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Numerical Weather and Climate Prediction

Warner, Thomas Tomkins

1, 2011

Volltextzugriff (PDF)

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches

Lancet neurology, 2019-12, Vol.18 (12), p.1136-1146

2019

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Prognosis and Neuropathologic Correlation of Clinical Subtypes of Parkinson Disease

JAMA neurology, 2019-04, Vol.76 (4), p.470

2019

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Wilson's disease: update on pathogenesis, biomarkers and treatments

Journal of neurology, neurosurgery and psychiatry, 2021-10, Vol.92 (10), p.1053

2021

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Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms

Lancet neurology, 2008-12, Vol.7 (12), p.1127-1138

2008

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Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

Movement disorders, 2016-04, Vol.31 (4), p.436-457

2016

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Pathological Validation of the MDS Criteria for the Diagnosis of Multiple System Atrophy

Movement disorders, 2023-03, Vol.38 (3), p.444-452

2023

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A Histologic Study of the Circadian System in Parkinson Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy

JAMA neurology, 2018-08, Vol.75 (8), p.1008

2018

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Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology

Brain (London, England : 1878), 2016-12, Vol.139 (Pt 12), p.3237-3252

2016

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White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy

Acta neuropathologica, 2020-01, Vol.139 (1), p.135-156

2020

Volltextzugriff (PDF)

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

American journal of human genetics, 2013-04, Vol.92 (4), p.605-613

2013

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Plasma melatonin is reduced in Huntington's disease

Movement disorders, 2014-10, Vol.29 (12), p.1511-1515

2014

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Dystonia rating scales: Critique and recommendations

Movement disorders, 2013-06, Vol.28 (7), p.874-883

2013

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A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome

Nature genetics, 2015-07, Vol.47 (7), p.814-817

2015

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Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy

Brain (London, England : 1878), 2021-05, Vol.144 (4), p.1138-1151

2021

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Early presentation of urinary retention in multiple system atrophy: can the disease begin in the sacral spinal cord?

Journal of neurology, 2020-03, Vol.267 (3), p.659-664

2020

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A systematic evaluation of integration free reprogramming methods for deriving clinically relevant patient specific induced pluripotent stem (iPS) cells

PloS one, 2013-11, Vol.8 (11), p.e81622-e81622

2013

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The contribution of DNA methylation to the (dys)function of oligodendroglia in neurodegeneration

Acta neuropathologica communications, 2023-06, Vol.11 (1), p.106-106, Article 106

2023

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Young‐onset multiple system atrophy: Clinical and pathological features

Movement disorders, 2018-07, Vol.33 (7), p.1099-1107

2018

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A Metabolic Study of Huntington's Disease

PloS one, 2016-01, Vol.11 (1), p.e0146480-e0146480

2016

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Pathological substrate of memory impairment in multiple system atrophy

Neuropathology and applied neurobiology, 2022-12, Vol.48 (7), p.e12844-n/a

2022

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SGCE mutations cause psychiatric disorders: clinical and genetic characterization

Brain (London, England : 1878), 2013, Vol.136 (Pt 1), p.294-303

2013

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Association between diabetes and subsequent Parkinson disease: A record-linkage cohort study

Neurology, 2018-07, Vol.91 (2), p.e139

2018

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Genetic and environmental factors in the cause of Parkinson's disease

Annals of neurology, 2003, Vol.53 (S3), p.S16-S25

2003

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Systematic review and meta-analysis of salivary protein concentration in Parkinson's disease

Movement disorders, 2015-12, Vol.30 (14), p.1971-1972

2015

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Numerical Weather and Climate Prediction

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches

Prognosis and Neuropathologic Correlation of Clinical Subtypes of Parkinson Disease

Wilson's disease: update on pathogenesis, biomarkers and treatments

Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

Pathological Validation of the MDS Criteria for the Diagnosis of Multiple System Atrophy

A Histologic Study of the Circadian System in Parkinson Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy

Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology

White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Plasma melatonin is reduced in Huntington's disease

Dystonia rating scales: Critique and recommendations

A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome

Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy

Early presentation of urinary retention in multiple system atrophy: can the disease begin in the sacral spinal cord?

A systematic evaluation of integration free reprogramming methods for deriving clinically relevant patient specific induced pluripotent stem (iPS) cells

The contribution of DNA methylation to the (dys)function of oligodendroglia in neurodegeneration

Young‐onset multiple system atrophy: Clinical and pathological features

A Metabolic Study of Huntington's Disease

Pathological substrate of memory impairment in multiple system atrophy

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

Association between diabetes and subsequent Parkinson disease: A record-linkage cohort study

Genetic and environmental factors in the cause of Parkinson's disease

Systematic review and meta-analysis of salivary protein concentration in Parkinson's disease

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