Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Giulia Carignani"'
Autor:
Margherita Barbuti, Giulia Carignani, Francesco Weiss, Alba Calderone, Paola Fierabracci, Guido Salvetti, Giulia Menculini, Alfonso Tortorella, Ferruccio Santini, Giulio Perugi
Purpose subjects with obesity, especially those seeking bariatric surgery, exhibit high rates of mental disorders and marked psychopathological traits. The primary objective of this prospective, non-interventional study was to investigate whether the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb3fcf934decc9fdfc01c6ce97837d6b
https://hdl.handle.net/11391/1553347
https://hdl.handle.net/11391/1553347
Autor:
Guido Salvetti, Margherita Barbuti, A Calderone, Giulia Carignani, Giulio E. Brancati, Francesco Weiss, Giulio Perugi, Paola Fierabracci, Ferruccio Santini
Publikováno v:
Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity. 27:1021-1027
Purpose We aimed at investigating the lifetime prevalence of mood, eating and panic disorders in a large sample of obese patients referred to bariatric surgery. We also explored the patterns of psychiatric comorbidity and their relationship with Body
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d35a1b4647a215a57d4b3a3b4a3c7492
https://doi.org/10.1007/s40519-021-01236-y
https://doi.org/10.1007/s40519-021-01236-y
Autor:
Francesco Weiss, Ferruccio Santini, Giulia Carignani, Giulio Perugi, Margherita Barbuti, A Calderone
Publikováno v:
Journal of affective disorders. 279
Background Obese patients seeking bariatric surgery are known to show high rates of mental disorders, mainly mood and eating disorders. The aim of the present study is to evaluate psychiatric comorbidities, affective temperamental dimensions, emotion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d963e10493cf72b404606a80966f1f4
https://pubmed.ncbi.nlm.nih.gov/33038699
https://pubmed.ncbi.nlm.nih.gov/33038699
Autor:
Alessandra Rufa, Alessandra Renieri, Antonio Federico, Maria Antonietta Mencarelli, Francesca Mari, Giulia Carignani, Chiara Fallerini, Alessandro Rossi, Giorgio Capoccitti, Caterina Lo Rizzo, Fabio Giannini, Anna Maria Pinto
Publikováno v:
Journal of the Neurological Sciences. 359:409-417
Hereditary motor and sensory neuropathies (HMSN) are genetically heterogeneous disorders affecting peripheral motor and sensory functions. Many different pathogenic variants in several genes involved in the demyelinating, the axonal and the intermedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8be7cdc3243e72c094c2bef755e12db9
https://doi.org/10.1016/j.jns.2015.09.377
https://doi.org/10.1016/j.jns.2015.09.377
Autor:
Marina Vascotto, Margherita Baldassarri, Pietro Rubegni, Giulia Carignani, Francesca Mari, Ranuccio Nuti, Joussef Hayek, Alessandra Renieri, Joris Vermeesch, Elena Pretegiani, Carla Caffarelli, Livia Garavelli, Angelo Selicorni, Maria Teresa Dotti, Francesca Cristofoli, Chiara Di Marco, Paola Cianci, Salvatore Grosso, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Michele Fimiani, Paolo Balestri, Chiara Fallerini, Laura Dosa, Annabella Marozza, R. Vivarelli
Publikováno v:
Brain and Development. 37:527-536
Background Nicolaides–Baraitser and Coffin–Siris syndromes are emerging conditions with overlapping clinical features including intellectual disability and typical somatic characteristics, especially sparse hair, low frontal hairline, large mouth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b8bb8c1f9d61456f6b865e98446e95b
https://doi.org/10.1016/j.braindev.2014.08.009
https://doi.org/10.1016/j.braindev.2014.08.009
Autor:
Giulia Carignani, Maria Antonietta Mencarelli, Paolo Toti, Francesca Mari, Chiara Di Marco, Francesca Ariani, Daniela Galimberti, Annabella Marozza, Serena Somma, Theodora Hadjistilianou, Ilaria Meloni, Pietro Piu, Caterina Lo Rizzo, Sonia De Francesco, Valentina Imperatore, Sara Amitrano, Laura Dosa, Francesco Cetta, Alessandra Renieri
Publikováno v:
European Journal of Human Genetics. 23:1523-1530
In about 50% of sporadic cases of retinoblastoma, no constitutive RB1 mutations are detected by conventional methods. However, recent research suggests that, at least in some of these cases, there is somatic mosaicism with respect to RB1 normal and m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e0092d3365856b220ad8bb2e976100a
https://doi.org/10.1038/ejhg.2015.6
https://doi.org/10.1038/ejhg.2015.6
Autor:
Thomas Wieland, Guido M. Kukuk, Dagmar Wieczorek, Anne Dieux-Coeslier, Alessandra Renieri, Jessica Becker, Tim M. Strom, Julia K. Ehret, Beate Albrecht, Mohnish Suri, Kirsten Cremer, Alexander M. Zink, Joris Andrieux, Nicola Dennert, Giulia Carignani, Hermann-Josef Lüdecke, Hartmut Engels, Eva Wohlleber
Loss-of-function mutations and deletions of the SOX2 gene are known to cause uni- and bilateral anophthalmia and microphthalmia as well as related disorders such as anophthalmia-esophageal-genital syndrome. Thus, anophthalmia/microphthalmia is the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf500ee8c60fc5e84bac75fb8c83c663
http://hdl.handle.net/11365/1006634
http://hdl.handle.net/11365/1006634