Werner syndrome: a rare mutation.

Castagna, Alberto; Gareri, Pietro; Falvo, Francesca; Sestito, Simona; Rocca, Maurizio; Pensabene, Licia; Concolino, Daniela; Coppolino, Giuseppe; Ruotolo, Giovanni

Castagna, Alberto; Gareri, Pietro; Falvo, Francesca; Sestito, Simona; Rocca, Maurizio; Pensabene, Licia; Concolino, Daniela; Coppolino, Giuseppe; Ruotolo, Giovanni.

Afiliación

Castagna A; Center for Cognitive Disorders and Dementia, DSS Catanzaro Lido, ASP Catanzaro, Viale Crotone, 88100, Catanzaro, Italy.
Gareri P; Center for Cognitive Disorders and Dementia, DSS Catanzaro Lido, ASP Catanzaro, Viale Crotone, 88100, Catanzaro, Italy. pietro.gareri@alice.it.
Falvo F; Department of Pediatrics, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Sestito S; Department of Pediatrics, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Rocca M; Center for Cognitive Disorders and Dementia, DSS Catanzaro Lido, ASP Catanzaro, Viale Crotone, 88100, Catanzaro, Italy.
Pensabene L; Department of Pediatrics, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Concolino D; Department of Pediatrics, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Coppolino G; Nephrology and Dialysis Unit, "Pugliese-Ciaccio" Hospital of Catanzaro, Catanzaro, Italy.
Ruotolo G; SOC Geriatrics, Azienda Ospedaliera Pugliese-Ciaccio, Catanzaro, Italy.

Aging Clin Exp Res ; 31(3): 425-429, 2019 03.

Article en En | MEDLINE | ID: mdl-29876830

Palabras clave

Atherosclerosis; Diabetes mellitus; Hypercholesterolemia; Progeroid syndrome; Werner syndrome

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Aging Clin Exp Res Asunto de la revista: GERIATRIA Año: 2019 Tipo del documento: Article País de afiliación: Italia

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