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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2012 1
2014 2
2016 2
2017 2
2018 1
2019 2
2020 1
2021 1
2022 1
2024 1

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12 results

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Page 1
Congenital hyperinsulinism in Gran Canaria, Canary Isles.
Nóvoa-Medina Y, Domínguez García A, Quinteiro González S, García Cruz LM, Santana Rodríguez A. Nóvoa-Medina Y, et al. Among authors: santana rodriguez a. An Pediatr (Engl Ed). 2021 Aug;95(2):93-100. doi: 10.1016/j.anpede.2020.08.006. Epub 2021 Jul 10. An Pediatr (Engl Ed). 2021. PMID: 34253504 Free article.
Prenatal diagnosis of Greig Cephalopolysyndactyly Syndrome. When to suspect it.
Garcia-Rodriguez R, Rodriguez-Rodriguez R, Garcia-Delgado R, Romero-Requejo A, Medina-Castellano M, Garcia Cruz L, Santana Rodriguez A, Garcia-Hernandez JA. Garcia-Rodriguez R, et al. Among authors: santana rodriguez a. J Matern Fetal Neonatal Med. 2022 Jun;35(11):2162-2165. doi: 10.1080/14767058.2020.1774541. Epub 2020 Jun 4. J Matern Fetal Neonatal Med. 2022. PMID: 32495660
The solitary median maxillary central incisor (SMMCI) syndrome: Associations, prenatal diagnosis, and outcomes.
Garcia Rodriguez R, Garcia Cruz L, Novoa Medina Y, Garcia Delgado R, Perez Gonzalez J, Palma Milla C, Lopez Siles J, Medina Castellano M, Garcia Hernandez JA, Santana Rodriguez A. Garcia Rodriguez R, et al. Among authors: santana rodriguez a. Prenat Diagn. 2019 May;39(6):415-419. doi: 10.1002/pd.5451. Epub 2019 Apr 26. Prenat Diagn. 2019. PMID: 30900264 Review.
[Three cases of Pallister-Killian syndrome].
Toledo-Bravo de Laguna L, del Campo-Casanelles M, Santana-Rodriguez A, Santana-Artiles A, Sebastian-Garcia I, Cabrera-Lopez JC. Toledo-Bravo de Laguna L, et al. Among authors: santana rodriguez a. Rev Neurol. 2014 Jan 16;58(2):63-8. Rev Neurol. 2014. PMID: 24399622 Free article. Spanish.
Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction.
Amor-Salamanca A, Santana Rodríguez A, Rasoul H, Rodríguez-Palomares JF, Moldovan O, Hey TM, Delgado MG, Cuenca DL, de Castro Campos D, Basurte-Elorz MT, Macías-Ruiz R, Fuentes Cañamero ME, Galvin J, Bilbao Quesada R, de la Higuera Romero L, Trujillo-Quintero JP, García-Cruz LM, Cárdenas-Reyes I, Jiménez-Jáimez J, García-Hernández S, Valverde-Gómez M, Gómez-Díaz I, Limeres Freire J, García-Pinilla JM, Gimeno-Blanes JR, Savattis K, García-Pavía P, Ochoa JP. Amor-Salamanca A, et al. Among authors: santana rodriguez a. Circ Genom Precis Med. 2024 Apr;17(2):e004404. doi: 10.1161/CIRCGEN.123.004404. Epub 2024 Feb 14. Circ Genom Precis Med. 2024. PMID: 38353104 Free PMC article.
X-linked adrenal hypoplasia congenita: Novel missense mutation of DAX-1 gene.
Domínguez García Á, Santana Rodríguez A, Cabrera Guedes MF. Domínguez García Á, et al. Among authors: santana rodriguez a. Med Clin (Barc). 2019 Mar 15;152(6):242-243. doi: 10.1016/j.medcli.2018.04.022. Epub 2018 Jun 7. Med Clin (Barc). 2019. PMID: 29887178 English, Spanish. No abstract available.
Evaluation of family history of permanent hearing loss in childhood as a risk indicator in universal screening.
Valido Quintana M, Oviedo Santos Á, Borkoski Barreiro S, Santana Rodríguez A, Ramos Macías Á. Valido Quintana M, et al. Among authors: santana rodriguez a. Acta Otorrinolaringol Esp (Engl Ed). 2017 May-Jun;68(3):157-163. doi: 10.1016/j.otorri.2016.08.001. Epub 2016 Oct 21. Acta Otorrinolaringol Esp (Engl Ed). 2017. PMID: 27776808 English, Spanish.
[Familial hemiplegic migraine type 2: two paediatric case reports].
Toledo-Bravo de Laguna L, Santana-Rodríguez A, Cabrera-López JC, Santana-Artiles A, Sebastián-García I. Toledo-Bravo de Laguna L, et al. Among authors: santana rodriguez a. Rev Neurol. 2012 Feb 16;54(4):222-6. Rev Neurol. 2012. PMID: 22314763 Free article. Spanish.
12 results