CONTINUUM Lifelong Learning in Neurology




One-year access to more than 500 world journals available in the system
    http://medilib.ir
  • Duration of Time : 365 Day
  • Price : 300$
  • Special Price : 100$
Order

Table of Contents.

doi : 10.1212/CON.0000000000001255

Volume 28(6) pgs. 1564-1566 December 2022

Buy The Package and View The Article Online



Editorial Privilege, and the Continuum of Continuum.

LEWIS, STEVEN L. MD, FAAN

doi : 10.1212/CON.0000000000001280

Buy The Package and View The Article Online


A Symptoms and Signs Approach to the Patient With Neuromuscular Weakness.

Silvestri, Nicholas J. MD, FAAN

doi : 10.1212/CON.0000000000001150

Muscle weakness is a common feature of many neuromuscular disorders. This article outlines a symptoms and signs approach to the patient presenting with neuromuscular weakness, highlighting key aspects of the clinical history and examination.

Buy The Package and View The Article Online


Lambert-Eaton Myasthenic Syndrome and Botulism.

Raja, Shruti M. MD

doi : 10.1212/CON.0000000000001205

This article reviews the pathophysiology, epidemiology, clinical features, diagnosis, and treatment of Lambert-Eaton myasthenic syndrome (LEMS) and botulism, presynaptic disorders of neuromuscular transmission in which rapid diagnosis improves long-term outcomes.

Buy The Package and View The Article Online


Diagnosis and Management of Myasthenia Gravis.

Hehir, Michael K. II MD; Li, Yuebing MD, PhD, FAAN

doi : 10.1212/CON.0000000000001161

This article reviews updated diagnostic procedures and currently available treatment modalities for myasthenia gravis (MG).

Buy The Package and View The Article Online


Inflammatory Myopathies.

Manousakis, Georgios MD, FAAN

doi : 10.1212/CON.0000000000001179

This article outlines the salient clinical, serologic, electrophysiologic, imaging, and histopathologic findings and treatment options for the idiopathic inflammatory myopathies, including those related to immune checkpoint inhibitors and SARS-CoV-2.

Buy The Package and View The Article Online


Inclusion Body Myositis.

Goyal, Namita A. MD, FAAN

doi : 10.1212/CON.0000000000001204

This article highlights the clinical and diagnostic features of inclusion body myositis (IBM) and provides recent insights into the pathomechanisms and therapeutic strategies of the disease.

Buy The Package and View The Article Online


The Dystrophinopathies.

Lee, Bo Hoon MD

doi : 10.1212/CON.0000000000001208

This article reviews the history, epidemiology, genetics, clinical presentation, multidisciplinary management, and established and emerging therapies for the dystrophinopathies.

Buy The Package and View The Article Online


The Limb-Girdle Muscular Dystrophies.

Johnson, Nicholas E. MD, FAAN; Statland, Jeffrey M. MD

doi : 10.1212/CON.0000000000001178

The limb-girdle muscular dystrophies (LGMDs) are a group of inherited muscle disorders with a common feature of limb-girdle pattern of weakness, caused by over 29 individual genes.

Buy The Package and View The Article Online


Myotonic Dystrophy.

Hamel, Johanna I. MD

doi : 10.1212/CON.0000000000001184

Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are genetic disorders affecting skeletal and smooth muscle, heart, brain, eyes, and other organs.

Buy The Package and View The Article Online


Facioscapulohumeral Muscular Dystrophy.

Mul, Karlien MD, PhD

doi : 10.1212/CON.0000000000001155

This article reviews the current knowledge on the clinical characteristics and disease mechanism of facioscapulohumeral muscular dystrophy (FSHD), as well as advances in targeted therapy development.

Buy The Package and View The Article Online


Metabolic Myopathies.

Tarnopolsky, Mark A. MD, PhD, FRCP

doi : 10.1212/CON.0000000000001182

Metabolic myopathies are disorders that affect skeletal muscle substrate oxidation. Although some drugs and hormones can affect metabolism in skeletal muscle, this review will focus on the genetic metabolic myopathies.

Buy The Package and View The Article Online


Muscle Channelopathies.

Trivedi, Jaya R. MD, FAAN

doi : 10.1212/CON.0000000000001183

This article describes the clinical features, diagnosis, pathophysiology, and management of nondystrophic myotonia and periodic paralysis.

Buy The Package and View The Article Online


Genetic-Based Treatment Strategies for Muscular Dystrophy and Congenital Myopathies.

Findlay, Andrew R. MD; Weihl, Conrad C. MD, PhD

doi : 10.1212/CON.0000000000001203

This article discusses the foundational concepts of genetic treatment strategies employed in neuromuscular medicine, as well as the importance of genetic testing as a requirement for applying gene-based therapy.

Buy The Package and View The Article Online


The Practice of Experimental Neurotherapeutics in Neuromuscular Disease.

Reoma, Lauren B. MD, FAAN; Nath, Avindra MD, MBBS, FAAN; Griggs, Robert C. MD, FAAN

doi : 10.1212/CON.0000000000001240

The discipline of experimental neurotherapeutics targets the process and operation of translating scientific discoveries into new treatments for neurologic diseases and has been instrumental in the progression of many areas of neurology.

Buy The Package and View The Article Online



Postreading Self-Assessment and CME Test.

Owens, James W. M. Jr MD, PhD; Zazulia, Allyson R. MD

doi : 10.1212/CON.0000000000001252

Buy The Package and View The Article Online


Postreading Self-Assessment and CME Test-Preferred Responses.

Owens, James W. M. Jr MD, PhD; Zazulia, Allyson R. MD

doi : 10.1212/CON.0000000000001253

Buy The Package and View The Article Online



Learning Objectives and Core Competencies.

doi : 10.1212/CON.0000000000001256

Buy The Package and View The Article Online





Do you want to add Medilib to your home screen?