Zobrazeno 1 - 10
of 23
pro vyhledávání: '"María de Lourdes Ramírez-Dueñas"'
Autor:
Yaira Chamorro, Salvador Trejo, Pablo Alvarez-Tostado, María de Lourdes Ramírez-Dueñas, Lourdes Bolaños, Esmeralda Matute, Omar Barrios, Alan Cervantes
Publikováno v:
Neuropsychiatric Disease and Treatment
Yaira Chamorro,1 Lourdes Bolaños,1 Salvador Trejo,2 Omar Barrios,3 María de Lourdes Ramírez-Dueñas,1 Pablo Alvarez-Tostado,4 Alan Cervantes,5 Esmeralda Matute1,6 1Instituto de Neurociencias, Centro Universitario de Ciencias Biológicas y Agropecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df1e3116bdc13c59abcf53c2b20f6ce6
http://europepmc.org/articles/PMC8216073
http://europepmc.org/articles/PMC8216073
Publikováno v:
Psychiatric Genetics. 30:65-72
OBJECTIVE Diminished inhibitory control has been proposed as a core characteristic and potential endophenotype of attention deficit hyperactivity disorder (ADHD). If this is the case, one would expect to find this trait among first-degree relatives o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1966a0558c2456520f928f9d32be55de
https://doi.org/10.1097/ypg.0000000000000252
https://doi.org/10.1097/ypg.0000000000000252
Autor:
Salvador Trejo, Yaira Chamorro, José A. Morales, María de Lourdes Ramírez-Dueñas, Esmeralda Matute, Adriana P. Mendizabal-Ruiz
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 177:676-684
The objective of this study was to characterize an attention deficit hyperactivity disorder (ADHD) endophenotype in non-affected parents of adolescents with a history of ADHD, based on the relationship between performance on a sustained attention tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c012815053fc8ced0c6850378e0d4fb
https://doi.org/10.1002/ajmg.b.32676
https://doi.org/10.1002/ajmg.b.32676
Autor:
José Elías García-Ortiz, Eunice López-Muñoz, Jose J. Toscano-Flores, Luis E. Becerra-Solano, Jorge Román Corona-Rivera, Manuel Díaz-Rodríguez, Gema Castañeda-Cisneros, Jose A. Nastasi-Catanese, María de Lourdes Ramírez-Dueñas, Luis E. Figuera
Publikováno v:
Fetal and Pediatric Pathology. 37:27-37
Background: Disruptive amniotic band sequence (DABS) is a sporadic, non-familial disorder with unclear etiology. Diagnosis is based on clinical features because there is currently no reliable laboratory diagnostic tests. Objective: We describe six ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9bd5ef59d8357a4a90689f4d8a34324
https://doi.org/10.1080/15513815.2017.1392663
https://doi.org/10.1080/15513815.2017.1392663
Autor:
Luis E. Becerra-Solano, Liliana Chacon, José Elías García-Ortiz, Dinorah Morales-Mata, María de Lourdes Ramírez-Dueñas
Publikováno v:
Clinical Dysmorphology. 24:1-6
Spondylospinal thoracic dysostosis can be considered a type of spondylocostal dysostosis because of the occurrence of vertebral defects (hemivertebrae and vertebral body fusion) and thoracic anomalies (short thorax and pulmonary hypoplasia). This syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::876d9b275674a2da495b77bbb18aca98
https://doi.org/10.1097/mcd.0000000000000058
https://doi.org/10.1097/mcd.0000000000000058
Autor:
César Borjas Gutiérrez, Martín Daniel Domínguez Cruz, María de Lourdes Ramírez Dueñas, Reyna Lucía Barajas Torres, María Teresa Magaña Torres, Juan Ramón González García
Publikováno v:
Cytogenetic and genome research. 148(2-3)
1,3-Butadiene, a colorless gas regularly used in the production of plastics, thermoplastic resins, and styrene-butadiene rubber, poses an increased leukemia mortality risk to workers in this field. 1,3-Butadiene is also produced by incomplete combust
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc1c205620149bef18e16c96ee39a44b
https://pubmed.ncbi.nlm.nih.gov/27193269
https://pubmed.ncbi.nlm.nih.gov/27193269
Autor:
Carlos Alva-Espinoza, Rodrigo Torres-Saldúa, José Alfredo Sierra-Ramírez, María de Lourdes Ramírez-Dueñas, Héctor Rangel-Villalobos, Carlos Galaviz-Hernández, Eliakym Arámbula-Meraz, Ricardo García-Cavazos, Rocío Sánchez-Urbina
Publikováno v:
Revista Española de Cardiología. 65:158-163
Resumen Introduccion y objetivos Mexico tiene alta frecuencia de la mutacion 677C>T del gen de la enzima metilentetrahidrofolato reductasa. Se ha demostrado que esta mutacion en estado homocigoto y la hiperhomocisteinemia se asocian a cardiopatias co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0258fcbf763beea7d57781fe81e304a7
https://doi.org/10.1016/j.recesp.2011.09.022
https://doi.org/10.1016/j.recesp.2011.09.022
Autor:
Rodrigo Torres-Saldúa, Ricardo García-Cavazos, Héctor Rangel-Villalobos, Carlos Alva-Espinoza, Rocío Sánchez-Urbina, Carlos Galaviz-Hernández, Eliakym Arámbula-Meraz, María de Lourdes Ramírez-Dueñas, José Alfredo Sierra-Ramírez
Publikováno v:
Revista Española de Cardiología (English Edition). 65:158-163
A B S T R A C T Introduction and objectives: The frequency of the 677C>T mutation in the methylenetetrahydrofolate reductase gene in Mexico is one of the highest worldwide. Some studies have shown that both the homozygous state of this mutation and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2772c18868ecc46e2117f45f69c62312
https://doi.org/10.1016/j.rec.2011.09.024
https://doi.org/10.1016/j.rec.2011.09.024
Autor:
Luis E. Becerra-Solano, Ana I. Vásquez-Velásquez, Horacio Rivera, María de Lourdes Ramírez-Dueñas
Publikováno v:
Journal of Applied Genetics. 48:95-98
We report on a 3-year-old girl with a typical 9p trisomy syndrome, whose 45-chromosome karyotype includes a 9p+. As assessed by G, C and Ag-NOR bands, the rearranged chromosome resulted from a 9p13--p24 direct duplication coupled with a translocation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88a1d25526e3cc806bce05bc79f8a7cb
https://doi.org/10.1007/bf03194665
https://doi.org/10.1007/bf03194665
Autor:
José Elías García-Ortiz, Liliana Chacon, Luis E. Becerra-Solano, María de Lourdes Ramírez-Dueñas, Dinorah Morales-Mata, Juan Carlos Zenteno
Publikováno v:
Clinical dysmorphology. 25(1)
The association of anophthalmia, arrhinia, and hypogonadism constitutes the major clinical features for Bosma arrhinia microphthalmia syndrome. However, there is variability in the presentation of this disease; arrhinia is the most constant clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4acc4543dd835b35b91722d7927670bd
https://pubmed.ncbi.nlm.nih.gov/26440771
https://pubmed.ncbi.nlm.nih.gov/26440771