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Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada

Neurology, 2005-05, Vol.64 (9), p.1586-1591

2005

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Marked increase of neuronal prion protein immunoreactivity in Alzheimer's disease and human prion diseases

Acta neuropathologica, 2001-05, Vol.101 (5), p.417-423

2001

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Phenotype variability in 130 adult patients with respiratory chain disorders

Journal of inherited metabolic disease, 2001-10, Vol.24 (5), p.560-576

2001

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Understanding Patterns of Residency and Space Use of Arctic Skates (Amblyraja hyperborea) in Scott Inlet, Canada to Inform Indigenous Fisheries

Bradley, Jarius C

2023

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Sequential MRI in a case of Creutzfeldt-Jakob disease

Neuroradiology, 2002-03, Vol.44 (3), p.223-226

2002

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Fibrous meningeal tumours with extensive non-calcifying collagenous whorls and glial fibrillary acidic protein expression: the whorling-sclerosing variant of meningioma

Neuropathology and applied neurobiology, 2002-02, Vol.28 (1), p.42-47

2002

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Parkinson's disease associated with impaired oxidative phosphorylation

Neuroradiology, 2001-11, Vol.43 (11), p.997-1000

2001

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Lactate-stress testing in 54 patients with mitochondriopathy

European archives of psychiatry and clinical neuroscience, 2000, Vol.250 (1), p.36-39

2000

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Oxidative damage to nucleic acids in human prion disease

Neurobiology of disease, 2002-04, Vol.9 (3), p.275-281

2002

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Immunohistochemistry for the Prion Protein: Comparison of Different Monoclonal Antibodies in Human Prion Disease Subtypes

Brain pathology (Zurich, Switzerland), 2002-01, Vol.12 (1), p.1-11

2002

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Creutzfeldt-Jakob disease in Austria: an autopsy-controlled study

Neuroepidemiology, 2008-01, Vol.30 (4), p.215-221

2008

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Enhanced expression of 14-3-3 proteins in reactive astrocytes in Creutzfeldt-Jakob disease brains

Acta neuropathologica, 2004-10, Vol.108 (4), p.302-308

2004

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Increased CSF protein in chloroquine-induced axonal polyneuropathy and myopathy

Clinical neurology and neurosurgery, 2003-09, Vol.105 (4), p.231-236

2003

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Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease

Acta neuropathologica, 2003-05, Vol.105 (5), p.449-454

2003

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A novel phenotype in familial Creutzfeldt-Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein

Annals of neurology, 1999-06, Vol.45 (6), p.812-816

1999

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Familial Creutzfeldt-Jakob disease initially presenting with alien hand syndrome

Journal of neurology, 2002-05, Vol.249 (5), p.631-632

2002

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Alteration of the serotonergic nervous system in fatal familial insomnia

Annals of neurology, 2000-11, Vol.48 (5), p.788-791

2000

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Left ventricular hypertrabeculation in myotonic dystrophy type 1

Herz, 2001-06, Vol.26 (4), p.287-290

2001

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Hypothyroidism and muscular respiratory failure successfully treated with liothyronine

Southern medical journal (Birmingham, Ala.), 2002-11, Vol.95 (11), p.1347-1349

2002

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Malnutrition-Induced Hypokalemic Myopathy in Chronic Alcoholism

Clinical toxicology (Philadelphia, Pa.), 1998, Vol.36 (4), p.369-373

1998

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MOG encephalomyelitis: international recommendations on diagnosis and antibody testing

Journal of neuroinflammation, 2018-05, Vol.15 (1), p.134-134, Article 134

2018

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Xanthogranuloma of the Anterior Skull Base: A Case Report

Skull base, 1998, Vol.8 (4), p.215-219

1998

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ACUTE DISSEMINATED ENCEPHALOMYELITIS FOLLOWING VACCINATION AGAINST HUMAN PAPILLOMA VIRUS

Neurology, 2009-06, Vol.72 (24), p.2132-2133

2009

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Update on the diagnosis and treatment of neuromyelitis optica: Recommendations of the Neuromyelitis Optica Study Group (NEMOS)

Journal of neurology, 2014-01, Vol.261 (1), p.1-16

2014

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Xanthogranuloma of the anterior skull base: a case report

Skull base surgery, 1998, Vol.8 (4), p.215-219

1998

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Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada

Marked increase of neuronal prion protein immunoreactivity in Alzheimer's disease and human prion diseases

Phenotype variability in 130 adult patients with respiratory chain disorders

Understanding Patterns of Residency and Space Use of Arctic Skates (Amblyraja hyperborea) in Scott Inlet, Canada to Inform Indigenous Fisheries

Sequential MRI in a case of Creutzfeldt-Jakob disease

Fibrous meningeal tumours with extensive non-calcifying collagenous whorls and glial fibrillary acidic protein expression: the whorling-sclerosing variant of meningioma

Parkinson's disease associated with impaired oxidative phosphorylation

Lactate-stress testing in 54 patients with mitochondriopathy

Oxidative damage to nucleic acids in human prion disease

Immunohistochemistry for the Prion Protein: Comparison of Different Monoclonal Antibodies in Human Prion Disease Subtypes

Creutzfeldt-Jakob disease in Austria: an autopsy-controlled study

Enhanced expression of 14-3-3 proteins in reactive astrocytes in Creutzfeldt-Jakob disease brains

Increased CSF protein in chloroquine-induced axonal polyneuropathy and myopathy

Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease

A novel phenotype in familial Creutzfeldt-Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein

Familial Creutzfeldt-Jakob disease initially presenting with alien hand syndrome

Alteration of the serotonergic nervous system in fatal familial insomnia

Left ventricular hypertrabeculation in myotonic dystrophy type 1

Hypothyroidism and muscular respiratory failure successfully treated with liothyronine

Malnutrition-Induced Hypokalemic Myopathy in Chronic Alcoholism

MOG encephalomyelitis: international recommendations on diagnosis and antibody testing

Xanthogranuloma of the Anterior Skull Base: A Case Report

ACUTE DISSEMINATED ENCEPHALOMYELITIS FOLLOWING VACCINATION AGAINST HUMAN PAPILLOMA VIRUS

Update on the diagnosis and treatment of neuromyelitis optica: Recommendations of the Neuromyelitis Optica Study Group (NEMOS)

Xanthogranuloma of the anterior skull base: a case report

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