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Benitez-Alonso, Edmar
12
results:
Search for persons
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Format
Online (12)
Mediatypes
Articles (Online) (7)
OpenAccess-fulltext (5)
Sorted by: Relevance
Sorted by: Year
?
1
Miopatías genéticas en adultos: experiencia de un centro de..:
Vargas-Cañas, Edwin Steven
;
Martínez-Jiménez, Eunice
;
Galnares-Olalde, Javier Andrés
...
Archivos de Neurociencias. 28 (2022) 1 - p. , 2022
Link:
https://doi.org/10.31157..
?
2
Miopatías genéticas en adultos: experiencia de un centro de..:
Vargas-Cañas, Edwin Steven
;
Martínez-Jiménez, Eunice
;
Galnares-Olalde, Javier Andrés
...
Archivos de Neurociencias. , 2022
Link:
https://doi.org/10.31157..
?
3
Vacuolar Myopathy Associated to CACNA1S Mutation as a Rare ..:
López-Hernández, Juan Carlos
;
Galnares-Olalde, JavierA
;
Benitez-Alonso, Edmar
..
Cureus. , 2021
Link:
https://doi.org/10.7759/..
?
4
FUS as a cause of familial Amyotrophic lateral sclerosis, a..:
Bazán-Rodríguez, Lisette
;
Ruíz-Avalos, Jesús A.
;
Bernal-López, Oscar
...
Neurocase. 28 (2022) 3 - p. 323-330 , 2022
Link:
https://doi.org/10.1080/..
?
5
Short-Communication: Variable Expression of Clinical Sympto..:
Benítez-Alonso, Edmar O
;
López-Hernández, Juan C
;
Galnares-Olalde, Javier A
..
Cureus. , 2022
Link:
https://doi.org/10.7759/..
?
6
Mitochondrial encephalomyopathy, lactic acidosis and stroke..:
Galnares-Olalde, Javier Andrés
;
López-Hernández, Juan Carlos
;
Benitez-Alonso, Edmar Obed
...
Neurology. 96 (2021) 15_supplement - p. , 2021
Link:
https://doi.org/10.1212/..
?
7
Severe Congenital Neutropenia Type 4: A Rare Disease Harbor..:
López-Rodríguez, Larissa
;
Svyryd, Yevgeniya
;
Benítez-Alonso, Edmar O
...
10.24875/ric.22000234. , 2022
Link:
http://www.scielo.org.mx..
?
8
Genetic Testing to Inform Epilepsy Treatment Management Fro..:
McKnight, Dianalee
;
Morales, Ana
;
Hatchell, Kathryn E
...
https://jamanetwork.com/journals/jamaneurology/fullarticle/2797510. , 2023
Link:
https://hdl.handle.net/2..
?
9
Genetic Testing to Inform Epilepsy Treatment Management Fro..:
McKnight, Dianalee
;
Morales, Ana
;
Hatchell, Kathryn E
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623482/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
10
Genetic Testing to Inform Epilepsy Treatment Management Fro..:
McKnight, Dianalee
;
Morales, Ana
;
Hatchell, Kathryn E
...
https://jdc.jefferson.edu/pedsfp/127. , 2022
Link:
https://jdc.jefferson.ed..
?
11
Severe congenital neutropenia type 4: a rare disease harbor..:
Larissa López-Rodríguez
;
Yevgeniya Svyryd
;
Edmar O. Benítez-Alonso
...
https://www.clinicalandtranslationalinvestigation.com/frame_esp.php?id=445. , 2022
Link:
https://doi.org/10.24875..
?
12
Clinical and genetic spectrum of a large cohort of patients..:
Alonso-Pérez, Jorge
;
González-Quereda, Lidia
;
Bruno, Claudio
...
Brain. 145 (2021) 2 - p. 596-606 , 2021
Link:
https://doi.org/10.1093/..
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