Gaming Technology for Pediatric Neurorehabilitation: A Systematic Review

Autor: Marco Iosa, Cristiano Maria Verrelli, Amalia Egle Gentile, Martino Ruggieri, Agata Polizzi

Publikováno v: Frontiers in Pediatrics, Vol 10 (2022)

IntroductionThe emergence of gaming technologies, such as videogames and virtual reality, provides a wide variety of possibilities in intensively and enjoyably performing rehabilitation for children with neurological disorders. Solid evidence-based r

Externí odkaz: https://doaj.org/article/fd4901817d7f4dfeaebd95b0ab8912f3

Neurocutaneous syndromes in art and antiquities

Autor: Massimo Papi, Agata Polizzi, Domenica Taruscio, Amalia Egle Gentile, Albert Mudry, Martino Ruggieri, Vincenza Ferrara, Giuseppe Micali, Andrea D. Praticò

Publikováno v: American Journal of Medical Genetics. Part C, Seminars in Medical Genetics

Neurocutaneous syndromes are a group of genetic disorders affecting the skin, the central and peripheral nervous system, and the eye with congenital abnormalities and/or tumors. Manifestations may also involve the heart, vessels, lungs, kidneys, endo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e5adc6096a39a7b72be914920e67e18
https://doi.org/10.1002/ajmg.c.31917

Health Systems Sustainability and Rare Diseases

Autor: Rita Maria, Ferrelli, Marta, De Santis, Amalia, Egle Gentile, Domenica, Taruscio

Publikováno v: Advances in experimental medicine and biology. 1031

The paper is addressing aspects of health system sustainability for rare diseases in relation to the current economic crisis and equity concerns. It takes into account the results of the narrative review carried out in the framework of the Joint Acti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f6a4617b5d2ea1cdb232dc052a66252e
https://pubmed.ncbi.nlm.nih.gov/29214595

EUROPLAN: A Project to Support the Development of National Plans on Rare Diseases in Europe

Autor: L. Fregonese, Valentina Bottarelli, M. Posada de la Paz, Amalia Egle Gentile, Ariane Weinman, M. De Santis, C Donati, Rumen Stefanov, Kate Bushby, Y Le Cam, E Jessop, Pierpaolo Mincarone, J. Huizer, Luciano Vittozzi, Manuel Hens, Rosa Giuseppa Frazzica, Rita Maria Ferrelli, Désirée Gavhed, Domenica Taruscio

Publikováno v: Public health genomics (Online) 16 (2013): 278–287. doi:10.1159/000355932
info:cnr-pdr/source/autori:Taruscio, D [ 1 ] ; Gentile, AE [ 1 ] ; De Santis, M [ 1 ] ; Ferrelli, RM [ 2 ] ; de la Paz, MP [ 4 ] ; Hens, M [ 4 ] ; Huizer, J [ 5 ] ; Fregonese, L [ 5 ] ; Stefanov, R [ 6 ] ; Bottarelli, V [ 7 ] ; Weinman, A [ 7 ] ; Le Cam, Y [ 7 ] ; Gavhed, D [ 8 ] ; Mincarone, P [ 3 ] ; Bushby, K [ 9 ] ; Frazzica, RG [ 1 ] ; Donati, C [ 1 ] ; Vittozzi, L [ 1 ] ; Jessop, E [ 10/titolo:EUROPLAN: a project to support the development of national plans on rare diseases in Europe./doi:10.1159%2F000355932/rivista:Public health genomics (Online)/anno:2013/pagina_da:278/pagina_a:287/intervallo_pagine:278–287/volume:16

Background/Aims: National Plans for Rare Diseases (RDs) are the common denominator of current public health policy concerns on RDs across the EU. With the aim of a better distribution of the available resources, they conjugate the European objective

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a007372d83cd21f1ac8bb1829368d22b
https://doi.org/10.1159/000355932

National Plans on Rare Diseases

Autor: Rumen Stefanov, Georgi Iskrov, Marta De Santis, Domenica Taruscio, Rosa Giuseppa Frazzica, Rita Maria Ferrelli, Amalia Egle Gentile

Publikováno v: Rare Diseases ISBN: 9789401792134

This paper aims to describe the state-of-the-art of national plans for rare diseases (RD) in EU Member States, pointing out common as well as country-specific features and approaches. It critically assesses the national achievements in this field, dr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d6947339d3ed0fffc5f244b83306f8ae
https://doi.org/10.1007/978-94-017-9214-1_1