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• W2899243337 abstract "Pediatrics InternationalVolume 61, Issue 2 p. 193-197 Clinical Notes Bartter syndrome and growth hormone deficiency: Three siblings with a novel CLCNKB mutation Ilaria Brambilla, Ilaria Brambilla Department of Pediatrics, University of Pavia, Pavia, ItalySearch for more papers by this authorDimitri Poddighe, Corresponding Author Dimitri Poddighe dimimedpv@yahoo.it orcid.org/0000-0001-6431-9334 Department of Medicine, Nazarbayev University School of Medicine, Astana, KazakhstanCorrespondence: Dimitri Poddighe, MD MSc, Department of Medicine, Nazarbayev University School of Medicine, 4th Floor, Room 455, Kerei-Zhanibek Street 5/1, Astana 010000, Kazakhstan. Email: dimimedpv@yahoo.itSearch for more papers by this authorSimona Semeria Mantelli, Simona Semeria Mantelli Department of Pediatrics, University of Pavia, Pavia, ItalySearch for more papers by this authorCarmen Guarracino, Carmen Guarracino Department of Pediatrics, University of Pavia, Pavia, ItalySearch for more papers by this authorGian Luigi Marseglia, Gian Luigi Marseglia Department of Pediatrics, University of Pavia, Pavia, ItalySearch for more papers by this author Ilaria Brambilla, Ilaria Brambilla Department of Pediatrics, University of Pavia, Pavia, ItalySearch for more papers by this authorDimitri Poddighe, Corresponding Author Dimitri Poddighe dimimedpv@yahoo.it orcid.org/0000-0001-6431-9334 Department of Medicine, Nazarbayev University School of Medicine, Astana, KazakhstanCorrespondence: Dimitri Poddighe, MD MSc, Department of Medicine, Nazarbayev University School of Medicine, 4th Floor, Room 455, Kerei-Zhanibek Street 5/1, Astana 010000, Kazakhstan. Email: dimimedpv@yahoo.itSearch for more papers by this authorSimona Semeria Mantelli, Simona Semeria Mantelli Department of Pediatrics, University of Pavia, Pavia, ItalySearch for more papers by this authorCarmen Guarracino, Carmen Guarracino Department of Pediatrics, University of Pavia, Pavia, ItalySearch for more papers by this authorGian Luigi Marseglia, Gian Luigi Marseglia Department of Pediatrics, University of Pavia, Pavia, ItalySearch for more papers by this author First published: 02 November 2018 https://doi.org/10.1111/ped.13726 Ilaria Brambilla and Dimitri Poddighe contributed equally to the study. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Volume61, Issue2February 2019Pages 193-197 RelatedInformation" @default.
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• W2899243337 title "Bartter syndrome and growth hormone deficiency: Three siblings with a novel <i>CLCNKB</i> mutation" @default.
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