اختلالات عصبی-عضلانی نوزادی، کودکی و نوجوانی: رویکردی از دید پزشک

Neuromuscular disorders are diagnosed across the lifespan and create many challenges especially with infants, children and adolescents. This new edition of the definitive reference, edited by the established world renowned authorities on the science, diagnosis and treatment of neuromuscular disorders in childhood is a timely and needed resource for all clinicians and researchers studying neuromuscular disorders, especially in childhood. The Second Edition is completely revised to remain current with advances in the field and to insure this remains the standard reference for clinical neurologists and clinical research neurologists. The Second Edition retains comprehensive coverage while shortening the total chapter count to be an even more manageable and effective reference. * Carefully revised new edition of the classic reference on neuromuscular disorders in infancy, childhood and adolescence. * Definitive coverage of the basic science of neuromuscular disease and the latest diagnosis and treatment best practices. * Includes coverage of clinical phenomenology, electrophysiology, histopathology, molecular genetics and protein chemistry Content: Front-matter, Pages i,iii Copyright, Page iv Dedication, Pages v-vi Foreword, Pages xxiii-xxiv, Joseph J. Volpe Preface to the Second Edition, Pages xxv-xxvi, Basil T. Darras, Monique M. Ryan, Darryl C. De Vivo Preface to the First Edition, Pages xxvii-xxviii, H. Royden Jones Jr., Darryl C. De Vivo, Basil T. Darras List of Contributors, Pages xxix-xxxii, Hasan O. Akman, Felicia B. Axelrod, Jonathan Baets, Alan H. Beggs, Carsten G. Bönnemann, Kathryn M. Brennan, Robert H. Brown Jr., Kate Bushby, Stirling Carpenter, Wendy Chung, Emma Ciafaloni, Pedro D.S.C. Ciarlini, Thomas O. Crawford, Basil T. Darras, William S. David, Umberto De Girolami, Darryl C. De Vivo, Feza Deymeer, Salvatore DiMauro, James J. Dowling, Hacer Durmus, et al. Chapter 1 - Introduction: Historical Perspectives, Pages 3-16, Darryl C. De Vivo, Basil T. Darras, Monique M. Ryan, H. Royden Jones Jr. Chapter 2 - Genetics of Neuromuscular Disorders, Pages 17-31, Wendy Chung Chapter 3 - Electromyography in Pediatrics, Pages 32-45, Matthew Pitt, Peter B. Kang Chapter 4 - Muscle Biopsy for Diagnosis of Neuromuscular and Metabolic Diseases, Pages 46-65, Harvey B. Sarnat, Stirling Carpenter Chapter 5 - Nerve Biopsy, Pages 66-81, Jo M. Wilmshurst, Pedro D.S.C. Ciarlini, Umberto De Girolami Chapter 6 - Neonatal Hypotonia, Pages 85-95, Joseph J. Volpe Chapter 7 - Arthrogryposis, Pages 96-114, Judith G. Hall, Angela Vincent Chapter 8 - Spinal Muscular Atrophies, Pages 117-145, Basil T. Darras, Jennifer A. Markowitz, Umrao R. Monani, Darryl C. De Vivo Chapter 9 - Juvenile Amyotrophic Lateral Sclerosis, Pages 146-159, Jemeen Sreedharan, Robert H. Brown Jr. Chapter 10 - Infectious or Acquired Motor Neuron Diseases, Pages 160-187, Manikum Moodley, William S. David, Alan R. Seay Chapter 11 - The Stiff-man Syndrome in Children and Adolescents, Pages 188-196, Jennifer A. Tracy, Andrew McKeon Chapter 12 - Radiculopathies and Plexopathies, Pages 199-224, H. Royden Jones Jr., Monique M. Ryan, Kerry H. Levin Chapter 13 - Congenital and Acquired Facial Palsies, Pages 225-242, Francis Renault, Susana Quijano-Roy Chapter 14 - Mononeuropathies, Pages 243-273, Monique M. Ryan, H. Royden Jones Jr. Chapter 15 - Overview of Pediatric Peripheral Neuropathies, Pages 274-288, Hugh J. McMillan, Monique M. Ryan Chapter 16 - Congenital and Early Infantile Neuropathies, Pages 289-318, Eppie M. Yiu, Jonathan Baets Chapter 17 - Hereditary Neuropathies in Late Childhood and Adolescence, Pages 319-339, Kathryn M. Brennan, Michael E. Shy Chapter 18 - Hereditary Sensory and Autonomic Neuropathies, Pages 340-352, Felicia