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HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients

✍ Scribed by Simona Capponi; Alessandro Geroldi; Paola Fossa; Marina Grandis; Paola Ciotti; Rossella Gulli; Angelo Schenone; Paola Mandich; Emilia Bellone


Book ID
109116418
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
551 KB
Volume
16
Category
Article
ISSN
1085-9489

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Apoptosis in CADASIL: An in vitro study
✍ Patrizia Formichi; Elena Radi; Carla Battisti; Giuseppe Di Maio; Ermelinda Tarqu πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 500 KB

## Abstract Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary disease affecting vascular smooth muscle cells of nearly all tissues. Clinical manifestations mainly concern the central nervous system with repeated TIA/stroke, migraine