Zobrazeno 1 - 10
of 40
pro vyhledávání: '"I. Loddo"'
Autor:
I, Loddo, F, Barbera, G, Di Gesaro, M C, Cutrupi, M P, Calabrò, G, Ceravolo, C, Salpietro, S M C, Gramaglia, A, Ceravolo, D, Concolino, R, De Sarro, C, Cuppari, E, Gitto, F, Clemenza, D, Di Carlo
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::295b1f86c99b7887f77da4ecf40c5cc5
https://hdl.handle.net/11570/3184493
https://hdl.handle.net/11570/3184493
Autor:
Diego Chila, Saverio Loddo, Nancy Morabito, Federica Bellone, Antonino Catalano, I. Loddo, Gabriella Martino, Salvatore Benvenga, Giacomo Nicocia
Publikováno v:
Journal of Clinical & Translational Endocrinology
Highlights • Disorders of calcium metabolism are frequently encountered in clinical practice. • Hypocalcemia accounted for 27.72% and hypercalcemia for 4.74% of inpatients. • Incidence of hypo- and hypercalcemia changed over time.
Disorder
Disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d845aa1013ce2023cf88f1b0ad70a258
http://hdl.handle.net/11570/3129597
http://hdl.handle.net/11570/3129597
Akademický článek
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Autor:
Luigi Meloni, I. Loddo, Sergio Muntoni, Pierluigi Cocco, A. Schwartz, Sa. Muntoni, Marco Manca, G. Cioglia
Publikováno v:
Journal of inherited metabolic disease. 31(3)
Previous studies suggest a reduction in cardiovascular risk among subjects expressing the glucose-6-phosphate dehydrogenase (G6PD, EC 1.1.1.49) deficient phenotype. We aimed to test this hypothesis in male subjects expressing the G6PD-deficient pheno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed9b33c9c3d032915795dc5e9d47afb3
https://pubmed.ncbi.nlm.nih.gov/18392752
https://pubmed.ncbi.nlm.nih.gov/18392752
Publikováno v:
Digestive and Liver Disease. 45:e294-e295
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba7c36678f45c9c88a942f57afbfda3
https://doi.org/10.1016/j.dld.2013.08.206
https://doi.org/10.1016/j.dld.2013.08.206
Publikováno v:
Digestive and Liver Disease. 45:e295
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c586ec9101f7deee79425cbf9237fad2
https://doi.org/10.1016/j.dld.2013.08.207
https://doi.org/10.1016/j.dld.2013.08.207
Autor:
I. Loddo, R. Centorrino, Tommaso Alterio, S. Cardile, F. Sancetta, R. Mallamace, Claudio Romano
Publikováno v:
Journal of Crohn's and Colitis. 7:S281
Background: Genome wide association studies (GWAS) find a significative correlation between several single nucleotide polymorphisms (SNPs) involved in autophagy and the occurrence of Crohn’s disease (CD) risk both in children and in adult patients.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b5285501ca918d48c04410bcbc8fcb9
https://doi.org/10.1016/s1873-9946(13)60695-9
https://doi.org/10.1016/s1873-9946(13)60695-9
Publikováno v:
Digestive and Liver Disease. 44:S283
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa1e39f2da9c621729693c28de6e7414
https://doi.org/10.1016/s1590-8658(12)60722-1
https://doi.org/10.1016/s1590-8658(12)60722-1
Publikováno v:
Journal of Crohn's and Colitis. 6:S56
Background: In adults, Faecal Calprotectin (FC) ELISA has a sensitivity and specificity of >93% for detecting IBD (1). However, small case series have shown that other factors (eg NSAIDs, cirrhosis, obesity etc) may lead to false +ve results. It is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcb07ab17203640b43880a00325fea02
https://doi.org/10.1016/s1873-9946(12)60135-4
https://doi.org/10.1016/s1873-9946(12)60135-4
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.