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Larotrectinib as an Effective Therapy in Congenital Infantile Fibrosarcoma: Report of Two Cases.
Lapeña LM, Caldas MCS, Ramírez C, Basilio MS, Junco PT, Rodríguez-Laguna L, Martínez-González V, Marín-Manzano E, Perez-Martinez A, Lopez-Gutierrez JC. Lapeña LM, et al. European J Pediatr Surg Rep. 2022 Jun 25;10(1):e76-e79. doi: 10.1055/s-0042-1748866. eCollection 2022 Jan. European J Pediatr Surg Rep. 2022. PMID: 35761904 Free PMC article.
Nodular Proliferation in Parkes Weber Syndrome.
Rojas Esquivel DJ, Marín Manzano E, Concepción NA, Lopéz Gutierréz JC, Riera de Cubas L. Rojas Esquivel DJ, et al. Ann Vasc Surg. 2017 Jan;38:321.e1-321.e4. doi: 10.1016/j.avsg.2016.06.015. Epub 2016 Aug 26. Ann Vasc Surg. 2017. PMID: 27575310
CLAPO syndrome: identification of somatic activating PIK3CA mutations and delineation of the natural history and phenotype.
Rodriguez-Laguna L, Ibañez K, Gordo G, Garcia-Minaur S, Santos-Simarro F, Agra N, Vallespín E, Fernández-Montaño VE, Martín-Arenas R, Del Pozo Á, González-Pecellín H, Mena R, Rueda-Arenas I, Gomez MV, Villaverde C, Bustamante A, Ayuso C, Ruiz-Perez VL, Nevado J, Lapunzina P, Lopez-Gutierrez JC, Martinez-Glez V. Rodriguez-Laguna L, et al. Genet Med. 2018 Aug;20(8):882-889. doi: 10.1038/gim.2017.200. Epub 2018 Feb 15. Genet Med. 2018. PMID: 29446767 Free article.
Suprapubic vein shunt and iliac vein hypoplasia.
Marín-Manzano E, López-Gutiérrez JC. Marín-Manzano E, et al. Med Clin (Barc). 2019 May 17;152(10):e59. doi: 10.1016/j.medcli.2018.09.001. Epub 2018 Oct 30. Med Clin (Barc). 2019. PMID: 30389106 English, Spanish. No abstract available.
Somatic activating mutations in PIK3CA cause generalized lymphatic anomaly.
Rodriguez-Laguna L, Agra N, Ibañez K, Oliva-Molina G, Gordo G, Khurana N, Hominick D, Beato M, Colmenero I, Herranz G, Torres Canizalez JM, Rodríguez Pena R, Vallespín E, Martín-Arenas R, Del Pozo Á, Villaverde C, Bustamante A, Ayuso C, Lapunzina P, Lopez-Gutierrez JC, Dellinger MT, Martinez-Glez V. Rodriguez-Laguna L, et al. J Exp Med. 2019 Feb 4;216(2):407-418. doi: 10.1084/jem.20181353. Epub 2018 Dec 27. J Exp Med. 2019. PMID: 30591517 Free PMC article.
Capillary malformation with segmental distribution and central atrophy: A series of 7 cases.
Ivars M, Azaña JM, Weibel L, Theiler M, Boixeda P, Norris DI, Martinez-Glez V, Agra N, Rodríguez-Laguna L, Colmenero I, Beato-Merino MJ, López-Gutiérrez JC. Ivars M, et al. J Am Acad Dermatol. 2020 Jul;83(1):213-214. doi: 10.1016/j.jaad.2019.09.016. Epub 2019 Sep 18. J Am Acad Dermatol. 2020. PMID: 31541744 No abstract available.
Congenital hepatic hemangiomas: Clinical, histologic, and genetic correlation.
Triana P, Rodríguez-Laguna L, Giacaman A, Salinas-Sanz JA, Martín-Santiago A, López-Santamaría M, Palacios E, Beato MJ, Martinez-González V, López-Gutierrez JC. Triana P, et al. J Pediatr Surg. 2020 Oct;55(10):2170-2176. doi: 10.1016/j.jpedsurg.2020.02.008. Epub 2020 Feb 19. J Pediatr Surg. 2020. PMID: 32115227
A case of naevus vascularis mixtus with hypotrophy and hypotrichosis due to mosaic GNA11 mutation.
Rodríguez-Jiménez P, Chicharro P, Llamas-Velasco M, Moyano B, Sánchez-Carpintero I, López-Gutiérrez JC, Martinez-Glez V, Rodríguez-Laguna L, Torrelo A. Rodríguez-Jiménez P, et al. J Eur Acad Dermatol Venereol. 2020 Aug;34(8):e420-e422. doi: 10.1111/jdv.16369. Epub 2020 Apr 30. J Eur Acad Dermatol Venereol. 2020. PMID: 32180285 No abstract available.
220 results