Detalhe da pesquisa
1.
Further delineation of the clinical spectrum of KAT6B disorders and allelic series of pathogenic variants.
Genet Med
; 22(8): 1338-1347, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32424177
2.
Interactive and additive influences of Gender, BMI and Apolipoprotein 4 on cognition in children chronically exposed to high concentrations of PM2.5 and ozone. APOE 4 females are at highest risk in Mexico City.
Environ Res
; 150: 411-422, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27376929
3.
Alzheimer and Parkinson diseases, frontotemporal lobar degeneration and amyotrophic lateral sclerosis overlapping neuropathology start in the first two decades of life in pollution exposed urbanites and brain ultrafine particulate matter and industrial nanoparticles, including Fe, Ti, Al, V, Ni, Hg, Co, Cu, Zn, Ag, Pt, Ce, La, Pr and W are key players. Metropolitan Mexico City health crisis is in progress.
Front Hum Neurosci
; 17: 1297467, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38283093
4.
A recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencing.
Bol Med Hosp Infant Mex
; 76(1): 49-53, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30657467
5.
[Clinical profile of a cohort of Silver-Russell syndrome patients followed at the Hospital Infantil de México Federico Gómez from 1998 to 2012]. / Perfil clínico de una cohorte de pacientes con síndrome de Silver-Russell atendidos en el Hospital Infantil de México Federico Gómez de 1998 a 2012.
Bol Med Hosp Infant Mex
; 71(4): 218-226, 2014.
Artigo
em Espanhol
| MEDLINE | ID: mdl-29421254
6.
A recurrent de novo mutation in ATP1A3 gene in a Mexican patient with alternating hemiplegia of childhood detected by massively parallel sequencing / Mutación de novo recurrente en el gen ATP1A3 en una paciente mexicana con hemiplejia alternante de la infancia detectada por secuenciación masiva en paralelo
Bol. méd. Hosp. Infant. Méx
; 76(1): 49-53, ene.-feb. 2019. graf
Artigo
em Inglês
| LILACS | ID: biblio-1038891
7.
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
BMC Med Genomics
; 7: 55, 2014 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25223409
8.
Perfil clínico de una cohorte de pacientes con síndrome de Silver-Russell atendidos en el Hospital Infantil de México Federico Gómez de 1998 a 2012 / Clinical profile of a cohort of Silver-Russell syndrome patients followed at the Hospital Infantil de México Federico Gómez from 1998 to 2012
Bol. méd. Hosp. Infant. Méx
; 71(4): 218-226, jul.-ago. 2014. ilus, tab
Artigo
em Espanhol
| LILACS | ID: lil-747760