B. Axelrod, Horacio Kaufmann Chapter 19 - Peripheral Neuropathy in Inherited Metabolic Disease, Pages 353-378, Marc C. Patterson, Alan K. Percy Chapter 20 - Acute Polyneuropathies, Pages 379-397, H. Royden Jones Jr., Padraic J. Grattan-Smith, Monique M. Ryan Chapter 21 - Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Pages 398-417, Hugh J. McMillan, Peter B. Kang Chapter 22 - Neuropathies Secondary to Systemic Disorders, Pages 418-430, Jo M. Wilmshurst, Robert A. Ouvrier Chapter 23 - Toxic Neuropathies, Pages 431-437, David Pleasure Chapter 24 - Hansen’s Disease (Leprosy): Leprous Neuropathy, Pages 438-441, Wilson Marques Jr. Chapter 25 - Acquired Presynaptic Neuromuscular Junction Disorders: Infant Botulism and Lambert-Eaton Myasthenic Syndrome, Pages 445-455, Ai Sakonju, Thomas O. Crawford Chapter 26 - Congenital Myasthenic Syndromes, Pages 456-481, Andrew G. Engel Chapter 27 - Juvenile and Neonatal Myasthenia Gravis, Pages 482-496, Peter B. Kang, Wendy K.M. Liew, Maryam Oskoui, Angela Vincent Chapter 28 - Congenital and Other Structural Myopathies, Pages 499-537, James J. Dowling, Kathryn N. North, Hans H. Goebel, Alan H. Beggs Chapter 29 - Congenital Muscular Dystrophies, Pages 538-550, Eugenio Mercuri, Francesco Muntoni Chapter 30 - Dystrophinopathies, Pages 551-592, Basil T. Darras, Caroline C. Menache-Starobinski, Veronica Hinton, Louis M. Kunkel Chapter 31 - Clinical Management of Dystrophinopathies: A Systematic Approach, Pages 593-619, Michela Guglieri, Katharine Bushby Chapter 32 - Facioscapulohumeral Dystrophy, Pages 620-630, Wendy K.M. Liew, Silvère M. van der Maarel, Rabi Tawil Chapter 33 - Distal Myopathies, Pages 631-634, Bjarne Udd Chapter 34 - Limb-girdle Muscular Dystrophies, Pages 635-666, Payam Mohassel, Carsten G. Bönnemann Chapter 35 - Emery-Dreifuss Muscular Dystrophy: Nuclear Envelopathies, Pages 667-678, Hacer Durmus, Piraye Serdaroglu-Oflazer, Feza Deymeer Chapter 36 - Myopathies of Systemic Disease, Pages 679-696, Thornton B.A. Mason, Darryl C. De Vivo Chapter 37 - Myotonic Dystrophy, Pages 697-718, Richard T. Moxley, Emma Ciafaloni, Debra Guntrum Chapter 38 - Muscle Channelopathies: Myotonias and Periodic Paralyses, Pages 719-734, Karin Jurkat-Rott, Reinhardt Rüdel, Frank Lehmann-Horn Chapter 39 - Glycogen Storage Diseases of Muscle, Pages 735-760, Hasan O. Akman, Anders Oldfors, Salvatore DiMauro Chapter 40 - Lipid Storage Myopathies Due to Fatty Acid Oxidation Defects, Pages 761-795, Ingrid Tein Chapter 41 - Mitochondrial Encephalomyopathies, Pages 796-833, Darryl C. De Vivo, Carmen Paradas, Salvatore DiMauro Chapter 42 - Juvenile Dermatomyositis and Other Inflammatory Myopathies in Children, Pages 834-881, Lauren M. Pachman Chapter 43 - Neuromuscular Problems of the Critically Ill Neonate and Child, Pages 885-903, Basil T. Darras, H. Royden Jones Jr. Chapter 44 - Intensive Care Management, Including Cardiorespiratory Care, Pages 904-912, William A. Scott, Susan T. Iannaccone Chapter 45 - Malignant Hyperthermia: An Inherited Disorder of Muscle Calcium Metabolism, Pages 913-921, Werner Klingler, Frank Lehmann-Horn Chapter 46 - Disorders of the Ocular Motor Cranial Nerves and Extraocular Muscles, Pages 922-957, Monique M. Ryan, Elizabeth C. Engle Chapter 47 - Oromotor Dysfunction in Neuromuscular Disorders: Evaluation and Treatment, Pages 958-975, Manuel Roig-Quilis Chapter 48 - Complex Regional Pain Syndromes I and II (Reflex Sympathetic Dystrophy, Causalgia), Pages 976-983, Navil F. Sethna, Deirdre Logan Chapter 49 - Friedreich Ataxia, Pages 984-1002, Massimo Pandolfo Chapter 50 - Dominantly Inherited Spinocerebellar Syndromes, Pages 1003-1032, Stephen M. Maricich, Huda Y. Zoghbi Chapter 51 - Principles and Practice of Molecular Therapies, Pages 1035-1052, Louise R. Rodino-Klapac, Jerry R. Mendell Chapter 52 - Orthopedic Management, Pages 1053-1071, David P. Roye, Evan D. Sheha, Nanfang Xu Chapter 53 - Rehabilitation of the Child with a Neuromuscular Disorder, Pages 1072-1077, Nancy E. Strauss, Jacqueline Montes, Barry S. Russman Chapter 54 - Outcome Measures in Neuromuscular Diseases, Pages 1078-1089, Jacqueline Montes, Petra Kaufmann Index, Pages 1091-1123

