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