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Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

Nature genetics, 2015-06, Vol.47 (6), p.579-581

2015

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Consonant identification in N -talker babble is a nonmonotonic function of N

The Journal of the Acoustical Society of America, 2005-11, Vol.118 (5), p.2775-2778

2005

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Synthesising electrical demand profiles for UK dwellings

Energy and buildings, 2014-06, Vol.76, p.605-614

2014

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Management of Alcohol Withdrawal in the Emergency Department: Current Perspectives

Open access emergency medicine, 2020-01, Vol.12, p.53-65

2020

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Methods for assessing domestic overheating for future building regulation compliance

Energy policy, 2013-05, Vol.56, p.684-692

2013

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Prescribing Buprenorphine for Opioid Use Disorders in the ED: A Review of Best Practices, Barriers, and Future Directions

Open access emergency medicine, 2020-01, Vol.12, p.261-274

2020

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The long-term safety and efficacy of bilateral transplantation of human fetal striatal tissue in patients with mild to moderate Huntington's disease

Journal of neurology, neurosurgery and psychiatry, 2013-06, Vol.84 (6), p.657-665

2013

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To tell or not to tell: barriers and facilitators in family communication about genetic risk

Clinical genetics, 2003-10, Vol.64 (4), p.317-326

2003

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Exercise testing and training in people with Huntington’s disease

Clinical rehabilitation, 2015-02, Vol.29 (2), p.196-206

2015

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Tracking the Long-Term Decline and Recovery of an Isolated Population

Science (American Association for the Advancement of Science), 1998-11, Vol.282 (5394), p.1695-1698

1998

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Bicavitary effusion secondary to liver lobe torsion in a dog

Veterinary medicine (Auckland), 2016-01, Vol.7 (Issue 1), p.53-58

2016

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How young people find out about their family history of Huntington's disease

Social science & medicine (1982), 2009-05, Vol.68 (10), p.1892-1900

2009

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Late stage care in Huntington's disease

Brain research bulletin, 2007-04, Vol.72 (2), p.179-181

Simpson, Sheila A

2007

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Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course

Brain (London, England : 1878), 2003-04, Vol.126 (4), p.946-955

2003

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Young people's experiences of growing up in a family affected by Huntington's disease

Clinical genetics, 2007-02, Vol.71 (2), p.120-129

2007

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Cannabis use, cognitive performance and mood in a sample of workers

Journal of psychopharmacology (Oxford), 2006-01, Vol.20 (1), p.14-23

2006

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Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene

Brain (London, England : 1878), 2004-06, Vol.127 (6), p.1415-1426

2004

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Differential deficits in expression recognition in gene-carriers and patients with Huntington’s disease

Neuropsychologia, 2003, Vol.41 (11), p.1484-1492

2003

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Genetic professionals' reports of nondisclosure of genetic risk information within families

European journal of human genetics : EJHG, 2005-05, Vol.13 (5), p.556-562

2005

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Family Communication about Genetic Risk: The Little That Is Known

Community genetics, 2004-01, Vol.7 (1), p.15-24

2004

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Entry of Herpes Simplex Virus Type 1 into Primary Sensory Neurons In Vitro Is Mediated by Nectin-1/HveC

Journal of Virology, 2003-03, Vol.77 (5), p.3307-3311

2003

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Minor injuries, cognitive failures and accidents at work: incidence and associated features

Occupational medicine (Oxford), 2005-03, Vol.55 (2), p.99-108

2005

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Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

American journal of human genetics, 1996-07, Vol.59 (1), p.16-22

1996

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SSRIs and cognitive performance in a working sample

Human psychopharmacology, 2005-12, Vol.20 (8), p.561-572

2005

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Stability and Folding Kinetics of a Ubiquitin Mutant with a Strong Propensity for Nonnative β-Hairpin Conformation in the Unfolded State

Biochemistry (Easton), 2003-11, Vol.42 (46), p.13762-13771

2003

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Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

Consonant identification in N -talker babble is a nonmonotonic function of N

Synthesising electrical demand profiles for UK dwellings

Management of Alcohol Withdrawal in the Emergency Department: Current Perspectives

Methods for assessing domestic overheating for future building regulation compliance

Prescribing Buprenorphine for Opioid Use Disorders in the ED: A Review of Best Practices, Barriers, and Future Directions

The long-term safety and efficacy of bilateral transplantation of human fetal striatal tissue in patients with mild to moderate Huntington's disease

To tell or not to tell: barriers and facilitators in family communication about genetic risk

Exercise testing and training in people with Huntington’s disease

Tracking the Long-Term Decline and Recovery of an Isolated Population

Bicavitary effusion secondary to liver lobe torsion in a dog

How young people find out about their family history of Huntington's disease

Late stage care in Huntington's disease

Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course

Young people's experiences of growing up in a family affected by Huntington's disease

Cannabis use, cognitive performance and mood in a sample of workers

Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene

Differential deficits in expression recognition in gene-carriers and patients with Huntington’s disease

Genetic professionals' reports of nondisclosure of genetic risk information within families

Family Communication about Genetic Risk: The Little That Is Known

Entry of Herpes Simplex Virus Type 1 into Primary Sensory Neurons In Vitro Is Mediated by Nectin-1/HveC

Minor injuries, cognitive failures and accidents at work: incidence and associated features

Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

SSRIs and cognitive performance in a working sample

Stability and Folding Kinetics of a Ubiquitin Mutant with a Strong Propensity for Nonnative β-Hairpin Conformation in the Unfolded State

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