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Brain Pathology, ISSN 1015-6305, 07/2018, Volume 28, Issue 4, pp. 495 - 506
Hereditary cerebral hemorrhage with amyloidosis‐Dutch type (HCHWA‐D) is an early onset hereditary form of cerebral amyloid angiopathy (CAA) pathology, caused... 
TGFβ | amyloid β mutation E22Q | postmortem human brain tissue | cerebral amyloid angiopathy | phospho‐SMAD2/3 granules | hereditary cerebral hemorrhage with amyloidosis‐Dutch type | hereditary cerebral hemorrhage with amyloidosis-Dutch type | phospho-SMAD2/3 granules | phospho-SMAD2 | SMALL VESSEL DISEASE | PROTEIN | ALZHEIMERS-DISEASE | PATHOLOGY | NEUROSCIENCES | COLOCALIZES | CLINICAL NEUROLOGY | amyloid beta mutation E22Q | 3 granules | MICROVASCULAR DEGENERATION | TRANSFORMING GROWTH-FACTOR-BETA-1 | ANGIOPATHY | TGF beta | EXPRESSION | TRANSGENIC MICE | TGF-BETA-1 | Up-Regulation | Phosphorylation | Frontal Lobe - metabolism | Signal Transduction | Humans | Middle Aged | Smad2 Protein - metabolism | Cerebral Amyloid Angiopathy, Familial - metabolism | Cerebral Amyloid Angiopathy, Familial - pathology | Male | Smad3 Protein - metabolism | Occipital Lobe - pathology | Occipital Lobe - blood supply | Aged, 80 and over | Female | Aged | Frontal Lobe - blood supply | Transforming Growth Factor beta - metabolism | Frontal Lobe - pathology | Occipital Lobe - metabolism | Immunohistochemistry | Brain | Deregulation | Pathogenesis | Transforming growth factor-a | Transgenic mice | Blood vessels | Gene expression | Hemorrhage | Lobes | Pathology | Cerebral amyloid angiopathy | Autopsy | Smad2 protein | Fibrosis | Biomarkers | β-Amyloid | Amyloidosis | Microvasculature | Occipital lobes
Journal Article
Epilepsy Research, ISSN 0920-1211, 2014, Volume 108, Issue 10, pp. 1694 - 1704
Journal Article
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