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Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|February 6, 2002
Flumazenil responsive ornithine transcarbamylase deficiency encephalopathy: clinical and radiographic featuresMichael A Meyer, Ralitza H GavrilovaJournal of Child Neurology|April 2, 2011
Valproate-induced worsening of seizures: clue to underlying diagnosisRadhika Dhamija, Ralitza H Gavrilova, Elaine C WirrellNeuromuscular Disorders : NMD|May 19, 2012
Myalgic phenotype and preserved muscle strength in adult-onset acid maltase deficiencyLyell K Jones, Teerin Liewluck, Ralitza H GavrilovaBMJ Case Reports|January 22, 2017
De novo 2p16.1 microdeletion with metastatic esophageal adenocarcinomaDon Chamil Codipilly, Ralitza H Gavrilova, Eric G TangalosBrain Communications|March 4, 2024
Mitochondrial myopathies diagnosed in adulthood: clinico-genetic spectrum and long-term outcomesGrayson Beecher, Ralitza H Gavrilova, Jay Mandrekar, et al.The American Journal of Case Reports|March 26, 2018
Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati SyndromeMohammad Almeqdadi, Jennifer L Kemppainen, Pavel N Pichurin, et al.Frontiers in Neurology|December 29, 2023
The clinical spectrum of MELAS and associated disorders across ages: a retrospective cohort studyBenjamin C Cox, Jennifer Y Pearson, Jay Mandrekar, et al.Frontiers in Neurology|December 16, 2021
Seizure Semiology, EEG, and Imaging Findings in Epilepsy Secondary to Mitochondrial DiseaseAnthony L Fine, Greta Liebo, Ralitza H Gavrilova, et al.Archives of Neurology|March 16, 2011
Sporadic corticobasal syndrome with progranulin mutation presenting as progressive apraxic agraphiaVictoria Passov, Ralitza H Gavrilova, Edythe Strand, et al.Molecular Genetics & Genomic Medicine|September 12, 2021
Clinicoradiographic and genetic features of cerebral small vessel disease indicate variability in mode of inheritance for monoallelic HTRA1 variantsKarthik Muthusamy, Alejandro Ferrer, Eric W Klee, et al.Pageof 6