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

Year Number of Results
2003 1
2005 1
2006 2
2007 2
2008 2
2009 1
2010 3
2011 1
2012 4
2013 1
2015 1
2016 1
2017 4
2018 2
2019 1
2020 2
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2022 4
2023 3
2024 1

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Page 1
Generalized hypertrichosis syndromes in Mexico.
Aguayo-Orozco TA, Ríos-González BE, Castro-Martínez AG, Ruiz-Ramírez AV, Figuera LE. Aguayo-Orozco TA, et al. Among authors: figuera le. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):1014-1022. doi: 10.1002/ajmg.c.31864. Epub 2020 Dec 7. Am J Med Genet C Semin Med Genet. 2020. PMID: 33283427
SOD2 Gene Variants (rs4880 and rs5746136) and Their Association with Breast Cancer Risk.
Gallegos-Arreola MP, Ramírez-Patiño R, Sánchez-López JY, Zúñiga-González GM, Figuera LE, Delgado-Saucedo JI, Gómez-Meda BC, Rosales-Reynoso MA, Puebla-Pérez AM, Lemus-Varela ML, Garibaldi-Ríos AF, Marín-Domínguez NA, Pacheco-Verduzco DP, Mohamed-Flores EA. Gallegos-Arreola MP, et al. Among authors: figuera le. Curr Issues Mol Biol. 2022 Oct 26;44(11):5221-5233. doi: 10.3390/cimb44110355. Curr Issues Mol Biol. 2022. PMID: 36354667 Free PMC article.
Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14).
Minatogawa M, Unzaki A, Morisaki H, Syx D, Sonoda T, Janecke AR, Slavotinek A, Voermans NC, Lacassie Y, Mendoza-Londono R, Wierenga KJ, Jayakar P, Gahl WA, Tifft CJ, Figuera LE, Hilhorst-Hofstee Y, Maugeri A, Ishikawa K, Kobayashi T, Aoki Y, Ohura T, Kawame H, Kono M, Mochida K, Tokorodani C, Kikkawa K, Morisaki T, Kobayashi T, Nakane T, Kubo A, Ranells JD, Migita O, Sobey G, Kaur A, Ishikawa M, Yamaguchi T, Matsumoto N, Malfait F, Miyake N, Kosho T. Minatogawa M, et al. Among authors: figuera le. J Med Genet. 2022 Sep;59(9):865-877. doi: 10.1136/jmedgenet-2020-107623. Epub 2021 Nov 23. J Med Genet. 2022. PMID: 34815299 Free PMC article.
Severe Craniofacial Involvement due to Amniotic Band Sequence.
Becerra-Solano LE, Castañeda-Cisneros G, Corona-Rivera JR, Díaz-Rodríguez M, Figuera LE, López-Muñoz E, Nastasi-Catanese JA, Toscano-Flores JJ, Ramírez-Dueñas ML, García-Ortíz JE. Becerra-Solano LE, et al. Fetal Pediatr Pathol. 2018 Feb;37(1):27-37. doi: 10.1080/15513815.2017.1392663. Epub 2018 Jan 16. Fetal Pediatr Pathol. 2018. PMID: 29336649
Therapeutic goals in the treatment of Fabry disease.
Mehta A, West ML, Pintos-Morell G, Reisin R, Nicholls K, Figuera LE, Parini R, Carvalho LR, Kampmann C, Pastores GM, Lidove O. Mehta A, et al. Among authors: figuera le. Genet Med. 2010 Nov;12(11):713-20. doi: 10.1097/GIM.0b013e3181f6e676. Genet Med. 2010. PMID: 20975569 Free article.
35 results