E-LIB Suche - Ergebnisse für: Durón, Reyna María

1

Proyecto colaborativo inicial con Honduras para el centro d..:

Durón, Reyna María ; Breda Yepes, Michele ; Hernández Vanegas, Laura..
Innovare: Revista de ciencia y tecnología. 8 (2019) 1 - p. 38-45 , 2019

Link: https://doi.org/10.5377/..

2

La tosferina, enfermedad re-emergente en Honduras:

Sierra, Manuel ; Duron, Reyna Maria ; Luque, Marco...
Innovare: Revista de ciencia y tecnología. 7 (2018) 2 - p. 31-46 , 2018

Link: https://doi.org/10.5377/..

3

A New Database Platform for Clinical and Genetic Investigat..:

Discua, David ; Duron, Reyna M. ; Martinez, Iris E....
Neurology. 90 (2018) 15_supplement - p. , 2018

Link: https://doi.org/10.1212/..

4

Analyzing Phenotypes Using Artificial Intelligence Tools in..:

Durón, Reyna M. ; Arias, Carlos ; Martínez-Juárez, Iris E....
Neurology. 90 (2018) 15_supplement - p. , 2018

Link: https://doi.org/10.1212/..

5

EFHC1 variants in juvenile myoclonic epilepsy: reanalysis a..:

Bailey, Julia N. ; Patterson, Christopher ; de Nijs, Laurence...
Genetics in Medicine. 19 (2017) 2 - p. 144-156 , 2017

Link: https://doi.org/10.1038/..

6

Corrigendum to "Late onset Lafora disease and novel EPM2A m..:

Jara-Prado, Aurelio ; Ochoa, Adriana ; Alonso, María Elisa...
Epilepsy Research. 110 (2015) - p. 228 , 2015

Link: https://doi.org/10.1016/..

7

Late onset Lafora disease and novel EPM2A mutations: Breaki..:

Jara-Prado, Aurelio ; Ochoa, Adriana ; Alonso, María Elisa...
Epilepsy Research. 108 (2014) 9 - p. 1501-1510 , 2014

Link: https://doi.org/10.1016/..

8

Ontogeny of Lafora bodies and neurocytoskeleton changes in ..:

Machado-Salas, Jesús ; Avila-Costa, María Rosa ; Guevara, Patricia...
Experimental Neurology. 236 (2012) 1 - p. 131-140 , 2012

Link: https://doi.org/10.1016/..

9

DNA variants in coding region of EFHC1: SNPs do not associa..:

Bai, Dongsheng ; Bailey, Julia N. ; Durón, Reyna M....
Epilepsia. 50 (2009) 5 - p. 1184-1190 , 2009

Link: https://doi.org/10.1111/..

10

Hyperglycosylation and Reduced GABA Currents of Mutated GAB..:

Tanaka, Miyabi ; Olsen, Richard W. ; Medina, Marco T....
The American Journal of Human Genetics. 82 (2008) 6 - p. 1249-1261 , 2008

Link: https://doi.org/10.1016/..

11

Juvenile myoclonic epilepsy subsyndromes: family studies an..:

Martínez-Juárez, Iris E. ; Alonso, María Elisa ; Medina, Marco T....
Brain. 129 (2006) 5 - p. 1269-1280 , 2006

Link: https://doi.org/10.1093/..

12

Seizures of Idiopathic Generalized Epilepsies:

Durón, Reyna M. ; Medina, Marco T. ; Martínez‐Juárez, Iris E....
Epilepsia. 46 (2005) s9 - p. 34-47 , 2005

Link: https://doi.org/10.1111/..

13

Autophagy in Juvenile Myoclonic Epilepsy (JME) (P2.275):

Tanaka, Miyabi ; Martinez-Juarez, Iris ; Duron, Reyna...
Neurology. 90 (2018) 15_supplement - p. , 2018

Link: https://doi.org/10.1212/..

14

Absence Seizures in Juvenile Myoclonic Epilepsy: Whole Exom..:

Duron, Reyna ; Medina, Marco ; Martínez-Juarez, Iris...
Neurology. 86 (2016) 16_supplement - p. , 2016

Link: https://doi.org/10.1212/..

15

A Novel Gene (Myclonin 3) for Classic Juvenile Myoclonic Ep..:

Bai, Dongsheng ; Medina, Marco ; Duron, Reyna...
Neurology. 82 (2014) 10_supplement - p. , 2014

Link: https://doi.org/10.1212/..