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Apolipoprotein E genotype as a risk factor for susceptibility to and dementia in Parkinson’s Disease

Journal of neurology, 2009-03, Vol.256 (3), p.493-498

2009

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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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Abnormally phosphorylated tau is associated with neuronal and axonal loss in experimental autoimmune encephalomyelitis and multiple sclerosis

Brain (London, England : 1878), 2008-07, Vol.131 (7), p.1736-1748

2008

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Retinoid-independent motor neurogenesis from human embryonic stem cells reveals a medial columnar ground state

Nature communications, 2011-03, Vol.2 (1), p.214-214, Article 214

2011

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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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HLA-DRB1 and multiple sclerosis in Malta

Neurology, 2008-01, Vol.70 (2), p.101

2008

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Interleukin 7 receptor α chain ( IL7R ) shows allelic and functional association with multiple sclerosis

Nature genetics, 2007-09, Vol.39 (9), p.1083-1091

2007

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Myasthenia gravis: a population based epidemiological study in Cambridgeshire, England

Journal of neurology, neurosurgery and psychiatry, 1998-10, Vol.65 (4), p.492-496

1998

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Effects of Direct Transplantation of Multipotent Mesenchymal Stromal/Stem Cells into the Demyelinated Spinal Cord

Cell transplantation, 2008-01, Vol.17 (7), p.865-873

2008

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Interleukin 7 receptor [alpha] chain (IL7R) shows allelic and functional association with multiple sclerosis

Nature genetics, 2007-09, Vol.39 (9), p.1083-1091

2007

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Primary spinal cord neurodegeneration in Leber hereditary optic neuropathy

Neurology, 2007-07, Vol.69 (2), p.214

2007

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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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Astrocytes promote neurogenesis from oligodendrocyte precursor cells

The European journal of neuroscience, 2006-02, Vol.23 (4), p.945-956

2006

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Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease

Journal of neurology, 2007-07, Vol.254 (7), p.846-848

2007

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Continuing optic nerve atrophy following optic neuritis: a serial MRI study

Multiple sclerosis, 2002-08, Vol.8 (4), p.339-342

2002

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OCCURRENCE OF A MULTIPLE SCLEROSIS-LIKE ILLNESS IN WOMEN WHO HAVE A LEBER'S HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL DNA MUTATION

Brain (London, England : 1878), 1992-08, Vol.115 (4), p.979-989

1992

Volltextzugriff (PDF)

Alemtuzumab vs. Interferon Beta-1a in Early Multiple Sclerosis

The New England journal of medicine, 2008-10, Vol.359 (17), p.1786-1801

2008

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Genetic variation in nitric oxide synthase 2A ( ) and risk for multiple sclerosis

Genes and immunity, 2008-09, Vol.9 (6), p.493-500

2008

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IMMUNOCYTOCHEMICAL LOCALIZATION OF THE TERMINAL COMPLEMENT COMPLEX IN MULTIPLE SCLEROSIS

Neuropathology and applied neurobiology, 1989-08, Vol.15 (4), p.307-316

1989

Volltextzugriff (PDF)

Effects of intravenous methylprednisolone on outcome in MRI-based prognostic subgroups in acute optic neuritis

Neurology, 1998-01, Vol.50 (1), p.230

1998

Volltextzugriff (PDF)

HLA-DR 15 is associated with female sex and younger age at diagnosis in multiple sclerosis

Journal of neurology, neurosurgery and psychiatry, 2002-02, Vol.72 (2), p.184-187

2002

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A proliferative adult human oligodendrocyte progenitor

Neuroreport, 1995-02, Vol.6 (3), p.441-445

1995

Volltextzugriff (PDF)

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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No Evidence for Association with Parkinson Disease for 13 Single-Nucleotide Polymorphisms Identified by Whole-Genome Association Screening

American journal of human genetics, 2006-06, Vol.78 (6), p.1088-1090

2006

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Apolipoprotein E genotype as a risk factor for susceptibility to and dementia in Parkinson’s Disease

Increasing prevalence and incidence of multiple sclerosis in South East Wales

Abnormally phosphorylated tau is associated with neuronal and axonal loss in experimental autoimmune encephalomyelitis and multiple sclerosis

Retinoid-independent motor neurogenesis from human embryonic stem cells reveals a medial columnar ground state

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

HLA-DRB1 and multiple sclerosis in Malta

Interleukin 7 receptor α chain ( IL7R ) shows allelic and functional association with multiple sclerosis

Myasthenia gravis: a population based epidemiological study in Cambridgeshire, England

Effects of Direct Transplantation of Multipotent Mesenchymal Stromal/Stem Cells into the Demyelinated Spinal Cord

Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity

Interleukin 7 receptor [alpha] chain (IL7R) shows allelic and functional association with multiple sclerosis

Primary spinal cord neurodegeneration in Leber hereditary optic neuropathy

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

Astrocytes promote neurogenesis from oligodendrocyte precursor cells

Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease

Continuing optic nerve atrophy following optic neuritis: a serial MRI study

OCCURRENCE OF A MULTIPLE SCLEROSIS-LIKE ILLNESS IN WOMEN WHO HAVE A LEBER'S HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL DNA MUTATION

Alemtuzumab vs. Interferon Beta-1a in Early Multiple Sclerosis

Genetic variation in nitric oxide synthase 2A ( ) and risk for multiple sclerosis

IMMUNOCYTOCHEMICAL LOCALIZATION OF THE TERMINAL COMPLEMENT COMPLEX IN MULTIPLE SCLEROSIS

Effects of intravenous methylprednisolone on outcome in MRI-based prognostic subgroups in acute optic neuritis

HLA-DR 15 is associated with female sex and younger age at diagnosis in multiple sclerosis

A proliferative adult human oligodendrocyte progenitor

Urinary, faecal and sexual dysfunction in patients with multiple sclerosis

No Evidence for Association with Parkinson Disease for 13 Single-Nucleotide Polymorphisms Identified by Whole-Genome Association Screening

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