Luisa Politano

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 41

Top Topics

Myasthenia Gravis

Top Venues

International journal of molecular sciences

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

This page only lists publications with an associated author ORCID identifier.

Publications

Maria Elena Onore, Esther Picillo, Paola D'Ambrosio, Salvatore Morra, Vincenzo Nigro, Luisa Politano
Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene-A New Family Case Report. Biomolecules 14 (4) (2024)
Luisa Politano
Is Cardiac Transplantation Still a Contraindication in Patients with Muscular Dystrophy-Related End-Stage Dilated Cardiomyopathy? A Systematic Review. International journal of molecular sciences 25 (10) (2024)
Maria Elena Onore, Esther Picillo, Paola D'Ambrosio, Salvatore Morra, Vincenzo Nigro, Luisa Politano
Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene-A New Family Case Report. Biomolecules 14 (4) (2024)
Alessandra Govoni, Giulia Ricci, Silvia Bonanno, Luca Bello, Francesca Magri, Megi Meneri, Francesca Torri, Claudia Caponnetto, Luigia Passamano, Marina Grandis, Francesca Trojsi, Federica Cerri, Giulio Gadaleta, Giuliana Capece, Luca Caumo, Raffaella Tanel, Elena Saccani, Veria Vacchiano, Gianni Sorarù, Eustachio D'Errico, Irene Tramacere, Sara Bortolani, Enrica Rolle, Cinzia Gellera, Riccardo Zanin, Mauro Silvestrini, Luisa Politano, Angelo Schenone, Stefano Carlo Previtali, Angela Berardinelli, Mara Turri, Lorenzo Verriello, Michela Coccia, Renato Mantegazza, Rocco Liguori, Massimiliano Filosto, Maria Antonietta Maioli, Isabella Laura Simone, Tiziana Mongini, Stefania Corti, Maria Laura Manca, Elena Pegoraro, Gabriele Siciliano, Giacomo Pietro Comi, Lorenzo Maggi
Six-minute walk test as outcome measure of fatigability in adults with spinal muscular atrophy treated with nusinersen. Muscle & nerve (2024)
Maria Elena Onore, Esther Picillo, Paola D'Ambrosio, Salvatore Morra, Vincenzo Nigro, Luisa Politano
Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene-A New Family Case Report. Biomolecules 14 (4) (2024)
Luisa Politano
Is Cardiac Transplantation Still a Contraindication in Patients with Muscular Dystrophy-Related End-Stage Dilated Cardiomyopathy? A Systematic Review. International journal of molecular sciences 25 (10) (2024)
Antonella Pizza, Esther Picillo, Maria Elena Onore, Marianna Scutifero, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 42 (1) (2023)
Antonella Pizza, Esther Picillo, Maria Elena Onore, Marianna Scutifero, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 42 (1) (2023)
Emanuela Viggiano, Esther Picillo, Luigia Passamano, Maria Elena Onore, Giulio Piluso, Marianna Scutifero, Anna Laura Torella, Vincenzo Nigro, Luisa Politano
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy. Genes 14 (1) (2023)
Antonella Pizza, Esther Picillo, Maria Elena Onore, Marianna Scutifero, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 42 (1) (2023)
Antonella Pizza, Esther Picillo, Maria Elena Onore, Marianna Scutifero, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 42 (1) (2023)
Claudia Brogna, Marika Pane, Giorgia Coratti, Adele D'Amico, Elena Pegoraro, Luca Bello, Valeria Ada Maria Sansone, Emilio Albamonte, Sonia Messina, Antonella Pini, Maria Grazia D'Angelo, Claudio Bruno, Tiziana Mongini, Federica Silvia Ricci, Angela Berardinelli, Roberta Battini, Riccardo Masson, Enrico Silvio Bertini, Luisa Politano, Eugenio Mercuri, null Italian Dmd Group
Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study. Children (Basel, Switzerland) 10 (4) (2023)
Claudia Brogna, Marika Pane, Giorgia Coratti, Adele D'Amico, Elena Pegoraro, Luca Bello, Valeria Ada Maria Sansone, Emilio Albamonte, Sonia Messina, Antonella Pini, Maria Grazia D'Angelo, Claudio Bruno, Tiziana Mongini, Federica Silvia Ricci, Angela Berardinelli, Roberta Battini, Riccardo Masson, Enrico Silvio Bertini, Luisa Politano, Eugenio Mercuri, null Italian Dmd Group
Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study. Children (Basel, Switzerland) 10 (4) (2023)
Emanuela Viggiano, Esther Picillo, Luigia Passamano, Maria Elena Onore, Giulio Piluso, Marianna Scutifero, Anna Laura Torella, Vincenzo Nigro, Luisa Politano
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy. Genes 14 (1) (2023)
Luisa Politano, Filippo Maria Santorelli
Editorial for the Genetics of Muscular Dystrophies from the Pathogenesis to Gene Therapy Special Issue. Genes 14 (4) (2023)
Luisa Politano, Filippo Maria Santorelli
Editorial for the Genetics of Muscular Dystrophies from the Pathogenesis to Gene Therapy Special Issue. Genes 14 (4) (2023)
Emanuela Viggiano, Esther Picillo, Luigia Passamano, Maria Elena Onore, Giulio Piluso, Marianna Scutifero, Anna Laura Torella, Vincenzo Nigro, Luisa Politano
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy. Genes 14 (1) (2023)
Luisa Politano, Filippo Maria Santorelli
Editorial for the Genetics of Muscular Dystrophies from the Pathogenesis to Gene Therapy Special Issue. Genes 14 (4) (2023)
Luisa Politano
Females with dystrophinopathy: A neglected patient population. Developmental medicine and child neurology (2023)
Luisa Politano, Filippo Maria Santorelli
Editorial for the Genetics of Muscular Dystrophies from the Pathogenesis to Gene Therapy Special Issue. Genes 14 (4) (2023)
Anna Laura Torella, Alberto Budillon, Mariateresa Zanobio, Francesca Del Vecchio Blanco, Esther Picillo, Luisa Politano, Vincenzo Nigro, Giulio Piluso
Alu-Mediated Insertions in the DMD Gene: A Difficult Puzzle to Interpret Clinically. International journal of molecular sciences 24 (11) (2023)
Esther Picillo, Annalaura Torella, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Autosomal dominant Ullrich congenital muscular dystrophy due to a de novo mutation in COL6A3 gene. A case report. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 41 (2) (2022)
Maria Elena Onore, Marco Savarese, Esther Picillo, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function. International journal of molecular sciences 23 (24) (2022)
Maria Elena Onore, Marco Savarese, Esther Picillo, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function. International journal of molecular sciences 23 (24) (2022)
Maria Elena Onore, Marco Savarese, Esther Picillo, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function. International journal of molecular sciences 23 (24) (2022)
Marianna Scutifero, Michele Lanza, Roberta Petillo, Maddalena De Bernardo, Luigia Passamano, Nicola Rosa, Luisa Politano
Gender effect on onset, prevalence and surgical treatment of cataract in patients with Myotonic Dystrophy type 1. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 41 (3) (2022)
Giorgia Coratti, Jacopo Lenkowicz, Giulia Norcia, Simona Lucibello, Elisabetta Ferraroli, Adele d'Amico, Luca Bello, Elena Pegoraro, Sonia Messina, Federica Ricci, Tiziana Mongini, Angela Berardinelli, Riccardo Masson, Stefano C Previtali, Grazia D'angelo, Francesca Magri, Giacomo P Comi, Luisa Politano, Luigia Passamano, Gianluca Vita, Valeria A Sansone, Emilio Albamonte, Chiara Panicucci, Claudio Bruno, Antonella Pini, Enrico Bertini, Stefano Patarnello, Marika Pane, Eugenio Mercuri, null null
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy. PloS one 17 (7) (2022)
Maria Elena Onore, Marco Savarese, Esther Picillo, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function. International journal of molecular sciences 23 (24) (2022)
Lorenza Magliano, Giulia Citarelli, Maria Grazia Esposito, Vito Torre, Luisa Politano
Impact of the COVID-19 pandemic on neuromuscular rehabilitation setting. Part 2: patients and families' views on the received health care during the pandemic. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 41 (2) (2022)
