A Multicountry Analysis of Prevalence and Mortality among Neonates and Children with Bladder Exstrophy.

Autor: Kancherla V; Department of Epidemiology, Emory University Rollins School of Public Health, Atlanta, Georgia., Tandaki L; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke-University, Magdeburg, Germany., Sundar M; Department of Epidemiology, Emory University Rollins School of Public Health, Atlanta, Georgia., Lux A; Institute for Biometrics and Medical Informatics, Medical Faculty, Otto-von-Guericke-University, Magdeburg, Germany., Bakker MK; Department of Genetics, University of Groningen, University Medical Center Groningen, Eurocat Northern The Netherlands, Groningen, The Netherlands., Bergman JE; Department of Genetics, University of Groningen, University Medical Center Groningen, Eurocat Northern The Netherlands, Groningen, The Netherlands., Bermejo-Sánchez E; 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, Spain., Canfield MA; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas., Feldkamp ML; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah., Groisman B; 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, Argentina., Hurtado-Villa P; Department of Basic Sciences of Health, School of Health, Pontificia Universidad Javeriana Cali, Colombia and Clínica Imbanaco, Cali, Colombia., Källén K; National Board of Health and Welfare, Stockholm, Sweden., Landau D; Department of Neonatology, Soroka Medical Center, Beer-Sheva, Israel., Lelong N; Université de Paris, Inserm U1153, Obstetrical, Perinatal and Pediatric Epidemiology Research Team (Epopé), Center for Epidemiology and Statistics Sorbonne Paris Cité (CRESS) Paris, France., Lopez-Camelo J; ECLAMC, Center for Medical Education and Clinical Research (CEMIC-CONICET), Buenos Aires, Argentina., Mastroiacovo P; International Center on Birth Defects, International Clearinghouse for Birth Defects Surveillance and Research, Rome, Italy., Morgan M; CARIS, the Congenital Anomaly Register for Wales, Singleton Hospital, Swansea, Wales, United Kingdom., Mutchinick OM; RYVEMCE (Registry and Epidemiologic Surveillance of Congenital Malformations), Department of Genetics, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico., Nance AE; Utah Department of Health, Bureau of Children with Special Health Care Needs, Utah Birth Defects Network, Salt Lake City, Utah., Nembhard WN; 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, Little Rock, Arkansas., Pierini A; Institute of Clinical Physiology, National Research Council and Fondazione Toscana Gabriele Monasterio, Tuscany Registry of Congenital Defects, Pisa, Italy., Šípek A; Department of Medical Genetics, Thomayer Hospital, Prague, Czech Republic., Stallings EB; Division of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities, US Centers for Disease Control and Prevention, Atlanta, Georgia., Szabova E; Slovak Teratologic Information Centre (FPH), Slovak Medical University, Bratislava, Slovak Republic., Wertelecki W; OMNI-Net Ukraine, Rivne, Ukraine., Zarante I; Human Genetics Institute, Pontificia Universidad Javeriana, Bogotá, Colombia and Hospital Universitario San Ignacio, Bogotá, Colombia., Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke-University, Magdeburg, Germany.

Publikováno v: American journal of perinatology [Am J Perinatol] 2024 Jul; Vol. 41 (9), pp. 1143-1154. Date of Electronic Publication: 2022 May 29.

Esophageal atresia and prenatal exposure to mycophenolate

Autor: Martín, M.C., Cristiano, E., Villanueva, M., Bonora, M.L., Berguio, N., Tocci, A., Groisman, B., Bidondo, M.P., Liascovich, R., Barbero, P.

Publikováno v: In Reproductive Toxicology December 2014 50:117-121

Birth prevalence of congenital anomalies in Argentina, according to socioeconomic level.

Autor: Bronberg R; Ramos Mejía Hospital, Buenos Aires, Argentina. rabronberg@intramed.net.; National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina. rabronberg@intramed.net.; Buenos Aires Government Research Committee, Buenos Aires, Argentina. rabronberg@intramed.net., Groisman B; National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina.; National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina., Bidondo MP; National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina.; Medicine College, University of Buenos Aires (UBA), Buenos Aires, Argentina., Barbero P; National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina., Liascovich R; National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics, National Administration of Health Laboratories and Institutes, National Ministry of Health, Buenos Aires, Argentina.; National Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.

Publikováno v: Journal of community genetics [J Community Genet] 2021 Jul; Vol. 12 (3), pp. 345-355. Date of Electronic Publication: 2021 Mar 31.

T-cell engineered with a fully humanized B-cell maturation antigen-specific T-cell antigen coupler receptor effectively target multiple myeloma.

