Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Giuseppa Patti"'
Autor:
Margherita Squillario, Carola Bonaretti, Alberto La Valle, Eddi Di Marco, Gianluca Piccolo, Nicola Minuto, Giuseppa Patti, Flavia Napoli, Marta Bassi, Mohamad Maghnie, Giuseppe d’Annunzio, Roberto Biassoni
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-16 (2023)
Abstract The fecal microbiome of 55 obese children and adolescents (BMI-SDS 3.2 ± 0.7) and of 25 normal-weight subjects, matched both for age and sex (BMI-SDS − 0.3 ± 1.1) was analysed. Streptococcus, Acidaminococcus, Sutterella, Prevotella, Sutt
Externí odkaz:
https://doaj.org/article/56e79b6431c44361bfe8e18dc2680329
Autor:
Marco Salvatore, Paola Torreri, Graziano Grugni, Adele Rocchetti, Mohamad Maghnie, Giuseppa Patti, Antonino Crinò, Maurizio Elia, Donatella Greco, Corrado Romano, Adriana Franzese, Enza Mozzillo, Annamaria Colao, Gabriella Pugliese, Uberto Pagotto, Valentina Lo Preiato, Emanuela Scarano, Concetta Schiavariello, Gianluca Tornese, Danilo Fintini, Sarah Bocchini, Sara Osimani, Luisa De Sanctis, Michele Sacco, Irene Rutigliano, Maurizio Delvecchio, Maria Felicia Faienza, Malgorzata Wasniewska, Domenico Corica, Stefano Stagi, Laura Guazzarotti, Pietro Maffei, Francesca Dassie, Domenica Taruscio
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-9 (2023)
Abstract Background Prader–Willi syndrome (PWS) is a rare and complex genetic disease, with numerous implications on metabolic, endocrine, neuropsychomotor systems, and with behavioural and intellectual disorders. Rare disease patient registries ar
Externí odkaz:
https://doaj.org/article/e788ecaab80a41e2a602680820cf9f57
Autor:
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, Giulia Rosti, Maria Teresa Divizia, Tiziana Camia, Elena Lucia De Rose, Alice Zucconi, Emilio Casalini, Flavia Napoli, Natascia Di Iorgi, Mohamad Maghnie
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundNoonan syndrome (NS) is a genetic multisystem disorder characterised by variable clinical manifestations including dysmorphic facial features, short stature, congenital heart disease, renal anomalies, lymphatic malformations, chest deformit
Externí odkaz:
https://doaj.org/article/72330c4209af431b938af2d047b796b9
Autor:
Giuseppa Patti, Federica Malerba, Maria Grazia Calevo, Maurizio Schiavone, Marco Scaglione, Emilio Casalini, Silvia Russo, Daniela Fava, Marta Bassi, Flavia Napoli, Anna Elsa Maria Allegri, Giuseppe D’Annunzio, Roberto Gastaldi, Mohamad Maghnie, Natascia Di Iorgi
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/2157d110a282474c99eb73597a384b3f
Autor:
Gianluca Piccolo, Elena Lucia De Rose, Marta Bassi, Flavia Napoli, Nicola Minuto, Mohamad Maghnie, Giuseppa Patti, Giuseppe d’Annunzio
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Diabetes mellitus (DM) has been frequently associated with an impaired immune response against infectious agents, making affected patients at risk for more severe disease and sometimes causing worse outcomes. The recent COVID-19 pandemic has seriousl
Externí odkaz:
https://doaj.org/article/b34aa4667c834b65a668dedb93969b28
Autor:
Giuseppa Patti, Federica Malerba, Maria Grazia Calevo, Maurizio Schiavone, Marco Scaglione, Emilio Casalini, Silvia Russo, Daniela Fava, Marta Bassi, Flavia Napoli, Anna Elsa Maria Allegri, Giuseppe D’Annunzio, Roberto Gastaldi, Mohamad Maghnie, Natascia Di Iorgi
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ContextData on pubertal timing in Silver Russell syndrome (SRS) are limited.Design and methodsRetrospective observational study including twenty-three SRS patients [11p15 loss of methylation, (11p15 LOM, n=10) and maternal uniparental disomy of chrom
Externí odkaz:
https://doaj.org/article/6d3d40a3253d447497bb22f2eb81f286
Autor:
Anastasia Ibba, Francesca Corrias, Chiara Guzzetti, Letizia Casula, Mariacarolina Salerno, Natascia di Iorgi, Gianluca Tornese, Giuseppa Patti, Giorgio Radetti, Mohamad Maghnie, Marco Cappa, Sandro Loche
Publikováno v:
Endocrine Connections, Vol 9, Iss 11, Pp 1095-1102 (2020)
A number of studies have evaluated the role of IGF1 measurement in the diagnosis of growth hormone deficiency (GHD). This study aimed to evaluate th e accuracy and the best cut-off of IGF1 SDS in the diagnosis of GHD in a large coho rt of short child
Externí odkaz:
https://doaj.org/article/ac589648cd4c4896ad163f78e3a612fa
Autor:
Annachiara Libraro, Vito D’Ascanio, Marco Cappa, Mariangela Chiarito, Maria Cristina Digilio, Silvia Einaudi, Anna Grandone, Mohamad Maghnie, Laura Mazzanti, Alessandro Mussa, Giuseppa Patti, Emanuela Scarano, Antonietta Spinuzza, Silvia Vannelli, Malgorzata Gabriela Wasniewska, Giovanni Battista Ferrero, Maria Felicia Faienza
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
ObjectivesGrowth impairment is a common manifestation in Noonan syndrome (NS). Recombinant human GH (rhGH) treatment has been shown to increase growth and adult height (AH) in a few studies. We aimed to evaluate the growth trajectory towards the AH,
Externí odkaz:
https://doaj.org/article/db32319567be40a49ba047ac6fda8813
Autor:
Gianluca Tornese, Giuseppa Patti, Maria Chiara Pellegrin, Paola Costa, Flavio Faletra, Elena Faleschini, Egidio Barbi
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-4 (2020)
Abstract Background Growth failure and growth hormone deficiency (GHD) have been reported as one accessory feature of GLUT1 deficiency syndrome (GLUT1DS), considered so far as a long-term adverse effects of ketogenic diet which is used to treat this
Externí odkaz:
https://doaj.org/article/4f45439989f5461db3b37b9a00fdc03e
Autor:
Giuseppa Patti, Erika Calandra, Annamaria De Bellis, Annalisa Gallizia, Marco Crocco, Flavia Napoli, Anna Maria Elsa Allegri, Hanan F. Thiabat, Giuseppe Bellastella, Maria Ida Maiorino, Maria Luisa Garrè, Stefano Parodi, Mohamad Maghnie, Natascia di Iorgi
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Purpose: To detect the presence of antipituitary (APA) and antihypothalamus antibodies (AHA) in subjects treated for brain cancers, and to evaluate their potential association with pituitary dysfunction.Methods: We evaluated 63 patients with cranioph
Externí odkaz:
https://doaj.org/article/649ffdc08bf7471cabc8ef489c82a4bc