Maria Elena Onore, Marco Savarese, Esther Picillo, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function. International journal of molecular sciences 23 (24) (2022)
Alberto Palladino, Andrea Antonio Papa, Roberta Petillo, Marianna Scutifero, Salvatore Morra, Luigia Passamano, Vincenzo Nigro, Luisa Politano
The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution. Genes 13 (2) (2022)
Maria Elena Onore, Marco Savarese, Esther Picillo, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function. International journal of molecular sciences 23 (24) (2022)
Maria Elena Onore, Marco Savarese, Esther Picillo, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function. International journal of molecular sciences 23 (24) (2022)
Rabah Ben Yaou, Pomi Yun, Ivana Dabaj, Gina Norato, Sandra Donkervoort, Hui Xiong, Andrés Nascimento, Lorenzo Maggi, Anna Sarkozy, Soledad Monges, Marta Bertoli, Hirofumi Komaki, Michèle Mayer, Eugenio Mercuri, Edmar Zanoteli, Claudia Castiglioni, Chiara Marini-Bettolo, Adele D'Amico, Nicolas Deconinck, Isabelle Desguerre, Ricardo Erazo-Torricelli, Juliana Gurgel-Giannetti, Akihiko Ishiyama, Karin S Kleinsteuber, Emmanuelle Lagrue, Vincent Laugel, Sandra Mercier, Sonia Messina, Luisa Politano, Monique M Ryan, Pascal Sabouraud, Ulrike Schara, Gabriele Siciliano, Liliana Vercelli, Thomas Voit, Grace Yoon, Rachel Alvarez, Francesco Muntoni, Tyler Mark Pierson, David Gómez-Andrés, A Reghan Foley, Susana Quijano-Roy, Carsten G Bönnemann, Gisèle Bonne
International retrospective natural history study of LMNA-related congenital muscular dystrophy. Brain communications 3 (3) (2021)
Giulia Citarelli, Ciro Garofalo, Maria Grazia Esposito, Vito Torre, Lorenza Magliano, Luisa Politano
Impact of the COVID-19 pandemic on rehabilitation setting. Part 1: professionals' views on the changes in routine care provided by a rehabilitation centre for patients with muscle diseases. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 40 (3) (2021)
Emanuela Viggiano, Luisa Politano
X Chromosome Inactivation in Carriers of Fabry Disease: Review and Meta-Analysis. International journal of molecular sciences 22 (14) (2021)
Giorgia Coratti, Marika Pane, Claudia Brogna, Valeria Ricotti, Sonia Messina, Adele D'Amico, Claudio Bruno, Gian Luca Vita, Angela Berardinelli, Elena Mazzone, Francesca Magri, Federica Ricci, Tiziana Mongini, Roberta Battini, Luca Bello, Elena Pegoraro, Giovanni Baranello, Previtali Stefano Carlo, Luisa Politano, Giacomo P Comi, Valeria A Sansone, Alice Donati, Jean Yves Hogrel, Volker Straub, Silvana De Lucia, Erik H Niks, Laurent Servais, Imelda De Groot, Mary Chesshyre, Enrico Bertini, Nathalie M Goemans, Francesco Muntoni, Eugenio Mercuri, null null
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up. PloS one 16 (6) (2021)
Vincenzo Russo, Luisa Politano
Unmet needs on the management of COVID-19 vaccination in patients with neuromuscular disorders. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 40 (3) (2021)
Cristina Cappelletti, Irene Tramacere, Paola Cavalcante, Elisa Schena, Luisa Politano, Nicola Carboni, Alessandra Gambineri, Adele D'Amico, Lucia Ruggiero, Giulia Ricci, Gabriele Siciliano, Giuseppe Boriani, Tiziana Enrica Mongini, Liliana Vercelli, Elena Biagini, Matteo Ziacchi, Maria Rosaria D'Apice, Giovanna Lattanzi, Renato Mantegazza, Lorenzo Maggi, Pia Bernasconi
Cytokine Profile in Striated Muscle Laminopathies: New Promising Biomarkers for Disease Prediction. Cells 9 (6) (2020)
Manuela Ergoli, Massimo Venditti, Esther Picillo, Sergio Minucci, Luisa Politano
Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function. Molecular reproduction and development 87 (1) (2019)
Emanuela Viggiano, Esther Picillo, Manuela Ergoli, Alessandra Cirillo, Stefania Del Gaudio, Luisa Politano
Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy. The journal of gene medicine 19 (4) (2017)