Severe ocular involvement in hereditary gelsolin amyloidosis

Author:

da Silva Nisa Filipa Pinho,Beirão João Nuno Melo

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Biochemistry, Genetics and Molecular Biology

Reference9 articles.

1. Molecular mechanisms of amyloidosis;Merlini;N Engl J Med.,2003

2. Clinical aspects of systemic amyloid diseases;Obici;Biochim Biophys Acta.,2005

3. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome;Meretoja;Ann Clin Res.,1969

4. A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves;Andrade;Brain.,1952

5. Hereditary gelsolin amyloidosis;Kiuru-Enari;Handbook of Clinical Neurology.,2013

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