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Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues

Journal of neurology, neurosurgery and psychiatry, 2008-01, Vol.79 (1), p.6-11

2008

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Incidence of amyotrophic lateral sclerosis in Europe

Journal of neurology, neurosurgery and psychiatry, 2010-04, Vol.81 (4), p.385-390

2010

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Cause of death and clinical grading criteria in a cohort of amyotrophic lateral sclerosis cases undergoing autopsy from the Scottish Motor Neurone Disease Register

Journal of neurology, neurosurgery and psychiatry, 2009-01, Vol.80 (1), p.84-87

2009

Volltextzugriff (PDF)

Survival and cause of death in multiple sclerosis: a prospective population-based study

Journal of neurology, neurosurgery and psychiatry, 2008-09, Vol.79 (9), p.1016-1021

2008

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Increasing prevalence and incidence of multiple sclerosis in South East Wales

Journal of neurology, neurosurgery and psychiatry, 2009-04, Vol.80 (4), p.386-391

2009

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Unexpected decline in survival from amyotrophic lateral sclerosis/motor neurone disease

Journal of neurology, neurosurgery and psychiatry, 2004-12, Vol.75 (12), p.1753-1755

2004

Volltextzugriff (PDF)

The incidence of motor nueron disease in Scotland

Journal of neurology, 2007-07, Vol.254 (7), p.866-869

2007

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The prognosis of motor neurone disease

Journal of neurology, neurosurgery and psychiatry, 2010-10, Vol.81 (10), p.1062-1062

Swingler, R J

2010

Volltextzugriff (PDF)

Change in disability in patients with multiple sclerosis: a 20-year prospective population-based analysis

Journal of neurology, neurosurgery and psychiatry, 2008-10, Vol.79 (10), p.1137-1143

2008

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Population based cost utility study of interferon beta-1b in secondary progressive multiple sclerosis

BMJ (Online), 1999-12, Vol.319 (7224), p.1529

International edition, 1999

Volltextzugriff (PDF)

Molecular genetic analysis of the APEX nuclease gene in amyotrophic lateral sclerosis

Neurology, 1999-06, Vol.52 (9), p.1899

1999

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Urinary, faecal and sexual dysfunction in patients with multiple sclerosis

Journal of neurology, 1999-11, Vol.246 (11), p.1027-1032

1999

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Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register

Journal of neurology, neurosurgery and psychiatry, 1996-02, Vol.60 (2), p.147-151

1996

Volltextzugriff (PDF)

Review: Optical Micrometer Resolution Scanning for Non-invasive Grading of Precancer in the Human Uterine Cervix

Technology in cancer research & treatment, 2008-12, Vol.7 (6), p.483-496

2008

Volltextzugriff (PDF)

RE: “ANTIBIOTIC USE AND RISK OF MULTIPLE SCLEROSIS”

American journal of epidemiology, 2006-12, Vol.164 (12), p.1253-1253

2006

Volltextzugriff (PDF)

Estimating the Prevalence of Multiple Sclerosis in the United Kingdom by Using Capture-Recapture Methodology

American journal of epidemiology, 1999-06, Vol.149 (11), p.1016-1024

1999

Volltextzugriff (PDF)

Deep brain stimulation plus best medical therapy versus best medical therapy alone for advanced Parkinson's disease (PD SURG trial): a randomised, open-label trial

Lancet neurology, 2010-06, Vol.9 (6), p.581-591

2010

Volltextzugriff (PDF)

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis

Nature genetics, 2006-04, Vol.38 (4), p.411-413

2006

Volltextzugriff (PDF)

Not hysteria: ovarian teratoma-associated anti-N-methyl-D-aspartate receptor encephalitis

Scottish medical journal, 2012-08, Vol.57 (3), p.182

2012

Volltextzugriff (PDF)

Rapid mutation detection by the Transgenomic wave analyser DHPLC identifies MYOC mutations in patients with ocular hypertension and/or open angle glaucoma

British journal of ophthalmology, 2002-02, Vol.86 (2), p.191-195

2002

Volltextzugriff (PDF)

Effect of referral bias on assessing survival in als

Neurology, 2007-08, Vol.69 (9), p.939; author reply 939

2007

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Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus

Human molecular genetics, 1993-10, Vol.2 (10), p.1619-1624

1993

Volltextzugriff (PDF)

Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis

Journal of medical genetics, 1998-02, Vol.35 (2), p.174-174

1998

Volltextzugriff (PDF)

The prevalence of multiple sclerosis in Tayside, Scotland: do latitudinal gradients really exist?

Journal of neurology, 1999-11, Vol.246 (11), p.1033-1040

1999

Volltextzugriff (PDF)

Multiple sclerosis in Tayside, Scotland: detection of clusters using a spatial scan statistic

Multiple sclerosis, 2005-08, Vol.11 (4), p.403-408

2005

Volltextzugriff (PDF)

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Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues

Incidence of amyotrophic lateral sclerosis in Europe

Cause of death and clinical grading criteria in a cohort of amyotrophic lateral sclerosis cases undergoing autopsy from the Scottish Motor Neurone Disease Register

Survival and cause of death in multiple sclerosis: a prospective population-based study

Increasing prevalence and incidence of multiple sclerosis in South East Wales

Unexpected decline in survival from amyotrophic lateral sclerosis/motor neurone disease

The incidence of motor nueron disease in Scotland

The prognosis of motor neurone disease

Change in disability in patients with multiple sclerosis: a 20-year prospective population-based analysis

Population based cost utility study of interferon beta-1b in secondary progressive multiple sclerosis

Molecular genetic analysis of the APEX nuclease gene in amyotrophic lateral sclerosis

Urinary, faecal and sexual dysfunction in patients with multiple sclerosis

Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register

Review: Optical Micrometer Resolution Scanning for Non-invasive Grading of Precancer in the Human Uterine Cervix

RE: “ANTIBIOTIC USE AND RISK OF MULTIPLE SCLEROSIS”

Estimating the Prevalence of Multiple Sclerosis in the United Kingdom by Using Capture-Recapture Methodology

Deep brain stimulation plus best medical therapy versus best medical therapy alone for advanced Parkinson's disease (PD SURG trial): a randomised, open-label trial

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis

Not hysteria: ovarian teratoma-associated anti-N-methyl-D-aspartate receptor encephalitis

Rapid mutation detection by the Transgenomic wave analyser DHPLC identifies MYOC mutations in patients with ocular hypertension and/or open angle glaucoma

Effect of referral bias on assessing survival in als

Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus

Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis

The prevalence of multiple sclerosis in Tayside, Scotland: do latitudinal gradients really exist?

Multiple sclerosis in Tayside, Scotland: detection of clusters using a spatial scan statistic

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