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Did you mean rangel zuniga (76 results)?
[Antiphospholipid syndrome updating].
Orts JA, Zúñiga A, Orera M. Orts JA, et al. Among authors: zuniga a. Med Clin (Barc). 2003 Oct 11;121(12):459-71. Med Clin (Barc). 2003. PMID: 14572372 Review. Spanish.
Familial hyperaldosteronism type III a novel case and review of literature.
Pons Fernández N, Moreno F, Morata J, Moriano A, León S, De Mingo C, Zuñiga Á, Calvo F. Pons Fernández N, et al. Among authors: zuniga a. Rev Endocr Metab Disord. 2019 Mar;20(1):27-36. doi: 10.1007/s11154-018-9481-0. Rev Endocr Metab Disord. 2019. PMID: 30569443 Review.
Genotype FBN1/phenotype relationship in a cohort of patients with Marfan syndrome.
Hernándiz A, Zúñiga A, Valera F, Domingo D, Ontoria-Oviedo I, Marí JF, Román JA, Calvo I, Insa B, Gómez R, Cervera JV, Miralles M, Montero JA, Martínez-Dolz L, Sepúlveda P. Hernándiz A, et al. Among authors: zuniga a. Clin Genet. 2021 Feb;99(2):269-280. doi: 10.1111/cge.13879. Epub 2020 Nov 23. Clin Genet. 2021. PMID: 33174221
Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome.
Sánchez-Heras AB, Dámaso E, Castillejo A, Robledo M, Teulé A, Lázaro C, Sánchez-Martínez R, Zúñiga Á, López-Fernández A, Balmaña J, Robles L, Ramon Y Cajal T, Castillejo MI, Ibañez RP, Sevila CM, Sánchez-Mira A, Escandell I, Gómez L, Berbel P, Soto JL. Sánchez-Heras AB, et al. Among authors: zuniga a. Orphanet J Rare Dis. 2024 Jan 26;19(1):26. doi: 10.1186/s13023-024-03017-z. Orphanet J Rare Dis. 2024. PMID: 38279137 Free PMC article.
[Genetic analysis of a family with Von Hippel-Lindau syndrome].
Lafuente-Sanchis A, Cuevas JM, Alemany P, Cremades A, Zúñiga Á. Lafuente-Sanchis A, et al. Among authors: zuniga a. Rev Esp Patol. 2017 Jan-Mar;50(1):64-67. doi: 10.1016/j.patol.2015.12.004. Epub 2016 Feb 28. Rev Esp Patol. 2017. PMID: 29179968 Spanish.
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization.
Sánchez-Heras AB, Castillejo A, García-Díaz JD, Robledo M, Teulé A, Sánchez R, Zúñiga Á, Lastra E, Durán M, Llort G, Yagüe C, Ramon Y Cajal T, López San Martin C, López-Fernández A, Balmaña J, Robles L, Mesa-Latorre JM, Chirivella I, Fonfria M, Perea Ibañez R, Castillejo MI, Escandell I, Gomez L, Berbel P, Soto JL. Sánchez-Heras AB, et al. Among authors: zuniga a. Cancers (Basel). 2020 Nov 5;12(11):3277. doi: 10.3390/cancers12113277. Cancers (Basel). 2020. PMID: 33167498 Free PMC article.
Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in the LYST Gene in a Patient With a Severe Phenotype of Chédiak-Higashi Syndrome.
Boluda-Navarro M, Ibáñez M, Liquori A, Franco-Jarava C, Martínez-Gallo M, Rodríguez-Vega H, Teresa J, Carreras C, Such E, Zúñiga Á, Colobran R, Cervera JV. Boluda-Navarro M, et al. Among authors: zuniga a. Front Immunol. 2021 Mar 31;12:625591. doi: 10.3389/fimmu.2021.625591. eCollection 2021. Front Immunol. 2021. PMID: 33868243 Free PMC article.
24 results