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Table representation of search results timeline featuring number of search results per year.

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1964 1
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2004 1
2011 1
2014 1
2022 1
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Hypersensitivity reaction to ioversol.
Alvarez-Fernández JA, Valero AM, Pulido Z, de la Hoz B, Cuevas M, Sánchez-Cano M. Alvarez-Fernández JA, et al. Among authors: valero am. Allergy. 2000 Jun;55(6):581-2. doi: 10.1034/j.1398-9995.2000.00563.x. Allergy. 2000. PMID: 10858993 No abstract available.
A highly sensitive genetic protocol to detect NF1 mutations.
Valero MC, Martín Y, Hernández-Imaz E, Marina Hernández A, Meleán G, Valero AM, Javier Rodríguez-Álvarez F, Tellería D, Hernández-Chico C. Valero MC, et al. Among authors: valero am. J Mol Diagn. 2011 Mar;13(2):113-22. doi: 10.1016/j.jmoldx.2010.09.002. J Mol Diagn. 2011. PMID: 21354044 Free PMC article.
Neurofibromatosis type 1 families with first-degree relatives harbouring distinct <i>NF1</i> pathogenic variants. Genetic counselling and familial diagnosis: what should be offered?
Garcia B, Catasus N, Ros A, Rosas I, Negro A, Guerrero-Murillo M, Valero AM, Duat-Rodriguez A, Becerra JL, Bonache S, Lázaro Garcia C, Comas C, Bielsa I, Serra E, Hernández-Chico C, Martin Y, Castellanos E, Blanco I. Garcia B, et al. Among authors: valero am. J Med Genet. 2022 Oct;59(10):1017-1023. doi: 10.1136/jmedgenet-2021-108301. Epub 2022 Feb 4. J Med Genet. 2022. PMID: 35121649