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Does parkin play a role in the peripheral nervous system? A family reportABBRUZZESE, Giovanni; PIGULLO, Simona; AJMAR, Franco et al.Movement disorders. 2004, Vol 19, Num 8, pp 978-981, issn 0885-3185, 4 p.Article

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) geneLEE, Ming-Jen; STEPHENSON, Dennis A; AUER-GRUMBACH, Michaela et al.Human molecular genetics (Print). 2003, Vol 12, Num 15, pp 1917-1925, issn 0964-6906, 9 p.Article

The Refinement of the Critical Region for the 2q31.2q32.3 Deletion Syndrome Indicates Candidate Genes for Mental Retardation and Speech ImpairmentCOCCHELLA, Alessandro; MALACARNE, Michela; FORZANO, Francesca et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 7, pp 1342-1346, issn 1552-4841, 5 p.Article

Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathiesVENKEN, Koen; DI MARIA, Emilio; BELLONE, Emilia et al.Neurogenetics (Oxford. Print). 2002, Vol 4, Num 1, pp 37-41, issn 1364-6745Article

Essential tremor is not associated with α-synuclein gene haplotypesPIGULLO, Simona; DI MARIA, Emilio; AJMAR, Franco et al.Movement disorders. 2003, Vol 18, Num 7, pp 823-826, issn 0885-3185, 4 p.Article