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Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance

Brain (London, England : 1878), 2007-05, Vol.130 (5), p.1350-1359

2007

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Antioxidant treatment protects striatal neurons against excitotoxic insults

Neuroscience, 1996-07, Vol.73 (1), p.185-200

1996

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Analysis of Mitochondrial Targeting Sequence and Coding Region Polymorphisms of the Manganese Superoxide Dismutase Gene in German Parkinson Disease Patients

Biochemical and biophysical research communications, 1999-02, Vol.255 (3), p.749-752

1999

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Phenotypic development of the human embryonic striatal primordium: A study of cultured and grafted neurons from the lateral and medial ganglionic eminences

Neuroscience, 1996-07, Vol.73 (1), p.171-183

1996

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Microglia and the Development of Spongiform Change in Creutzfeldt-Jakob Disease

Journal of neuropathology and experimental neurology, 1998-03, Vol.57 (3), p.246-256

1998

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Intrastriatal grafts of embryonic mesencephalic rat neurons genetically modified using an adenovirus encoding human Cu/Zn superoxide dismutase

Neuroscience, 1997-06, Vol.78 (3), p.703-713

1997

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Mesencephalic neuron death induced by congeners of nitrogen monoxide is prevented by the lazaroid U-83836E

Experimental brain research, 1997, Vol.113 (1), p.138-143

1997

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Microglia only weakly present glioma antigen to cytotoxic T cells

International journal of developmental neuroscience, 1999-08, Vol.17 (5-6), p.547-556

1999

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Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents

Neurogenetics, 2001-07, Vol.3 (3), p.163-170

2001

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Lazaroid Treatment Prevents Death of Cultured Rat Embryonic Mesencephalic Neurons Following Glutathione Depletion

Journal of neurochemistry, 1996-10, Vol.67 (4), p.1653-1660

1996

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Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease

Neurogenetics, 1998-03, Vol.1 (3), p.197-204

1998

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Predominant influence of MGMT methylation in non-resectable glioblastoma after radiotherapy plus temozolomide

Journal of neurology, neurosurgery and psychiatry, 2011-04, Vol.82 (4), p.441-446

2011

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DARPP-32-rich zones in grafts of lateral ganglionic eminence govern the extent of functional recovery in skilled paw reaching in an animal model of Huntington's disease

Neuroscience, 1996-10, Vol.74 (4), p.959-970

1996

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Methylprednisolone prevents rejection of intrastriatal grafts of xenogeneic embryonic neural tissue in adult rats

Brain research, 1996-03, Vol.712 (2), p.199-212

1996

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Sequence analysis of the MTCYB gene in Parkinson disease

Neurogenetics, 2000-10, Vol.3 (1), p.47-48

2000

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A new approach to the genetic analysis of nervous system diseases: retrospective genotyping of archival brains

Progress in brain research, 1998, Vol.117, p.307-313

1998

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CuZn superoxide dismutase transgenic retinal transplants

Graefe's archive for clinical and experimental ophthalmology, 1999-04, Vol.237 (4), p.336-341

1999

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Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease

Neurogenetics, 1999-04, Vol.2 (2), p.121-127

1999

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The α1-antichymotrypsin A-allele in German Parkinson disease patients

Journal of neural transmission, 1999, Vol.106 (7-8), p.729-736

1999

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Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment

Acta neuropathologica, 2005-04, Vol.109 (4), p.443-448

2005

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The α 1 -antichymotrypsin A-allele in German Parkinson disease patients

Journal of Neural Transmission, 1999-08, Vol.106 (7-8), p.729-736

1999

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The lazaroid U-83836E improves the survival of rat embryonic mesencephalic tissue stored at 4°C and subsequently used for cultures or intracerebral transplantation

Brain research bulletin, 1996, Vol.39 (6), p.341-347

1996

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Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein gene

Neurogenetics, 2005-05, Vol.6 (2), p.97-100

2005

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Developmental Features of Human Striatal Tissue Transplanted in a Rat Model of Huntington's Disease

Neurobiology of disease, 1997, Vol.3 (4), p.299-311

1997

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Sequence analysis of two nuclear encoded subunits (10 and 51 kDa) of mitochondrial complex I in Parkinson disease

Neurogenetics, 2002-03, Vol.4 (1), p.55-57

2002

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Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance

Antioxidant treatment protects striatal neurons against excitotoxic insults

Analysis of Mitochondrial Targeting Sequence and Coding Region Polymorphisms of the Manganese Superoxide Dismutase Gene in German Parkinson Disease Patients

Phenotypic development of the human embryonic striatal primordium: A study of cultured and grafted neurons from the lateral and medial ganglionic eminences

Microglia and the Development of Spongiform Change in Creutzfeldt-Jakob Disease

Intrastriatal grafts of embryonic mesencephalic rat neurons genetically modified using an adenovirus encoding human Cu/Zn superoxide dismutase

Mesencephalic neuron death induced by congeners of nitrogen monoxide is prevented by the lazaroid U-83836E

Microglia only weakly present glioma antigen to cytotoxic T cells

Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents

Lazaroid Treatment Prevents Death of Cultured Rat Embryonic Mesencephalic Neurons Following Glutathione Depletion

Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease

Predominant influence of MGMT methylation in non-resectable glioblastoma after radiotherapy plus temozolomide

DARPP-32-rich zones in grafts of lateral ganglionic eminence govern the extent of functional recovery in skilled paw reaching in an animal model of Huntington's disease

Methylprednisolone prevents rejection of intrastriatal grafts of xenogeneic embryonic neural tissue in adult rats

Sequence analysis of the MTCYB gene in Parkinson disease

A new approach to the genetic analysis of nervous system diseases: retrospective genotyping of archival brains

CuZn superoxide dismutase transgenic retinal transplants

Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease

The α1-antichymotrypsin A-allele in German Parkinson disease patients

Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment

The α 1 -antichymotrypsin A-allele in German Parkinson disease patients

The lazaroid U-83836E improves the survival of rat embryonic mesencephalic tissue stored at 4°C and subsequently used for cultures or intracerebral transplantation

Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein gene

Developmental Features of Human Striatal Tissue Transplanted in a Rat Model of Huntington's Disease

Sequence analysis of two nuclear encoded subunits (10 and 51 kDa) of mitochondrial complex I in Parkinson disease

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