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The effect of onset age on the clinical features of Parkinson's disease

European journal of neurology, 2009-04, Vol.16 (4), p.450-456

2009

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Differentiation of atypical parkinsonian syndromes with routine MRI

Neurology, 2000-02, Vol.54 (3), p.697-697

2000

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The prevalence of progressive supranuclear palsy (Steele–Richardson–Olszewski syndrome) in the UK

Brain (London, England : 1878), 2001-07, Vol.124 (7), p.1438-1449

2001

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Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins

Neurology, 2010-07, Vol.75 (4), p.367-372

2010

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SGCZ mutations are unlikely to be associated with myoclonus dystonia

Neuroscience, 2014-07, Vol.272, p.88-91

2014

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Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP

Neurology, 2003-07, Vol.61 (1), p.102-104

2003

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Dentatorubral pallidoluysian atrophy in South Wales

Journal of neurology, neurosurgery and psychiatry, 2008-07, Vol.79 (7), p.804-807

2008

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Identification of candidate cerebrospinal fluid biomarkers in parkinsonism using quantitative proteomics

Parkinsonism & related disorders, 2017-04, Vol.37, p.65-71

2017

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Case control analysis of repeat expansion size in ataxia

Neuroscience letters, 2007-12, Vol.429 (1), p.28-32

2007

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Early myoclonic status and outcome after cardiorespiratory arrest

Journal of neurology, neurosurgery and psychiatry, 1998-02, Vol.64 (2), p.267-268

1998

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Effects of exercise intensity on clot microstructure and mechanical properties in healthy individuals

Thrombosis research, 2016-07, Vol.143, p.130-136

2016

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Olfaction in Parkin single and compound heterozygotes in a cohort of young onset Parkinson's disease patients

Acta neurologica Scandinavica, 2016-10, Vol.134 (4), p.271-276

2016

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A clinical and pathological study of motor neurone disease on Guam

Brain (London, England : 1878), 2001-11, Vol.124 (11), p.2215-2222

2001

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Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation

Neurology, 2002-04, Vol.58 (8), p.1161

2002

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Late onset startle induced tics

Journal of neurology, neurosurgery and psychiatry, 1999-12, Vol.67 (6), p.782-784

1999

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Human calcitonin gene related peptide: a potent endogenous vasodilator in man

Clinical science (1979), 1986-04, Vol.70 (4), p.389-393

1986

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Primary antiphospholipid syndrome presenting as a corticobasal degeneration syndrome

Movement disorders, 1999-05, Vol.14 (3), p.530-532

1999

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Differences Between Neonates and Adults in Tissue-Type-Plasminogen Activator (t-PA)-Catalyzed Plasminogen Activation With Various Effectors and in Carbohydrate Sequences of Fibrinogen Chains

Thrombosis research, 2001-08, Vol.103 (3), p.173-184

2001

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Antithrombin‐TRI (Ala 382 to Thr) causing severe thromboembolic tendency undergoes the S‐to‐R transition and is associated with a plasma‐inactive high‐molecular‐weight complex of aggregated antithrombin

British journal of haematology, 1995-03, Vol.89 (3), p.589-601

1995

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Sign language tics in a prelingually deaf man

Movement disorders, 2000-03, Vol.15 (2), p.318-320

2000

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Parkinsonism following electrical injury to the hand

Movement disorders, 1998-05, Vol.13 (3), p.600-602

1998

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Potent Vasodilator Activity of Calcitonin Gene-Related Peptide in Human Skin

Journal of investigative dermatology, 1986-10, Vol.87 (4), p.533-536

1986

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Leukotriene release by endometrium and myometrium throughout the menstrual cycle in dysmenorrhoea and menorrhagia

Journal of endocrinology, 1987-05, Vol.113 (2), p.291-295

1987

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Antithrombin Glasgow II: alanine 382 to threonine mutation in the serpin P12 position, resulting in a substrate reaction with thrombin

British journal of haematology, 1991-09, Vol.79 (1), p.70-74

1991

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G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction

Glycobiology (Oxford), 2011-07, Vol.21 (7), p.914-924

2011

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The effect of onset age on the clinical features of Parkinson's disease

Differentiation of atypical parkinsonian syndromes with routine MRI

The prevalence of progressive supranuclear palsy (Steele–Richardson–Olszewski syndrome) in the UK

Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins

SGCZ mutations are unlikely to be associated with myoclonus dystonia

Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP

Dentatorubral pallidoluysian atrophy in South Wales

Identification of candidate cerebrospinal fluid biomarkers in parkinsonism using quantitative proteomics

Case control analysis of repeat expansion size in ataxia

Early myoclonic status and outcome after cardiorespiratory arrest

Effects of exercise intensity on clot microstructure and mechanical properties in healthy individuals

Olfaction in Parkin single and compound heterozygotes in a cohort of young onset Parkinson's disease patients

A clinical and pathological study of motor neurone disease on Guam

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation

Late onset startle induced tics

Human calcitonin gene related peptide: a potent endogenous vasodilator in man

Primary antiphospholipid syndrome presenting as a corticobasal degeneration syndrome

Differences Between Neonates and Adults in Tissue-Type-Plasminogen Activator (t-PA)-Catalyzed Plasminogen Activation With Various Effectors and in Carbohydrate Sequences of Fibrinogen Chains

Antithrombin‐TRI (Ala 382 to Thr) causing severe thromboembolic tendency undergoes the S‐to‐R transition and is associated with a plasma‐inactive high‐molecular‐weight complex of aggregated antithrombin

Sign language tics in a prelingually deaf man

Parkinsonism following electrical injury to the hand

Potent Vasodilator Activity of Calcitonin Gene-Related Peptide in Human Skin

Leukotriene release by endometrium and myometrium throughout the menstrual cycle in dysmenorrhoea and menorrhagia

Antithrombin Glasgow II: alanine 382 to threonine mutation in the serpin P12 position, resulting in a substrate reaction with thrombin

G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction

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