García-Alix A - Search Results

1

Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome.

Fernández L, Lapunzina P, Arjona D, López Pajares I, García-Guereta L, Elorza D, Burgueros M, De Torres ML, Mori MA, Palomares M, García-Alix A, Delicado A. Fernández L, et al. Clin Genet. 2005 Oct;68(4):373-8. doi: 10.1111/j.1399-0004.2005.00493.x. Clin Genet. 2005. PMID: 16143025

2

De novo t(5p;21q) in a patient previously diagnosed as monosomy 21.

López-Pajares I, Martin-Ancel A, Cabello P, Delicado A, Garcia-Alix A, San Roman C. López-Pajares I, et al. Clin Genet. 1993 Feb;43(2):94-7. doi: 10.1111/j.1399-0004.1993.tb04457.x. Clin Genet. 1993. PMID: 8448910

3

[Clinical guide to the management of patients with Beckwith-Wiedemann syndrome].

Lapunzina Badía P, del Campo Casanelles M, Delicado Navarro A, Fernández-Toral J, García-Alix A, García-Guereta L, Pérez Jurado LA, Ramos Fuentes FJ, Sánchez Díaz A, Urioste Azcorra M. Lapunzina Badía P, et al. An Pediatr (Barc). 2006 Mar;64(3):252-9. doi: 10.1157/13085513. An Pediatr (Barc). 2006. PMID: 16527093 Free article. Spanish.

4

Multiple organ involvement in perinatal asphyxia.

Martín-Ancel A, García-Alix A, Gayá F, Cabañas F, Burgueros M, Quero J. Martín-Ancel A, et al. J Pediatr. 1995 Nov;127(5):786-93. doi: 10.1016/s0022-3476(95)70174-5. J Pediatr. 1995. PMID: 7472837

5

[Trisomy 5p: a report of 2 cases].

Alvarez-Coca J, García-Alix A, Delicado A, González M, Escribá R, López Pajares I, Morena V, Peralta A. Alvarez-Coca J, et al. An Esp Pediatr. 1985 Mar 31;22(4):288-92. An Esp Pediatr. 1985. PMID: 4003955 Spanish.

6

Early neurological manifestations and brain anomalies in Marden-Walker syndrome.

García-Alix A, Blanco D, Cabañas F, Garcia Sanchez P, Pellicer A, Quero J. García-Alix A, et al. Am J Med Genet. 1992 Sep 1;44(1):41-5. doi: 10.1002/ajmg.1320440110. Am J Med Genet. 1992. PMID: 1519648

7

Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion.

García-Cabezas MA, García-Alix A, Martín Y, Gutiérrez M, Hernández C, Rodríguez JI, Morales C. García-Cabezas MA, et al. Acta Neuropathol. 2004 May;107(5):475-8. doi: 10.1007/s00401-004-0825-3. Epub 2004 Feb 13. Acta Neuropathol. 2004. PMID: 14968368

8

Microcephaly-lymphedema-chorioretinal dysplasia associated with pachymicrogyria and atrophy of the cerebellar vermis: an integration of brain-ocular migration disorders.

Pastora N, Peralta J, Canal-Fontcuberta I, Grabowska A, Pulido JS, Abelairas J, Armada F, Garcia-Alix A. Pastora N, et al. Ophthalmic Genet. 2012 Jun;33(2):116-8. doi: 10.3109/13816810.2011.626012. Epub 2012 Mar 15. Ophthalmic Genet. 2012. PMID: 22420539

9

[The Adams-Oliver syndrome in Spain: the epidemiological aspects].

Martínez-Frías ML, Arroyo Carrera I, Muñoz-Delgado NJ, Nieto Conde C, Rodríguez-Pinilla E, Urioste Azcorra M, Omeñaca Teres F, García Alix A. Martínez-Frías ML, et al. An Esp Pediatr. 1996 Jul;45(1):57-61. An Esp Pediatr. 1996. PMID: 8849132 Spanish.

10

[Duration of resuscitation in neonates with Apgar scores at 10 minutes of less than 3 in the hypothermia era].

Martín-Ancel A, Balaguer A, García-Alix A. Martín-Ancel A, et al. An Pediatr (Barc). 2015 Mar;82(3):129-30. doi: 10.1016/j.anpedi.2014.09.002. Epub 2014 Oct 7. An Pediatr (Barc). 2015. PMID: 25300781 Free article. Spanish. No abstract available.

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