Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Anastasia Ibba"'
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:
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
Autor:
Anna Elsa Maria Allegri, Anastasia Ibba, Giuseppa Patti, Marco Crocco, Mohamad Maghnie, Flavia Napoli, Daniela Fava, Marilea Lezzi, Deborah Bianco, Natascia Di Iorgi, Andrea Rossi, Maurizio Schiavone, Giovanni Morana, Andrea Calandrino, Angela Pistorio, Hanan F. Thiabat, Mariasavina Severino, Tiziana Camia, Domenico Tortora
Publikováno v:
The Journal of clinical endocrinology and metabolism. 105(11)
Context The etiology of central diabetes insipidus (CDI) in children is often unknown. Clinical and radiological features at disease onset do not allow discrimination between idiopathic forms and other conditions or to predict anterior pituitary dysf
Autor:
Sandro Loche, Elisa Pisaneschi, Letizia Casula, Mafalda Mucciolo, Antonio Novelli, Anastasia Ibba, Emanuele Bellacchio, Carla Bizzarri, Marco Cappa, Chiara Guzzetti
Publikováno v:
Hormone Research in Paediatrics. 90:203-211
Background: The development of gonadotropin-independent (peripheral) precocious puberty in male children with primary adrenal insufficiency (PAI) is consistent with a defect in the genes encoding for the enzymes involved in steroid hormone biosynthes
Autor:
Sandro, Loche, Natascia, Di Iorgi, Giuseppa, Patti, Serena, Noli, Marta, Giaccardi, Irene, Olivieri, Anastasia, Ibba, Mohamad, Maghnie
Publikováno v:
Endocrine development. 33
Growth hormone (GH) is essential not only for normal growth during childhood, but also for the acquisition of bone mass and muscle strength in both sexes. This process is completed after the achievement of adult height in the phase of transition from
Autor:
Natascia Di Iorgi, Sandro Loche, Irene Olivieri, Marta Giaccardi, Anastasia Ibba, Serena Noli, Mohamad Maghnie, Giuseppa Patti
Growth hormone (GH) is essential not only for normal growth during childhood, but also for the acquisition of bone mass and muscle strength in both sexes. This process is completed after the achievement of adult height in the phase of transition from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0a4e5c6229885fd1501a0bb4734f5e2
https://doi.org/10.1159/000487525
https://doi.org/10.1159/000487525
Publikováno v:
Journal of Endocrinological Investigation. 37:51-56
In obese subjects it has been shown that cortisol (F) contributes to the reduction in insulin sensitivity, suggesting a role in the development of the metabolic syndrome (MS).The aim of this retrospective study was to evaluate the relationship betwee
Autor:
Sandro Loche, Natascia Di Iorgi, Nadia Beltrami, Sabrina Pilia, Mohammad Maghnie, Nadia Fratangeli, Giorgio Radetti, Alessandra Rollo, Chiara Guzzetti, Marco Cappa, Anastasia Ibba, Stefano Zucchini
Publikováno v:
European journal of endocrinology. 175(1)
ObjectiveThe diagnosis of GH deficiency (GHD) in children and adolescents is established when GH concentrations fail to reach an arbitrary cut-off level after at least two provocative tests. The objective of the study was to define the optimal GH cut
Autor:
Anastasia Ibba, Maria Rosaria Casini, Sandro Loche, Alberto Loche, Luigi Minerba, Patrizia Zavattari, Chiara Guzzetti, Sabrina Pilia
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 26
Aim: We aimed to study the influence of the fat mass and obesity-associated ( FTO ) gene on eating behavior in 412 obese Sardinian children and adolescents. Genome-wide association studies (GWAS) have identified several susceptibility loci for obesit