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- SKELETAL MUSCLE CHANNELOPATHIES Mus7 (1)
- Facioscapulohumeral Muscular Dystrophy
- Approach to Myopathy Introduction
- Familial Hyperkalemic Periodic Paralysis Caused by a De Novo Mutation in the Sodium Channel Gene SCN4A
- A-Band 5, 59, 128 AAA Proteases 378 AC133+ Cells 32-33 ACADVL
- Update on Congenital Myopathies in Adulthood
- Periodic Paralysis: What Clinician Needs to Know?
- Investigation of Muscle Disease
- Neuromuscular Update I
- Familial Periodic Paralysis and Charcot-Marie-Tooth Disease in a 7-Generation Family
- Noninflammatory Myopathies As Genetic Diagnosis Increases, Noninflammatory Myopathies Are Being Seen More in Clinical Practice
- Blueprint Genetics Periodic Paralysis Panel
- Classification of Myopathy
- Evaluation and Treatment of Myopathies
- Muscle Channelopathies and Critical Points in Functional and Genetic Studies
- Acute Muscular Weakness in Children Fraqueza Muscular Aguda Em Crianças Ricardo Pablo Javier Erazo Torricelli1,2
- Treatment Updates for Neuromuscular Channelopathies Nantaporn Jitpimolmard, MD1,2 Emma Matthews, MRCP, Phd1,3 Doreen Fialho, FRCP, Phd1,*
- Familial Cramp Due to Potassium-Aggravated Myotonia
- Inherited Neuromuscular Disorders: Which Role Forserum Biomarkers?
- Electrodiagnostic Evaluation of Myopathies
- Muscle Ion Channel Diseases
- Myopathies Crossfires
- MYOPATHY Evaluation and Diagnosis- Kirsten Gruis, MD 2010
- Differential Diagnosis and Important Diagnostic Tests
- Periodic Paralysis with Generalized Epilepsy in a Nigerian Child: a Case Report
- AANEM Monograph
- Adult Onset Myopathies Lecture Series Case Reports Invited Reviews Workshop Handouts Edxsaes/Nmsaes Case Studies Educational CD/Dvds Podcasts Practice Guidelines
- Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy
- Neuromuscular Guide
- BIOGRAPHICAL SKETCH Provide the Following Information for the Senior/Key Personnel and Other Significant Contributors
- Potassium Dependent Rescue of a Myopathy with Core-Like Structures in Mouse M Gartz Hanson1, Jonathan J Wilde1,2, Rosa L Moreno3, Angela D Minic1, Lee Niswander1,2*
- Paroxysmal Neuromyotonia: a New Sporadic Channelopathy
- Electrodiagnosis of Myotonic Disorders
- A Clinical Approach to Muscle Diseases
- Familial Hypokalaemic Periodic Paralysis in Finland
- Hypothyroid Myopathy with Periodic Paralysis As the Main Symptom: a Case Report and Literature Review
- Myotonic Disorders
- Muscle Diseases.Pdf
- Milestones in Duchenne Muscular Dystrophy Research