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Dokumententyp
Institution
Spezialsammlung
Sprache
- Englisch (1)
Autor
-
Devys, D. (1)
- Haller, S. (1)
- Haufschild, T. (1)
- Lyrer, P. (1)
- Mihatsch, M. (1)
- Probst, A. (1)
- Steck, A. (1)
- Tolnay, M. (1)
- Willi, N. (1)
- Winkler, D. (1)
Schlagwort
- ADAMTS : a disintegrin-like and metalloproteinase with thrombospondin motifs (1)
- CADASIL (1)
- CADASIL : cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (1)
- CARASIL : cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (1)
- CRV (1)
- CRV : cerebroretinal vasculopathy (1)
- HERNS (1)
- HERNS : hereditary endotheliopathy with retinopathy, nephropathy, and stroke (1)
- HIHRTL : hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy (1)
- HSA : hereditary systemic angiopathy (1)
- HVR (1)
- MELAS : mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (1)
- angiopathy (1)
- cerebral calcification (1)
- small vessel disease (1)
- vWF : von Willebrand factor (1)
- vasculopathy (1) Mehr Weniger