Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit?

Guerrot, Dominique

Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit? [electronic resource] - American journal of kidney diseases : the official journal of the National Kidney Foundation Aug 2008 - 340-5 p. digital

Publication Type: Case Reports; Journal Article

1523-6838

10.1053/j.ajkd.2008.04.017 doi


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