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Edmar Obed Benitez-Alonso

Observed names: Edmar Benitez-Alonso, Edmar O Benitez-Alonso, Edmar O Benítez-Alonso, Edmar O. Benitez-Alonso, Edmar O. Benítez, Edmar O. Benítez Alonso, Edmar O. Benítez-Alonso, Edmar O. Benítez‐Alonso, Edmar Obed Benítez-Alonso
ORCID: 0000-0002-3813-0359
Observed ORCID: 0000-0002-3813-0359
OpenAlex ID: A5035040951
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice
2022 · Dianalee McKnight, Ana Morales, et al. · JAMA Neurology · 95
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A Novel GMPPA Mutation in Two Adult Sisters with Achalasia, Alacrima, Short Stature, Dysmorphism, and Intellectual Disability
2018 · Edmar O. Benítez, Juan J. Morales, et al. · Molecular Syndromology · 16
Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population
2022 · Larissa López-Rodríguez, Yevgeniya Svyryd, et al. · Revista de investigaci�n Cl�nica · 5
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Vacuolar Myopathy Associated to CACNA1S Mutation as a Rare Cause of Late-Onset Limb-Girdle Myopathy: A Case Report
2021 · Juan Carlos López-Hernández, Javier A Galnares-Olalde, et al. · Cureus · 4
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Unraveling the role of relative telomere length and CAG expansion on initial symptoms of juvenile Huntington disease
2022 · Adriana PerezGrovas‐Saltijeral, Adriana Ochoa‐Morales, et al. · European Journal of Neurology · 3
FUS as a cause of familial Amyotrophic lateral sclerosis, a case report in a pregnant patient
2022 · Lisette Bazán-Rodríguez, Jesús A. Ruíz-Avalos, et al. · Neurocase · 3
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
2021 · Javier A. Galnares-Olalde, Juan C. López-Hernández, et al. · The Neurologist · 3
Juvenile Huntington’s Disease: Diagnostic challenges in the Clinic
2025 · Naomi Nazareth Becerra-Aguiar, Carlos Javier Moreno-Bernardino, et al. · Clinical Pediatrics · 2
DLG4-Related Synaptopathy and Coexisting Fabry’s Disease: A Case Report
2026 · Daniel San-Juan, Edmar O Benitez-Alonso, et al. · Annals of Indian Academy of Neurology · 1
Miopatías genéticas en adultos: experiencia de un centro de tercer nivel en México.
2022 · Edwin Steven Vargas-Cañas, Eunice Martínez-Jiménez, et al. · Archivos de Neurociencias · 1
Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome: frequency, clinical features, imaging, histopathologic and molecular genetic findings in a third-level healthcare center in Mexico. (1280)
2021 · Javier Andrés Galnares-Olalde, Juan Carlos López-Hernández, et al. · Neurology · 1
Vohwinkel syndrome with de novo heterozygous mutation in the GJB2 gene - c.175G>A (p. Gly59Ser)
2024 · María Caridad Duran-Lemarie, Luis Enrique Cano-Aguilar, et al. · Anais Brasileiros de Dermatologia
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
2022 · Edmar O Benítez-Alonso, Juan C López-Hernández, et al. · Cureus
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Porcentaje de infecciones micóticas por uso del dispositivo intrauterino en la ciudad de Puebla, México
2009 · José Antonio Sánchez-Hernández, Edmar Obed Benítez-Alonso, et al.
Works count: 14
Citation count: 134
H-index: 4
I10-index: 2
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