Keyphrases
Neuroimaging
100%
Inborn Errors of Metabolism
100%
Adulthood
100%
Neuroimaging Findings
33%
Disease Progression
16%
Pediatric
16%
Gaucher Disease
16%
Phenylketonuria
16%
Treatment Response
16%
Urea Cycle Disorders
16%
Magnetic Resonance Imaging
16%
Adrenoleukodystrophy
16%
Therapeutic Potential
16%
Brain Iron
16%
Fabry
16%
Neurodegenerative Diseases
16%
Mitochondrial Disease
16%
Disease Treatment
16%
Huntington's Disease
16%
Leukodystrophy
16%
Cockayne Syndrome
16%
Lysosomal Storage Disease
16%
Metachromatic Leukodystrophy
16%
Delayed Diagnosis
16%
Photosystem II
16%
Patient Relatives
16%
Gene Defects
16%
Peroxisomal Disorders
16%
Disease Syndrome
16%
Wilson Disease
16%
Globoid Cell Leukodystrophy
16%
Lactic Acidosis
16%
PLP1
16%
Polymerase III
16%
Leigh Disease
16%
Fahr's Disease
16%
Leukoencephalopathy
16%
Vanishing White Matter Disease
16%
Calcinosis
16%
Kearns-Sayre Syndrome
16%
Krabbe
16%
Salla Disease
16%
4H Syndrome
16%
Subcortical Cysts
16%
Childhood Ataxia with Central Nervous System Hypomyelination
16%
Glutaric Aciduria
16%
Aciduria
16%
Transporter Molecules
16%
Organic Acidemia
16%
Megalencephalic Leukoencephalopathy with Subcortical Cysts
16%
Pelizaeus-Merzbacher Disease
16%
Methylmalonic Academia
16%
Fibrinoid
16%
L-2-hydroxyglutaric Aciduria
16%
Mitochondrial Encephalomyopathy
16%
Niemann-Pick Disease
16%
Maple Syrup Urine Disease
16%
Van Der Knaap Disease
16%
Imaging Sequences
16%
Myoclonus Epilepsy with Ragged-red Fibers (MERRF)
16%
Medicine and Dentistry
Disease
100%
Inborn Error of Metabolism
100%
Leukoencephalopathy
33%
Aciduria
33%
Diseases
33%
Magnetic Resonance Imaging
16%
Pediatrics
16%
Mucopolysaccharidosis
16%
Central Nervous System
16%
Iron
16%
Treatment Response
16%
Adrenoleukodystrophy
16%
Synapsin I
16%
Neurodegenerative Disorder
16%
Storage Disease
16%
Lysosomal Storage Disease
16%
Ataxia
16%
Phenylketonuria
16%
White Matter Disease
16%
Huntington's Disease
16%
Lactic Acidosis
16%
Calciphylaxis
16%
Proteolipid Protein
16%
Metachromatic Leukodystrophy
16%
Gaucher's Disease
16%
Globoid Cell Leukodystrophy
16%
Polymerase
16%
Wilson's Disease
16%
Cockayne Syndrome
16%
Kearns-Sayer Syndrome
16%
Fahr's Syndrome
16%
Leigh's Disease
16%
Organic Acidemia
16%
Leukodystrophy
16%
MERRF Syndrome
16%
Mitochondrial Encephalomyopathy
16%
Peroxisomal Disorder
16%
Pelizaeus Merzbacher Disease
16%
Salla Disease
16%
Disorders of Mitochondrial Functions
16%
Maple Syrup Urine Disease
16%
Methylmalonic aciduria
16%
Niemann-Pick Disease
16%
Urea Cycle Disorder
16%