Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Laura Congiu"'
Autor:
P. Di Marco, Maria Flora Scusa, A Romanelli, Michele Zappella, P. Morescalchi, Laura Congiu, Giorgio Pini, Fabrizio Bianchi, Alessandra Ferlini, Alberto Benincasa, Stefania Bigoni, Daniela Tropea
Publikováno v:
Orphanet Journal of Rare Diseases
Background Rett Syndrome is a neurodevelopmental disorder almost exclusively affecting females, characterized by a broad clinical spectrum of signs and symptoms and a peculiar course. The disease affects different body systems: nervous, muscolo-skele
Autor:
Adam H Dyer, Laura Congiu, Kevin J. Mitchell, Giorgio Pini, Niall Mortimer, Alberto Benincasa, Seán O’Leary, Stefania Bigoni, Michael Gill, Daniela Tropea, Rachel McNamara, Pietro DiMarco, Andrea Della-Chiesa
Publikováno v:
Autism Research and Treatment, Vol 2016 (2016)
Autism Research and Treatment
Autism Research and Treatment
Rett Syndrome (RTT) is a severe neurodevelopmental disorder characterized by an apparently normal development followed by an arrest and subsequent regression of cognitive and psychomotor abilities. At present, RTT has no definitive cure and the treat
Autor:
Maria Flora Scusa, Stefano Stagi, Giorgio Pini, Laura Congiu, Loredana Cavalli, Bruno Rossi, Alberto Benincasa, Stefania Bigoni, Alessandra Ferlini
Introduction: Thyroid function in Rett syndrome (RTT) has rarely been studied with unanimous results. However, this aspect is of great concern regarding the effect thyroid hormones (TH) have on proper mammalian brain development. Objective: To evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d283eac39496a3d5620a6fed6261917
http://hdl.handle.net/11392/2332458
http://hdl.handle.net/11392/2332458
Repeated Insulin-Like Growth Factor 1 Treatment in a Patient with Rett Syndrome: A Single Case Study
Autor:
Ilaria Bottiglioni, Chetti Puccetti, Giorgio Pini, Michael Gill, M. Flora Scusa, Seán O’Leary, Laura Congiu, Cyrus Vadhatpour, Ilaria Gemo, Daniela Tropea, Rachel McNamara, Anna Maria Romanelli, Alberto Benincasa, Aiden Corvin
Publikováno v:
Frontiers in Pediatrics
Rett syndrome (RTT) is a devastating neurodevelopmental disorder that has no cure. Patients show regression of acquired skills, motor, and speech impairment, cardio-respiratory distress, microcephaly, and stereotyped hand movements. The majority of R
Autor:
Peter O.O. Julu, Lucia Billeci, Giovanni Pioggia, I. Gemo, E. Fonsa, P. Di Marco, Maria Flora Scusa, Laura Congiu, Giorgio Pini, Alessandro Tonacci
Publikováno v:
Autonomic Neuroscience. 192:83-84
Autor:
Laura Congiu, Ilaria Bottiglioni, Alberto Benincasa, Andrea Della-Chiesa, Paolina Morescalchi, Adriele Prina-Mello, Ubaldo Bonuccelli, Paolo Borelli, Pietro Di Marco, Giorgio Pini, Daniela Tropea, Maria Flora Scusa
Publikováno v:
Autism Research and Treatment
Hindawi Publishing Corporation
Autism Research and Treatment, Vol 2012 (2012)
Hindawi Publishing Corporation
Autism Research and Treatment, Vol 2012 (2012)
Rett syndrome (RTT) is a devastating neurodevelopmental disorder that affects one in ten thousand girls and has no cure. The majority of RTT patients display mutations in the gene that codes for the methyl-CpG-binding protein 2 (MeCP2). Clinical obse