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Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000-2014 multi-country registry-based study.
Gili, Juan Antonio; López-Camelo, Jorge Santiago; Nembhard, Wendy N; Bakker, Marian; de Walle, Hermien E K; Stallings, Erin B; Kancherla, Vijaya; Contiero, Paolo; Dastgiri, Saeed; Feldkamp, Marcia L; Nance, Amy; Gatt, Miriam; Martínez, Laura; Canessa, María Aurora; Groisman, Boris; Hurtado-Villa, Paula; Källén, Karin; Landau, Danielle; Lelong, Nathalie; Morgan, Margery; Arteaga-Vázquez, Jazmín; Pierini, Anna; Rissmann, Anke; Sipek, Antonin; Szabova, Elena; Wertelecki, Wladimir; Zarante, Ignacio; Canfield, Mark A; Mastroiacovo, Pierpaolo.
Afiliação
  • Gili JA; ECLAMC, Centro de Educación Médica e Investigaciones Clínicas (CEMIC-CONICET), Buenos Aires, Argentina.
  • López-Camelo JS; Instituto Académico Pedagógico de Ciencias Humanas, Universidad Nacional de Villa María, Córdoba, Argentina.
  • Nembhard WN; ECLAMC, Centro de Educación Médica e Investigaciones Clínicas (CEMIC-CONICET), Buenos Aires, Argentina.
  • Bakker M; 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, USA.
  • de Walle HEK; Department of Genetics, University of Groningen, University Medical Center Groningen, EUROCAT Northern Netherlands, Groningen, The Netherlands.
  • Stallings EB; Department of Genetics, University of Groningen, University Medical Center Groningen, EUROCAT Northern Netherlands, Groningen, The Netherlands.
  • Kancherla V; Metro Atlanta Congenital Defects Program (MACDP), Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia, USA.
  • Contiero P; As listed in http://www.fundacion1000.es/Estructura-del-ECEMC for year 2021, Spain.
  • Dastgiri S; Lombardy Congenital Anomalies Registry, Cancer Registry Unit, Fondazione IRCCS, Istituto Nazionale Tumori, Milan, Italy.
  • Feldkamp ML; Health Services Management Research Centre, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Nance A; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Gatt M; Utah Birth Defect Network, Bureau of Children with Special Health Care Needs, Division of Family Health and Preparedness, Utah Department of Health, Salt Lake City, Utah, USA.
  • Martínez L; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, Tal-Pietà, Malta.
  • Canessa MA; Genetics Department, Hospital Universitario Dr. José E. González, Universidad Autonóma de Nuevo León, San Nicolás de los Garza, Mexico.
  • Groisman B; Regional Register Congenital Malformation Maule Health Service (RRMC-SSM), Maule, Chile.
  • Hurtado-Villa P; 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, Argentina.
  • Källén K; Department of Basic Sciences of Health, School of Health, Pontificia Universidad Javeriana, Cali, Colombia.
  • Landau D; National Board of Health and Welfare, Stockholm, Sweden.
  • Lelong N; Department of Neonatology, Soroka Medical Center, Beer-Sheva, Israel.
  • Morgan M; Université de Paris, CRESS Obstetrical, Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA, Paris, France.
  • Arteaga-Vázquez J; CARIS, The Congenital Anomaly Register for Wales, Singleton Hospital, Swansea, Wales, UK.
  • Pierini A; Department of Genetics, RYVEMCE, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, México City, Mexico.
  • Rissmann A; Institute of Clinical Physiology, National Research Council and Fondazione Toscana Gabriele Monasterio, Tuscany Registry of Congenital Defects, Pisa, Italy.
  • Sipek A; Medical Faculty, Malformation Monitoring Centre Saxony-Anhalt, Otto-von-Guericke University, Magdeburg, Germany.
  • Szabova E; Department of Medical Genetics, Thomayer University Hospital, Prague, Czech Republic.
  • Wertelecki W; Slovak Teratologic Information Centre (FPH), Slovak Medical University, Bratislava, Slovak Republic.
  • Zarante I; Omni-Net for Children International Charitable Fund, Rivne, Ukraine.
  • Canfield MA; Human Genetics Institute, Pontificia Universidad Javeriana, Bogotá, Colombia.
  • Mastroiacovo P; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas, USA.
Birth Defects Res ; 114(12): 631-644, 2022 07 15.
Article em En | MEDLINE | ID: mdl-35633200
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Natimorto / Hidrocefalia Tipo de estudo: Prevalence_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Argentina
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Natimorto / Hidrocefalia Tipo de estudo: Prevalence_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Argentina