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

Year Number of Results
1994 1
1996 1
1999 2
2001 3
2003 1
2005 2
2006 2
2007 1
2008 1
2009 2
2012 1
2013 2
2014 5
2015 4
2019 1
2021 1
2022 1
2023 3
2024 1

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29 results

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Page 1
Liraglutide in Children and Adolescents with Type 2 Diabetes.
Tamborlane WV, Barrientos-Pérez M, Fainberg U, Frimer-Larsen H, Hafez M, Hale PM, Jalaludin MY, Kovarenko M, Libman I, Lynch JL, Rao P, Shehadeh N, Turan S, Weghuber D, Barrett T; Ellipse Trial Investigators. Tamborlane WV, et al. N Engl J Med. 2019 Aug 15;381(7):637-646. doi: 10.1056/NEJMoa1903822. Epub 2019 Apr 28. N Engl J Med. 2019. PMID: 31034184 Clinical Trial.
Relevancia de la secuenciación de nueva generación en el diagnóstico de cáncer de mama y dos mutaciones descritas por primera vez en población mexicana.
González-Huerta LM, Hernández-Vázquez A, Toral-López J, Rivera-Vega MDR, Escobar-Gómez M, Hernández-Zamora E. González-Huerta LM, et al. Among authors: rivera vega mdr. Salud Publica Mex. 2023 Mar 10;65(2 mar-abr). doi: 10.21149/14026. Salud Publica Mex. 2023. PMID: 38060862 Spanish. No abstract available.
Inguinal hernia in recessive X-linked ichthyosis.
Cuevas-Covarrubias SA, Kofman-Alfaro SH, Rivera-Vega MD, Palencia AB, Díaz-Zagoya JC. Cuevas-Covarrubias SA, et al. Among authors: rivera vega md. J Dermatol. 1994 Dec;21(12):985. doi: 10.1111/j.1346-8138.1994.tb03327.x. J Dermatol. 1994. PMID: 7868777 No abstract available.
New Genetic Variants of RUNX2 in Mexican Families Cause Cleidocranial Dysplasia.
Toral López J, Gómez Martinez S, Rivera Vega MDR, Hernández-Zamora E, Cuevas Covarrubias S, Ibarra Castrejón BA, González Huerta LM. Toral López J, et al. Among authors: rivera vega mdr. Biology (Basel). 2024 Mar 8;13(3):173. doi: 10.3390/biology13030173. Biology (Basel). 2024. PMID: 38534443 Free PMC article.
Higher prevalence of X-linked ichthyosis vs. ichthyosis vulgaris in Mexico.
Cuevas-Covarrubias SA, Díaz-Zagoya JC, Rivera-Vega MR, Beirana A, Carrasco E, Orozco E, Kofman-Alfaro SH. Cuevas-Covarrubias SA, et al. Among authors: rivera vega mr. Int J Dermatol. 1999 Jul;38(7):555-6. doi: 10.1046/j.1365-4362.1999.00532.x. Int J Dermatol. 1999. PMID: 10440291 No abstract available.
Two novel compound heterozygous families with a trimutation in the GJB2 gene causing sensorineural hearing loss.
Martínez-Saucedo M, Rivera-Vega Mdel R, Gonzalez--Huerta Luz M, Urueta-Cuellar H, Toral-López J, Berruecos-Villalobos P, Cuevas-Covarrubias S. Martínez-Saucedo M, et al. Among authors: rivera vega mdel r. Int J Pediatr Otorhinolaryngol. 2015 Dec;79(12):2295-9. doi: 10.1016/j.ijporl.2015.10.030. Epub 2015 Oct 28. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26553399
Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event.
Morán-Barroso VF, Cervantes A, Rivera-Vega MDR, Del Castillo-Moreno A, Moreno-Chacón A, Mejía-Cauich E, Contreras-Ortiz LE, Fernández-Ramírez F. Morán-Barroso VF, et al. Among authors: rivera vega mdr. Mol Genet Genomic Med. 2021 Sep;9(9):e1762. doi: 10.1002/mgg3.1762. Epub 2021 Jul 20. Mol Genet Genomic Med. 2021. PMID: 34288579 Free PMC article.
29 results