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Type de document
Institution
Collection spécifique
Langue
- Anglais (3)
Auteur
- Accarino, Anna (1)
- Bakker, Jaap A. (1)
- Barba, Pere (1)
- Beguin, Yves (1)
- Benoist, J.F. (1)
- Boelens, Jaap J. (1)
- Brekenfeld, C. (1)
- Burgunder, J.M. (1)
- Casali, Carlo (1)
- Chinnery, Patrick F. (1)
- Collin, Matthew (1)
- Devys, D. (1)
- Dotti, Maria T. (1)
- Elhasid, Ronit (1)
- Fay, Keith (1)
- Ferra, Christelle (1)
- Filosto, Massimiliano (1)
- Gallati, S. (1)
- Gratwohl, Alois (1)
- Haller, S. (1)
- Halter, Joerg P. (1)
- Hammans, Simon R. (1)
- Haufschild, T. (1)
- Hirano, Michio (1)
- Illa, Isabel (1)
- Kappeler, L. (1)
- Lyrer, P. (1)
- Mandel, Hanna (1)
- Marotta, Giuseppe (1)
- Martí, Ramon (1) Plus Moins
Mot clé
- thymidine phosphorylase (2)
- 1070 (1)
- 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)
- Original Articles (1)
- allogeneic haematopoietic stem cell transplantation (1)
- angiopathy (1)
- cerebral calcification (1)
- magnetic resonance spectroscopy (1)
- mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) (1)
- mitochondrial neurogastrointestinal encephalomyopathy MNGIE (1)
- outcome (1)
- risk factors (1)
- small vessel disease (1)
- vWF : von Willebrand factor (1)
- vasculopathy (1) Plus Moins