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Year Number of Results
1989 1
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1998 3
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2004 5
2005 10
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2007 10
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198 results

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Page 1
Epigenetic Mechanisms in Hirschsprung Disease.
Torroglosa A, Villalba-Benito L, Luzón-Toro B, Fernández RM, Antiñolo G, Borrego S. Torroglosa A, et al. Among authors: antinolo g. Int J Mol Sci. 2019 Jun 26;20(13):3123. doi: 10.3390/ijms20133123. Int J Mol Sci. 2019. PMID: 31247956 Free PMC article. Review.
Influencers on Thyroid Cancer Onset: Molecular Genetic Basis.
Luzón-Toro B, Fernández RM, Villalba-Benito L, Torroglosa A, Antiñolo G, Borrego S. Luzón-Toro B, et al. Among authors: antinolo g. Genes (Basel). 2019 Nov 8;10(11):913. doi: 10.3390/genes10110913. Genes (Basel). 2019. PMID: 31717449 Free PMC article. Review.
What is new about the genetic background of Hirschsprung disease?
Luzón-Toro B, Villalba-Benito L, Torroglosa A, Fernández RM, Antiñolo G, Borrego S. Luzón-Toro B, et al. Among authors: antinolo g. Clin Genet. 2020 Jan;97(1):114-124. doi: 10.1111/cge.13615. Epub 2019 Aug 5. Clin Genet. 2020. PMID: 31355911 Review.
Epigenetics in ENS development and Hirschsprung disease.
Torroglosa A, Alves MM, Fernández RM, Antiñolo G, Hofstra RM, Borrego S. Torroglosa A, et al. Among authors: antinolo g. Dev Biol. 2016 Sep 15;417(2):209-16. doi: 10.1016/j.ydbio.2016.06.017. Epub 2016 Jun 16. Dev Biol. 2016. PMID: 27321561 Free article. Review.
ESR2 Gene and Medullary Thyroid Carcinoma.
Ruiz-Ferrer M, Fernández RM, Navarro E, Antiñolo G, Borrego S. Ruiz-Ferrer M, et al. Among authors: antinolo g. Thyroid. 2017 Nov;27(11):1456-1457. doi: 10.1089/thy.2017.0171. Epub 2017 Oct 11. Thyroid. 2017. PMID: 28891392 No abstract available.
Unusual clinical phenotype of Stargardt disease.
Molina-Solana P, Morillo-Sánchez MJ, Méndez-Vidal C, Ramos-Jiménez M, Domínguez-Serrano B, Antiñolo G, Rodríguez-de-la-Rúa-Franch E. Molina-Solana P, et al. Among authors: antinolo g. Arq Bras Oftalmol. 2021 Jul-Aug;84(4):391-394. doi: 10.5935/0004-2749.20210064. Arq Bras Oftalmol. 2021. PMID: 34008801 Free article.
Expanding the phenotype of THRB: a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing variant.
Fernández-Suárez E, González-Del Pozo M, García-Núñez A, Méndez-Vidal C, Martín-Sánchez M, Mejías-Carrasco JM, Ramos-Jiménez M, Morillo-Sánchez MJ, Rodríguez-de la Rúa E, Borrego S, Antiñolo G. Fernández-Suárez E, et al. Among authors: antinolo g. Front Cell Dev Biol. 2023 Jul 21;11:1197744. doi: 10.3389/fcell.2023.1197744. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37547476 Free PMC article.
Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model.
Alves MM, Sribudiani Y, Brouwer RW, Amiel J, Antiñolo G, Borrego S, Ceccherini I, Chakravarti A, Fernández RM, Garcia-Barcelo MM, Griseri P, Lyonnet S, Tam PK, van Ijcken WF, Eggen BJ, te Meerman GJ, Hofstra RM. Alves MM, et al. Among authors: antinolo g. Dev Biol. 2013 Oct 1;382(1):320-9. doi: 10.1016/j.ydbio.2013.05.019. Epub 2013 May 23. Dev Biol. 2013. PMID: 23707863 Free article. Review.
198 results