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Diseases of Muscle
Georgios Manousakis
,
Peter B Kang
Neurology
Research output
:
Chapter in Book/Report/Conference proceeding
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Chapter
Overview
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Keyphrases
Myopathy
100%
Accurate Diagnosis
40%
Molecular Biology
20%
Duchenne muscular Dystrophy
20%
Muscular Dystrophy
20%
Enzyme Replacement Therapy
20%
Treatment Options
20%
Pompe Disease
20%
Dystrophy
20%
Family History
20%
AAV Gene Therapy
20%
Specific Treatment
20%
Disease Modeling
20%
Inherited Disorders
20%
Genetic Testing
20%
Endocrinopathy
20%
Differential Diagnosis
20%
Muscle Biopsy
20%
Muscle Enzymes
20%
Enzyme Level
20%
Acuity
20%
Antisense Oligonucleotides
20%
Congenital Myopathy
20%
Diagnostic Approach
20%
Clinical Diagnostics
20%
Imaging Genetics
20%
Medication Exposure
20%
Mitochondrial Myopathy
20%
Channelopathy
20%
Systemic Conditions
20%
Metabolic Myopathy
20%
Proximal Weakness
20%
Limb-girdle
20%
Inherited Myopathies
20%
Evolution Family
20%
Toxic Myopathy
20%
Toxic Exposure
20%
FDA Approval
20%
Acquired Disorders
20%
Biology Modeling
20%
Inflammatory Myopathy
20%
Acquired Myopathies
20%
Molecular Disease
20%
Medicine and Dentistry
Myopathy
100%
Diseases
100%
Weakness
42%
Gene Therapy
14%
Duchenne Muscular Dystrophy
14%
Adeno-Associated Virus
14%
Limb
14%
Muscular Dystrophy
14%
Hope
14%
Chronicity
14%
Dystrophy
14%
Family History
14%
Genetic Screening
14%
Differential Diagnosis
14%
Muscle Biopsy
14%
Antisense Oligonucleotide
14%
Electromyography
14%
Enzyme Replacement Therapy
14%
Muscle Enzyme
14%
Mitochondrial Myopathy
14%
Acquired Disorder
14%
Channelopathy
14%
Glycogen Storage Disease Type II
14%
Endocrine Disease
14%
Toxic Myopathy
14%
Treatment Option
14%
Genetics
14%
Neuroscience
Muscle Disorder
100%
Muscular Dystrophy
22%
Genetics
22%
Electromyography
11%
Differential Diagnosis
11%
Enzyme Replacement Therapy
11%
Endocrine Disease
11%
Disease Modeling
11%
Antisense Oligonucleotide
11%
Muscle Enzyme
11%
Adeno-Associated Virus
11%
Channelopathy
11%