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Paolo Aridon

Researcher at University of Palermo

Publications -  81
Citations -  3873

Paolo Aridon is an academic researcher from University of Palermo. The author has contributed to research in topics: Population & Medicine. The author has an hindex of 30, co-authored 74 publications receiving 3550 citations. Previous affiliations of Paolo Aridon include Vita-Salute San Raffaele University.

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Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.

TL;DR: Results show that mutations in the gene ATP1A2 that encodes the α2 subunit of the Na+/K+ pump are associated with familial hemiplegic migraine type 2 (FHM2) linked to chromosome 1q23 (OMIM 602481).
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Autosomal dominant restless legs syndrome maps on chromosome 14q.

TL;DR: Significant evidence is shown of linkage to a new locus for RLS on chromosome 14q13-21 region in a 30-member, three-generation Italian family affected by RLS and periodic leg movements in sleep (PLMS), the second RLS locus identified so far and the first consistent with an autosomal dominant inheritance pattern.
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Risk of Parkinson disease in women: Effect of reproductive characteristics

TL;DR: An association between factors reducing estrogen stimulation during life and PD was found, and the hypothesis that endogenous estrogens play a role in the development of PD is supported.
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Autosomal recessive Rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp : Delineation of the syndrome and gene mapping to chromosome 16p12-11.2

TL;DR: It is shown that idiopathic focal disorders such as epilepsy and dystonia, can be caused by the same genetic abnormality, may have a transient expression, and may be inherited as an autosomal recessive trait.