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Publications by Henry Houlden
PUS3 Mutations Are Associated With Intellectual Disability, Leukoencephalopathy, and Nephropathy
Neurology: Genetics
Neurology
Genetics
An Update on the Genetics, Clinical Presentation, and Pathomechanisms of Human Riboflavin Transporter Deficiency
Journal of Inherited Metabolic Disease
Genetics
Cerebral Mitochondrial Electron Transport Chain Dysfunction in Multiple System Atrophy and Parkinson’s Disease
Scientific Reports
Multidisciplinary
Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients
PLoS ONE
Multidisciplinary
Response to the Commentary of Yates RL and DeLuca GC on the Study: HLA-DRB1*1501 Associations With Magnetic Resonance Imaging Measures of Grey Matter Pathology in Multiple Sclerosis
Multiple Sclerosis and Related Disorders
Medicine
Neurology
C9orf72 and Its Relevance in Parkinsonism and Movement Disorders: A Comprehensive Review of the Literature
Movement Disorders Clinical Practice
Neurology
Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases
Journal of Clinical Medicine
Loss of UGP2 in Brain Leads to a Severe Epileptic Encephalopathy, Emphasizing That Bi-Allelic Isoform Specific Start-Loss Mutations of Essential Genes Can Cause Genetic Diseases
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