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Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASIL.
- Published in:
- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0844-x
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- Publication type:
- Article
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1.
- Published in:
- 2017
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- Publication type:
- letter
Gelsolin amyloid angiopathy causes severe disruption of the arterial wall.
- Published in:
- APMIS, 2016, v. 124, n. 8, p. 639, doi. 10.1111/apm.12554
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- Publication type:
- Article
Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases.
- Published in:
- Neuropathology & Applied Neurobiology, 2016, v. 42, n. 2, p. 194, doi. 10.1111/nan.12248
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- Publication type:
- Article
Autophagy in neuropathology.
- Published in:
- 2015
- By:
- Publication type:
- Editorial
X-linked myopathy with excessive autophagy: a failure of self-eating.
- Published in:
- Acta Neuropathologica, 2015, v. 129, n. 3, p. 383, doi. 10.1007/s00401-015-1393-4
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- Publication type:
- Article
CADASIL and CARASIL.
- Published in:
- Brain Pathology, 2014, v. 24, p. 525, doi. 10.1111/bpa.12181
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- Publication type:
- Article
CADASIL and CARASIL.
- Published in:
- 2014
- By:
- Publication type:
- Other
Regeneration of injured skeletal muscle after the injury.
- Published in:
- Muscles, Ligaments & Tendons Journal (MLTJ), 2013, v. 3, n. 4, p. 337
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- Publication type:
- Article
Quantitative Vascular Pathology and Phenotyping Familial and Sporadic Cerebral Small Vessel Diseases.
- Published in:
- Brain Pathology, 2013, v. 23, n. 5, p. 547, doi. 10.1111/bpa.12041
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- Publication type:
- Article
Monoclonal antibodies selective for α-synuclein oligomers/protofibrils recognize brain pathology in Lewy body disorders and α-synuclein transgenic mice with the disease-causing A30P mutation.
- Published in:
- Journal of Neurochemistry, 2013, v. 126, n. 1, p. 131, doi. 10.1111/jnc.12175
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- Publication type:
- Article
Polymorphonuclear neutrophil infiltration into ischemic infarctions: myth or truth?
- Published in:
- 2013
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- Publication type:
- Editorial
VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 439, doi. 10.1007/s00401-012-1073-6
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- Publication type:
- Article
CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cells.
- Published in:
- Journal of Cerebral Blood Flow & Metabolism, 2012, v. 32, n. 12, p. 2171, doi. 10.1038/jcbfm.2012.123
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- Publication type:
- Article
Prolonged Myalgia in Sindbis Virus Infection: Case Description and In Vitro Infection of Myotubes and Myoblasts.
- Published in:
- Journal of Infectious Diseases, 2012, v. 206, n. 3, p. 407, doi. 10.1093/infdis/jis358
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- Publication type:
- Article
APOE and AβPP Gene Variation in Cortical and Cerebrovascular Amyloid-β Pathology and Alzheimer's Disease: A Population-Based Analysis.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 26, n. 2, p. 377, doi. 10.3233/JAD-2011-102049
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- Publication type:
- Article
Cerebral amyloid angiopathy, neurodegeneration, and dementia in a population-based study on the very elderly Finns (Vantaa 85+)
- Published in:
- 2010
- By:
- Publication type:
- Abstract
α-Synuclein pathology in the spinal cord autonomic nuclei associates with α-synuclein pathology in the brain: a population-based Vantaa 85+ study.
- Published in:
- Acta Neuropathologica, 2010, v. 119, n. 6, p. 715, doi. 10.1007/s00401-009-0629-6
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- Publication type:
- Article
Bedside diagnosis of rippling muscle disease in CAV3 p.A46T mutation carriers.
- Published in:
- Muscle & Nerve, 2010, v. 41, n. 6, p. 751, doi. 10.1002/mus.21589
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- Publication type:
- Article
Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.
- Published in:
- Acta Neuropathologica, 2010, v. 119, n. 4, p. 465, doi. 10.1007/s00401-010-0637-6
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- Publication type:
- Article
Pyroglutamate Abeta pathology in APP/PS1KI mice, sporadic and familial Alzheimer’s disease cases.
- Published in:
- Journal of Neural Transmission, 2010, v. 117, n. 1, p. 85, doi. 10.1007/s00702-009-0314-x
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- Publication type:
- Article
Neuropathologic Findings of Dementia with Lewy Bodies (DLB) in a Population-based Vantaa 85+ Study.
- Published in:
- Journal of Alzheimer's Disease, 2009, v. 18, n. 3, p. 677, doi. 10.3233/JAD-2009-1169
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- Publication type:
- Article
Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.
- Published in:
- Brain: A Journal of Neurology, 2009, v. 132, n. 4, p. 933, doi. 10.1093/brain/awn364
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- Publication type:
- Article
Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.
