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Items: 20

1.

Resolution of maternal Mirror syndrome after succesful fetal intrauterine therapy: a case series.

Chimenea A, García-Díaz L, Calderón AM, Heras MML, Antiñolo G.

BMC Pregnancy Childbirth. 2018 Apr 6;18(1):85. doi: 10.1186/s12884-018-1718-0.

2.

The Role of Cultural and Family Values on Social Connectedness and Loneliness among Ethnic Minority Elders.

Garcia Diaz L, Savundranayagam MY, Kloseck M, Fitzsimmons D.

Clin Gerontol. 2017 Oct 31:1-13. doi: 10.1080/07317115.2017.1395377. [Epub ahead of print]

PMID:
29206574
3.

TGA+VSD and Subpulmonary Conus: From Fetus to a 3-dimensional Model.

Manso B, García-Díaz L, Valverde I.

Rev Esp Cardiol (Engl Ed). 2017 Nov;70(11):1007. doi: 10.1016/j.rec.2017.04.023. Epub 2017 May 19. English, Spanish. No abstract available.

PMID:
28532978
4.

Ultrasound, Echocardiography, MRI, and Genetic Analysis of a Fetus with Congenital Diaphragmatic Hernia and Partial 11q Trisomy.

Fernández-Perea Y, García-Díaz L, Sánchez J, Antiñolo G, Borrego S.

Case Rep Obstet Gynecol. 2017;2017:1471704. doi: 10.1155/2017/1471704. Epub 2017 Mar 2.

5.

Public health impact and economic benefits of quadrivalent influenza vaccine in Latin America.

Jamotte A, Clay E, Macabeo B, Caicedo A, Lopez JG, Bricks L, Romero Prada M, Marrugo R, Alfonso P, Moreno Arévalo B, Franco D, Garcia Diaz L, Isaza de Molto Y.

Hum Vaccin Immunother. 2017 Apr 3;13(4):877-888. doi: 10.1080/21645515.2016.1256928. Epub 2017 Jan 24.

6.

Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations.

Fernández RM, Sánchez J, García-Díaz L, Peláez-Nora Y, González-Meneses A, Antiñolo G, Borrego S.

Am J Med Genet A. 2016 May;170A(5):1268-73. doi: 10.1002/ajmg.a.37559. Epub 2016 Jan 14.

PMID:
26762557
7.

Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects.

Alcántara-Ortigoza MA, De Rubens-Figueroa J, Reyna-Fabian ME, Estandía-Ortega B, González-del Angel A, Molina-Álvarez B, Velázquez-Aragón JA, Villagómez-Martínez S, Pereira-López GI, Martínez-Cruz V, Álvarez-Gómez RM, Díaz-García L.

Pediatr Cardiol. 2015 Apr;36(4):802-8. doi: 10.1007/s00246-014-1091-3. Epub 2014 Dec 19. Erratum in: Pediatr Cardiol. 2015 Oct;36(7):1551.

PMID:
25524324
8.

EXIT procedure in twin pregnancy: a series of three cases from a single center.

García-Díaz L, de Agustín JC, Ontanilla A, Marenco ML, Pavón A, Losada A, Antiñolo G.

BMC Pregnancy Childbirth. 2014 Jul 30;14:252. doi: 10.1186/1471-2393-14-252.

9.

Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome.

García-Díaz L, Coserria F, Antiñolo G.

Case Rep Obstet Gynecol. 2013;2013:472356. doi: 10.1155/2013/472356. Epub 2013 Jan 3.

10.

Prenatal diagnosis of a fetus with congenital heart defect and ring chromosome 14.

Sánchez J, García-Díaz L, Chinchón D, Antiñolo G.

Case Rep Genet. 2012;2012:794075. doi: 10.1155/2012/794075. Epub 2012 Nov 5.

11.

[Intrauterine myelomeningocele repair: experience of the fetal medicine and therapy program of the Virgen de Rocío University Hospital].

Marenco ML, Márquez J, Ontanilla A, García-Díaz L, Rivero M, Losada A, Torrejón R, Sainz JA, Antiñolo G.

Rev Esp Anestesiol Reanim. 2013 Jan;60(1):47-53. doi: 10.1016/j.redar.2012.07.011. Epub 2012 Oct 31. Spanish.

PMID:
23121708
12.

Prenatal management and outcome of junctional ectopic tachycardia and hydrops.

García-Díaz L, Coserria F, Costa S, Antiñolo G.

Arq Bras Cardiol. 2012 Oct;99(4):e145-8. English, Portuguese. No abstract available.

13.

Prenatal management and perinatal outcome in giant placental chorioangioma complicated with hydrops fetalis, fetal anemia and maternal mirror syndrome.

García-Díaz L, Carreto P, Costa-Pereira S, Antiñolo G.

BMC Pregnancy Childbirth. 2012 Jul 28;12:72. doi: 10.1186/1471-2393-12-72.

14.

Isolated absence of septum pellucidum: prenatal diagnosis and outcome.

García-Arreza A, García-Díaz L, Fajardo M, Carreto P, Antiñolo G.

Fetal Diagn Ther. 2013;33(2):130-2. doi: 10.1159/000338009. Epub 2012 Apr 27.

PMID:
22572040
15.

Association of X-linked hydrocephalus and Hirschsprung disease: report of a new patient with a mutation in the L1CAM gene.

Fernández RM, Núñez-Torres R, García-Díaz L, de Agustín JC, Antiñolo G, Borrego S.

Am J Med Genet A. 2012 Apr;158A(4):816-20. doi: 10.1002/ajmg.a.35244. Epub 2012 Feb 17.

PMID:
22344793
16.

Hemimegalencephaly: prenatal diagnosis and outcome.

Alvarez RM, García-Díaz L, Márquez J, Fajardo M, Rivas E, García-Lozano JC, Antiñolo G.

Fetal Diagn Ther. 2011;30(3):234-8. doi: 10.1159/000329937. Epub 2011 Sep 14.

PMID:
21921574
17.

Aortopulmonary window with atrial septal defect: prenatal diagnosis, management and outcome.

Alvarez R, García-Díaz L, Coserria F, Hosseinpour R, Antiñolo G.

Fetal Diagn Ther. 2011;30(4):306-8. doi: 10.1159/000324173. Epub 2011 Feb 18.

PMID:
21335954
18.

Diagnosis and management of fetal intrapericardial Morgagni diaphragmatic hernia with massive pericardial effussion.

Antiñolo G, De Agustin JC, Losada A, Marenco ML, Garcia-Diaz L, Morcillo J.

J Pediatr Surg. 2010 Feb;45(2):424-6. doi: 10.1016/j.jpedsurg.2009.11.009.

PMID:
20152367
19.

[Pathogenesis of severe vision deficiency in school-age children in Hungary].

Czeizel E, Törzs E, Kovács J, Szabó G, Vitéz M, Garcia Diaz L.

Orv Hetil. 1991 Jul 21;132(29):1593-8. Hungarian.

PMID:
1861857
20.

[Congenital monomorph adenoma of the parotid gland (author's transl)].

Jover P, Quirós L, García Díaz L, Terrón F, Contreras F, Solas I.

An Esp Pediatr. 1978 Apr;11(4):351-4. Spanish.

PMID:
697207

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