Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Pier L Calvo"'
Publikováno v:
Minerva Pediatrics.
Bowel ultrasound (US) is a low cost, non-invasive, bed side practice and a reproducible procedure that represents a high yield tool in clinical practice and in the diagnostic workup of a consistent group of acute and chronic gastrointestinal (GI) tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9be59141a726d19f42a1599341201cc5
https://doi.org/10.23736/s2724-5276.21.06371-0
https://doi.org/10.23736/s2724-5276.21.06371-0
Publikováno v:
Minerva Pediatrica. 72
Introduction Calprotectin is a calcium and zinc-binding protein, formed by a hetero complex of S100A8 and S100A9 proteins, which belong to the S-100 protein family consisting in more than 20 different proteins with a tissue-specific expression patter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e22cc7df6683f6a24c9ef57364300f08
https://doi.org/10.23736/s0026-4946.20.06002-8
https://doi.org/10.23736/s0026-4946.20.06002-8
Autor:
Massimiliano Bergallo, Stefano Gambarino, Valentina Daprà, Michele Pinon, Pier L Calvo, Paola Montanari, Ilaria Galliano
Publikováno v:
Minerva Pediatrica. 72
Background Human endogenous retrovirus (HER Vs) constitute approximately 8% of the human genome. Induction of HER V transcription is possible under certain circumstances, and may have a possible role in some pathological conditions. Aim of the presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012efa3c433f957d5d244604e50a34e5
https://doi.org/10.23736/s0026-4946.16.04472-8
https://doi.org/10.23736/s0026-4946.16.04472-8
Autor:
Diana Carli, Elisa Giorgio, Francesca Pantaleoni, Alessandro Bruselles, Sabina Barresi, Evelise Riberi, Francesco Licciardi, Andrea Gazzin, Giuseppina Baldassarre, Simone Pizzi, Marcello Niceta, Francesca C. Radio, Cristina Molinatto, Davide Montin, Pier L. Calvo, Andrea Ciolfi, Nicole Fleischer, Giovanni B. Ferrero, Alfredo Brusco, Marco Tartaglia
Publikováno v:
Human Mutation. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::530308328acde90fe4609ff84c5ea2a4
https://doi.org/10.1002/humu.23795
https://doi.org/10.1002/humu.23795
Publikováno v:
Minerva pediatrica. 72(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2812b90c2ca5e3893a7edbbe94e57458
https://pubmed.ncbi.nlm.nih.gov/26605702
https://pubmed.ncbi.nlm.nih.gov/26605702
Autor:
Nedim Hadzic, Dorothea Haas, Evelyn Zöhrer, Dominique Debray, Jörg Jahnel, Antal Dezsofi, Emmanuel Gonzales, Pier L Calvo, Björn Fischler, Loreto Hierro, Lorenzo D'Antiga, Thierry Lamireau, P. McKiernan, Ulrich Baumann, Henkjan J. Verkade, Valérie A. McLin, Giuseppe Maggiore, Emmanuel Jacquemin
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition, Vol. 64, No 6 (2017) pp. 864-868
Journal of Pediatric Gastroenterology and Nutrition, 64(6), 864-868. Lippincott Williams and Wilkins
Journal of Pediatric Gastroenterology and Nutrition, 64(6), 864-868. Lippincott Williams and Wilkins
Objective: Inborn errors of primary bile acid (BA) synthesis are genetic cholestatic disorders leading to accumulation of atypical BA with deficiency of normal BA. Unless treated with primary BA, chronic liver disease usually progresses to cirrhosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c01892fddfbe279d6851e4ccb437c98e
https://pubmed.ncbi.nlm.nih.gov/28333767
https://pubmed.ncbi.nlm.nih.gov/28333767
Autor:
Henkjan J. Verkade, F. Lacaille, S. Sankaranarayanan, Yael Mozer-Glassberg, Dominique Debray, E. Gonzales, Carolina Gonçalves, DA Kelly, Patryk Lipiński, Ekkehard Sturm, Pier L Calvo, Daniele Serranti, Cigdem Arikan, Irena Jankowska, A. Spraul, Piotr Czubkowski, Loreto Hierro, Henrik Arnell, Bettina E. Hansen, D. Schmitt, Amer Azaz, Dieter C. Broering, Björn Fischler, D. van Wessel, Gema Muñoz Bartolo, A. Pizzol, Tassos Grammatikopoulos, Jernej Brecelj, Emanuele Nicastro, Talal Algoufi, Antal Dezsofi, Esra Polat, Jan B F Hulscher, Mohammed Shagrani, W. van der Woerd, Gabriella Nebbia, E. Jacquemin, Etienne Sokal, Nejat Mazhar, Richard J. Thompson, Agustina Kadaristiana
Publikováno v:
Journal of Hepatology, 68, S626-S627. ELSEVIER SCIENCE BV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3365f701c15b62eac35cc198ee60026
https://doi.org/10.1016/s0168-8278(18)31509-5
https://doi.org/10.1016/s0168-8278(18)31509-5
Autor:
Antonella Lezo, Cristiana Barbera, Isabella Morra, P. Lerro, Maurizio Baldi, Giovanna Cenacchi, Vincenza Valenti, Angelo B. Cefalù, Fabio Tramuto, Pier L Calvo, Maurizio Averna, Davide Noto
Publikováno v:
Metabolism. 59:463-467
Chylomicron retention disease is a recessive inherited disorder characterized by fat malabsorption and steatorrhea and is associated with failure to thrive in infancy. We describe a kindred carrying a mutation of Sara2 gene causing a chylomicron rete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1021cbc81f8f85fc80bc7d4d2b08096b
https://doi.org/10.1016/j.metabol.2009.07.042
https://doi.org/10.1016/j.metabol.2009.07.042
Autor:
G. Forni, M. Cuozzo, M. Baldi, E. Croveri, G. Bechis, G. Oropeza, Pier L Calvo, Cristiana Barbera
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 39:S225-S226
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8096d56c253e72d75899c2e5386c856b
https://doi.org/10.1097/00005176-200406001-00571
https://doi.org/10.1097/00005176-200406001-00571
Autor:
A. Vernetto, Loredana Serpe, Angelo Pera, L. Crocellà, Franco Castagno, Roberto Canaparo, Raffaello Sostegni, Pier L. Calvo, Sergio D'Antico, Marco Daperno, Rodolfo Rocca, Gian Paolo Zara
Publikováno v:
Gastroenterology. 134:A-206
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0db80637bc8a6113f71b9c024045cf50
https://doi.org/10.1016/s0016-5085(08)60951-8
https://doi.org/10.1016/s0016-5085(08)60951-8