1. DSpace-CRIS @ ANLIS
  2. Centro Nacional de Genética Médica
  3. Publicaciones CeNaGeM
Por favor, use este identificador para citar o enlazar este ítem: http://sgc.anlis.gob.ar/handle/123456789/2742
Campo DC Valor Lengua/Idioma
dc.contributor.authorCarreño, Angiees
dc.contributor.authorAguilera, Maria Paulaes
dc.contributor.authorIbañez, Linaes
dc.contributor.authorSarmiento, Karenes
dc.contributor.authorGili, Juan Aes
dc.contributor.authorSiffel, Csabaes
dc.contributor.authorNembhard, Wendy Nes
dc.contributor.authorBergman, Jorieke E Hes
dc.contributor.authorBermejo-Sánchez, Evaes
dc.contributor.authorTagliabue, Giovannaes
dc.contributor.authorDastgiri, Saeedes
dc.contributor.authorFeldkamp, Marcia Les
dc.contributor.authorPocius, Stephaniees
dc.contributor.authorGatt, Miriames
dc.contributor.authorMartinez, Lauraes
dc.contributor.authorCanessa, María Auroraes
dc.contributor.authorGroisman, Borises
dc.contributor.authorKällén, Karines
dc.contributor.authorLandau, Daniellees
dc.contributor.authorLelong, Nathaliees
dc.contributor.authorMorgan, Margeryes
dc.contributor.authorArteaga-Vázquez, Jazmínes
dc.contributor.authorSantoroi, Michelees
dc.contributor.authorRissmann, Ankees
dc.contributor.authorSipek, Antonines
dc.contributor.authorSzabova, Elenaes
dc.contributor.authorWertelecki, Wladimires
dc.contributor.authorCanfield, Mark Aes
dc.contributor.authorMastroiacovo, Pierpaoloes
dc.contributor.authorZarante, Ignacioes
dc.date.accessioned2026-05-07T18:35:49Z-
dc.date.available2026-05-07T18:35:49Z-
dc.date.issued2026-04-20-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/2742-
dc.descriptionFil: Carreño, Angie. Birth Defect Surveillance Program, Faculty of Health Sciences, Pontificia Universidad Javeriana, Cali, Colombia. Fil: Aguilera, Maria Paula. Human Genetics Institute, Faculty of Medicine, Pontificia Universidad Javeriana, Bogotá, Colombia. Fil: Ibañez, Lina. Faculty of Health Sciences, Universidad Libre Sectional Cali, Cali, Colombia. Fil: Sarmiento, Karen. Department of Physiologic Science, Faculty of Medicine, Pontificia Universidad Javeriana, Bogotá, Colombia. Fil: Gili, Juan A. Estudio Colaborativo Latino Americano de Malformaciones Congénitas ECLAMC (ECLAMC), Centro de Educación Médica e Investigaciones Clínicas (CEMIC-CONICET), Buenos Aires, Argentina; Universidad Nacional de Villa María, Córdoba, Argentina. Fil: Siffel, Csaba. College of Allied Health Sciences, Augusta University, Augusta, Georgia, USA. Fil: Nembhard, Wendy N. Arkansas Center for Birth Defects Research and Prevention and Arkansas Reproductive Health Monitoring System, University of Arkansas for Medical Sciences, Department of Epidemiology, Little Rock, Arkansas, USA. Fil: Bergman, Jorieke E H. Department of Genetics, EUROCAT Northern Netherlands, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands. Fil: Bermejo-Sánchez, Eva. Estudio Colaborativo Español de Malformaciones Congénitas (ECEMC), Unidad de Investigación sobre Anomalías Congénitas (UIAC), Instituto de Investigación de Enfermedades Raras (IIER), Instituto de Salud Carlos III, Madrid, España. Fil: Tagliabue, Giovanna. Lombardy Congenital Anomalies Registry, Cancer Registry Unit, Fondazione IRCCS, National Cancer Institute, Roma, Italia. Fil: Dastgiri, Saeed. Health Services Management Research Centre, Tabriz University of Medical Sciences, Tabriz, Iran. Fil: Feldkamp, Marcia L. Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA. Fil: Pocius, Stephanie. Utah Birth Defect Network, Office of Children With Special Health Care Needs, Division of Family Health, Utah Department of Health and Human Services, Salt Lake City, Utah, USA. Fil: Gatt, Miriam. Malta Congenital Anomalies Registry, Directorate for Health Information and Research, La Valeta, Malta. Fil: Martinez, Laura. Departamento de Genética, Hospital Universitario. Dr. José Eleuterio González, Universidad Autónoma de Nuevo León, Nuevo León, Mexico. Fil: Canessa, María Aurora. Registro Regional Malformacional Congénita Maule Health Service (RRMC-SSM), Maule, Chile. Fil: Groisman, Boris. Red Nacional de Anomalías Congénitas de Argentina (RENAC), Centro Nacional de Genética Médica, Administración Nacional de Laboratorios e Institutos de Salud (ANLIS) Ministerio de Salud, Buenos Aires, Argentina. Fil: Källén, Karin. National Board of Health and Welfare, Stockholm, Sweden. Fil: Landau, Danielle. Department of Neonatology, Soroka Medical Center, Beer-Sheva, Israel. Fil: Lelong, Nathalie. University of Paris, CRESS Obstetrical, Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA, Paris, France. Fil: Morgan, Margery. CARIS, the Congenital Anomaly Register for Wales, Singleton Hospital, Swansea, Wales, UK. Fil: Arteaga-Vazquez, Jazmin. Department of Genetics, RYVEMCE, National Institute of Medical Sciences and Nutrition Salvador Zubirán, Mexico City, Mexico. Fil: Santoroi, Michele. Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy. Fil: Rissmann, Anke. Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke University, Magdeburg, Germany. Fil: Sipek, Antonin. Department of Medical Genetics, Thomayer Hospital, Prague, Czech Republic. Fil: Szabova, Elena. Slovak Teratologic Information Centre (FPH), Slovak Medical University, Bratislava, Slovak Republic. Fil: Wertelecki, Wladimir. Omni-Net for Children International Charitable Fund, Rivne, Ukraine. Fil: Canfield,Mark A. Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas, USA. Fil: Mastroiacovo, Pierpaolo. International Center on Birth Defects, International Clearinghouse for Birth Defects Surveillance and Research, Rome, Italy. Fil: Zarante, Ignacio. Human Genetics Institute, Faculty of Medicine, Pontificia Universidad Javeriana, Bogotá, Colombia; San Ignacio University Hospital, Bogotá, Colombia.es
dc.description.abstractSmall intestinal atresia (SIA) consists of a congenital obstruction of the lumen of the duodenum, jejunum, or ileum with varying severity. The aim of the investigation was to analyze the prevalence and mortality of SIA, using data from the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR).es
dc.language.isoenes
dc.publisherWileyes
dc.subjectEpidemiologíaes
dc.subjectMortalidades
dc.subjectAtresia Intestinales
dc.subjectVigilanciaes
dc.titleAnalysis of Prevalence and Mortality Among Neonates and Children With Intestinal Atresia: A Multinational Study, 1974-2015es
dc.typeArtículoes
dc.identifier.doi10.1002/bdr2.70032-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.openairetypeArtículo-
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)-
Aparece en las colecciones: Publicaciones CeNaGeM
Ficheros en este ítem:
Fichero Descripción Tamaño Formato
10.1002.70032.pdfEnglish; 15 pages577.5 kBAdobe PDFVisualizar/Abrir
Mostrar el registro sencillo del ítem

Visualizaciones de página(s)

16
comprobado en 11-may-2026

Descarga(s)

1
comprobado en 11-may-2026

Google ScholarTM

Consultar

Altmetric

Altmetric


Los ítems de DSpace están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.