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Overview

Antonio V. Delgado-Escueta is affiliated with the University of California, Los Angeles in the United States. Their research predominantly spans the fields of Medicine and Biochemistry, Genetics and Molecular Biology, with subfields that include Rheumatology, Genetics, Neurology, Oncology, and Pediatrics, Perinatology and Child Health.

The scientist's work focuses on several main topics, such as Glycogen Storage Diseases and Myoclonus, Genetics and Neurodevelopmental Disorders, Neurological disorders and treatments, Drug Transport and Resistance Mechanisms, Pharmacological Effects and Toxicity Studies, Epilepsy research and treatment, and Autoimmune Neurological Disorders and Treatments.

Antonio V. Delgado-Escueta has published papers in several venues, notably:

  • Epilepsy & Behavior
  • Neurological Sciences
  • Child Neurology Open
  • Neurology

Frequent co-authors of Antonio V. Delgado-Escueta include:

  • Matthew S. Gentry
  • Roberto Michelucci
  • Berge A. Minassian
  • Pascual Sanz
  • José M. Serratosa

Recent publications by Antonio V. Delgado-Escueta cover various aspects of epilepsy and related neurological conditions. Some notable papers include:

  • The 5th International Lafora Epilepsy Workshop: Basic science elucidating therapeutic options and preparing for therapies in the clinic, 2020, Epilepsy & Behavior
  • Association of variants in the ABCB1, CYP2C19 and CYP2C9 genes for Juvenile Myoclonic Epilepsy, 2023, Neurological Sciences
  • The 9th annual Lafora science symposium: a rare epilepsy community makes progress towards clinical readiness, 2025, Epilepsy & Behavior
  • A Novel Mutation in Lafora Disease and Update on Pathophysiology and Future Treatments, 2022, Child Neurology Open
  • Early Stages of Lafora Progressive Myoclonus Epilepsy (5489), 2020, Neurology

Best Publications

  • Comparison of carbamazepine, phenobarbital, phenytoin, and primidone in partial and secondarily generalized tonic-clonic seizures

    Mattson Rh;Cramer Ja;Collins Jf;Smith Db

  • Altered patterns of dynorphin immunoreactivity suggest mossy fiber reorganization in human hippocampal epilepsy

    CR Houser;JE Miyashiro;BE Swartz;GO Walsh

  • Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy.

    Berge A. Minassian;R. Lee Jeffrey;Jo Anne Herbrick;Jack Huizenga

  • Juvenile myoclonic epilepsy of Janz

    A. V. Delgado-Escueta;Fe Enrile-Bacsal

  • Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

    T. M. DeLorey;A. Handforth;S. G. Anagnostaras;G. E. Homanics

  • Jasper's basic mechanisms of the epilepsies

    Jeffrey L Noebels;Massimo Avoli;Michael A Rogawski;Richard W Olsen

  • Rapid preparation of synaptosomes from mammalian brain using nontoxic isoosmotic gradient material (Percoll).

    Agnes Nagy;Antonio V. Delgado-Escueta

  • Mutations in EFHC1 cause juvenile myoclonic epilepsy

    Toshimitsu Suzuki;Toshimitsu Suzuki;Antonio V Delgado-Escueta;Kripamoy Aguan;Maria E Alonso

  • Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6.

    David A. Greenberg;David A. Greenberg;Antonio V. Delgado-Escueta;Antonio V. Delgado-Escueta;Heidi Widelitz;Robert S. Sparkes

  • Mutations in NHLRC1 cause progressive myoclonus epilepsy

    Elayne M Chan;Edwin J Young;Leonarda Ianzano;Iulia Munteanu

  • Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice

    Subramaniam Ganesh;Antonio V. Delgado-Escueta;Antonio V. Delgado-Escueta;Toshiro Sakamoto;Maria Rosa Avila

  • Management of Status Epilepticus

    A. V. Delgado-Escueta;C. Wasterlain;D. M. Treiman;R. J. Porter

  • Calcific neurocysticercosis and epileptogenesis

    Theodore E. Nash;O. H. Del Brutto;J. A. Butman;T. Corona

  • Consensus guidelines: preconception counseling, management, and care of the pregnant woman with epilepsy.

    A V Delgado-Escueta;D Janz

  • Special report. The nature of aggression during epileptic seizures

    Antonio V. DelgadoEscueta;Richard H. Mattson;Lambert King;Eli S. Goldensohn

  • Laforin is a glycogen phosphatase, deficiency of which leads to elevated phosphorylation of glycogen in vivo

    Vincent S. Tagliabracci;Julie Turnbull;Wei Wang;Wei Wang;Jean Marie Girard

  • Hyperglycosylation and Reduced GABA Currents of Mutated GABRB3 Polypeptide in Remitting Childhood Absence Epilepsy

    Miyabi Tanaka;Richard W. Olsen;Marco T. Medina;Emily Schwartz

  • Treatment of neurocysticercosis: Current status and future research needs

    T. E. Nash;G. Singh;A. C. White;V. Rajshekhar

  • Juvenile myoclonic epilepsy subsyndromes : family studies and long-term follow-up

    Iris E. Martínez-Juárez;María Elisa Alonso;Marco T. Medina;Reyna M. Durón

  • Angelman syndrome: Correlations between epilepsy phenotypes and genotypes

    Berge A. Minassian;Berge A. Minassian;Timothy M. DeLorey;Richard W. Olsen;Michel Philippart

  • Neuronal Synchronization and Thalamocortical Rhythms in Sleep, Wake and Epilepsy -- Jasper's Basic Mechanisms of the Epilepsies

    Noebels Jl;Avoli M;Rogawski Ma;Olsen Rw

Frequent Co-Authors

Michael A. Rogawski
Michael A. Rogawski University of California, Davis
Massimo Avoli
Massimo Avoli McGill University
Kazuhiro Yamakawa
Kazuhiro Yamakawa Nagoya City University
José M. Serratosa
José M. Serratosa Hospital Universitario Fundación Jiménez Díaz
Berge A. Minassian
Berge A. Minassian The University of Texas Southwestern Medical Center
Richard W. Olsen
Richard W. Olsen University of California, Los Angeles
Roger J. Porter
Roger J. Porter University of Pennsylvania
David A. Greenberg
David A. Greenberg Nationwide Children's Hospital
Robert S. Sparkes
Robert S. Sparkes University of California, Los Angeles
David M. Treiman
David M. Treiman Barrow Neurological Institute

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