Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Gianpaolo Grumieri"'
Autor:
Paola, Roggero, Emanuela, Carissimi, Elena, Pozzi, Elena, Cataliotti, Francesca, Santus, Pasquina, Piemontese, Gianpaolo, Grumieri, Bruno, Gridelli, V, Carnelli
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 36(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2eae927cc50bf93d68a118d7d2ea55cd
https://pubmed.ncbi.nlm.nih.gov/12669709
https://pubmed.ncbi.nlm.nih.gov/12669709
Autor:
Carla Navone, Milvia Cecconi, Michele Sacco, Gianpaolo Grumieri, Cristina Curcio, Alberto Bettinelli, Augusto Rosini, Giuseppe Ruffa, Giovanna Leozappa, Silvana Tedeschi, Aldo Claris Appiani, Sonia Ciarmatori, Giorgio Casari, Layla Cesareo, Silvana Binda, Marie Louise Syren, Bruno Mercuri
Publikováno v:
Scopus-Elsevier
Limited phenotypic variability has been reported in patients with Bartter syndrome type I, with mutations in the Na-K-2Cl cotransporter gene (BSC). The diagnosis of this hereditary renal tubular disorder is usually made in the antenatal-neonatal peri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87154dfac900b9bb58571ee6a2de01bc
https://pubmed.ncbi.nlm.nih.gov/10975303
https://pubmed.ncbi.nlm.nih.gov/10975303
Autor:
Joseph F. Fitzgerald, Riccardo Troncone, Paola Roggero, Emanuela Carissimi, Elena Pozzi, Elena Cataliotti, Francesca Santus, Pasquina Piemontese, Gianpaolo Grumieri, Bruno Gridelli, V. Carnelli
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 36:375
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::588edf9bc95fd0adcae525b732c0d44c
https://doi.org/10.1097/00005176-200303000-00014
https://doi.org/10.1097/00005176-200303000-00014
Autor:
Cinzia Sforzini, Angelo Selicorni, Donatella Milani, Mario G. Bianchetti, Anna Barbato, Emilio F. Fossali, Gianpaolo Grumieri
Publikováno v:
ResearcherID
Renal ultrasound scan, circulating creatinine and calcium, and the urinary calcium excretion rate were investigated in 57 patients with clinically and genetically typical Williams-Beuren syndrome (25 female and 32 male subjects, aged from 1.0 year to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fe15875e4bd9d1f44d00f5509b0e991
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=MEDLINE&KeyUT=MEDLINE:12432430&KeyUID=MEDLINE:12432430
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=MEDLINE&KeyUT=MEDLINE:12432430&KeyUID=MEDLINE:12432430
