Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Anastasia Ibba"'
Autor:
Agnese Murianni, Anna Lussu, Chiara Guzzetti, Anastasia Ibba, Letizia Casula, Mariacarolina Salerno, Marco Cappa, Sandro Loche
Publikováno v:
Endocrines, Vol 4, Iss 1, Pp 169-178 (2023)
Background: Several studies have evaluated the role of IGF-1 in the diagnosis of growth hormone deficiency (GHD). According to a recent study, an IGF-1 concentration of a −1.5 standard deviation score (SDS) appeared to be the best cut-off for disti
Externí odkaz:
https://doaj.org/article/691ded72cc67439788032dd462bb8c9d
Autor:
Anastasia Ibba, Sandro Loche
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Growth hormone deficiency (GHD) is the most commonly affected pituitary hormone in childhood with a prevalence of 1 in 4000–10000 live births. GH stimulation testing (GHST) is commonly used in the diagnostic workup of GHD. However, GHD can be diagn
Externí odkaz:
https://doaj.org/article/7c7d5ca26c11474296899eb5095b3a31
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
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
Objectives: To evaluate the effect of gender and puberty on cardiovascular risk factors (CVRF) in obese children and adolescents.Methods: One thousand four hundred and nine obese patients [age 9.7 (2.2–17.9) y; 646 Male] were studied. Subjects were
Externí odkaz:
https://doaj.org/article/a72fc39f11c04b32a8f20c22363a1031
Autor:
Giuseppa Patti, Serena Noli, Donatella Capalbo, Anna Maria Elsa Allegri, Flavia Napoli, Marco Cappa, Grazia Maria Ubertini, Annalisa Gallizia, Sara Notarnicola, Anastasia Ibba, Marco Crocco, Stefano Parodi, Mariacarolina Salerno, Sandro Loche, Maria Luisa Garré, Elena Tornari, Mohamad Maghnie, Natascia Di Iorgi
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
Background: Re-testing for GH secretion is needed to confirm the diagnosis of GH deficiency (GHD) after adult height achievement in childhood-onset GHD (COGHD).Aim: To define the cut-off of GH peak after retesting with GH-releasing hormone plus argin
Externí odkaz:
https://doaj.org/article/48870823fb624b5095e5971dbde8ee68
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 19, Iss 1, Pp 1-7 (2014)
Until 1985 growth hormone (GH) was obtained from pituitary extracts, and was available in limited amounts only to treat severe growth hormone deficiency (GHD). With the availability of unlimited quantities of GH obtained from recombinant DNA technolo
Externí odkaz:
https://doaj.org/article/04611d2c93ab44b18500796960b31fe1
Autor:
Tycho R Tromp, Merel L Hartgers, G Kees Hovingh, Antonio J Vallejo-Vaz, Kausik K Ray, Handrean Soran, Tomas Freiberger, Stefano Bertolini, Mariko Harada-Shiba, Dirk J Blom, Frederick J Raal, Marina Cuchel, Tycho R. Tromp, Merel L. Hartgers, G. Kees Hovingh, Antonio J. Vallejo-Vaz, Kausik K. Ray, Stefano A. Bertolini, Jing Pang, Gerald F. Watts, Susanne Greber-Platzer, Martin Mäser, Thomas M. Stulnig, Christoph F. Ebenbichler, Khalid Bin Thani, David Cassiman, Olivier S. Descamps, Daisy Rymen, Peter Witters, Raul D. Santos, Liam R. Brunham, Gordon A. Francis, Jacques Genest, Robert A. Hegele, Brooke A. Kennedy, Isabelle Ruel, Mark H. Sherman, Long Jiang, Luya Wang, Željko Reiner, Vladimir Blaha, Richard Ceska, Jana Dvorakova, Lubomir Dlouhy, Pavel Horak, Vladimir Soska, Lukas Tichy, Robin Urbanek, Helena Vaverkova, Michal Vrablik, Stanislav Zemek, Lukas Zlatohlavek, Sameh Emil, Tarek Naguib, Ashraf Reda, Sophie Béliard, Eric Bruckert, Antonio Gallo, Moses S. Elisaf, Genovefa Kolovou, Hofit Cohen, Ronen Durst, Eldad J. Dann, Avishay Elis, Osama Hussein, Eran Leitersdorf, Daniel Schurr, Nitika Setia, Ishwar C. Verma, Mohammed D. Alareedh, Mutaz Al-Khnifsawi, Ali F. Abdalsahib Al-Zamili, Sabah H. Rhadi, Foaad K. Shaghee, Marcello Arca, Maurizio Averna, Andrea Bartuli, Marco Bucci, Paola S. Buonuomo, Paolo Calabrò, Sebastiano Calandra, Manuela Casula, Alberico L. Catapano, Angelo B. Cefalù, Arrigo F.G. Cicero, Sergio D'Addato, Laura D'Erasmo, Alessia Di Costanzo, Tommaso Fasano, Marta