Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/2552
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dc.contributor.authorGili, Juan Antonioes
dc.contributor.authorLópez-Camelo, Jorge Santiagoes
dc.contributor.authorNembhard, Wendy Nes
dc.contributor.authorBakker, Marian Kes
dc.contributor.authorde Walle, Hermien E Kes
dc.contributor.authorStallings, Erin Bes
dc.contributor.authorKancherla, Vijayaes
dc.contributor.authorContiero, Paoloes
dc.contributor.authorDastgiri, Saeedes
dc.contributor.authorFeldkamp, Marcia Les
dc.contributor.authorNance, Amy Ees
dc.contributor.authorGatt, Miriames
dc.contributor.authorMartínez, Lauraes
dc.contributor.authorCanessa, María Auroraes
dc.contributor.authorGroisman, Borises
dc.contributor.authorHurtado-Villa, Paulaes
dc.contributor.authorKällén, Karines
dc.contributor.authorLandau, Daniellees
dc.contributor.authorLelong, Nathaliees
dc.contributor.authorMorgan, Margeryes
dc.contributor.authorArteaga-Vázquez, Jazmínes
dc.contributor.authorPierini, Annaes
dc.contributor.authorRissmann, Ankees
dc.contributor.authorSipek, Antonines
dc.contributor.authorSzabova, Elenaes
dc.contributor.authorWertelecki, Wladimires
dc.contributor.authorZarante, Ignacioes
dc.contributor.authorCanfield, Mark Aes
dc.contributor.authorMastroiacovo, Pierpaoloes
dc.date.accessioned2023-04-06T19:49:27Z-
dc.date.available2023-04-06T19:49:27Z-
dc.date.issued2022-07-15-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/2552-
dc.descriptionFil: Gili, Juan Antonio. Instituto Académico Pedagógico de Ciencias Humanas, Universidad Nacional de Villa María; Córdoba, Argentinaes
dc.descriptionFil: López-Camelo, Jorge Santiago. ECLAMC, Centro de Educación Médica e Investigaciones Clínicas (CEMIC-CONICET); Buenos Aires, Argentinaes
dc.descriptionFil: Nembhard, Wendy N. Department of Epidemiology, Arkansas Center for Birth Defects Research and Prevention and Arkansas Reproductive Health Monitoring System, University of Arkansas for Medical Sciences; Little Rock, Arkansas, USAes
dc.descriptionFil: Bakker, Marian. Department of Genetics, University of Groningen, University Medical Center Groningen, EUROCAT Northern Netherlands; Groningen, The Netherlandses
dc.descriptionFil: de Walle, Hermien E K. Department of Genetics, University of Groningen, University Medical Center Groningen, EUROCAT Northern Netherlands; Groningen, The Netherlandses
dc.descriptionFil: Stallings, Erin B. Metro Atlanta Congenital Defects Program (MACDP), Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities; USAes
dc.descriptionFil: Kancherla, Vijaya. Department of Epidemiology, Emory University Rollins School of Public Health; USAes
dc.descriptionFil: Contiero, Paolo. Lombardy Congenital Anomalies Registry, Cancer Registry Unit, Fondazione IRCCS, Istituto Nazionale Tumori; Italiaes
dc.descriptionFil: Dastgiri, Saeed. Health Services Management Research Centre, Tabriz University of Medical Sciences; Iranes
dc.descriptionFil: Feldkamp, Marcia L. Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine; USAes
dc.descriptionFil: Nance, Amy. Utah Birth Defect Network, Bureau of Children with Special Health Care Needs, Division of Family Health and Preparedness, Utah Department of Health; USAes
dc.descriptionFil: Gatt, Miriam. Malta Congenital Anomalies Registry, Directorate for Health Information and Research; Maltaes
dc.descriptionFil: Martínez, Laura. Genetics Department, Hospital Universitario Dr. José E. González, Universidad Autonóma de Nuevo León; Mexicoes
dc.descriptionFil: Canessa, María Aurora. Regional Register Congenital Malformation Maule Health Service (RRMC-SSM); Chilees
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 and Social Development; Buenos Aires, Argentinaes
dc.descriptionFil: Hurtado-Villa, Paula. Department of Basic Sciences of Health, School of Health, Pontificia Universidad Javeriana; 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, CRESS Obstetrical, Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA; Franciaes
dc.descriptionFil: Morgan, Margery. CARIS, The Congenital Anomaly Register for Wales, Singleton Hospital; UKes
dc.descriptionFil: Arteaga-Vázquez, Jazmín. Department of Genetics, RYVEMCE, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán; Mexicoes
dc.descriptionFil: Pierini, Anna. Institute of Clinical Physiology, National Research Council and Fondazione Toscana Gabriele Monasterio, Tuscany Registry of Congenital Defects; Italiaes
dc.descriptionFil: Rissmann, Anke. Medical Faculty, Malformation Monitoring Centre Saxony-Anhalt, Otto-von-Guericke University; Alemaniaes
dc.descriptionFil: Sipek, Antonin. Department of Medical Genetics, Thomayer University Hospital; República Checaes
dc.descriptionFil: Szabova, Elena. Slovak Teratologic Information Centre (FPH), Slovak Medical University; Eslovaquiaes
dc.descriptionFil: Wertelecki, Wladimir. Omni-Net for Children International Charitable Fund; Ucraniaes
dc.descriptionFil: Zarante, Ignacio. Human Genetics Institute, Pontificia Universidad Javeriana; Colombiaes
dc.descriptionFil: Canfield, Mark A. Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services; USAes
dc.descriptionFil: Mastroiacovo, Pierpaolo. International Center on Birth Defects, International Clearinghouse for Birth Defects Surveillance and Research; Italiaes
dc.description.abstractCongenital hydrocephalus (CH) comprises a heterogeneous group of birth anomalies with a wide-ranging prevalence across geographic regions and registry type. The aim of the present study was to analyze the early neonatal case fatality rate (CFR) and total birth prevalence of newborns diagnosed with CH.es
dc.language.isoenes
dc.relation.ispartofBirth defects researches
dc.relation.ispartofseriesBirth Defects Res;114(12):631-644-
dc.subjectAnomalías Congénitases
dc.subjectMortalidades
dc.subjectHidrocefaliaes
dc.subjectVigilancia de la Poblaciónes
dc.subjectPrevalenciaes
dc.subjectCrecimiento Demográficoes
dc.titleAnalysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000-2014 multi-country registry-based studyes
dc.typeArtículoes
dc.identifier.doi10.1002/bdr2.2045-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.openairetypeArtículo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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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