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Page 1
Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution.
Murillo-Melo NM, Márquez-Quiróz LC, Gómez R, Orozco L, Mendoza-Caamal E, Tapia-Guerrero YS, Camacho-Mejorado R, Cortés H, López-Reyes A, Santana C, Noris G, Hernández-Hernández O, Cisneros B, Magaña JJ. Murillo-Melo NM, et al. Among authors: cortes h. Neuromuscul Disord. 2017 Dec;27(12):1106-1114. doi: 10.1016/j.nmd.2017.09.004. Epub 2017 Sep 21. Neuromuscul Disord. 2017. PMID: 29054426
Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population.
Magaña JJ, Gómez R, Maldonado-Rodríguez M, Velázquez-Pérez L, Tapia-Guerrero YS, Cortés H, Leyva-García N, Hernández-Hernández O, Cisneros B. Magaña JJ, et al. Among authors: cortes h. Cerebellum. 2013 Dec;12(6):902-5. doi: 10.1007/s12311-013-0505-8. Cerebellum. 2013. PMID: 23828024
Dopaminergic denervation switches dopamine D3 receptor signaling and disrupts its Ca(2+) dependent modulation by CaMKII and calmodulin in striatonigral projections of the rat.
Avalos-Fuentes A, Albarrán-Bravo S, Loya-Lopéz S, Cortés H, Recillas-Morales S, Magaña JJ, Paz-Bermúdez F, Rangel-Barajas C, Aceves J, Erlij D, Florán B. Avalos-Fuentes A, et al. Among authors: cortes h. Neurobiol Dis. 2015 Feb;74:336-46. doi: 10.1016/j.nbd.2014.12.008. Epub 2014 Dec 14. Neurobiol Dis. 2015. PMID: 25517101
Effects of Physical Rehabilitation in Patients with Spinocerebellar Ataxia Type 7.
Tercero-Pérez K, Cortés H, Torres-Ramos Y, Rodríguez-Labrada R, Cerecedo-Zapata CM, Hernández-Hernández O, Pérez-González N, González-Piña R, Leyva-García N, Cisneros B, Velázquez-Pérez L, Magaña JJ. Tercero-Pérez K, et al. Among authors: cortes h. Cerebellum. 2019 Jun;18(3):397-405. doi: 10.1007/s12311-019-1006-1. Cerebellum. 2019. PMID: 30701400 Clinical Trial.
Oropharyngeal dysphagia in early stages of myotonic dystrophy type 1.
Franco-Guerrero AA, Márquez-Quiroz LC, Valadéz-Jiménez VM, Cortés H, Murillo-Melo NM, Muñoz B, Cisneros B, Magaña JJ. Franco-Guerrero AA, et al. Among authors: cortes h. Muscle Nerve. 2019 Jul;60(1):90-95. doi: 10.1002/mus.26485. Epub 2019 May 6. Muscle Nerve. 2019. PMID: 30994189
Altered Plasma Acylcarnitines and Amino Acids Profile in Spinocerebellar Ataxia Type 7.
Nambo-Venegas R, Valdez-Vargas C, Cisneros B, Palacios-González B, Vela-Amieva M, Ibarra-González I, Cerecedo-Zapata CM, Martínez-Cruz E, Cortés H, Reyes-Grajeda JP, Magaña JJ. Nambo-Venegas R, et al. Among authors: cortes h. Biomolecules. 2020 Mar 3;10(3):390. doi: 10.3390/biom10030390. Biomolecules. 2020. PMID: 32138195 Free PMC article. Clinical Trial.
High prevalence of autosomal recessive congenital ichthyosis in a Mexican population caused by a new mutation in the TGM1 gene: epidemiological evidence of a founder effect.
González-Del Carmen M, Montaño S, Reyes-Hernández OD, Vizcaíno-Dorado PA, Leyva-García N, Morales-Morfín JC, Diaz-Beltran W, Quinto-Santiago E, Cariño-Calvo L, Magaña JJ, Leyva-Gómez G, Cortés H. González-Del Carmen M, et al. Among authors: cortes h. Int J Dermatol. 2020 Aug;59(8):969-977. doi: 10.1111/ijd.14952. Epub 2020 May 21. Int J Dermatol. 2020. PMID: 32436339
223 results