy.
Francesca Luisa Conforti, Teresa Sprovieri, Rosalucia Mazzei, Alessandra Patitucci, Carmine Ungaro

Amyotroph Lateral Scler· February 2009

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A longitudinal observation of brain-derived neurotrophic factor mRNA levels in patients with relapsing-remitting multiple sclerosis.
Maria Liguori, Francesco Fera, Alessandra Patitucci, Ida Manna, Francesca Condino

Brain Res· February 2009

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Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.
Alessandro Malandrini, Simona Gambelli, Maria Muglia, Gianna Berti, Carmen Gaudiano, Alessandra Patitucci

Brain Dev· April 2008

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A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies.
Maria Muglia, Alessandra Patitucci, Romana Rizzi, Carmine Ungaro, Francesca Luisa Conforti

J Neurol Sci· December 2007

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Putative role of specific JAG1 gene exons in modulating clinical features in patients with leukoencephalopathy.
Carmine Ungaro, Teresa Sprovieri, Francesca L Conforti, Maria Muglia, Alessandra Patitucci

Neurosci Lett· May 2007

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Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia.
Angela Magariello, Maria Muglia, Alessandra Patitucci, Rosalucia Mazzei, Francesca Luisa Conforti

Neuromuscul Disord· June 2006

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Sporadic ALS is not associated with VAPB gene mutations in Southern Italy.
Francesca Luisa Conforti, Teresa Sprovieri, Rosalucia Mazzei, Carmine Ungaro, Alessandro Tessitore, Alessandra Patitucci

J Negat Results Biomed· May 2006

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Comparison of different techniques for detecting 17p12 duplication in CMT1A.
Alessandra Patitucci, Maria Muglia, Angela Magariello, Anna Lia Gabriele, Giuseppina Peluso

Neuromuscul Disord· July 2005

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Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy.
Luca Passamonti, Maria Muglia, Angela Magariello, Michele Bellesi, Francesca Luisa Conforti, Alessandra Patitucci

Neuromuscul Disord· November 2004

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Stephan Züchner, Irina V Mersiyanova, Maria Muglia, Nisrine Bissar-Tadmouri, Julie Rochelle, Alessandra Patitucci

Nat Genet· May 2004

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Abnormally high levels of SOD1 mRNA in a patient with amyotrophic lateral sclerosis.
Francesca Luisa Conforti, Angela Magariello, Rosalucia Mazzei, Teresa Sprovieri, Alessandra Patitucci

Muscle Nerve· April 2004

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