Publications by authors named "Andrea Solari"

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Classic Prader-Willi Syndrome Phenotype Caused by an Atypical Deletion in the 15q11 Region Not Involving the SNORD Genes.
Jazmín Belén Martínez, Josefina María Álvarez Arancedo, Andrea Solari, Aldana Claps, Tania Castro

Clin Genet· April 2025

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Novel variant in the KAT6B gene associated with Say Barber Biesecker Young Simpson.
Stefania A Miller, Andrea P Solari, Guillermo Alberto, Ana C Benitez Medina, Brenda M García Ayré

Clin Dysmorphol· October 2023

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TRIO-related intellectual disability with microcephaly: a case report of a patient with novel clinical findings.
Florencia Bevilacqua, Guillermo Alberto, Santiago Pablo Duarte, Marina Serra, Julieta Basterra, Andrea Paula Solari

Clin Dysmorphol· January 2021

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Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.
Lucía Daniela Espeche, Andrea Paula Solari, María Ángeles Mori, Rubén Martín Arenas, María Palomares

Mol Biol Rep· September 2020

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Identification of a pharmacological inhibitor of Epac1 that protects the heart against acute and chronic models of cardiac stress.
Marion Laudette, Antonio Coluccia, Yannis Sainte-Marie, Andrea Solari, Loubina Fazal

Cardiovasc Res· October 2019

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[Fragile X syndrome and other entities associated with the FMR1 gene: Study of 28 affected families].
Mariel Ormazábal, Andrea Solari, Lucía Espeche, Tania Castro, Noemí Buzzalino

Arch Argent Pediatr· June 2019

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[16p11.2 Microdeletion: first report in Argentina].
Agostina Tardivo, Bárbara Masotto, Lucía Espeche, Andrea P Solari, Julián Nevado

Arch Argent Pediatr· December 2017

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Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency.
Lucía Daniela Espeche, Violeta Chiauzzi, Ianina Ferder, Mehrnoosh Arrar, Andrea Paula Solari

Genes (Basel)· August 2017

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Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations.
Carlos D Bruque, Marisol Delea, Cecilia S Fernández, Juan V Orza, Melisa Taboas, Andrea Solari

Sci Rep· December 2016

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[Clinical diagnosis of Kabuki syndrome: phenotype and associated abnormalities in two new cases].
María Soledad Andersen, Sebastián Menazzi, Paloma Brun, Cecilia Cocah, Giuseppe Merla, Andrea Solari

Arch Argent Pediatr· February 2014

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[Phenotypic variability in 47, XXX patients: Clinical report of four new cases].
Ernesto Goldschmidt, Marisa Márquez, Andrea Solari, María I Ziembar, Alejandro Laudicina

Arch Argent Pediatr· August 2010

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[Complete androgen insensitivity syndrome: diagnosis and clinical characteristics].
Andrea Solari, Boris Groisman, María P Bidondo, Constanza Cinca, Liliana Alba

Arch Argent Pediatr· June 2008

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