A new mutation in ABCC8 gene discoverd in an infant with congenital hyperinsulinism

Autor: DiCandia S., Bosio L., Proverbio MC, Zamproni I., Mora S., Valin PS, Bove M, Grechi E., Biagiotti L., Biunno I., Patricelli MG., Chiumello G

Publikováno v: Hormone research (2007).
info:cnr-pdr/source/autori:DiCandia S., Bosio L., Proverbio MC, Zamproni I., Mora S., Valin PS, Bove M, Grechi E., Biagiotti L., Biunno I., Patricelli MG., Chiumello G/titolo:A new mutation in ABCC8 gene discoverd in an infant with congenital hyperinsulinism/doi:/rivista:Hormone research/anno:2007/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::65c59591f9ee2bd84299c7c21b9e5030
http://www.cnr.it/prodotto/i/55914

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A Psycho-Oncological Rehabilitation intervention: the pathway of CeRiOn (Centre for Oncological Rehabilitation) and preliminary results of efficacy, Florence 2007–2010

Autor: Giovanna, Franchi, Grechi, E., Maruelli, A., Francesco, Bulli, Grazia, Muraca Maria, Miccinesi, G.

Publikováno v: In European Journal of Integrative Medicine September 2012 4 Supplement 1:23-23

Prader-Willi Syndrome: Clinical Aspects

Autor: Grechi Elena, Cammarata Bruna, Mariani Benedetta, Di Candia Stefania, Chiumello Giuseppe

Publikováno v: Journal of Obesity, Vol 2012 (2012)

Prader-Willi Syndrome (PWS) is a complex multisystem genetic disorder that shows great variability, with changing clinical features during a patient’s life. The syndrome is due to the loss of expression of several genes encoded on the proximal long

Externí odkaz: https://doaj.org/article/2bb4dc9ad2dc462a84b89f2d187c73b6

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