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Page 1
Neurofibromatosis type I: mutation spectrum of NF1 in spanish patients.
Ann Hum Genet. 2018 Nov;82(6):425-436. doi: 10.1111/ahg.12272. Epub 2018 Jul 16.
Ann Hum Genet. 2018.
PMID: 30014477
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. Among authors: lopez siles j.
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.
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[Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy].
Carrasco Salas P, Palma Milla C, López Montiel J, Benito C, Franco Freire S, López Siles J.
Carrasco Salas P, et al. Among authors: lopez siles j.
Med Clin (Barc). 2016 Feb 19;146(4):163-6. doi: 10.1016/j.medcli.2015.10.015. Epub 2015 Dec 10.
Med Clin (Barc). 2016.
PMID: 26683077
Spanish.
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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: lopez siles j.
Prenat Diagn. 2019 May;39(6):415-419. doi: 10.1002/pd.5451. Epub 2019 Apr 26.
Prenat Diagn. 2019.
PMID: 30900264
Review.
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[Influenza virus in pediatrics. A reason for hospitalization].
Cruz-Cañete M, Moreno-Pérez D, Jurado-Ortiz A, García-Martín FJ, López-Siles J, Olalla-Martín L.
Cruz-Cañete M, et al. Among authors: lopez siles j.
Enferm Infecc Microbiol Clin. 2007 Mar;25(3):177-83. doi: 10.1157/13099369.
Enferm Infecc Microbiol Clin. 2007.
PMID: 17335696
Spanish.
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High prevalence of hepatitis C virus subtypes 4c and 4d in Malaga (Spain): phylogenetic and epidemiological analyses.
Fernández-Arcás N, López-Siles J, Trapero S, Ferraro A, Ibáñez A, Orihuela F, Maldonado J, Alonso A.
Fernández-Arcás N, et al. Among authors: lopez siles j.
J Med Virol. 2006 Nov;78(11):1429-35. doi: 10.1002/jmv.20706.
J Med Virol. 2006.
PMID: 16998884
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A carboxylesterase 2 gene polymorphism as predictor of capecitabine on response and time to progression.
Ribelles N, López-Siles J, Sánchez A, González E, Sánchez MJ, Carabantes F, Sánchez-Rovira P, Márquez A, Dueñas R, Sevilla I, Alba E.
Ribelles N, et al. Among authors: lopez siles j.
Curr Drug Metab. 2008 May;9(4):336-43. doi: 10.2174/138920008784220646.
Curr Drug Metab. 2008.
PMID: 18473752
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Newborn screening for severe combined immunodeficiency does not identify bare lymphocyte syndrome.
Kuo CY, Chase J, Garcia Lloret M, Stiehm ER, Moore T, Aguilera MJ, Lopez Siles J, Church JA.
Kuo CY, et al. Among authors: lopez siles j.
J Allergy Clin Immunol. 2013 Jun;131(6):1693-5. doi: 10.1016/j.jaci.2013.01.019. Epub 2013 Feb 26.
J Allergy Clin Immunol. 2013.
PMID: 23453137
No abstract available.
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