García-Alix A - Search Results

1

Okur-Chung neurodevelopmental syndrome in a patient from Spain.

Martinez-Monseny AF, Casas-Alba D, Arjona C, Bolasell M, Casano P, Muchart J, Ramos F, Martorell L, Palau F, García-Alix A, Serrano M. Martinez-Monseny AF, et al. Am J Med Genet A. 2020 Jan;182(1):20-24. doi: 10.1002/ajmg.a.61405. Epub 2019 Nov 15. Am J Med Genet A. 2020. PMID: 31729156

2

Thrombin, protein C, and protein S values in mother-infant dyads in the postpartum period.

Garrido-Barbero M, Arnaez J, Martín-Ancel A, González H, García-Alix A. Garrido-Barbero M, et al. An Pediatr (Engl Ed). 2023 May;98(5):338-343. doi: 10.1016/j.anpede.2023.03.005. Epub 2023 Apr 17. An Pediatr (Engl Ed). 2023. PMID: 37076369 Free article.

3

Retained central venous lines in the newborn: report of one case and systematic review of the literature.

Serrano M, García-Alix A, López JC, Pérez J, Quero J. Serrano M, et al. Neonatal Netw. 2007 Mar-Apr;26(2):105-10. doi: 10.1891/0730-0832.26.2.105. Neonatal Netw. 2007. PMID: 17402602 Review.

4

Early identification of brain injury in infants with hypoxic ischemic encephalopathy at high risk for severe impairments: accuracy of MRI performed in the first days of life.

Agut T, León M, Rebollo M, Muchart J, Arca G, Garcia-Alix A. Agut T, et al. BMC Pediatr. 2014 Jul 8;14:177. doi: 10.1186/1471-2431-14-177. BMC Pediatr. 2014. PMID: 25005267 Free PMC article.

5

Language learning and brain reorganization in a 3.5-year-old child with left perinatal stroke revealed using structural and functional connectivity.

François C, Ripollés P, Bosch L, Garcia-Alix A, Muchart J, Sierpowska J, Fons C, Solé J, Rebollo M, Gaitán H, Rodriguez-Fornells A. François C, et al. Cortex. 2016 Apr;77:95-118. doi: 10.1016/j.cortex.2016.01.010. Epub 2016 Feb 4. Cortex. 2016. PMID: 26922507

6

A Population-Based Study on Congenital Disorders of Protein N- and Combined with O-Glycosylation Experience in Clinical and Genetic Diagnosis.

Pérez-Cerdá C, Girós ML, Serrano M, Ecay MJ, Gort L, Pérez Dueñas B, Medrano C, García-Alix A, Artuch R, Briones P, Pérez B. Pérez-Cerdá C, et al. J Pediatr. 2017 Apr;183:170-177.e1. doi: 10.1016/j.jpeds.2016.12.060. Epub 2017 Jan 27. J Pediatr. 2017. PMID: 28139241

7

[The human genome and medicine].

Palau F, García-Alix A. Palau F, et al. An Pediatr (Engl Ed). 2018 Jul;89(1):1-2. doi: 10.1016/j.anpedi.2018.04.009. Epub 2018 May 10. An Pediatr (Engl Ed). 2018. PMID: 29753559 Free article. Spanish. No abstract available.

8

Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations.

Casas-Alba D, Martínez-Monseny A, Pino-Ramírez RM, Alsina L, Castejón E, Navarro-Vilarrubí S, Pérez-Dueñas B, Serrano M, Palau F, García-Alix A. Casas-Alba D, et al. Hum Mutat. 2018 Dec;39(12):1752-1763. doi: 10.1002/humu.23638. Epub 2018 Sep 17. Hum Mutat. 2018. PMID: 30176098 Review.

9

Right Structural and Functional Reorganization in Four-Year-Old Children with Perinatal Arterial Ischemic Stroke Predict Language Production.

François C, Ripollés P, Ferreri L, Muchart J, Sierpowska J, Fons C, Solé J, Rebollo M, Zatorre RJ, Garcia-Alix A, Bosch L, Rodriguez-Fornells A. François C, et al. eNeuro. 2019 Aug 28;6(4):ENEURO.0447-18.2019. doi: 10.1523/ENEURO.0447-18.2019. Print 2019 Jul/Aug. eNeuro. 2019. PMID: 31383726 Free PMC article.

10

Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion.

Fernández L, Lapunzina P, Pajares IL, Palomares M, Martínez I, Fernández B, Quero J, García-Guereta L, García-Alix A, Burgueros M, Galán-Gómez E, Carbonell-Pérez JM, Pérez-Granero A, Torres-Juan L, Heine-Suñer D, Rosell J, Delicado A. Fernández L, et al. Am J Med Genet A. 2008 May 1;146A(9):1134-41. doi: 10.1002/ajmg.a.32256. Am J Med Genet A. 2008. PMID: 18384142

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