IJND/
Editorial Board

Editorial Board

  • Editor-in-Chief

    • Prof.  Corrado Angelini

      Neuromuscular Laboratory, Department of Neurosciences, University of Padova, Padua, Italy.

      Research Interests: metabolic myopathies; muscular dystrophy; neutral lipid storage disorders; spinal muscular atrophy; McArdle disease.

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  • Associate Editor-in-Chief

    • Prof. Dr.  Pasquale Striano

      • 1. Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini", Genova, Italy.
      • 2. Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.

      Research Interests: neurology; paediatrics; molecular genetics of epilepsies; microbiota; omics.

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  • Editorial Board Members

    • Prof. Dr.  Gabriele Siciliano

      Section of Neurology, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

      Research Interests: neurodegenerative and neurogenetic disorders; acquired and genetic diseases of peripheral nervous system; neuromuscular disorders; muscular dystrophies; Steinert disease; myotonic syndromes; mitochondrial myopathies; inflammatory peripheral neuropathies; amyotrophic lateral sclerosis.

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    • Prof. Dr.  Edoardo Malfatti

      Institut Mondor de Recherche Biomédicale (IMRB), UPEC - Paris-Est Créteil University, 94010 Créteil, France.

      Research Interests: genetics; neuromuscular disorders; limb-girdle muscular dystrophies.

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    • Prof. Dr.  Daniela Tavian

      Department of Psychology, Università Cattolica del Sacro Cuor, Milan, Italy.

      Research Interests: neutral lipid storage disorders in muscle; skin; and brain.

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    • Prof. Dr.  Giuseppe Novelli

      Direttore U.O.C. Laboratorio Genetica Medica, Dipartimento di Oncoematologia, Università di Roma Tor Vergata, Italy.

      Research Interests: human genetics; Laron dwarfism; cystic fibrosis; DiGeorge syndrome; Mandibuloacral dysplasia; Friedrich ataxia vitamin-E-deficiency; myotonic dystrophy; psoriasis; galactosemia; hereditary nonspherocytic haemolytic anemia.

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    • Prof. Dr.  Massimiliano Filosto

      Department of Clinical and Experimental Sciences, NeMO-Brescia Clinical Center for Neuromuscular Diseases, University of Brescia, 25121 Brescia, Italy.

      Research Interests: mitochondrial DNA; mitochondrial diseases; mitochondria; neurodegenerative diseases; neuromuscular diseases; motor neuron disease; muscular diseases; neuropathy; rare diseases; glycogen storage disease.

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    • Prof. Dr.  Maggie C. Walter

      LMU Klinikum, Ludwig-Maximilians-Universität in Munich, 80336 München, Germany.

      Research Interests: muscular dystrophy; myopathies; spinal muscular atrophy; NMT neuropathies.

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    • Dr.  David Israeli

      Généthon, Evry, France.

      Research Interests: pathophysiology of muscular dystrophies; Duchenne muscular dystrophy disease; Duchenne muscular dystrophy (DMD) disease.

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    • Prof. Dr.  Marianne de Visser

      Department of Neurology, University of Amsterdam, Amsterdam 1012 WP, Netherlands.

      Research Interests: neuromuscular disorders: motor neuron disease; hereditary neuropathies; inflammatory myopathies.

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    • Prof. Dr.  Ana Ferreiro

      • 1. Basic and Translational Myology Laboratory, Université Paris, BFA, UMR 8251, CNRS, 75013 Paris, France
      • 2. APHP, Reference Center for Neuromuscular Disorders Nord-Est-Ile de France, Neuromyology Department, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

      Research Interests: neuromuscular disorders; translational research; human genetics.

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    • Prof. Dr.  Aleksovska Katina

      European Academy of Neurology, Vienna, Austria.

      Research Interests: clinical practice guidelines in neurology and related methodology; EAN guidelines on asymptomatic hyperemia.

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