Liliana Alba

Acitretin embryopathy: A case report

Pablo Barbero, Vanesa Lotersztein, Rubén Bronberg et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2004 · 41 citations

Medicine, Pediatrics, Pharmacology +17

Classical and nonclassical 21‐hydroxylase deficiency: a molecular study of Argentine patients

Liliana Daín, Noemí Buzzalino, Adriana Oneto et al. · Clinical Endocrinology · 2002 · 31 citations

Life Sciences, Endocrinology, Genetics +17

Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

Jair Tenorio, Pablo Alarcón, Pedro Arias et al. · European Journal of Human Genetics · 2019 · 31 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Structure-Based Analysis of Five Novel Disease-Causing Mutations in 21-Hydroxylase-Deficient Patients

Carolina Minutolo, Alejandro D. Nadra, Cecilia Fernández et al. · PLoS ONE · 2011 · 30 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Methimazole embryopathy: A contribution to defining the phenotype

Rita Valdéz, Pablo Barbero, Rosa Liascovich et al. · Reproductive Toxicology · 2006 · 30 citations

Life Sciences, Developmental Biology, Pathology +3