Melissa L DiBacco
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Explore the profile of Melissa L DiBacco including associated specialties, affiliations and a list of published articles.
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20
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95
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Recent Articles
1.
Tokatly Latzer I, Hanson E, Bertoldi M, DiBacco M, Aygun D, Afacan O, et al.
Mol Genet Metab
. 2025 Feb;
144(3):109051.
PMID: 39919676
Background And Objectives: Succinic semialdehyde dehydrogenase deficiency (SSADHD) is an inherited metabolic disorder resulting in hyper-physiologic concentrations of the neurotransmitter γ-aminobutyrate (GABA). This study aims to provide the most comprehensive...
2.
Sansevere A, DiBacco M, Cavan K, Rotenberg A
J Clin Neurophysiol
. 2024 Nov;
PMID: 39582111
Introduction: To assess the alpha-delta ratio (ADR) as a biomarker for cerebral injury and stroke in pediatric extracorporeal membrane oxygenation (ECMO). Methods: Retrospective study of children aged >44 weeks gestation...
3.
Tokatly Latzer I, Roullet J, Afshar-Saber W, Lee H, Bertoldi M, McGinty G, et al.
J Neurodev Disord
. 2024 Apr;
16(1):21.
PMID: 38658850
Background: Succinic semialdehyde dehydrogenase deficiency (SSADHD) represents a model neurometabolic disease at the fulcrum of translational research within the Boston Children's Hospital Intellectual and Developmental Disabilities Research Centers (IDDRC), including...
4.
Tokatly Latzer I, Bertoldi M, Blau N, DiBacco M, Elsea S, Garcia-Cazorla A, et al.
Mol Genet Metab
. 2024 Mar;
142(1):108363.
PMID: 38452608
Succinic semialdehyde dehydrogenase deficiency (SSADHD) (OMIM #271980) is a rare autosomal recessive metabolic disorder caused by pathogenic variants of ALDH5A1. Deficiency of SSADH results in accumulation of γ-aminobutyric acid (GABA)...
5.
Sansevere A, Janatti A, DiBacco M, Cavan K, Rotenberg A
Neurocrit Care
. 2024 Feb;
41(1):156-164.
PMID: 38302644
Background: Our objective was to assess the utility of the 1-h suppression ratio (SR) as a biomarker of cerebral injury and neurologic prognosis after cardiac arrest (CA) in the pediatric...
6.
Tokatly Latzer I, Roullet J, Cesaro S, DiBacco M, Arning E, Rotenberg A, et al.
Hum Genet
. 2023 Nov;
142(12):1755-1776.
PMID: 37962671
To investigate the genotype-to-protein-to-phenotype correlations of succinic semialdehyde dehydrogenase deficiency (SSADHD), an inherited metabolic disorder of γ-aminobutyric acid catabolism. Bioinformatics and in silico mutagenesis analyses of ALDH5A1 variants were performed...
7.
Papadelis C, Ntolkeras G, Tokatly Latzer I, DiBacco M, Afacan O, Warfield S, et al.
Brain Commun
. 2023 Nov;
5(6):fcad291.
PMID: 37953848
Succinic semialdehyde dehydrogenase deficiency is a rare autosomal recessively inherited metabolic disorder of γ-aminobutyric acid catabolism manifested by intellectual disability, expressive aphasia, movement disorders, psychiatric ailments and epilepsy. Subjects with...
8.
Tokatly Latzer I, Roullet J, Cesaro S, DiBacco M, Arning E, Rotenberg A, et al.
Res Sq
. 2023 Jul;
PMID: 37503297
Objective: To investigate the genotype-to-protein-to-phenotype correlations of succinic semialdehyde dehydrogenase deficiency (SSADHD), an inherited metabolic disorder of γ-aminobutyric acid catabolism. Methods: Bioinformatics and in silico mutagenesis analyses of ALDH5A1 variants...
9.
Tokatly Latzer I, Bertoldi M, DiBacco M, Arning E, Tsuboyama M, MacMullin P, et al.
Epilepsia
. 2023 Mar;
64(6):1516-1526.
PMID: 36961285
Objective: Succinic semialdehyde dehydrogenase deficiency (SSADHD) is a rare inherited metabolic disorder caused by a defect of γ-aminobutyrate (GABA) catabolism. Despite the resultant hyper-GABAergic environment facilitated by the metabolic defect,...
10.
DiBacco M, Cavan K, Sansevere A
J Child Neurol
. 2022 May;
37(7):562-567.
PMID: 35635225
Objective: To determine features of paroxysmal events and background electroencephalographic (EEG) abnormalities associated with electroclinical seizures in critically ill children who undergo continuous video EEG to characterize clinical events. Methods:...