Autor: Bezverbnaya K; McMaster Immunology Research Center, McMaster University, Hamilton, Canada; Department of Medicine, McMaster University, Hamilton, Canada., Hammill JA; McMaster Immunology Research Center, McMaster University, Hamilton, Canada; Department of Medicine, McMaster University, Hamilton, Canada; Center for Discovery in Cancer Research, McMaster University, Hamilton, Canada., Cummings D; McMaster Immunology Research Center, McMaster University, Hamilton, Canada; Department of Medicine, McMaster University, Hamilton, Canada; Center for Discovery in Cancer Research, McMaster University, Hamilton, Canada., Bojovic B; McMaster Immunology Research Center, McMaster University, Hamilton, Canada; Department of Medicine, McMaster University, Hamilton, Canada; Center for Discovery in Cancer Research, McMaster University, Hamilton, Canada., Groisman B; McMaster Immunology Research Center, McMaster University, Hamilton, Canada., Baker CL; McMaster Immunology Research Center, McMaster University, Hamilton, Canada; Department of Medicine, McMaster University, Hamilton, Canada; Center for Discovery in Cancer Research, McMaster University, Hamilton, Canada., Aarts C; McMaster Immunology Research Center, McMaster University, Hamilton, Canada; Department of Medicine, McMaster University, Hamilton, Canada; Center for Discovery in Cancer Research, McMaster University, Hamilton, Canada., Hayes DL; Triumvira Immunologics, Hamilton, Canada., Rill D; Triumvira Immunologics, Hamilton, Canada., Xu SX; Triumvira Immunologics, Hamilton, Canada., Bader AG; Triumvira Immunologics, Hamilton, Canada., Helsen CW; McMaster Immunology Research Center, McMaster University, Hamilton, Canada; Triumvira Immunologics, Hamilton, Canada., Bramson JL; McMaster Immunology Research Center, McMaster University, Hamilton, Canada; Department of Medicine, McMaster University, Hamilton, Canada; Center for Discovery in Cancer Research, McMaster University, Hamilton, Canada; Office of the Vice Dean, Research, Faculty of Health Sciences, McMaster University, Hamilton, Canada. Electronic address: bramsonj@mcmaster.ca.

Publikováno v: Cytotherapy [Cytotherapy] 2023 May; Vol. 25 (5), pp. 490-501. Date of Electronic Publication: 2023 Feb 11.

The Latin American network for congenital malformation surveillance: ReLAMC.

Autor: Orioli IM; ReLAMC (Latin American Network of Congenital Malformation Surveillance) at Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.; Instituto Nacional de Genética Médica Populacional INAGEMP, Porto Alegre, Brazil., Dolk H; Maternal Fetal and Infant Research Centre, Institute of Nursing and Health Research, Ulster University, Newtownabbey, Northern Ireland, United Kingdom., Lopez-Camelo J; Latin American Collaborative Study of Congenital Malformations (ECLAMC) at Center for Medical Education and Clinical Research (CEMIC-CONICET), Buenos Aires, Argentina., Groisman B; National Network of Congenital Anomalies of Argentina (RENAC), National Center of Medical Genetics (CNGM), National Administration of Laboratories and Health Institutes (ANLIS), National Ministry of Health, Buenos Aires, Argentina., Benavides-Lara A; Centro de Registro de Enfermedades Congénitas (CREC), Unidad de Enfermedades Congénitas, Instituto Costarricense de Investigación y Enseñanza en Nutrición y Salud-INCIENSA, Cartago, Costa Rica., Gimenez LG; Latin American Collaborative Study of Congenital Malformations (ECLAMC) at Center for Medical Education and Clinical Research (CEMIC-CONICET), Buenos Aires, Argentina., Correa DM; ReLAMC (Latin American Network of Congenital Malformation Surveillance) at Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil., Ascurra M; Registro Nacional de Defectos Congénitos Paraguay, Programa Nacional de Prevención de Defectos Congénitos (RENADECOPY-PNPDC), Ministerio de Salud Pública y Bienestar Social, Assuncion, Paraguay., de Aquino Bonilha E; Secretaria Municipal da Saúde de São Paulo, Coordenação de Epidemiologia e Informação, Gerência do SINASC, São Paulo, Brazil., Canessa-Tapia MA; Regional Register of Congenital Anomalies Maule Health Service, Linares, Chile., de França GVA; Secretaria de Vigilância em Saúde, Ministério da Saúde, Brasília, Distrito Federal, Brazil., Hurtado-Villa P; Facultad de Ciencias de la Salud, Pontificia Universidad Javeriana Cali, Cali, Colombia., Ibarra-Ramírez M; Departamento de Genética, Facultad de Medicina y Hospital Universitario José E. González, Universidad Autónoma de Nuevo León, Monterrey, Mexico., Pardo R; Unidad de Neonatologia, Sección de Genética, Hospital Clínico Universidad de Chile, Unidad de Genética y Enfermedades Metabólicas, Complejo Asistencial Dr. Sótero del Río: Registro Nacional de Anomalías Congénitas de Chile RENACH, Santiago, Chile., Pastora DM; Facultad de Ciencias Médicas UNAN-León, MINSA, León, Nicaragua., Zarante I; Instituto de Genética Humana, Pontificia Universidad Javeriana Bogotá, Bogotá, Colombia., Soares FS; ReLAMC (Latin American Network of Congenital Malformation Surveillance) at Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil., de Carvalho FM; Laboratory of Congenital Malformations Epidemiology (LEMC), Instituto Oswaldo Cruz (IOC), Fundação Oswaldo Cruz (Fiocruz), Rio de Janeiro, Rio de Janeiro, Brazil., Piola M; Latin American Collaborative Study of Congenital Malformations (ECLAMC) at Center for Medical Education and Clinical Research (CEMIC-CONICET), Buenos Aires, Argentina.

Publikováno v: American journal of medical genetics. Part C, Seminars in medical genetics [Am J Med Genet C Semin Med Genet] 2020 Dec; Vol. 184 (4), pp. 1078-1091. Date of Electronic Publication: 2020 Dec 14.