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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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Compulsive sexual behaviour in Parkinson’s disease is associated with higher doses of levodopa

Journal of neurology, neurosurgery and psychiatry, 2018-10, Vol.89 (10), p.1121-1123

2018

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Diurnal patterns of rainfall in northwestern South America. Part III: Diurnal gravity waves and nocturnal convection offshore

Monthly weather review, 2003-05, Vol.131 (5), p.830-844

2003

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Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

Nature genetics, 2004-03, Vol.36 (3), p.271-276

2004

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Using initial condition and model physics perturbations in short-range ensemble simulations of mesoscale convective systems

Monthly weather review, 2000-07, Vol.128 (7), p.2077-2107

2000

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The Outcome of Dopamine Dysregulation Syndrome in Parkinson's Disease: A Retrospective Postmortem Study

Movement disorders clinical practice (Hoboken, N.J.), 2018-09, Vol.5 (5), p.519-522

2018

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Diurnal patterns of rainfall in northwestern South America. Part I: Observations and context

Monthly weather review, 2003-05, Vol.131 (5), p.799-812

2003

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A novel RAB7 mutation associated with ulcero-mutilating neuropathy

Annals of neurology, 2004-10, Vol.56 (4), p.586-590

2004

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High-dose creatine therapy for Huntington disease: a 2-year clinical and MRS study

Neurology, 2005-05, Vol.64 (9), p.1655-1656

2005

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Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy

Annals of neurology, 2000-07, Vol.48 (1), p.72-76

2000

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D04 A Study Of The Hypothalamo-pituitary Axes In Huntington’s Disease

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A32-A33

2014

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Impact of cervical dystonia on quality of life

Movement disorders, 2002-07, Vol.17 (4), p.838-841

2002

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Diurnal patterns of rainfall in northwestern South America. Part II: Model simulations

Monthly weather review, 2003-05, Vol.131 (5), p.813-829

2003

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Expression of mutant α-synuclein causes increased susceptibility to dopamine toxicity

Human molecular genetics, 2000-11, Vol.9 (18), p.2683-2689

2000

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Human spastin has multiple microtubule‐related functions

Journal of neurochemistry, 2005-12, Vol.95 (5), p.1411-1420

2005

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Creatine therapy for Huntington's disease: clinical and MRS findings in a 1-year pilot study

Neurology, 2003-07, Vol.61 (1), p.141-142

2003

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Predictability of low-level winds by Mesoscale meteorological models

Monthly weather review, 2004-11, Vol.132 (11), p.2553-2569

2004

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A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

Brain (London, England : 1878), 2004-05, Vol.127 (5), p.973-980

2004

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ARE PSYCHIATRIC SYMPTOMS A CORE PHENOTYPE OF MYOCLONUS DYSTONIA SYNDROME CAUSED BY SGCE MUTATIONS?

Journal of neurology, neurosurgery and psychiatry, 2013-09, Vol.84 (9), p.e1-e1

2013

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A Tutorial on Lateral Boundary Conditions as a Basic and Potentially Serious Limitation to Regional Numerical Weather Prediction

Bulletin of the American Meteorological Society, 1997-11, Vol.78 (11), p.2599-2617

1997

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Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cells

Movement disorders, 2005-04, Vol.20 (4), p.432-440

2005

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The Silver Syndrome Variant of Hereditary Spastic Paraplegia Maps to Chromosome 11q12-q14, with Evidence for Genetic Heterogeneity within This Subtype

American journal of human genetics, 2001-07, Vol.69 (1), p.209-215

2001

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Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

Clinical genetics, 2009-05, Vol.75 (5), p.485-489

2009

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A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14

Journal of medical genetics, 2005-01, Vol.42 (1), p.80-82

2005

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MIR-NATs repress MAPT translation and aid proteostasis in neurodegeneration

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

Compulsive sexual behaviour in Parkinson’s disease is associated with higher doses of levodopa

Diurnal patterns of rainfall in northwestern South America. Part III: Diurnal gravity waves and nocturnal convection offshore

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

Using initial condition and model physics perturbations in short-range ensemble simulations of mesoscale convective systems

The Outcome of Dopamine Dysregulation Syndrome in Parkinson's Disease: A Retrospective Postmortem Study

Diurnal patterns of rainfall in northwestern South America. Part I: Observations and context

A novel RAB7 mutation associated with ulcero-mutilating neuropathy

High-dose creatine therapy for Huntington disease: a 2-year clinical and MRS study

Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy

D04 A Study Of The Hypothalamo-pituitary Axes In Huntington’s Disease

Impact of cervical dystonia on quality of life

Diurnal patterns of rainfall in northwestern South America. Part II: Model simulations

Expression of mutant α-synuclein causes increased susceptibility to dopamine toxicity

Human spastin has multiple microtubule‐related functions

Creatine therapy for Huntington's disease: clinical and MRS findings in a 1-year pilot study

Predictability of low-level winds by Mesoscale meteorological models

A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

ARE PSYCHIATRIC SYMPTOMS A CORE PHENOTYPE OF MYOCLONUS DYSTONIA SYNDROME CAUSED BY SGCE MUTATIONS?

A Tutorial on Lateral Boundary Conditions as a Basic and Potentially Serious Limitation to Regional Numerical Weather Prediction

Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cells

The Silver Syndrome Variant of Hereditary Spastic Paraplegia Maps to Chromosome 11q12-q14, with Evidence for Genetic Heterogeneity within This Subtype

Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14

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