Keyphrases
Cyprus
100%
Electron Microscopy
77%
Mitochondrial Encephalomyopathy
71%
Cervical Vestibular-evoked Myogenic Potential (cVEMP)
71%
Multiple Sclerosis
70%
Muscle Biopsy
54%
Age of Onset
52%
Myopathy
51%
Myasthenia Gravis
50%
Clinical Characteristics
50%
Amyotrophic Lateral Sclerosis
50%
Motor Neuron Disease
50%
Autosomal Recessive
48%
Charcot-Marie-Tooth Disease
47%
Neuropathy
41%
Phenotypic Spectrum
40%
Epidemiological Characteristics
40%
Transgenic Mouse Model
40%
Myalgia
40%
Cypriot
39%
Dystrophin
38%
Transthyretin
37%
Vestibular System
34%
V30M
33%
Amyloid Deposition
33%
Disease Severity
32%
Plasma Exchange
30%
Spinal muscular Atrophy
30%
Duchenne muscular Dystrophy
30%
Clinical Phenotype
27%
Cerebellum
27%
Autosomal Dominant
26%
Cypriot Population
26%
Amyloid Fibrils
25%
Musk
25%
Muscle Disease
24%
Neuromuscular Disease
24%
Transthyretin Amyloidosis
23%
Morphological Method
23%
Muscular Dystrophy
22%
Neuropathology
22%
Autoantibodies
21%
Cell-based Assay
21%
Clinical Significance
21%
Upper Limb
21%
Sarcolemma
20%
Mechanical Injury
20%
Laminin-1
20%
Muscle Pathology
20%
Familial Amyloid Polyneuropathy
20%
Medicine and Dentistry
Disease
90%
Autosomal Recessive Inheritance
45%
Multifocal Motor Neuropathy
45%
Muscle Biopsy
43%
DeJerine-Sottas Disease
42%
Amyloid Protein
33%
Myopathy
30%
Transthyretin
30%
Mitochondrial Encephalomyopathy
30%
Plasma Exchange
30%
Electron Microscopy
28%
Upper Limb
27%
Spinal Muscular Atrophy
27%
Onset Age
26%
Genetic Screening
25%
Clinical Significance
22%
Neuropathy
22%
Weakness
22%
Duchenne Muscular Dystrophy
20%
Familial Amyloid Neuropathy
20%
Cerebellum
20%
Amyloid Neuropathy
20%
Complement Component C1q
20%
Transgenic Mouse
20%
Respiratory Failure
20%
Refsum Disease
20%
Hypoventilation
20%
Nerve Block
20%
Glycine Transfer RNA Ligase
20%
Phytanic Acid
20%
Angelman Syndrome
20%
Temporal Lobe
20%
Chromosome 7p
20%
Parkinson's Disease
20%
Genetic Trait
20%
Variant Creutzfeldt-Jakob Disease
20%
Sporadic Creutzfeldt Jakob Disease
20%
Creutzfeldt-Jakob Disease
20%
Epidemiological Surveillance
20%
Contracture
20%
Vestibular Evoked Potential
20%
ATTR Amyloidosis
20%
Amyotrophic Lateral Sclerosis
20%
Neurologic Disease
20%
Frontal Lobe
20%
Bioluminescence
20%
Autosomal Dominant Inheritance
19%
Dystrophin
19%
Creatine Kinase
18%
Diagnosis
18%
