Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
6 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population.
Rev Invest Clin. 2022;74(6):328-339. doi: 10.24875/RIC.22000234.
Rev Invest Clin. 2022.
PMID: 36546889
Free article.
Unraveling the role of relative telomere length and CAG expansion on initial symptoms of juvenile Huntington disease.
PerezGrovas-Saltijeral A, Ochoa-Morales A, Jara-Prado A, Velázquez-Cruz R, Rivera-Paredez B, Dávila-OrtizdeMontellano D, Benítez-Alonso EO, Santamaría-Olmedo M, Sevilla-Montoya R, Marfil-Marín E, Valdés-Flores M, Martínez-Ruano L, Camacho-Molina A, Hidalgo-Bravo A.
PerezGrovas-Saltijeral A, et al. Among authors: benitez alonso eo.
Eur J Neurol. 2023 Mar;30(3):612-621. doi: 10.1111/ene.15644. Epub 2022 Dec 8.
Eur J Neurol. 2023.
PMID: 36421025
Item in Clipboard
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice.
McKnight D, Morales A, Hatchell KE, Bristow SL, Bonkowsky JL, Perry MS, Berg AT, Borlot F, Esplin ED, Moretz C, Angione K, Ríos-Pohl L, Nussbaum RL, Aradhya S; ELEVIATE Consortium; Haldeman-Englert CR, Levy RJ, Parachuri VG, Lay-Son G, de Montellano DJD, Ramirez-Garcia MA, Benítez Alonso EO, Ziobro J, Chirita-Emandi A, Felix TM, Kulasa-Luke D, Megarbane A, Karkare S, Chagnon SL, Humberson JB, Assaf MJ, Silva S, Zarroli K, Boyarchuk O, Nelson GR, Palmquist R, Hammond KC, Hwang ST, Boutlier SB, Nolan M, Batley KY, Chavda D, Reyes-Silva CA, Miroshnikov O, Zuccarelli B, Amlie-Wolf L, Wheless JW, Seinfeld S, Kanhangad M, Freeman JL, Monroy-Santoyo S, Rodriguez-Vazquez N, Ryan MM, Machie M, Guerra P, Hassan MJ, Candee MS, Bupp CP, Park KL, Muller E 2nd, Lupo P, Pedersen RC, Arain AM, Murphy A, Schatz K, Mu W, Kalika PM, Plaza L, Kellogg MA, Lora EG, Carson RP, Svystilnyk V, Venegas V, Luke RR, Jiang H, Stetsenko T, Dueñas-Roque MM, Trasmonte J, Burke RJ, Hurst ACE, Smith DM, Massingham LJ, Pisani L, Costin CE, Ostrander B, Filloux FM, Ananth AL, Mohamed IS, Nechai A, Dao JM, Fahey MC, Aliu E, Falchek S, Press CA, Treat L, Eschbach K, Starks A, Kammeyer R, Bear JJ, Jacobson M, Che…
See abstract for full author list ➔
McKnight D, et al. Among authors: benitez alonso eo.
JAMA Neurol. 2022 Dec 1;79(12):1267-1276. doi: 10.1001/jamaneurol.2022.3651.
JAMA Neurol. 2022.
PMID: 36315135
Free PMC article.
Item in Clipboard
FUS as a cause of familial Amyotrophic lateral sclerosis, a case report in a pregnant patient.
Bazán-Rodríguez L, Ruíz-Avalos JA, Bernal-López O, Benitez-Alonso EO, Villaseñor-Sánchez J, Fernandez-Valverde F, Vargas-Cañas S.
Bazán-Rodríguez L, et al. Among authors: benitez alonso eo.
Neurocase. 2022 Jun;28(3):323-330. doi: 10.1080/13554794.2022.2100265. Epub 2022 Jul 13.
Neurocase. 2022.
PMID: 35833217
Item in Clipboard
Short-Communication: Variable Expression of Clinical Symptoms and an Unexpected Finding of Vacuolar Myopathy Related to a Pathogenic Variant in the CACNA1S Gene in a Previous Case Report.
Benítez-Alonso EO, López-Hernández JC, Galnares-Olalde JA, Alcalá RE, Vargas-Cañas ES.
Benítez-Alonso EO, et al.
Cureus. 2022 Apr 2;14(4):e23760. doi: 10.7759/cureus.23760. eCollection 2022 Apr.
Cureus. 2022.
PMID: 35509735
Free PMC article.
Item in Clipboard
Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) Syndrome: Frequency, Clinical Features, Imaging, Histopathologic, and Molecular Genetic Findings in a Third-level Health Care Center in Mexico.
Galnares-Olalde JA, López-Hernández JC, Benitez-Alonso EO, de Montellano DJD, May-Mas RN, Briseño-Godínez ME, Pérez-Valdez EY, Pérez-Jovel E, Fernández-Valverde F, León-Manríquez E, Vargas-Cañas ES.
Galnares-Olalde JA, et al. Among authors: benitez alonso eo.
Neurologist. 2021 Jul 6;26(4):143-148. doi: 10.1097/NRL.0000000000000331.
Neurologist. 2021.
PMID: 34190208
Item in Clipboard
Cite
Cite