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Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain

Neuropathology and applied neurobiology, 2011-02, Vol.37 (1), p.94-113

2011

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PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease

Brain (London, England : 1878), 2008-07, Vol.131 (7), p.1845-1853

2008

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Prevalence and severity of cerebral amyloid angiopathy: a population-based study on very elderly Finns (Vantaa 85+)

Neuropathology and applied neurobiology, 2012-06, Vol.38 (4), p.329-336

2012

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Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases

Neuropathology and applied neurobiology, 2016-02, Vol.42 (2), p.194-209

2016

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Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease

Neurology, 2005-11, Vol.65 (10), p.1636

2005

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MR Imaging Characteristics and Neuropathology of the Spinal Cord in Adult-Onset Autosomal Dominant Leukodystrophy with Autonomic Symptoms

American journal of neuroradiology : AJNR, 2009-02, Vol.30 (2), p.328-335

2009

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MR Characteristics and Neuropathology in Adult-Onset Autosomal Dominant Leukodystrophy with Autonomic Symptoms

American Journal of Neuroradiology, 2006-04, Vol.27 (4), p.904-911

2006

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Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL

Brain (London, England : 1878), 2007-02, Vol.130 (2), p.357-367

2007

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Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest old

Current Alzheimer research, 2013-12, Vol.10 (10), p.1090

2013

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Relation between myofibers and connective tissue during muscle injury repair

Scandinavian journal of medicine & science in sports, 2000-12, Vol.10 (6), p.332-337

2000

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Neurophysiological and mitochondrial abnormalities in MuSK antibody seropositive myasthenia gravis compared to other immunological subtypes

Clinical neurophysiology, 2006-07, Vol.117 (7), p.1434-1443

2006

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Increased brain histamine levels in Parkinson's disease but not in multiple system atrophy

Journal of neurochemistry, 2002-06, Vol.81 (5), p.954-960

2002

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The pathogenesis of CADASIL: an update

Journal of the neurological sciences, 2004-11, Vol.226 (1), p.35-39

2004

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CADASIL and CARASIL

Brain pathology (Zurich, Switzerland), 2014-09, Vol.24 (5), p.525-544

2014

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The tau S305S mutation causes frontotemporal dementia with parkinsonism

European journal of neurology, 2008-02, Vol.15 (2), p.156-161

2008

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Stable expression of mutated and non-mutated mouse NOTCH3 in C2C12 mouse myoblast

Journal of the neurological sciences, 2009, Vol.283 (1), p.295-295

2009

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Neuronal histamine deficit in Alzheimer's disease

Neuroscience, 1997-11, Vol.82 (4), p.993-997

1997

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Satellite cell proliferation and the expression of myogenin and desmin in regenerating skeletal muscle: evidence for two different populations of satellite cells

Laboratory investigation, 1995-03, Vol.72 (3), p.341

1995

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G.P.7.03 Mutations in TPM2 and TPM3 causing nemaline myopathy or arthrogryposis

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.587-588

2009

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Reappraisal of a consecutive autopsy series of patients with primary degenerative dementia: Lewy-related pathology

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2007-07, Vol.115 (7), p.820-827

2007

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Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

Brain (London, England : 1878), 2009-04, Vol.132 (4), p.933-939

2009

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Neurologic symptoms are common during gestation and puerperium in CADASIL

Neurology, 2005-04, Vol.64 (8), p.1441

2005

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Muscle paralysis and myosin loss in a patient with cancer cachexia

Acta myologica, 2007-12, Vol.26 (3), p.136-144

2007

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Molecular genetic and clinical findings in identical twins with CADASIL

JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, Vol.283 (1), p.294-294

2009

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Low TENS treatment on post-stroke paretic arm: a three-year follow-up

Clinical rehabilitation, 2000-02, Vol.14 (1), p.14-19

2000

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Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain

PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease

Prevalence and severity of cerebral amyloid angiopathy: a population-based study on very elderly Finns (Vantaa 85+)

Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases

Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease

MR Imaging Characteristics and Neuropathology of the Spinal Cord in Adult-Onset Autosomal Dominant Leukodystrophy with Autonomic Symptoms

MR Characteristics and Neuropathology in Adult-Onset Autosomal Dominant Leukodystrophy with Autonomic Symptoms

Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL

Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest old

Relation between myofibers and connective tissue during muscle injury repair

Neurophysiological and mitochondrial abnormalities in MuSK antibody seropositive myasthenia gravis compared to other immunological subtypes

Increased brain histamine levels in Parkinson's disease but not in multiple system atrophy

The pathogenesis of CADASIL: an update

CADASIL and CARASIL

The tau S305S mutation causes frontotemporal dementia with parkinsonism

Stable expression of mutated and non-mutated mouse NOTCH3 in C2C12 mouse myoblast

Neuronal histamine deficit in Alzheimer's disease

Satellite cell proliferation and the expression of myogenin and desmin in regenerating skeletal muscle: evidence for two different populations of satellite cells

G.P.7.03 Mutations in TPM2 and TPM3 causing nemaline myopathy or arthrogryposis

Reappraisal of a consecutive autopsy series of patients with primary degenerative dementia: Lewy-related pathology

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

Neurologic symptoms are common during gestation and puerperium in CADASIL

Muscle paralysis and myosin loss in a patient with cancer cachexia

Molecular genetic and clinical findings in identical twins with CADASIL

Low TENS treatment on post-stroke paretic arm: a three-year follow-up

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