Publications by authors named "Mauro Pessia"

51Publications

Corrigendum to "Ion Channels Involvement in Neurodevelopmental Disorders" [Neuroscience 440C (2020) 337-359].

Authors:

Maria CristinaD'Adamo Antonella Liantonio Elena Conte Mauro Pessia Paola Imbrici

Neuroscience 2020 Sep 29;443:233. Epub 2020 Jul 29.

Department of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Italy. Electronic address:

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September 2020

Electromechanical coupling of the Kv1.1 voltage-gated K channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker.

Authors:

Sonia Hasan Alfredo Megaro Marta Cenciarini Lorena Coretti Fabio Massimo Botti Paola Imbrici Harry W M Steinbusch Therese Hunter Gary Hunter Mauro Pessia Maria Cristina D'Adamo

Pflugers Arch 2020 07 23;472(7):899-909. Epub 2020 Jun 23.

Department of Physiology & Biochemistry, Faculty of Medicine & Surgery, University of Malta, Msida, MSD 2080, Malta.

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July 2020

Ion Channels Involvement in Neurodevelopmental Disorders.

Authors:

Maria Cristina D'Adamo Antonella Liantonio Elena Conte Mauro Pessia Paola Imbrici

Neuroscience 2020 08 28;440:337-359. Epub 2020 May 28.

Department of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Italy. Electronic address:

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August 2020

Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia.

Authors:

Claudia Stendel Maria Cristina D'Adamo Manuela Wiessner Marina Dusl Marta Cenciarini Silvia Belia Ehsan Nematian-Ardestani Peter Bauer Jan Senderek Thomas Klopstock Mauro Pessia

Int J Mol Sci 2020 May 27;21(11). Epub 2020 May 27.

Faculty of Medicine, Department of Physiology & Biochemistry, University of Malta, MSD 2080 Msida, Malta.

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May 2020

Altered functional properties of a missense variant in the TRESK K channel (KCNK18) associated with migraine and intellectual disability.

Authors:

Paola Imbrici Ehsan Nematian-Ardestani Sonia Hasan Mauro Pessia Stephen J Tucker Maria Cristina D'Adamo

Pflugers Arch 2020 07 12;472(7):923-930. Epub 2020 May 12.

Department of Physiology & Biochemistry, Faculty of Medicine and Surgery, University of Malta, MSD, Msida, 2080, Malta.

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July 2020

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches.

Authors:

Maria Cristina D'Adamo Antonella Liantonio Jean-Francois Rolland Mauro Pessia Paola Imbrici

Int J Mol Sci 2020 Apr 22;21(8). Epub 2020 Apr 22.

Department of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", 70125 Bari, Italy.

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April 2020

Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies.

Authors:

Marta Cenciarini Mario Valentino Silvia Belia Luigi Sforna Paolo Rosa Simona Ronchetti Maria Cristina D'Adamo Mauro Pessia

Front Mol Neurosci 2019 29;12:65. Epub 2019 Mar 29.

Section of Physiology and Biochemistry, Department of Experimental Medicine, University of Perugia School of Medicine, Perugia, Italy.

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March 2019

Identification of a New Mutation Underlying Regressive Episodic Ataxia Type I.

Authors:

Zeynep S Karalok Alfredo Megaro Marta Cenciarini Alev Guven Sonia M Hasan Birce D Taskin Paola Imbrici Serdar Ceylaner Mauro Pessia Maria C D'Adamo

Front Neurol 2018 25;9:587. Epub 2018 Jul 25.

Department of Physiology and Biochemistry, Faculty of Medicine and Surgery, University of Malta, Msida, Malta.

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July 2018

Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia.

Authors:

Sonia Hasan Therese Hunter Gary Hunter Mauro Pessia Maria Cristina D'Adamo

Front Cell Neurosci 2018 20;12:174. Epub 2018 Jun 20.

Department of Physiology and Biochemistry, Faculty of Medicine and Surgery University of Malta, Msida, Malta.

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June 2018

Reply to 'F508del-CFTR is not corrected by thymosin α1'.

Authors:

Luigina Romani Claudia Stincardini Stefano Giovagnoli Maurizio Paci Valeria R Villella Luigi Sforna Giorgia Renga Marina M Bellet Claudio Costantini Paolo Puccetti Guido Kroemer Luigi Maiuri Mauro Pessia Allan Goldstein Enrico Garaci

Nat Med 2018 07;24(7):891-893

University San Raffaele, Rome, Italy.