- Published in:
- Neurogenetics, 2009, v. 10, n. 1, p. 27, doi. 10.1007/s10048-008-0155-z
- By:
- Publication type:
- Article
Absence of polysialylated NCAM is an unfavorable prognostic phenotype for advanced stage neuroblastoma.
- Published in:
- BMC Cancer, 2009, v. 9, p. 1, doi. 10.1186/1471-2407-9-57
- By:
- Publication type:
- Article
Heparan Sulfate Accumulation with Aβ Deposits in Alzheimer's Disease and Tg2576 Mice is Contributed by Glial Cells.
- Published in:
- Brain Pathology, 2008, v. 18, n. 4, p. 548, doi. 10.1111/j.1750-3639.2008.00152.x
- By:
- Publication type:
- Article
Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Neurofibrillary tau pathology modulated by genetic variation of α -synuclein.
- Published in:
- Annals of Neurology, 2008, v. 64, n. 3, p. 348, doi. 10.1002/ana.21446
- By:
- Publication type:
- Article
P1-097: The arctic Alzheimer mutation alters structure and composition of Aβ deposits
- Published in:
- 2008
- By:
- Publication type:
- Abstract
P2-033: Pet amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease
- Published in:
- 2008
- By:
- Publication type:
- Abstract
P3-416: Aβ stimulation leads to elevated levels of heparan sulfate proteoglycans in glial cells
- Published in:
- 2008
- By:
- Publication type:
- Abstract
Distal myopathy caused by homozygous missense mutations in the nebulin gene.
- Published in:
- Brain: A Journal of Neurology, 2007, v. 130, n. 6, p. 1465, doi. 10.1093/brain/awm094
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- Publication type:
- Article
Genetically distinct astrocytic and oligodendroglial components in oligoastrocytomas.
- Published in:
- Acta Neuropathologica, 2007, v. 113, n. 2, p. 129, doi. 10.1007/s00401-006-0142-0
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- Publication type:
- Article
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
- Published in:
- 2006
- By:
- Publication type:
- Correction notice
P1-038: Immunohistochemical and biochemical analyses of Aβ deposits in Tg-APP-ArcSwe and Tg-APP-Swe transgenic mouse brain
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P2-273: PET-imaging of amyloid depositions and astrocytosis in severe ad and histopathological correlations in one patient
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-150: Frontotemporal dementia and parkinsonism: A new phenotype of the tau S305S mutation
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-038: Immunohistochemical and biochemical analyses of Aβ deposits in Tg-APP-ArcSwe and Tg-APP-Swe transgenic mouse brain
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P2-273: PET-imaging of amyloid depositions and astrocytosis in severe ad and histopathological correlations in one patient
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-150: Frontotemporal dementia and parkinsonism: A new phenotype of the tau S305S mutation
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
- Published in:
- Neurogenetics, 2006, v. 7, n. 3, p. 185, doi. 10.1007/s10048-006-0049-x
- By:
- Publication type:
- Article
Chromogenic in situ hybridization-detected hotspot MYCN amplification associates with Ki-67 expression and inversely with nestin expression in neuroblastomas.
- Published in:
- 2005
- By:
- Publication type:
- journal article
The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperone.
- Published in:
- Nature Genetics, 2005, v. 37, n. 12, p. 1309, doi. 10.1038/ng1677
- By:
- Publication type:
- Article
Meconium aspiration induces neuronal injury in piglets.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Muscle Injuries: Biology and Treatment.
- Published in:
- American Journal of Sports Medicine, 2005, v. 33, n. 5, p. 745, doi. 10.1177/0363546505274714
- By:
- Publication type:
- Article
Mild eccentric stretch injury in skeletal muscle causes transient effects on tensile load and cell proliferation.
- Published in:
- Scandinavian Journal of Medicine & Science in Sports, 2004, v. 14, n. 6, p. 367, doi. 10.1111/j.1600-0838.2004.403.x
- By:
- Publication type:
- Article
Fibrosis and Stenosis of the Long Penetrating Cerebral Arteries: the Cause of the White Matter Pathology in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
- Published in:
- Brain Pathology, 2004, v. 14, n. 4, p. 358, doi. 10.1111/j.1750-3639.2004.tb00078.x
- By:
- Publication type:
- Article
Detection of the founder effect in Finnish CADASIL families.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 813, doi. 10.1038/sj.ejhg.5201221
- By:
- Publication type:
- Article
Low expression of p27 indicates a poor prognosis in patients with high-grade astrocytomas.
- Published in:
- Cancer (0008543X), 2003, v. 97, n. 3, p. 644, doi. 10.1002/cncr.11079
- By:
- Publication type:
- Article
Metabolic characterization of childhood brain tumors.
- Published in:
- Cancer (0008543X), 2002, v. 95, n. 6, p. 1376, doi. 10.1002/cncr.10798
- By:
- Publication type:
- Article