Volume 4, Number 4 / 2017 Available Online Review Articles Muscular Dystrophy with Ribitol-Phosphate Deficiency: A Novel Post-Translational Mechanism in Dystroglycanopathy – Open Access Kanagawa, Motoi | Toda, Tatsushi Congenital Myasthenic Syndromes or Inherited Disorders of Neuromuscular Transmission: Recent Discoveries and Open Questions – Open Access Nicole, Sophie | Azuma, Yoshiteru | Bauché, Stéphanie | Eymard, Bruno | Lochmüller, Hanns | Slater, Clarke Research Articles Patient Preferences for Treatments of Neuromuscular Diseases: A Systematic Literature Review Landfeldt, Erik | Edström, Josefin | Lindgren, Peter | Lochmüller, Hanns Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database – Open Access Koeks, Zaïda et al. Progression of Duchenne Cardiomyopathy Presenting with Chest Pain and Troponin Elevation Hor, Kan N. | Johnston, Pace | Kinnett, Kathi | Mah, May Ling | Stiver, Corey | Markham, Larry | Cripe, Linda Early-Onset Myopathies: Clinical Findings, Prevalence of Subgroups and Diagnostic Approach in a Single Neuromuscular Referral Center in Germany Vill, K. | Blaschek, A. | Gläser, D. | Kuhn, M. | Haack, T. | Alhaddad, B. | Wagner, M. | Kovacs-Nagy, R. | Tacke, M. | Gerstl, L. | Schroeder, A.S. | Borggraefe, I. | Mueller, C. | Schlotter-Weigel, B. | Schoser, B. | Walter, M.C. | Müller-Felber, W. Cytokine Profiling of Serum Allows Monitoring of Disease Progression in Inclusion Body Myositis Badrising, Umesh A. | Tsonaka, Roula | Hiller, Monika | Niks, Erik H. | Evangelista, Teresinha | Lochmüller, Hanns | Verschuuren, Jan JGM. | Aartsma-Rus, Annemieke | Spitali, Pietro Expanding the Clinical Spectrum of IgLON5-Syndrome – Open Access Wenninger, Stephan A Panel of Slow-Channel Syndrome Mice Reveals a Unique Locomotor Behavioral Signature Grajales-Reyes, José G. | García-González, Aurian | María-Ríos, José C. | Grajales-Reyes, Gary E. | Delgado-Vélez, Manuel | Báez-Pagán, Carlos A. | Quesada, Orestes | Gómez, Christopher M. | Lasalde-Dominicci, José A. Dominant Centronuclear Myopathy with Early Childhood Onset due to a Novel Mutation in BIN1 Kouwenberg, Carlyn | Bohm, Johann | Erasmus, Corrie | van Balken, Irene | Vos, Sandra | Kusters, Benno | Kamsteeg, Erik-Jan | Biancalana, Valerie | Koch, Catherine | Dondaine, Nicolas | Laporte, Jocelyn | Voermans, Nicol Two Cases of Spinal Muscular Atrophy Type II with Eosinophilic Oesophagitis Fuller, Heidi R. | Shorrock, Hannah K. | Gillingwater, Thomas H. | Pigott, Anna | Smith, Victoria | Kulshrestha, Richa | Sewry, Caroline S. | Willis, Tracey A. | Most Read JND Articles in 2017 Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism – Open Access (Research Article in Vol.2, Iss.s2, 2015) Meola, Giovanni | Cardani, Rosanna Mortality and Causes of Death in Patients with Sporadic Inclusion Body Myositis: Survey Study Based on the Clinical Experience of Specialists in Australia, Europe and the USA – Open Access (Research Article in Vol.3, Iss.1, 2016) Price, Mark A. | Barghout, Victoria | Benveniste, Olivier | Christopher-Stine, Lisa | Corbett, Alastair | de Visser, Marianne | Hilton-Jones, David | Kissel, John T. | Lloyd, Thomas E. | Lundberg, Ingrid E. | Mastaglia, Francis | Mozaffar, Tahseen | Needham, Merrilee | Schmidt, Jens | Sivakumar, Kumaraswamy | DeMuro, Carla | Tseng, Brian S. Genome Editing Gene Therapy for Duchenne Muscular Dystrophy – Open Access (Review Article in Vol.2, Iss.4, 2015) Hotta, Akitsu Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy – Open Access (Review Article in Vol.4, Iss.1, 2017) Fayssoil, Abdallah | Abasse, Soumeth | Silverston, Katy Feeding and Swallowing Disorders in Pediatric Neuromuscular Diseases: An Overview – Open Access (Review Article in Vol.2, Iss.4, 2015) van den Engel-Hoek, Lenie | de Groot, Imelda J.M. | de Swart, Bert J.M. | Erasmus, Corrie E. | Announcing Partnership with TREAT-NMD | We are pleased to announce a new partnership between JND and TREAT-NMD, a network for the neuromuscular field that provides an infrastructure to ensure that the most promising new therapies reach patients as quickly as possible. The partnership will see our respective teams working together to give a platform to the latest developments in neuromuscular diseases research. Our journal is dedicated to providing an open forum for original research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases. JND aims to support the development of important tools for clinicials and scientists in the field, which aligns with TREAT-NMD's focus, as well as it its goal to establish best-practice care for neuromuscular patients worldwide. The organisation recently celebrated its 10th anniversary at its symposium in Freiburg, Germany (pictured), where copies of the journal were available to delegates. | Submit your Paper As a member of our research community, we would like to invite you to contribute your own articles to the journal. JND offers contributing authors many benefits, including rigorous peer review and speedy manuscript processing, rapid online publication (pre-print) and an affordable Open Access option (US$1250 / €900). JND is fully compliant with all mandates by major funders. Submit your manuscript online via MsTracker View detailed Instructions to Authors Aims and Scope | |