Cortico-motor neurone conduction in dopa responsive dystonia

Right gastroepiploic-to-coronary artery bypass. The first decade of use.

Circulation·1995

Western blot mapping of disease-specific amyloid in various animal species and humans with transmissible spongiform encephalopathies using a high-yield purification method.

The Journal of general virology·1995

Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum.

Brain : a journal of neurology·1995

First experimental transmission of fatal familial insomnia.

Nature·1995

Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy.

Annals of neurology·1995

Clinical and genetic studies of fatal familial insomnia.

Neurology·1995

Joint Risk Factor Combinations with Additive Interaction Increase the Risk of Parkinson's Disease.

Movement disorders : official journal of the Movement Disorder Society·2026

COVID-19 Amplifies Sex-Specific Dopamine and Glial Responses in a Parkinson's Disease Mouse Model.

Movement disorders : official journal of the Movement Disorder Society·2026

Early Longitudinal Brain Network Changes in Huntington's Disease Before Clinical Motor Onset.

Movement disorders : official journal of the Movement Disorder Society·2026

Expanded ATXN3 CAG Repeat is Stable in Human Purkinje Cells.

Movement disorders : official journal of the Movement Disorder Society·2026

Cannabis-Based Oil for Pain and Other Non-Motor Symptoms in Parkinson's Disease: A Randomized Controlled Trial.

Movement disorders : official journal of the Movement Disorder Society·2026

Rare Heterozygous Loss-of-Function Variants in MCOLN1 Identified in Two Sporadic Patients with α-Synucleinopathies.

Movement disorders : official journal of the Movement Disorder Society·2026

RFC1 Repeat Expansions in Chronic Idiopathic Axonal Polyneuropathy: Prevalence, Phenotype, and Diagnostic Implications.

Journal of the peripheral nervous system : JPNS·2026

Network Analysis in Central Disorders of Hypersomnolence: Insight Into Relationships Between Symptoms, Mental Health, and Quality of Life.

Journal of sleep research·2026

Association between sarcopenia and inflammation in non-geriatric patients with chronic kidney disease: a comparison of hemodialysis and non-hemodialysis patients.

Journal of nephrology·2026

Transmission ratio distortion of NF1 mutant alleles in familial Neurofibromatosis type 1.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Disease-Specific Glycopattern Signatures of Serum Small Extracellular Vesicles in Depression, Schizophrenia, and Glioblastoma.

Proteomics·2026

Blended Hereditary Neuropathy Phenotype Caused by Biallelic PRX and SCN9A Variants: A Case Report.

Molecular syndromology·2026

Related Experiment Videos

Cortico-motor neurone conduction in dopa responsive dystonia

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Right gastroepiploic-to-coronary artery bypass. The first decade of use.

Western blot mapping of disease-specific amyloid in various animal species and humans with transmissible spongiform encephalopathies using a high-yield purification method.

Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum.

First experimental transmission of fatal familial insomnia.

Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy.

Clinical and genetic studies of fatal familial insomnia.

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COVID-19 Amplifies Sex-Specific Dopamine and Glial Responses in a Parkinson's Disease Mouse Model.

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RFC1 Repeat Expansions in Chronic Idiopathic Axonal Polyneuropathy: Prevalence, Phenotype, and Diagnostic Implications.

Network Analysis in Central Disorders of Hypersomnolence: Insight Into Relationships Between Symptoms, Mental Health, and Quality of Life.

Association between sarcopenia and inflammation in non-geriatric patients with chronic kidney disease: a comparison of hemodialysis and non-hemodialysis patients.

Transmission ratio distortion of NF1 mutant alleles in familial Neurofibromatosis type 1.

Disease-Specific Glycopattern Signatures of Serum Small Extracellular Vesicles in Depression, Schizophrenia, and Glioblastoma.

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Cortico-motor neurone conduction in dopa responsive dystonia

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