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Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions

Acta neuropathologica communications, 2022-03, Vol.10 (1), p.28-17, Article 28

2022

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Cathepsin D-deficient Drosophila recapitulate the key features of neuronal ceroid lipofuscinoses

Neurobiology of disease, 2005-06, Vol.19 (1), p.194-199

2005

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Long-term outcome after removal of spinal schwannoma: a clinicopathological study of 187 cases

Journal of neurosurgery, 1995-10, Vol.83 (4), p.621-626

1995

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High-resolution magic angle spinning and 1H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3

Journal of neuroscience research, 2004-09, Vol.77 (5), p.762-769

2004

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Neuronal intranuclear inclusion disease is genetically heterogeneous

Annals of clinical and translational neurology, 2020-09, Vol.7 (9), p.1716-1725

2020

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Long-term outcome after removal of spinal neurofibroma

Journal of neurosurgery, 1995-04, Vol.82 (4), p.572-577

1995

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Spinal malignant nerve-sheath tumor or cellular schwannoma? A striking difference in prognosis

Journal of neurosurgery, 1993-10, Vol.79 (4), p.528-532

1993

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High‐resolution magic angle spinning and 1 H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3

Journal of neuroscience research, 2004-09, Vol.77 (5), p.762-769

2004

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High-resolution magic angle spinning and super(1)H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3

Journal of neuroscience research, 2004-01, Vol.77 (5), p.762-769

2004

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ApoE ϵ3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

American journal of medical genetics, 2002-04, Vol.114 (3), p.288-291

2002

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ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

American journal of medical genetics, 2002-04, Vol.114 (3), p.288-291

2002

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Systematic drug sensitivity testing reveals synergistic growth inhibition by dasatinib or mTOR inhibitors with paclitaxel in ovarian granulosa cell tumor cells

Gynecologic oncology, 2017-03, Vol.144 (3), p.621-630

2017

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DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features

The Journal of experimental medicine, 2003-08, Vol.198 (4), p.669-675

2003

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Finnish neuroscience from past to present

The European journal of neuroscience, 2020-09, Vol.52 (5), p.3273-3289

2020

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Hippocampal Pathology in the Human Neuronal Ceroid-Lipofuscinoses: Distinct Patterns of Storage Deposition, Neurodegeneration and Glial Activation

Brain pathology (Zurich, Switzerland), 2004-10, Vol.14 (4), p.349-357

2004

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CNS manifestations of Nasu-Hakola disease: a frontal dementia with bone cysts

Neurology, 2001-06, Vol.56 (11), p.1552-1558

2001

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A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration

The EMBO journal, 2000-06, Vol.19 (12), p.2786-2792

2000

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Neuropathological Diagnostic Criteria for Creutzfeldt-Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

Brain pathology (Zurich, Switzerland), 1995-10, Vol.5 (4), p.459-466

1995

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Revisiting the catalytic CuZ cluster of nitrous oxide (N2O) reductase. Evidence of a bridging inorganic sulfur

The Journal of biological chemistry, 2000-12, Vol.275 (52), p.41133-41136

2000

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The Active Site of the Bacterial Nitric Oxide Reductase Is a Dinuclear Iron Center

Biochemistry (Easton), 1998-09, Vol.37 (38), p.13102-13109

1998

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A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

Nature medicine, 1998-04, Vol.4 (4), p.452-455

1998

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An autosomal locus predisposing to deletions of mitochondrial DNA

Nature genetics, 1995-02, Vol.9 (2), p.146-151

1995

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Multiple schwannomas: schwannomatosis or neurofibromatosis type 2?

Journal of neurosurgery, 1998-07, Vol.89 (1), p.36-41

1998

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Northern Epilepsy: A Novel Form of Neuronal Ceroid-Lipofuscinosis

Brain pathology (Zurich, Switzerland), 2000-04, Vol.10 (2), p.215-222

2000

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Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions

Cathepsin D-deficient Drosophila recapitulate the key features of neuronal ceroid lipofuscinoses

Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)

Long-term outcome after removal of spinal schwannoma: a clinicopathological study of 187 cases

High-resolution magic angle spinning and 1H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3

Neuronal intranuclear inclusion disease is genetically heterogeneous

Long-term outcome after removal of spinal neurofibroma

Spinal malignant nerve-sheath tumor or cellular schwannoma? A striking difference in prognosis

High‐resolution magic angle spinning and 1 H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3

High-resolution magic angle spinning and super(1)H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3

ApoE ϵ3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

Systematic drug sensitivity testing reveals synergistic growth inhibition by dasatinib or mTOR inhibitors with paclitaxel in ovarian granulosa cell tumor cells

DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features

Finnish neuroscience from past to present

Hippocampal Pathology in the Human Neuronal Ceroid-Lipofuscinoses: Distinct Patterns of Storage Deposition, Neurodegeneration and Glial Activation

CNS manifestations of Nasu-Hakola disease: a frontal dementia with bone cysts

A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration

Neuropathological Diagnostic Criteria for Creutzfeldt-Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

Revisiting the catalytic CuZ cluster of nitrous oxide (N2O) reductase. Evidence of a bridging inorganic sulfur

The Active Site of the Bacterial Nitric Oxide Reductase Is a Dinuclear Iron Center

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

An autosomal locus predisposing to deletions of mitochondrial DNA

Multiple schwannomas: schwannomatosis or neurofibromatosis type 2?

Northern Epilepsy: A Novel Form of Neuronal Ceroid-Lipofuscinosis

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