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Your search keyword '"Volta, Umberto"' showing total 11 results
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11 results on '"Volta, Umberto"'

2. List of contributors

Author

Aimo, Cristina, primary, Aronico, Nicola, additional, Auricchio, Renata, additional, Barone, Michele, additional, Biagi, Federico, additional, Bianchi, Paola Ilaria, additional, Bibbò, Stefano, additional, Broglio, Giacomo, additional, Caio, Giacomo, additional, Calabrese, Emma, additional, Cammarota, Giovanni, additional, Caproni, Marzia, additional, Carroccio, Antonio, additional, Castellaneta, Stefania, additional, Catassi, Carlo, additional, Catassi, Giulia, additional, Ciacci, Carolina, additional, Ciccocioppo, Rachele, additional, Copparoni, Roberto, additional, Corazza, Gino Roberto, additional, Corrà, Alberto, additional, Cristofori, Fernanda, additional, Dargenio, Vanessa Nadia, additional, De Giorgio, Roberto, additional, De Lisi, Giuseppe, additional, De Micco, Ida, additional, Di Sabatino, Antonio, additional, Di Stasio, Luigia, additional, Di Stefano, Michele, additional, Discepolo, Valentina, additional, Fasano, Alessio, additional, Francavilla, Ruggiero, additional, Gasbarrini, Antonio, additional, Gasbarrini, Giovanni, additional, Gatti, Simona, additional, Gianfrani, Carmen, additional, Giuliano, Alessandra, additional, Greco, Luigi, additional, Guandalini, Stefano, additional, Ianiro, Gianluca, additional, Lenti, Marco Vincenzo, additional, Lionetti, Elena, additional, Lucioni, Marco, additional, Maimaris, Stiliano, additional, Mamone, Gianfranco, additional, Mandile, Roberta, additional, Mansueto, Pasquale, additional, Marafini, Irene, additional, Mariotti, Elena Biancamaria, additional, Mengoli, Caterina, additional, Monteleone, Giovanni, additional, Monteleone, Ivan, additional, Neuhold, Susanna, additional, Novellino, Luisa, additional, Pilo, Caterina, additional, Plutino, Giuseppe, additional, Sansotta, Naire, additional, Santacroce, Giovanni, additional, Schiepatti, Annalisa, additional, Seidita, Aurelio, additional, Silano, Marco, additional, Troncone, Edoardo, additional, Troncone, Riccardo, additional, Vanoli, Alessandro, additional, Vitale, Serena, additional, Volta, Umberto, additional, Zanini, Annalisa, additional, and Zingone, Fabiana, additional

Published
2024
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4. New entity of adult ultra-short coeliac disease: the first international cohort and case–control study

Author

Raju, Suneil A, primary, Greenaway, Emily A, additional, Schiepatti, Annalisa, additional, Arpa, Giovanni, additional, Vecchione, Nicoletta, additional, Jian, Chao LA, additional, Grobler, Charlotte, additional, Maregatti, Margherita, additional, Green, Olivia, additional, Bowker-Howell, Freya J, additional, Shiha, Mohamed G, additional, Penny, Hugo A, additional, Cross, Simon S, additional, Ciacci, Carolina, additional, Rostami, Kamran, additional, Ahmadipour, Shokoufeh, additional, Moradi, Afshin, additional, Rostami-Nejad, Mohammad, additional, Biagi, Federico, additional, Volta, Umberto, additional, Fiorentino, Michelangelo, additional, Lebwohl, Benjamin, additional, Green, Peter HR, additional, Lewis, Suzanne, additional, Molina-Infante, Javier, additional, Mata-Romero, Pilar, additional, Vaira, Valentina, additional, Elli, Luca, additional, Soykan, Irfan, additional, Ensari, Arzu, additional, and Sanders, David S, additional

Published
2024
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5. Celiac Disease: A Forty-Year Analysis in an Italian Referral Center.

