Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/2582
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dc.contributor.authorKancherla, Vijayaes
dc.contributor.authorTandaki, Lucitaes
dc.contributor.authorSundar, Manasvies
dc.contributor.authorLux, Ankees
dc.contributor.authorBakker, Marian Kes
dc.contributor.authorBergman, Jorieke Ehes
dc.contributor.authorBermejo-Sánchez, Evaes
dc.contributor.authorCanfield, Mark Aes
dc.contributor.authorFeldkamp, Marcia Les
dc.contributor.authorGroisman, Borises
dc.contributor.authorHurtado-Villa, Paulaes
dc.contributor.authorKällén, Karines
dc.contributor.authorLandau, Daniellees
dc.contributor.authorLelong, Nathaliees
dc.contributor.authorLópez Camelo, Jorgees
dc.contributor.authorMastroiacovo, Pierpaoloes
dc.contributor.authorMorgan, Margeryes
dc.contributor.authorMutchinick, Osvaldo Mes
dc.contributor.authorNance, Amy Ees
dc.contributor.authorNembhard, Wendy Nes
dc.contributor.authorPierini, Annaes
dc.contributor.authorSipek, Antonines
dc.contributor.authorStallings, Erin Bes
dc.contributor.authorSzabova, Elenaes
dc.contributor.authorWertelecki, Wladimires
dc.contributor.authorZarante, Ignacioes
dc.contributor.authorRissmann, Ankees
dc.date.accessioned2023-04-06T20:13:49Z-
dc.date.available2023-04-06T20:13:49Z-
dc.date.issued2022-05-29-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/2582-
dc.descriptionFil: Kancherla, Vijaya. Department of Epidemiology, Emory University Rollins School of Public Health; Georgiaes
dc.descriptionFil: Tandaki, Lucita. Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke-University; Germanyes
dc.descriptionFil: Sundar, Manasvi. Department of Epidemiology, Emory University Rollins School of Public Health; Georgiaes
dc.descriptionFil: Lux, Anke. Institute for Biometrics and Medical Informatics, Medical Faculty, Otto-von-Guericke-University; Germanyes
dc.descriptionFil: Bakker, Marian K. Department of Genetics, University of Groningen, University Medical Center Groningen, Eurocat Northern The Netherlands; The Netherlandses
dc.descriptionFil: Bergman, Jorieke Eh. Department of Genetics, University of Groningen, University Medical Center Groningen, Eurocat Northern The Netherlands; The Netherlandses
dc.descriptionFil: Bermejo-Sánchez, Eva. ECEMC (Spanish Collaborative Study of Congenital Malformations), UIAC (Unidad de Investigación sobre Anomalías Congénitas), Instituto de Investigación de Enfermedades Raras (IIER). Instituto de Salud Carlos III; Madrid, Españaes
dc.descriptionFil: Canfield, Mark A. Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services; Texases
dc.descriptionFil: Feldkamp, Marcia L. Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine; Utahes
dc.descriptionFil: Groisman, Boris. National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Laboratories and Health Institutes (ANLIS), National Ministry of Health; Buenos Aires, Argentinaes
dc.descriptionFil: Hurtado-Villa, Paula. Department of Basic Sciences of Health, School of Health, Pontificia Universidad Javeriana Cali, Colombia and Clínica Imbanaco; Colombiaes
dc.descriptionFil: Källén, Karin. National Board of Health and Welfare; Swedenes
dc.descriptionFil: Landau, Danielle. Department of Neonatology, Soroka Medical Center; Israeles
dc.descriptionFil: Lelong, Nathalie. Université de Paris, Inserm U1153, Obstetrical, Perinatal and Pediatric Epidemiology Research Team (Epopé), Center for Epidemiology and Statistics Sorbonne Paris Cité (CRESS); Franciaes
dc.descriptionFil: Lopez-Camelo, Jorge. ECLAMC, Center for Medical Education and Clinical Research (CEMIC-CONICET); Buenos Aires, Argentinaes
dc.descriptionFil: Mastroiacovo, Pierpaolo. International Center on Birth Defects, International Clearinghouse for Birth Defects Surveillance and Research; Italiaes
dc.descriptionFil: Morgan, Margery. CARIS, the Congenital Anomaly Register for Wales, Singleton Hospital; United Kingdomes
dc.descriptionFil: Mutchinick, Osvaldo M. RYVEMCE (Registry and Epidemiologic Surveillance of Congenital Malformations), Department of Genetics, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán; Mexicoes
dc.descriptionFil: Nance, Amy E. Utah Department of Health, Bureau of Children with Special Health Care Needs, Utah Birth Defects Network; Utahes
dc.descriptionFil: Nembhard, Wendy N. Arkansas Center for Birth Defects Research and Prevention and Arkansas Reproductive Health Monitoring System, University of Arkansas for Medical Sciences, Fay Boozman College of Public Health, Department of Epidemiology; Arkansases
dc.descriptionFil: Pierini, Anna. Institute of Clinical Physiology, National Research Council and Fondazione Toscana Gabriele Monasterio, Tuscany Registry of Congenital Defects; Pisa, Italyes
dc.descriptionFil: Šípek, Antonin. Department of Medical Genetics, Thomayer Hospital; Czech Republices
dc.descriptionFil: Stallings, Erin B. Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, US Centers for Disease Control and Prevention; Georgiaes
dc.descriptionFil: Szabova, Elena. Slovak Teratologic Information Centre (FPH), Slovak Medical University; Republices
dc.descriptionFil: Wertelecki, Wladimir. OMNI-Net Ukraine; Ukrainees
dc.descriptionFil: Zarante, Ignacio. Human Genetics Institute, Pontificia Universidad Javeriana, Bogotá, Colombia and Hospital Universitario San Ignacio; Bogotá, Colombiaes
dc.descriptionFil: Rissmann, Anke. Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke-University; Germanyes
dc.description.abstractBladder exstrophy (BE) is a rare but severe birth defect affecting the lower abdominal wall and genitourinary system. The objective of the study is to examine the total prevalence, trends in prevalence, and age-specific mortality among individuals with BE.es
dc.language.isoenes
dc.relation.ispartofAmerican journal of perinatologyes
dc.relation.ispartofseriesAm J Perinatol;2022:101055-
dc.subjectExtrofia de la Vejigaes
dc.subjectEpidermólisis Ampollosaes
dc.titleA Multicountry Analysis of Prevalence and Mortality among Neonates and Children with Bladder Exstrophyes
dc.typeArtículoes
dc.identifier.doi10.1055/s-0042-1748318-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArtículo-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptCentro Nacional de Genética Médica (CeNaGeM)-
crisitem.author.deptRegistro Nacional de Anomalías Congénitas (RENAC)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Epidemiología (INE)-
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