Gabriel Veneruzzo - Garrahan Hospital

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论文共 10 篇作者统计合作学者相似作者

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Expanding the Phenotypic Spectrum of GRIN1 Encephalopathy: Two Pediatric Patients with Atypical Findings

Mariana Loos,Matias Juanes,Adolfo Gallo, Maria Eugenia Martin,Gabriela Reyes,Gabriel Veneruzzo,Carlos Rugilo, Cristina Alonso,Roberto Caraballo

Journal of Pediatric Epilepsy (2024)

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Dravet Syndrome: an Electroclinical, Genetic, Treatment, and Outcome Study of 35 Patients in Argentina

Roberto Caraballo,Gabriel Veneruzzo,Mariana Loos,Gabriela Reyes,Matias Juanes, Eugenia Martin, Segio Melgarejo Duarte,Maria Sol Touzon,Cristina Alonso

Journal of Pediatric Epilepsyno. 02 (2024): 031-039

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Age-dependent and sex-specific changes of dna methylation within growth hormone receptor (GHR), insulin-like growth factor type 1 receptor (IGF1R) and insulin receptor (INSR) gene promoters in peripheral blood leukocytes from healthy prepubertal and pubertal children

Luciana Zoff,Francisco Garcia, Maria Florencia Fernandez,Giovanna Aschettino,Gabriel Veneruzzo,Carolina Pepe, Celeste Mattone,Natalia Perez Garrido,Matias Juanes,Nora Saraco,Gabriela Guercio,Cristina Alonso,Alicia Belgorosky,Maria Sonia Baquedano

HORMONE RESEARCH IN PAEDIATRICSno. SUPPL 2 (2023): 22-23

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THU157 Epigenetic Regulation of Genes Involved in the Signaling Cascade of the GH Axis - IGF1 and Insulin. Implication in Children Postnatal Growth

Luciana Zoff,Francisco Blanco García,Giovanna Aschettino,Gabriel Veneruzzo,María Celeste Mattone,Natalia Pérez Garrido,Matías Juanes,Nora Saraco,Cristina N. Alonso,Gabriela Guercio,Alicia Belgorosky,María Sonia Baquedano

Journal of the Endocrine Societyno. Supplement_1 (2023)

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Glucose transporter type 1 deficiency syndrome: clinical aspects, diagnosis, and treatment

Gabriel M. Veneruzzo,Mariana A. Loos,Marisa Armeno,Cristina N. Alonso,Roberto H. Caraballo

ARCHIVOS ARGENTINOS DE PEDIATRIA（2023）

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Glucose Transporter Type 1 Deficiency Syndrome: Clinical Aspects, Diagnosis, and Treatment

Gabriel Veneruzzo, Mariana Loos, Marisa Armeno, Cristina N. Alonso, Roberto Caraballo

Archivos argentinos de pediatría (2022)

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Clinical and genetic study of developmental and epileptic encephalopathy in argentinean pediatric patients

Matias Juanes,Mariana Loos,Gabriela Reyes,Gabriel Veneruzzo,Francisco Martin Garcia,Giovanna Aschettino, Silvana Calligaris, Maria Eugenia Martin,Maria Eugenia Foncuberta,Cristina N. Alonso,Roberto H. Caraballo

Medicina (B Aires)（2022）

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Expanding the knowledge spectrum of the genetic background in pediatric Argentinean patients with epileptic encephalopathy

Matias Hernan Juanes,Gabriel Veneruzzo,Mariana Loos,Gabriela Reyes Valenzuela,Gimena Gomez,Veronica Araoz,Francisco Garcia Martin,Giovanna Aschettino,Cristina N. Alonso,Roberto Caraballo

EPILEPSIA（2021）

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Molecular Diagnosis of Epileptic Encephalopathy of the First Year of Life Applying a Customized Gene Panel in a Group of Argentinean Patients

Matias Juanes,Gabriel Veneruzzo,Mariana Loos,Gabriela Reyes,Hilda Veronica Araoz,Francisco Martin Garcia,Gimena Gomez, Cristina Noemi Alonso,Lilien P. Chertkoff,Roberto Caraballo

Epilepsy & Behavior（2020）

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Next Generation Sequencing-Based Mutational Profile of Therapy-Related AML and De Novo AML: Results from a Single Pediatric Institution in Argentina

Patricia Laura Rubio,Maria Sara Felice,Matias Juanes,Gabriel Veneruzzo,Francisco Martin Garcia,Jorge Alberto Digiorge, Maria Eugenia Ducatelli,Adriana Medina,Matias Pujana,Myriam Ruth Guitter,Jorge Gabriel Rossi, Cristina Noemi Alonso

Blood（2018）

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