Cincinnato Baruzzi

Recent publications · Crossref

5 total works indexed

1. Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene

   · 1992 · cited 469x

2. Fatal Familial Insomnia and Dysautonomia with Selective Degeneration of Thalamic Nuclei

   · 1986 · cited 469x

3. Melanopsin retinal ganglion cell loss in <scp>A</scp>lzheimer disease

   · 2015 · cited 356x

4. <i>FBXO7</i> mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome

   · 2009 · cited 313x

5. Skin nerve α-synuclein deposits

   · 2014 · cited 270x

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