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Page 1
Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes.
D'Erasmo L, Minicocci I, Nicolucci A, Pintus P, Roeters Van Lennep JE, Masana L, Mata P, Sánchez-Hernández RM, Prieto-Matos P, Real JT, Ascaso JF, Lafuente EE, Pocovi M, Fuentes FJ, Muntoni S, Bertolini S, Sirtori C, Calabresi L, Pavanello C, Averna M, Cefalu AB, Noto D, Pacifico AA, Pes GM, Harada-Shiba M, Manzato E, Zambon S, Zambon A, Vogt A, Scardapane M, Sjouke B, Fellin R, Arca M. D'Erasmo L, et al. J Am Coll Cardiol. 2018 Jan 23;71(3):279-288. doi: 10.1016/j.jacc.2017.11.028. J Am Coll Cardiol. 2018. PMID: 29348020 Free article.
Clinical description, molecular delineation and genotype-phenotype correlation in 340 patients with KBG syndrome: addition of 67 new patients.
Martinez-Cayuelas E, Blanco-Kelly F, Lopez-Grondona F, Swafiri ST, Lopez-Rodriguez R, Losada-Del Pozo R, Mahillo-Fernandez I, Moreno B, Rodrigo-Moreno M, Casas-Alba D, Lopez-Gonzalez A, García-Miñaúr S, Ángeles Mori M, Pacio-Minguez M, Rikeros-Orozco E, Santos-Simarro F, Cruz-Rojo J, Quesada-Espinosa JF, Sanchez-Calvin MT, Sanchez-Del Pozo J, Bernado Fonz R, Isidoro-Garcia M, Ruiz-Ayucar I, Alvarez-Mora MI, Blanco-Lago R, De Azua B, Eiris J, Garcia-Peñas JJ, Gil-Fournier B, Gomez-Lado C, Irazabal N, Lopez-Gonzalez V, Madrigal I, Malaga I, Martinez-Menendez B, Ramiro-Leon S, Garcia-Hoyos M, Prieto-Matos P, Lopez-Pison J, Aguilera-Albesa S, Alvarez S, Fernández-Jaén A, Llano-Rivas I, Gener-Querol B, Ayuso C, Arteche-Lopez A, Palomares-Bralo M, Cueto-González A, Valenzuela I, Martinez-Monseny A, Lorda-Sanchez I, Almoguera B. Martinez-Cayuelas E, et al. Among authors: prieto matos p. J Med Genet. 2023 Jul;60(7):644-654. doi: 10.1136/jmg-2022-108632. Epub 2022 Nov 29. J Med Genet. 2023. PMID: 36446582
Clinical and molecular characteristics of homozygous familial hypercholesterolemia patients: Insights from SAFEHEART registry.
Alonso R, Díaz-Díaz JL, Arrieta F, Fuentes-Jiménez F, de Andrés R, Saenz P, Ariceta G, Vidal-Pardo JI, Almagro F, Argueso R, Prieto-Matos P, Miramontes JP, Pintó X, Rodriguez-Urrego J, Perez de Isla L, Mata P. Alonso R, et al. J Clin Lipidol. 2016 Jul-Aug;10(4):953-961. doi: 10.1016/j.jacl.2016.04.006. Epub 2016 Apr 21. J Clin Lipidol. 2016. PMID: 27578128
Autosomal recessive hypercholesterolemia in Spain.
Sánchez-Hernández RM, Prieto-Matos P, Civeira F, Lafuente EE, Vargas MF, Real JT, Goicoechea FG, Fuentes FJ, Pocovi M, Boronat M, Wägner AM, Masana L. Sánchez-Hernández RM, et al. Atherosclerosis. 2018 Feb;269:1-5. doi: 10.1016/j.atherosclerosis.2017.12.006. Epub 2017 Dec 6. Atherosclerosis. 2018. PMID: 29245109
[Turner syndrome: Study of 42 cases].
Bahíllo-Curieses MP, Prieto-Matos P, Quiroga González R, Regueras Santos L, Blanco Barrio A, Rupérez Peña S; Grupo de Endocrinología Pediátrica de Castilla y León. Bahíllo-Curieses MP, et al. Med Clin (Barc). 2016 Oct 21;147(8):348-351. doi: 10.1016/j.medcli.2016.06.033. Epub 2016 Aug 27. Med Clin (Barc). 2016. PMID: 27575526 Spanish.
Clinical response to growth hormone in children with intrauterine growth retardation without catch-up growth in Castilla y León (Spain).
Gutiérrez-Abejón E, Campo-Ortega EP, Prieto-Matos P, Bahíllo-Curieses MP, Breñas-Villalón MT, Martín-Sobrino N. Gutiérrez-Abejón E, et al. Endocrinol Diabetes Nutr (Engl Ed). 2018 Dec;65(10):584-591. doi: 10.1016/j.endinu.2018.06.007. Epub 2018 Aug 22. Endocrinol Diabetes Nutr (Engl Ed). 2018. PMID: 30143447 English, Spanish.
[Growth hormone treatment in 2 patients with 22q11.21 deletion syndrome].
Bahíllo-Curieses MP, Prieto-Matos P, Hernández-Fabián A, Vázquez-Martín S. Bahíllo-Curieses MP, et al. Med Clin (Barc). 2016 Mar 4;146(5):e27-8. doi: 10.1016/j.medcli.2015.09.003. Epub 2015 Oct 29. Med Clin (Barc). 2016. PMID: 26520612 Spanish. No abstract available.
Heterozygous aggrecan variants are associated with short stature and brachydactyly: Description of 16 probands and a review of the literature.
Sentchordi-Montané L, Aza-Carmona M, Benito-Sanz S, Barreda-Bonis AC, Sánchez-Garre C, Prieto-Matos P, Ruiz-Ocaña P, Lechuga-Sancho A, Carcavilla-Urquí A, Mulero-Collantes I, Martos-Moreno GA, Del Pozo A, Vallespín E, Offiah A, Parrón-Pajares M, Dinis I, Sousa SB, Ros-Pérez P, González-Casado I, Heath KE. Sentchordi-Montané L, et al. Clin Endocrinol (Oxf). 2018 Jun;88(6):820-829. doi: 10.1111/cen.13581. Epub 2018 Mar 24. Clin Endocrinol (Oxf). 2018. PMID: 29464738 Free article. Review.
[Epiphysiolysis and recombinant growth hormone].
Roncero-Toscano ML, Barea-Peinador F, Prieto-Matos P. Roncero-Toscano ML, et al. An Pediatr (Barc). 2016 Apr;84(4):239-40. doi: 10.1016/j.anpedi.2015.08.004. Epub 2015 Oct 9. An Pediatr (Barc). 2016. PMID: 26455559 Free article. Spanish. No abstract available.
Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia.
Barraza-García J, Rivera-Pedroza CI, Hisado-Oliva A, Belinchón-Martínez A, Sentchordi-Montané L, Duncan EL, Clark GR, Del Pozo A, Ibáñez-Garikano K, Offiah A, Prieto-Matos P, Cormier-Daire V, Heath KE. Barraza-García J, et al. Clin Genet. 2017 Jul;92(1):91-98. doi: 10.1111/cge.12964. Epub 2017 Feb 22. Clin Genet. 2017. PMID: 28067412 Free article.
23 results