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pro vyhledávání: '"Ilaria Bettocchi"'
Akademický článek
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Autor:
alberto burlina, Ilaria Bettocchi, Giacomo Biasucci, Andrea Bordugo, Serena Gasperini, Luisa La Spina, Evelina Maines, Concetta Meli, Francesca Menni, Sabrina Paci, Elena Procopio, Alessandro Rossi, Laura Rubert, Marco Spada, Flavia Tubili, Albina Tummolo
Publikováno v:
SSRN Electronic Journal.
Autor:
Valentina, Papa, Nunzio Cosimo Mario, Salfi, Roberta, Costa, Ilaria, Bettocchi, Emilia, Ricci, Duccio Maria, Cordelli, Francesca, Locatelli, Fabio, Caramelli, Giovanna, Cenacchi
Publikováno v:
Advances in experimental medicine and biology. 1369
TORCH (Toxoplasmosis, Rubella, Cytomegalovirus, Herpes Simplex Virus and Syphilis) infections are a major cause of intrauterine and perinatal infections with associated morbidity and mortality. Neonatal Herpes Simplex Virus infection caused by an env
Autor:
Valentina Papa, Nunzio Cosimo Mario Salfi, Roberta Costa, Ilaria Bettocchi, Emilia Ricci, Duccio Maria Cordelli, Francesca Locatelli, Fabio Caramelli, Giovanna Cenacchi
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783031019944
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e169f3aa53aef512fa9078ce5b400a4
https://doi.org/10.1007/5584_2021_688
https://doi.org/10.1007/5584_2021_688
Autor:
Emilia Ricci, Roberta Costa, Nunzio Salfi, Ilaria Bettocchi, Giovanna Cenacchi, Duccio Maria Cordelli, Fabio Caramelli, Francesca Locatelli, Valentina Papa
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783031019944
TORCH (Toxoplasmosis, Rubella, Cytomegalovirus, Herpes Simplex Virus and Syphilis) infections are a major cause of intrauterine and perinatal infections with associated morbidity and mortality. Neonatal Herpes Simplex Virus infection caused by an env
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b31a1e5178289dd62b6a1ed33cfe25b
https://doi.org/10.1007/5584_2021_659
https://doi.org/10.1007/5584_2021_659
Autor:
Ilaria Bettocchi, Giulio Marchesini, Alessandra Cassio, Sara Cataldi, Lucia Brodosi, Maria Letizia Petroni, Federico Baronio, Maria Turchese Caletti
Background and aims Phenylketonuria (PKU)-affected women may become pregnant, and dietary phenylalanine (Phe) intake must be adjusted according to Phe tolerance. We report our experience with maternal PKU in relation to genotype PKU heterogeneity. Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::533f66c645e3ec56d0a8b0c70994268b
http://hdl.handle.net/11585/782751
http://hdl.handle.net/11585/782751
Autor:
Francesca Righetti, Andrea Pession, Beatrice Righi, Roberto Rondelli, Giacomo Faldella, Ilaria Bettocchi, Rita Ortolano, Federico Baronio, Alessandra Cassio
Background: The aim of this study is to investigate free carnitine (C0) and total acylcarnitine levels (AC) in preterm infants with BW < 1800 g and the relationship with neonatal and perinatal factors. Methods: Ninety-three thousand two hundred and n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::101e0fa679335cefbcfa4e63b6690b68
http://hdl.handle.net/11585/726543
http://hdl.handle.net/11585/726543
Autor:
Elena Proncopio, Maria Alice Donati, Federico Baronio, Amelia Morrone, Giancarlo la Marca, Ilaria Bettocchi, Giacomo Biasucci, Binghuang Cai, Sean D. Mooney, Anna Caciotti, Silvia Funghini, Rodolfo Tonin, Andrea Bordugo, Renzo Guerrini, Elisabetta Pasquini, Alessandra Cassio
Publikováno v:
BBA Clinical
Short-chain acyl-coA dehydrogenase deficiency (SCADD) is an autosomal recessive inborn error of mitochondrial fatty acid oxidation caused by ACADS gene alterations. SCADD is a heterogeneous condition, sometimes considered to be solely a biochemical c
Autor:
Laura Nardi, Veronica Conti, Franco D'Alberton, Ilaria Bettocchi, Alessandro Cicognani, Graziana D'Addabbo, Sara Monti, Milva Orquidea Bal, Alessandra Cassio, Nicoletta Bisacchi
Publikováno v:
European Journal of Endocrinology. 164:269-276
ObjectiveTo compare the psychological adjustment and behaviour of congenital hypothyroidism (CH) children and their parents with a control group.Study designA cross-sectional study was carried out with 84 CH subjects diagnosed by neonatal screening (
Autor:
F. Chiodo, Monica Galliano, Monica Dagnino, Davide Tassinari, Ilaria Bettocchi, Gianluca Caridi, Monica Campagnoli, M. Marsciani, Filippo Bernardi, Lorenzo Minchiotti
Publikováno v:
European Journal of Clinical Investigation. 40:281-284
Eur J Clin Invest 2010; 40 (3): 281–284 Abstract Background Analbuminaemia (OMIM #103600) is a rare autosomal recessive disorder manifested by the absence or severe reduction of circulating serum albumin in homozygous or compound heterozygous subje