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Chronology of Lake El'gygytgyn sediments – a combined magnetostratigraphic, palaeoclimatic and orbital tuning study based on multi-parameter analyses

Climate of the past, 2013-11, Vol.9 (6), p.2413-2432

2013

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Magnetostratigraphy of sediments from Lake El'gygytgyn ICDP Site 5011-1: paleomagnetic age constraints for the longest paleoclimate record from the continental Arctic

Climate of the past, 2014-03, Vol.10 (2), p.623-642

2014

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The Neuronal Ceroid–Lipofuscinoses

Journal of neuropathology and experimental neurology, 2003-01, Vol.62 (1), p.1-13

HALTIA, MATTI

2003

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A new mini-invasive technique in treating pediatric diaphyseal forearm fractures by bioabsorbable elastic stable intramedullary nailing: a preliminary technical report

Scandinavian journal of surgery, 2013-12, Vol.102 (4), p.258-264

2013

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Prevalence of Alzheimer's disease in very elderly people: a prospective neuropathological study

Neurology, 2001-06, Vol.56 (12), p.1690-1696

2001

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Human prion diseases

Annals of medicine (Helsinki), 2000-10, Vol.32 (7), p.493-500

Haltia, Matti

2000

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Vascular growth factors and receptors in capillary hemangioblastomas and hemangiopericytomas

The American journal of pathology, 1996-03, Vol.148 (3), p.763-775

1996

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Amphoterin Includes a Sequence Motif Which Is Homologous to the Alzheimer's β-Amyloid Peptide (Aβ), Forms Amyloid Fibrils in Vitro, and Binds Avidly to Aβ

Biochemistry (Easton), 2001-08, Vol.40 (34), p.10032-10037

2001

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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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Status Epilepticus Induces Changes in the Expression and Localization of Endogenous Palmitoyl-Protein Thioesterase 1

Neurobiology of disease, 2002-08, Vol.10 (3), p.247-257

2002

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Alzheimer disease PS-1 exon 9 deletion defined

Nature medicine, 1999-10, Vol.5 (10), p.1090-1090

1999

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Ezrin expression in stromal cells of capillary hemangioblastoma. An immunohistochemical survey of brain tumors

The American journal of pathology, 1996-02, Vol.148 (2), p.367-373

1996

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Mutation in gelsolin gene in finnish hereditary amyloidosis

The Journal of experimental medicine, 1990-12, Vol.172 (6), p.1865-1867

1990

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The Expression of Palmitoyl-Protein Thioesterase Is Developmentally Regulated in Neural Tissues but Not in Nonneural Tissues

Molecular genetics and metabolism, 1999-04, Vol.66 (4), p.290-293

1999

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Self-reinforcement and hydrolytic degradation of amorphous lactic acid based poly(ester-amide), and of its composite with sol-gel derived fibers

Journal of materials science. Materials in medicine, 2002-10, Vol.13 (10), p.903-909

2002

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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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Hippocampal lesions in the neuronal ceroid lipofuscinoses

European journal of paediatric neurology, 2001, Vol.5 Suppl A, p.209-211

2001

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Congenital ovine neuronal ceroid lipofuscinosis--a cathepsin D deficiency with increased levels of the inactive enzyme

European journal of paediatric neurology, 2001, Vol.5 Suppl A, p.43-45

2001

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Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

American journal of medical genetics, 1992-02, Vol.42 (4), p.561-567

1992

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Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndrome

Investigative ophthalmology & visual science, 1994-09, Vol.35 (10), p.3759-3769

1994

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Sphingolipid activator proteins (SAPs) in neuronal ceroid lipofuscinoses (NCL)

Neuropediatrics, 1997-02, Vol.28 (1), p.49-52

1997

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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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An animal model of the infantile type of neuronal ceroid‐lipofuscinosis

Journal of inherited metabolic disease, 1993-03, Vol.16 (2), p.274-277

1993

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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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Chronology of Lake El'gygytgyn sediments – a combined magnetostratigraphic, palaeoclimatic and orbital tuning study based on multi-parameter analyses

Magnetostratigraphy of sediments from Lake El'gygytgyn ICDP Site 5011-1: paleomagnetic age constraints for the longest paleoclimate record from the continental Arctic

The Neuronal Ceroid–Lipofuscinoses

A new mini-invasive technique in treating pediatric diaphyseal forearm fractures by bioabsorbable elastic stable intramedullary nailing: a preliminary technical report

Prevalence of Alzheimer's disease in very elderly people: a prospective neuropathological study

Human prion diseases

The structure of the presenilin 1 ( S182 ) gene and identification of six novel mutations in early onset AD families

Vascular growth factors and receptors in capillary hemangioblastomas and hemangiopericytomas

Amphoterin Includes a Sequence Motif Which Is Homologous to the Alzheimer's β-Amyloid Peptide (Aβ), Forms Amyloid Fibrils in Vitro, and Binds Avidly to Aβ

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

Status Epilepticus Induces Changes in the Expression and Localization of Endogenous Palmitoyl-Protein Thioesterase 1

Alzheimer disease PS-1 exon 9 deletion defined

Ezrin expression in stromal cells of capillary hemangioblastoma. An immunohistochemical survey of brain tumors

Mutation in gelsolin gene in finnish hereditary amyloidosis

The Expression of Palmitoyl-Protein Thioesterase Is Developmentally Regulated in Neural Tissues but Not in Nonneural Tissues

Self-reinforcement and hydrolytic degradation of amorphous lactic acid based poly(ester-amide), and of its composite with sol-gel derived fibers

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

Hippocampal lesions in the neuronal ceroid lipofuscinoses

Congenital ovine neuronal ceroid lipofuscinosis--a cathepsin D deficiency with increased levels of the inactive enzyme

Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndrome

Sphingolipid activator proteins (SAPs) in neuronal ceroid lipofuscinoses (NCL)

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

An animal model of the infantile type of neuronal ceroid‐lipofuscinosis

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

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