Neuromuscular disorders are diagnosed across the lifespan and create many challenges especially with infants, children and adolescents. This new edition of the definitive reference, edited by the established world renowned authorities on the science, diagnosis and treatment of neuromuscular disorders in childhood is a timely and needed resource for all clinicians and researchers studying neuromuscular disorders, especially in childhood. The Second Edition is completely revised to remain current with advances in the field and to insure this remains the standard reference for clinical neurologists and clinical research neurologists. The Second Edition retains comprehensive coverage while shortening the total chapter count to be an even more manageable and effective reference.

• Carefully revised new edition of the classic reference on neuromuscular disorders in infancy, childhood and adolescence.
• Definitive coverage of the basic science of neuromuscular disease and the latest diagnosis and treatment best practices.
• Includes coverage of clinical phenomenology, electrophysiology, histopathology, molecular genetics and protein chemistry
  

Neuromuscular disorders are diagnosed across the lifespan and create many challenges especially with infants, children and adolescents. This new edition of the definitive reference, edited by the established world renowned authorities on the science, diagnosis and treatment of neuromuscular disorders in childhood is a timely and needed resource for all clinicians and researchers studying neuromuscular disorders, especially in childhood. TheSecond Edition is completely revised to remain current with advances in the field and to insure this remains the standard reference for clinical neurologists and clinical research neurologists. TheSecond Edition retains comprehensive coverage while shortening the total chapter count to be an even more manageable and effective reference. Carefully revised new edition of the classic reference on neuromuscular disorders in infancy, childhood and adolescence.Definitive coverage of the basic science of neuromuscular disease and the latest diagnosis and treatment best practices.Includes coverage of clinical phenomenology, electrophysiology, histopathology, molecular genetics and protein chemistry " "Neuromuscular disorders are diagnosed across the lifespan and create many challenges especially with infants, children and adolescents. This new edition of the definitive reference, edited by the established world renowned authorities on the science, diagnosis and treatment of neuromuscular disorders in childhood is a timely and needed resource for all clinicians and researchers studying neuromuscular disorders, especially in childhood. The Second Edition is completely revised to remain current with advances in the field and to insure this remains the standard reference for clinical neurologists and clinical research neurologists. The Second Edition retains comprehensive coverage while shortening the total chapter count to be an even more manageable and effective reference."--Publisher's website Neuromuscular disorders are diagnosed across the lifespan and create many challenges especially with infants, children and adolescents. This edition focuses on neuromuscular disorders in infancy, childhood and adolescence. It offers coverage of the basic science of neuromuscular disease and the diagnosis and treatment best practices.