Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Elena, Inzaghi"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 5, Pp n/a-n/a (2021)
ABSTRACT Background Dubowitz syndrome (DS) is a complex and rare condition characterized by postnatal growth retardation, microcephaly, short stature, mild developmental delay, facial dysmorphism, skin eruption and bone marrow failure. Though approxi
Externí odkaz:
https://doaj.org/article/6c00021b4c3342328947ba83e2fe086c
Autor:
Elena Inzaghi, Anna Kistner, Daniela Germani, Annalisa Deodati, Mireille Vanpee, Lena Legnevall, Katarina Berinder, Stefano Cianfarani
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0228075 (2020)
OBJECTIVE:microRNAs (miRNAs) associated with metabolic risk have never been extensively investigated in SGA subjects. The aim of the current study was to evaluate miRNAs in SGA and AGA subjects and their relationships with the metabolic status and gr
Externí odkaz:
https://doaj.org/article/42990f57a99e48b1850338191304cf8f
Publikováno v:
Frontiers in Genetics, Vol 10 (2020)
Epidemiological evidence has shown an association between prenatal malnutrition and a higher risk of developing metabolic disease in adult life. An inadequate intrauterine milieu affects both growth and development, leading to a permanent programming
Externí odkaz:
https://doaj.org/article/c15b314f2fa8435290e7fae5a0358c57
Publikováno v:
Hormone Research in Paediatrics. :1-7
Background: Daily recombinant human growth hormone (rhGH) is approved and marketed worldwide to treat children and adults with GH deficiency and other conditions. Efficacy of rhGH therapy is influenced by several variables. Drop of treatment adherenc
Autor:
Giorgia Catino, Marco Cappa, E. Sallicandro, Sara Loddo, Stefano Cianfarani, Annalisa Deodati, Mafalda Mucciolo, Antonio Novelli, F. Verdecchia, Elena Inzaghi
Publikováno v:
Journal of Endocrinological Investigation. 45:79-87
Multiple factors influence intrauterine growth and lead to low birth sizes. The impact of genetic alterations on both pre- and post-natal growth is still largely unknown. The aim of this study was to investigate the prevalence of CNVs in an Italian c
Publikováno v:
Yearbook of Paediatric Endocrinology.
Background: Children with 17p13.3 microdeletions including the YWHAE gene show intrauterine growth restriction, craniofacial dysmorphisms, postnatal growth failure, and cognitive impairment. This region is characterized by genomic instability and has
Publikováno v:
Yearbook of Paediatric Endocrinology.
Autor:
Stefania Pedicelli, Danilo Fintini, Lucilla Ravà, Elena Inzaghi, Annalisa Deodati, Maria Rita Spreghini, Carla Bizzarri, Michela Mariani, Stefano Cianfarani, Marco Cappa, Melania Manco
To evaluate prevalence of prediabetes (impaired fasting glucose, IFG; impaired glucose tolerance, IGT; and high glycated haemoglobin, h-HbA1c) in children and adolescents in relation to class of age and obesity; to appraise association with estimates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b666edb8f02ef9eae9c1276de309b5f8
http://hdl.handle.net/2108/294801
http://hdl.handle.net/2108/294801
Autor:
Manuela Caruso Nicoletti, Luisa De Sanctis, Anna Grandone, Alessandra Cassio, Carla Bizzarri, Flavia Barbieri, Elena Inzaghi
Publikováno v:
Minerva Pediatrics. 73
Puberty represents a milestone during a person's life and is characterized by several physical and psychological changes which end with the achievement of sexual maturation and of fertility. Puberty onset depends on a series of sophisticated, not com