Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit? [electronic resource]
Producer: 20080805Description: 340-5 p. digitalISSN:- 1523-6838
- Arteriolosclerosis -- genetics
- Biopsy
- CADASIL -- complications
- Cell Proliferation
- DNA -- genetics
- DNA Mutational Analysis
- Follow-Up Studies
- Glomerulonephritis, IGA -- complications
- Humans
- Immunohistochemistry
- Juxtaglomerular Apparatus -- blood supply
- Magnetic Resonance Imaging
- Male
- Mesangial Cells -- ultrastructure
- Microscopy, Electron
- Middle Aged
- Muscle, Smooth, Vascular -- metabolism
- Mutation, Missense
- Receptor, Notch3
- Receptors, Notch -- genetics
- Renal Artery -- diagnostic imaging
- Renal Circulation
- Ultrasonography, Doppler
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Publication Type: Case Reports; Journal Article
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