Investigación sobre Anomalías Congénitas

A Multicountry Analysis of Prevalence and Mortality among Neonates and Children with Bladder Exstrophy. Am J Perinatol. 2024 Jul;41(9):1143-1154

Kancherla V, Tandaki L, Sundar M, Lux A, Bakker MK, Bergman JE, Bermejo-Sánchez E, Canfield MA, Feldkamp ML, Groisman B, Hurtado-Villa P, Källén K, Landau D, Lelong N, Lopez-Camelo J, Mastroiacovo P, Morgan M, Mutchinick OM, Nance AE, Nembhard WN, Pierini A, Šípek A, Stallings EB, Szabova E, Wertelecki W, Zarante I, Rissmann A.

PUBMED DOI

A Nationwide Registry-Based Study on Mortality Due to Rare Congenital Anomalies. Int J Environ Res Public Health. 2018 Aug 10;15(8). pii:E1715

Alonso-Ferreira V, Sánchez-Díaz G, Villaverde-Hueso A, Posada de la Paz M, Bermejo-Sánchez E.

PUBMED DOI

Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000-2014 multi-country registry-based study. Defects Res. 2022 Jul 15;114(12):631-644

Gili JA, López-Camelo JS, Nembhard WN, Bakker M, de Walle HEK, Stallings EB, Kancherla V; ECEMC Peripheral Group; Contiero P, Dastgiri S, Feldkamp ML, Nance A, Gatt M, Martínez L, Canessa MA, Groisman B, Hurtado-Villa P, Källén K, Landau D, Lelong N, Morgan M, Arteaga-Vázquez J, Pierini A, Rissmann A, Sipek A, Szabova E, Wertelecki W, Zarante I, Canfield MA, Mastroiacovo P.

PUBMED DOI

Analysis of Mortality among Neonates and Children with Spina Bifida: An International Registry-Based Study, 2001-2012. Paediatr Perinat Epidemiol. 2019 Nov;33(6):436-448

Bakker MK, Kancherla V, Canfield MA, Bermejo-Sanchez E, Cragan JD, Dastgiri S, De Walle HEK, Feldkamp ML, Groisman B, Gatt M, Hurtado-Villa P, Kallen K, Landau D, Lelong N, Lopez Camelo JS, Martínez L, Morgan M, Mutchinick OM, Nembhard WN, Pierini A, Rissmann A, Sipek A, Szabova E, Tagliabue G, Wertelecki W, Zarante I, Mastroiacovo P.

PUBMED DOI

Changes in Alcohol Intake During Pregnancy in Spain, 1980 to 2014. Alcohol Clin Exp Res. 2019 Nov;43(11):2367-2373

Romero-Rodríguez E, Cuevas L, Simón L; ECEMC Peripheral Group; Bermejo-Sánchez E, Galán I.

PUBMED DOI

Congenital Anomalies: Cluster Detection and Investigation. Adv Exp Med Biol. 2017;1031:535-557

Bermejo-Sánchez E, Posada de la Paz M.

PUBMED DOI

Deletion 1q43-44 in a patient with clinical diagnosis of Warburg-Micro syndrome. Am J Med Genet A. 2015 Jun;167(6):1243-51

Arroyo-Carrera I, de Zaldívar Tristancho MS, Bermejo-Sánchez E, Martínez-Fernández ML, López-Lafuente A, MacDonald A, Zúñiga Á, Luis Gómez-Skarmeta J, Luisa Martínez-Frías M.

PUBMED DOI

Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date. Am J Med Genet A. 2015 Sep;167A(9):2034-41

Martínez-Fernández ML, Fernández-Toral J, Llano-Rivas I, Bermejo-Sánchez E, MacDonald A, Martínez-Frías ML.

PUBMED DOI

Investigación