Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Giulia Bassanese"'
Autor:
Giulia Bassanese, Tanja Wlodkowski, Aude Servais, Laurence Heidet, Dario Roccatello, Francesco Emma, Elena Levtchenko, Gema Ariceta, Justine Bacchetta, Giovambattista Capasso, Augustina Jankauskiene, Marius Miglinas, Pietro Manuel Ferraro, Giovanni Montini, Jun Oh, Stephane Decramer, Tanja Kersnik Levart, Jack Wetzels, Elisabeth Cornelissen, Olivier Devuyst, Aleksandra Zurowska, Lars Pape, Anja Buescher, Dieter Haffner, Natasa Marcun Varda, Gian Marco Ghiggeri, Giuseppe Remuzzi, Martin Konrad, Germana Longo, Detlef Bockenhauer, Atif Awan, Ilze Andersone, Jaap W. Groothoff, Franz Schaefer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background The European Rare Kidney Disease Reference Network (ERKNet) recently established ERKReg, a Web-based registry for all patients with rare kidney diseases. The main objectives of this core registry are to generate epidemiological in
Externí odkaz:
https://doaj.org/article/298d7b2d56344d9ab3fa1ca68f07142f
Autor:
Pietro Manuel Ferraro, Elena Levtchenko, Tanja Kersnik Levart, Jaap W. Groothoff, Olivier Devuyst, Giovanni Montini, Anja Buescher, Dario Roccatello, Justine Bacchetta, Francesco Emma, Jun Oh, Dieter Haffner, Elisabeth A.M. Cornelissen, Tanja Wlodkowski, Martin Konrad, Jack F.M. Wetzels, Natasa Marcun Varda, Gema Ariceta, Detlef Bockenhauer, Aleksandra Zurowska, Germana Longo, Augustina Jankauskiene, Aude Servais, Giuseppe Remuzzi, Ilze Andersone, Franz Schaefer, Laurence Heidet, Lars Pape, Stéphane Decramer, Giovambattista Capasso, Marius Miglinas, Gian Marco Ghiggeri, Giulia Bassanese, Atif Awan
Publikováno v:
Orphanet journal of rare diseases, London : BioMed Central Ltd., 2021, vol.16, no. 1, p. 1844-1859
Orphanet journal of rare diseases, 16(1):251. BioMed Central
Orphanet Journal of Rare Diseases, 16
Scientia
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Orphanet Journal of Rare Diseases, Vol. 16, no.1, p. 251 (2021)
Orphanet Journal of Rare Diseases, 16, 1
Orphanet journal of rare diseases, 16(1):251. BioMed Central
Orphanet Journal of Rare Diseases, 16
Scientia
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Orphanet Journal of Rare Diseases, Vol. 16, no.1, p. 251 (2021)
Orphanet Journal of Rare Diseases, 16, 1
Epidemiologia; Nefrologia pediàtrica; Registre Epidemiología; Nefrología pediátrica; Registro Epidemiology; Pediatric nephrology; Registry Background The European Rare Kidney Disease Reference Network (ERKNet) recently established ERKReg, a Web-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f580ddf5b1808b33370d6fb1bbd3079
https://www.ncbi.nlm.nih.gov/pubmed/34078418
https://www.ncbi.nlm.nih.gov/pubmed/34078418
Autor:
Giulia Bassanese, Aglaia Vignoli, Maria Valvassori Bolgè, Maria Paola Canevini, Katherine Turner, Cristina Baldi, Albertina Franza, Elena Zambrelli
Publikováno v:
Seizure. 73
Purpose Postpartum depression (PPD) is a non-psychotic depressive disorder that begins within 4 weeks of childbirth. This study aimed to evaluate the prevalence of PPD by screening mothers with the Edinburgh Postnatal Depression Scale (EPDS), to asse
Publikováno v:
Pediatric emergency care. 34(7)
Objective This study aimed to assess the spectrum of pathologies responsible for torticollis in children presenting to the emergency department and to evaluate the associated symptoms to determine clinical red flags for hospitalization. Methods This
Objective The main aim of the study was to investigate the incidence and the clinically relevant features of functional constipation in patients evaluated for acute abdominal pain in a tertiary care pediatric emergency department. Methods This is a r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a826dbe7c5b59f7a583bfc25b289de7
https://insights.ovid.com/crossref?an=00006565-201710000-00014
https://insights.ovid.com/crossref?an=00006565-201710000-00014
Autor:
Lorenzo Monasta, Alessandro Ventura, Laura Travan, Giulia Bassanese, Giuseppina D’Ottavio, Marco Pennesi
Publikováno v:
The Journal of urology. 190(5)
PURPOSE: Congenital hydronephrosis and isolated pyelectasis are frequently diagnosed by prenatal ultrasound. About 80% of cases resolve spontaneously in early childhood. Currently there is no agreed on protocol for prenatal followup. Most clinicians