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July 2018

Publisher Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis.

Nat Med 2018 Sep;24(9):1482

University San Raffaele and IRCCS San Raffaele, Rome, Italy.

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September 2018

Author Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis.

Nat Med 2018 Sep;24(9):1481

University San Raffaele and IRCCS San Raffaele, Rome, Italy.

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September 2018

Structure, Gating and Basic Functions of the Ca2+-activated K Channel of Intermediate Conductance.

Authors:

Luigi Sforna Alfredo Megaro Mauro Pessia Fabio Franciolini Luigi Catacuzzeno

Curr Neuropharmacol 2018 ;16(5):608-617

Department of Chemistry, Biology and Biotechnology, University of Perugia, via Pascoli 8, 06123, Perugia, Italy.

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September 2018

Lethal digenic mutations in the K channels Kir4.1 () and SLACK () associated with severe-disabling seizures and neurodevelopmental delay.

Authors:

Sonia Hasan Ameera Balobaid Alessandro Grottesi Omar Dabbagh Marta Cenciarini Rifaat Rawashdeh Afaf Al-Sagheir Cecilia Bove Lara Macchioni Mauro Pessia Mohammed Al-Owain Maria Cristina D'Adamo

J Neurophysiol 2017 10 26;118(4):2402-2411. Epub 2017 Jul 26.

Department of Physiology and Biochemistry, Faculty of Medicine and Surgery, University of Malta, Msida, Malta;

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October 2017

A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia.

Authors:

Sonia Hasan Cecilia Bove Gabriella Silvestri Elide Mantuano Anna Modoni Liana Veneziano Lara Macchioni Therese Hunter Gary Hunter Mauro Pessia Maria Cristina D'Adamo

Sci Rep 2017 07 4;7(1):4583. Epub 2017 Jul 4.

Faculty of Medicine & Surgery, Department of Physiology & Biochemistry, University of Malta, MSD 2080, Msida, Malta.

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July 2017

A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions.

Authors:

Paola Imbrici Concetta Altamura Francesca Gualandi Giuseppe Felice Mangiatordi Marcella Neri Giovanni De Maria Alessandra Ferlini Alessandro Padovani Maria Cristina D'Adamo Orazio Nicolotti Mauro Pessia Diana Conte Massimiliano Filosto Jean-Francois Desaphy

Mol Cell Neurosci 2017 09 28;83:6-12. Epub 2017 Jun 28.

Department of Biomedical Sciences and Human Oncology, University of Bari Aldo Moro, Bari, Italy.

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September 2017

Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis.

Nat Med 2017 May 10;23(5):590-600. Epub 2017 Apr 10.

University San Raffaele and IRCCS San Raffaele, Rome, Italy.

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May 2017

Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.

Authors:

Federico Sicca Elena Ambrosini Maria Marchese Luigi Sforna Ilenio Servettini Giulia Valvo Maria Stefania Brignone Angela Lanciotti Francesca Moro Alessandro Grottesi Luigi Catacuzzeno Sara Baldini Sonia Hasan Maria Cristina D'Adamo Fabio Franciolini Paola Molinari Filippo M Santorelli Mauro Pessia

Sci Rep 2016 Sep 28;6:34325. Epub 2016 Sep 28.

School of Medicine, Section of Physiology &Biochemistry, Department of Experimental Medicine, Piazzale Gambuli, University of Perugia, 06132-Perugia, Italy.

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September 2016

Overexpression of Large-Conductance Calcium-Activated Potassium Channels in Human Glioblastoma Stem-Like Cells and Their Role in Cell Migration.

Authors:

Paolo Rosa Luigi Sforna Silvia Carlomagno Giorgio Mangino Massimo Miscusi Mauro Pessia Fabio Franciolini Antonella Calogero Luigi Catacuzzeno

J Cell Physiol 2017 Sep 10;232(9):2478-2488. Epub 2017 Apr 10.

Department of Chemistry Biology and Biotechnology, University of Perugia, Perugia, Italy.

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September 2017

deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability.

J Med Genet 2016 Nov 31;53(11):786-792. Epub 2016 Aug 31.

College of Optometry, The Ohio State University, Columbus, Ohio, USA.

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November 2016