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Year Number of Results
2003 3
2005 3
2006 2
2007 2
2009 1
2011 1
2012 2
2013 4
2014 1
2015 4
2016 3
2017 1
2018 3
2019 4
2020 5
2021 5
2022 5
2023 8
2024 4

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54 results

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Page 1
Oblique facial clefts in Johanson-Blizzard syndrome.
Corona-Rivera JR, Zapata-Aldana E, Bobadilla-Morales L, Corona-Rivera A, Peña-Padilla C, Solis-Hernández E, Guzmán C, Richmond E, Zahl C, Zenker M, Sukalo M. Corona-Rivera JR, et al. Among authors: corona rivera a. Am J Med Genet A. 2016 Jun;170(6):1495-501. doi: 10.1002/ajmg.a.37630. Epub 2016 Mar 17. Am J Med Genet A. 2016. PMID: 26989884 Review.
Aneurysms involving the coronary arteries in a neonate with neurofibromatosis 1.
Corona-Rivera JR, Barrios-Prieto E, Rivera-Ramírez B, Sánchez-Uribe EH, Cortés-Pastrana RC, Aguilera CER, de Anda-Camacho RG, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Among authors: corona rivera a. Am J Med Genet A. 2023 Sep;191(9):2422-2427. doi: 10.1002/ajmg.a.63321. Epub 2023 Jun 6. Am J Med Genet A. 2023. PMID: 37278515 Review.
Clinical insights from an unusual Turner syndrome manifestation: Congenital cutis verticis gyrata.
Corona-Rivera JR, Bustos Rodríguez FJ, Vega-Silva LL, Hernández-Camarena F, Peña-Padilla C, Castillo-Reyes KA, Cruz-Cruz JP, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Among authors: corona rivera a. Am J Med Genet A. 2023 Jun;191(6):1669-1671. doi: 10.1002/ajmg.a.63183. Epub 2023 Mar 18. Am J Med Genet A. 2023. PMID: 36932882 Review.
Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome.
Zepeda-Romero LC, Zenker M, Schanze D, Schanze I, Peña-Padilla C, Quezada-Salazar CA, Pacheco-Torres PA, Rivera-Montellano ML, Aguirre-Guillén RL, Bobadilla-Morales L, Corona-Rivera A, Corona-Rivera JR. Zepeda-Romero LC, et al. Among authors: corona rivera a. Eur J Med Genet. 2022 Dec;65(12):104653. doi: 10.1016/j.ejmg.2022.104653. Epub 2022 Oct 28. Eur J Med Genet. 2022. PMID: 36330903
TRAPPC11-CDG muscular dystrophy: Review of 54 cases including a novel patient.
Corona-Rivera JR, Martínez-Duncker I, Morava E, Ranatunga W, Salinas-Marin R, González-Jaimes AM, Castillo-Reyes KA, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Orozco-Vela M, Brukman-Jiménez SA. Corona-Rivera JR, et al. Among authors: corona rivera a. Mol Genet Metab. 2024 May;142(1):108469. doi: 10.1016/j.ymgme.2024.108469. Epub 2024 Mar 28. Mol Genet Metab. 2024. PMID: 38564972 Review.
First Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological Manifestations.
Corona-Rivera JR, Zenteno JC, López-Pérez LG, Yokoyama-Rebollar E, Villarroel CE, Barragán-Arévalo T, Montes-Almanza LÁ, Zepeda-Romero LC, Morales-Domínguez GE, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Among authors: corona rivera a. Mol Syndromol. 2023 Apr;14(2):143-151. doi: 10.1159/000526975. Epub 2022 Dec 16. Mol Syndromol. 2023. PMID: 37064331 Free PMC article.
MTSS2-related neurodevelopmental disorder: Further delineation of the phenotype.
Corona-Rivera JR, Zenteno JC, Ordoñez-Labastida V, Cruz-Cruz JP, Cortés-Pastrana RC, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Martínez-Herrera A. Corona-Rivera JR, et al. Among authors: corona rivera a. Eur J Med Genet. 2023 Oct;66(10):104826. doi: 10.1016/j.ejmg.2023.104826. Epub 2023 Aug 30. Eur J Med Genet. 2023. PMID: 37657631
54 results