Gazzotti, Antonina Giammanco, Gabriella Iannuzzo, Anastasia Ibba, Emanuele A. Negri, Andrea Pasta, Chiara Pavanello, Livia Pisciotta, Claudio Rabacchi, Carlo Ripoli, Tiziana Sampietro, Francesco Sbrana, Fulvio Sileo, Patrizia Suppressa, Patrizia Tarugi, Chiara Trenti, Maria G. Zenti, Mika Hori, Mahmoud H. Ayesh, Sami T. Azar, Fadi F. Bitar, Akl C. Fahed, Elie M. Moubarak, Georges Nemer, Hapizah M. Nawawi, Ramón Madriz, Roopa Mehta, Arjen J. Cupido, Joep C. Defesche, M. Doortje Reijman, Jeanine E. Roeters-van Lennep, Erik S.G. Stroes, Albert Wiegman, Linda Zuurbier, Khalid Al-Waili, Fouzia Sadiq, Krzysztof Chlebus, Mafalda Bourbon, Isabel M. Gaspar, Katarina S. Lalic, Marat V. Ezhov, Andrey V. Susekov, Urh Groselj, Min-Ji Charng, Weerapan Khovidhunkit, Melih Aktan, Bulent B. Altunkeser, Sinan Demircioglu, Melis Kose, Cumali Gokce, Osman Ilhan, Meral Kayikcioglu, Leyla G. Kaynar, Irfan Kuku, Erdal Kurtoglu, Harika Okutan, Osman I. Ozcebe, Zafer Pekkolay, Saim Sag, Osman Z. Salcioglu, Ahmet Temizhan, Mustafa Yenercag, Mehmet Yilmaz, Hamiyet Yilmaz Yasar, Olena Mitchenko, Alexander R.M. Lyons, Christophe A.T. Stevens, Julie A. Brothers, Lisa C. Hudgins, Christina Nguyen, Rano Alieva, Aleksandr Shek, Doan-Loi Do, Ngoc-Thanh Kim, Hong-An Le, Thanh-Tung Le, Mai-Ngoc T. Nguyen, Thanh-Huong Truong, Dirk J. Blom, Frederick J. Raal
Publikováno v:
Homozygous Familial Hypercholesterolaemia International Clinical Collaborators 2022, ' Worldwide experience of homozygous familial hypercholesterolaemia : retrospective cohort study ', The Lancet, vol. 399, no. 10326, pp. 719-728 . https://doi.org/10.1016/S0140-6736(21)02001-8
The Lancet, 399(10326), 719-728. Elsevier Limited
The Lancet, 399(10326), 719-728. Elsevier Limited
[Background]: Homozygous familial hypercholesterolaemia (HoFH) is a rare inherited disorder resulting in extremely elevated low-density lipoprotein cholesterol levels and premature atherosclerotic cardiovascular disease (ASCVD). Current guidance abou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfdc3b132039534b5b3b16d9271de125
https://research.vumc.nl/en/publications/f39e2a3e-cdca-435e-8d43-781bf5d3735d
https://research.vumc.nl/en/publications/f39e2a3e-cdca-435e-8d43-781bf5d3735d
Autor:
Gianni Russo, Donatella Capalbo, Federico Baronio, Luisa De Sanctis, Antonio Balsamo, Marta Del Pistoia, Anastasia Ibba, Carla Bizzarri
Publikováno v:
Minerva pediatrics. 73(6)
Differences/disorders of sex development (DSD) are defined as a group of congenital conditions in which the development of chromosomal, gonadal or anatomical sex is atypical. The incidence of DSD is 1:4500 births. The current classification divides D
Autor:
Maurizio Averna, Gabriella Iannuzzo, Andrea Bartuli, Carlo Ripoli, Stefano Bertolini, Sebastiano Calandra, Patrizia Suppressa, Francesco Sbrana, Anastasia Ibba, Chiara Trenti, Alberico L. Catapano, Tommaso Fasano, Manuela Casula, Livia Pisciotta, Angelo B. Cefalù, Patrizia Tarugi, Tiziana Sampietro, Paolo Calabrò, Andrea Pasta, Paola Sabrina Buonuomo, Fulvio Sileo, M. G. Zenti, Chiara Pavanello, Sergio D'Addato, Marco Bucci, Marcello Arca, Arrigo F G Cicero, Emanuele A. Negri, Claudio Rabacchi, Laura D'Erasmo
Background and aims Homozygous familial hypercholesterolemia (HoFH) is a rare genetic disorder characterized by extremely elevated plasma levels of low density lipoprotein cholesterol (LDL-C) and high risk of premature atherosclerotic cardiovascular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afbf8ee0ca9d55982f70e295e27992f0
http://hdl.handle.net/11585/798740
http://hdl.handle.net/11585/798740
Autor:
Chiara Guzzetti, Sandro Loche, Mariacarolina Salerno, Anastasia Ibba, Anna Allegri, Marco Cappa, Mohamad Maghnie, Natascia Di Iorgi, Letizia Casula
Publikováno v:
Clinical Endocrinology. 89:765-770
OBJECTIVE: The diagnosis of growth hormone deficiency (GHD) is currently based on clinical, auxological, biochemical and neuro-radiological investigation. Provocative tests of GH secretion using physiological/pharmacological stimuli are required to c