Diffuse metabolic changes in the brain of patients with familial amyloid polyneuropathy. A proton MRSI study

Author:

Mazzeo Anna,Toscano Antonio,Stromillo Maria L.,Battaglini Marco,Messina Corrado,Federico Antonio,Vita Giuseppe,De Stefano Nicola

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference28 articles.

1. Hereditary and acquired amyloid neuropathies;Adams;J Neurol,2001

2. Type I familial amyloid polyneuropathy and pontine haemorrhage;Arpa Gutierrez;Acta Neuropathol (Berl),1993

3. Massive leptomeningeal amyloidosis associated with a Val30Met transthyretin gene;Herrick;Neurology,1996

4. Transthyretin amyloidosis (serine 44) with headache, hearing loss, and peripheral neuropathy;Klein;Neurology,1998

5. Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD 18G);Vidal;Am J Pathol,1996

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