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2015 2
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2018 2
2019 1
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Page 1
[Genetic predisposition to childhood cancer].
Carrasco Salas P, Lapunzina P, Pérez-Martínez A. Carrasco Salas P, et al. An Pediatr (Barc). 2017 Sep;87(3):125-127. doi: 10.1016/j.anpedi.2017.01.011. Epub 2017 Mar 7. An Pediatr (Barc). 2017. PMID: 28283310 Free article. Spanish. No abstract available.
Diversity of oncopharmacogenetic profile within Spanish population.
Ferrer Bolufer I, Galiana Vallés X, Izquierdo Álvarez S, Serrano Mira A, Guzmán Luján C, Safont Aguilera MJ, González Tarancón R, Bolaños Naranjo M, Carrasco Salas P, Santamaría González M, Rodríguez-López R. Ferrer Bolufer I, et al. Among authors: carrasco salas p. Pharmacogenet Genomics. 2024 Mar 18. doi: 10.1097/FPC.0000000000000530. Online ahead of print. Pharmacogenet Genomics. 2024. PMID: 38488402
Noonan syndrome: Severe phenotype and PTPN11 mutations.
Carrasco Salas P, Gómez-Molina G, Carreto-Alba P, Granell-Escobar R, Vázquez-Rico I, León-Justel A. Carrasco Salas P, et al. Med Clin (Barc). 2019 Jan 18;152(2):62-64. doi: 10.1016/j.medcli.2018.03.015. Epub 2018 Apr 25. Med Clin (Barc). 2019. PMID: 29703613 English, Spanish.
Unusual clinical presentation and new mutation in a case of triple A syndrome.
López Valverde ME, Rebollo Pérez MI, Martínez Fernández EM, Murillo Espejo E, Carrasco Salas P. López Valverde ME, et al. Among authors: carrasco salas p. Endocrinol Diabetes Nutr (Engl Ed). 2022 May;69(5):382-384. doi: 10.1016/j.endien.2022.04.002. Epub 2022 May 13. Endocrinol Diabetes Nutr (Engl Ed). 2022. PMID: 35570138 No abstract available.
Contingent prenatal screening for frequent aneuploidies with cell-free fetal DNA analysis.
Torres Aguilar MR, Carrasco Salas P, Santos Rosa C, Bueno Rodríguez G, Martínez-Bonet E, Carreto Alba P, León-Justel A, Granell Escobar MR. Torres Aguilar MR, et al. Among authors: carrasco salas p. Taiwan J Obstet Gynecol. 2021 Jul;60(4):745-751. doi: 10.1016/j.tjog.2021.05.028. Taiwan J Obstet Gynecol. 2021. PMID: 34247818 Free article.
The role of CDKN2A/B deletions in pediatric acute lymphoblastic leukemia.
Carrasco Salas P, Fernández L, Vela M, Bueno D, González B, Valentín J, Lapunzina P, Pérez-Martínez A. Carrasco Salas P, et al. Pediatr Hematol Oncol. 2016 Oct-Nov;33(7-8):415-422. doi: 10.1080/08880018.2016.1251518. Pediatr Hematol Oncol. 2016. PMID: 27960642
Unusual clinical presentation and new mutation in a case of triple A syndrome.
López Valverde ME, Rebollo Pérez MI, Martínez Fernández EM, Murillo Espejo E, Carrasco Salas P. López Valverde ME, et al. Among authors: carrasco salas p. Endocrinol Diabetes Nutr (Engl Ed). 2021 Jul 12:S2530-0164(21)00153-1. doi: 10.1016/j.endinu.2021.03.006. Online ahead of print. Endocrinol Diabetes Nutr (Engl Ed). 2021. PMID: 34266807 English, Spanish. No abstract available.
Hyperinsulinemic hypoglycemia in a patient with an intragenic NSD1 mutation.
Carrasco Salas P, Palma Milla C, Lezana Rosales JM, Benito C, Franco Freire S, López Siles J. Carrasco Salas P, et al. Am J Med Genet A. 2016 Feb;170A(2):544-546. doi: 10.1002/ajmg.a.37440. Epub 2015 Oct 21. Am J Med Genet A. 2016. PMID: 26487424 No abstract available.
12 results