Affiner les résultats
Type de document
Institution
Collection spécifique
Langue
- Anglais (1)
Auteur
- 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)
Mot clé
- 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) Plus Moins