Keyphrases
Spinal muscular Atrophy
100%
Onasemnogene Abeparvovec
62%
Israel
53%
Neurofibromatosis Type 1 (NF-1)
46%
Neurofibromatosis Type I
42%
Pediatric
42%
Immune-mediated Polyneuropathies
28%
COVID-19
28%
Congenital Myasthenic Syndrome
28%
Charcot-Marie-Tooth Disease
28%
Duchenne muscular Dystrophy
28%
Nusinersen
22%
Brain Magnetic Resonance Imaging
21%
Medical Center
20%
Consanguineous Family
17%
Clinical Presentation
17%
Imaging Findings
17%
Gene Replacement Therapy
17%
Homozygous Missense mutation
16%
Gene Copy number
16%
Motor Function
16%
Survival Motor Neuron
15%
Real-world Outcomes
14%
Receptor Assembly
14%
Genetic Characterization
14%
Impact Factor
14%
Museum
14%
Clinical Characterization
14%
Duchenne
14%
Becker muscular Dystrophy
14%
Acute Transverse Myelitis
14%
Citation Impact
14%
Self-citation Rate
14%
Rate Factor
14%
Gene Therapy
14%
Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
14%
Mitochondrial DNA mutation
14%
Phenotypic Heterogeneity
14%
Impressionists
14%
Atypical Presentation
14%
Population-based Carrier Screening
14%
Cerebellar Hypoplasia
14%
SCN1A mutation
14%
Adeno-associated Virus Serotype 9
14%
Hyperactivity Disorder
14%
Lactic Acidosis
14%
Electroencephalogram
14%
Corpus Callosum
14%
Graphology
14%
Guillain-Barré Syndrome
14%
Medicine and Dentistry
Spinal Muscular Atrophy
78%
Diseases
54%
Onasemnogene Abeparvovec
48%
Neurofibromatosis Type I
46%
Magnetic Resonance Imaging
28%
COVID-19
28%
Duchenne Muscular Dystrophy
28%
Pediatrics
28%
Nusinersen
22%
Motor Performance
19%
Cerebrospinal Fluid
17%
Gene Replacement Therapy
17%
Polyneuropathy
16%
Cutis Laxa
14%
Glycine Receptor
14%
Artery Disease
14%
Transverse Myelitis
14%
Corpus Callosum
14%
Patient Referral
14%
Autoinflammatory Disease
14%
Attention Deficit Disorder
14%
Polyradiculoneuropathy
14%
Ganglioglioma
14%
Apoplexy
14%
Strengths and Difficulties Questionnaire
14%
Language Delay
14%
Small Fiber Neuropathy
14%
Sputum Culture
14%
Kugelberg Welander Disease
14%
Lactic Acidosis
14%
Gene Therapy
14%
Congenital Myasthenic Syndrome
14%
Becker Muscular Dystrophy
14%
Social Interaction
14%
Cerebral Sinus Thrombosis
14%
Mitochondrial Encephalopathy
14%
microRNA
14%
Lung Function Test
14%
Mitochondrial DNA
14%
Brain Imaging
14%
Nimodipine
14%
Lafora Disease
14%
Giant Axonal Neuropathy
14%
Microgyria
14%
Autosomal Recessive Inheritance
14%
Hyperekplexia
14%
DeJerine-Sottas Disease
14%
Pneumonia
14%
Cohort Analysis
14%
Penicillin
14%