Author

Lungaro, Lisa, Costanzini, Anna, Manza, Francesca, Caputo, Fabio, Remelli, Francesca, Volpato, Stefano, De Giorgio, Roberto, Volta, Umberto, and Caio, Giacomo

Abstract

Background: Celiac disease (CD) is an autoimmune disorder triggered by gluten ingestion. Herein, we assessed clinical, serological and histopathological findings of a single-center, large cohort of CD patients diagnosed and followed-up over forty years. Methods: From January 1980 to December 2020, 1547 CD patients (1170 females; age range: 8–81 years; F:M ratio = 3.1:1) were diagnosed in an Italian tertiary referral center. Comorbidities and complications were recorded at diagnosis and during follow-up. Results: CD diagnoses quadrupled after 2000. The most frequent phenotype was the non-classical CD (63.3%), and the most prevalent histotype was Marsh 3C (44.7%). Gastrointestinal manifestations, detectable in 51% of patients, were diarrhea (24.3%), bloating (28%) and aphthous stomatitis (19.7%). The most common CD-associated disorder was osteopenia (59.9%), predominant in females (64.3%); extraintestinal manifestations included anemia (35.8% iron-deficiency; 87% folic acid malabsorption), cryptogenic hypertransaminasemia (27.9%), and recurrent miscarriages (11.5%). Thyroiditis (26.9%), type 1 diabetes mellitus (2.9%), and dermatitis herpetiformis (1.4%) were the most common CD-related autoimmune disorders. Six patients had inflammatory bowel disease. Complications and mortality rate occurred in 1.8% and 1.9%, respectively. Conclusions: This single-center, large cohort analysis confirmed that CD presentation changed over the years, with an increase of non-classical and subclinical clinical phenotypes. [ABSTRACT FROM AUTHOR]

Published
2024
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7. New entity of adult ultra-short coeliac disease: the first international cohort and case-control study.

Author

Raju, Suneil A., Greenaway, Emily A., Schiepatti, Annalisa, Arpa, Giovanni, Vecchione, Nicoletta, Jian, Chao LA, Grobler, Charlotte, Maregatti, Margherita, Green, Olivia, Bowker-Howell, Freya J., Shiha, Mohamed G., Penny, Hugo A., Cross, Simon S., Ciacci, Carolina, Rostami, Kamran, Ahmadipour, Shokoufeh, Moradi, Afshin, Rostami-Nejad, Mohammad, Biagi, Federico, and Volta, Umberto

Published
2024
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9. Su1885 THE IMPACT OF UNNECESSARY GLUTEN-FREE DIET ON GUT MICROBIOTA

Author

Manza, Francesca, Lungaro, Lisa, Costanzini, Anna, Segata, Nicola, Pinto, Federica, Puncochar, Michal, Asnicar, Francesco, Armanini, Federica, Carroccio, Antonio, Seidita, Aurelio, Mansueto, Pasquale, Calabrò, Antonino S., Cavalieri, Duccio, Barbara, Giovanni, Stanghellini, Vincenzo, Volta, Umberto, De Giorgio, Roberto, and Caio, Giacomo Pietro Ismaele

Published
2024
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10. Non-celiac gluten sensitivity: A work-in-progress entity in the spectrum of wheat-related disorders

Author

Volta, Umberto, Caio, Giacomo, De Giorgio, Roberto, Henriksen, Christine, Skodje, Gry, and Lundin, Knut E.

Abstract

Non-celiac gluten sensitivity is an undefined syndrome with gastrointestinal and extra-intestinal manifestations triggered by gluten in patients without celiac disease and wheat allergy. The pathogenesis involves immune-mediated mechanisms requiring further research. Symptoms disappear in a few hours or days after gluten withdrawal and recur rapidly after gluten ingestion. Besides gluten, other wheat proteins as well as fermentable oligo-, di-, mono-saccharides and polyols (FODMAPs) may contribute to this syndrome. This syndrome occurs mainly in young women, being rare in children. Its prevalence ranges from 0.6% to 6%, based on primary or tertiary care center estimates. No biomarker is available, but half of patients tests positive for IgG anti-gliadin antibodies, which disappear quickly after gluten-free diet together with symptoms. Also, genetic markers are still undefined. Although currently limited to a research setting, double-blind, placebo-controlled, cross-over trial strategy is recommended to confirm the diagnosis. Treatment is based on dietary restriction with special care to nutrient intake.

Published
2024
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11. Nonceliac Wheat Sensitivity

Author

Volta, Umberto, De Giorgio, Roberto, Caio, Giacomo, Uhde, Melanie, Manfredini, Roberto, and Alaedini, Armin

Abstract

Non-celiac wheat sensitivity (NCWS) is characterized by gastrointestinal and extra-intestinal symptoms following the ingestion of gluten-containing cereals in subjects without celiac disease or wheat allergy. The identity of the molecular triggers in these cereals responsible for the symptoms of NCWS remains to be delineated. Recent research has identified a biological basis for the condition, with the observation of systemic immune activation in response to microbial translocation that appears to be linked to intestinal barrier defects. Ongoing research efforts are aimed at further characterizing the etiology, mechanism, and biomarkers of the condition.

Published
2024
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