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Author

Gabriel Veneruzzo

Observed name: G. Veneruzzo
Institution: Garrahan Hospital
Observed institution: Garrahan Hospital
ORCID: 0000-0001-6635-0191
Observed ORCID: 0000-0001-6635-0191
OpenAlex ID: A5000420037
Molecular diagnosis of epileptic encephalopathy of the first year of life applying a customized gene panel in a group of Argentinean patients
2020 · Matias Juanes, Gabriel Veneruzzo, et al. · Epilepsy & Behavior · 7
Infantile Epileptic Spasms Syndrome: Unveiling clinical and genetic variability in a case series from Argentina
2025 · María Eugenia Martín, Lenin Intriago, et al. · Seizure · 2
Clinical and genetic study of developmental and epileptic encephalopathy in Argentinean pediatric patients.
2022 · Matías Juanes, Mariana Loos, et al. · PubMed · 2
Glucose transporter type 1 deficiency syndrome: Phenotypes, molecular findings, and ketogenic therapy implementation in Argentina
2026 · Marisa Laura Armeno, Mario Massaro, et al. · Epileptic Disorders
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SAT-203 Methylation Status of Growth Hormone Receptor (GHR), Insulin-like Growth Factor 1 Receptor (IGF1R) and Insulin Receptor (INSR) in Small for Gestational Age (SGA) Boys without Catch-up Growth
2025 · Luciana Zoff, Francisco M Garcia, et al. · Journal of the Endocrine Society
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SAT-202 DNA Methylation Changes in the GHR, IGF1R and INSR Genes in Foreskin from 46,XY DSD Children Born Adequate (AGA) or Small for Gestational Age (SGA)
2025 · Luciana Zoff, Francisco M Garcia, et al. · Journal of the Endocrine Society
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SAT-202 DNA Methylation Changes in the GHR, IGF1R and INSR Genes in Foreskin from 46,XY DSD Children Born Adequate (AGA) or Small for Gestational Age (SGA)
2025 · Luciana Zoff, Francisco M Garcia, et al. · Journal of the Endocrine Society
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Expanding the Phenotypic Spectrum of GRIN1 Encephalopathy: Two Pediatric Patients with Atypical Findings
2024 · Mariana Loos, Matias Juanes, et al. · Journal of Pediatric Epilepsy
Dravet Syndrome: An Electroclinical, Genetic, Treatment, and Outcome Study of 35 Patients in Argentina
2024 · Roberto H. Caraballo, Gabriel Veneruzzo, et al. · Journal of Pediatric Epilepsy
THU157 Epigenetic Regulation Of Genes Involved In The Signaling Cascade Of The GH Axis - IGF1 And Insulin. Implication In Children Postnatal Growth
2023 · Luciana Zoff, Francisco Garcia, et al. · Journal of the Endocrine Society
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Application of Next Generation Technologies
2021 · E. Foncuberta, F. Lubieniecki, et al. · Neuromuscular Disorders
Next Generation Sequencing-Based Mutational Profile of Therapy-Related AML and De Novo AML: Results from a Single Pediatric Institution in Argentina
2018 · Patricia Laura Rubio, Maria Sara Felice, et al. · Blood
Works count: 12
Citation count: 11
H-index: 2
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