Stefano Paolacci
www.mendeley.com
0000-0002-5551-7520
MAGI's Lab
13 papers found
Refreshing results…
Low Efficacy of Genetic Tests for the Diagnosis of Primary Lymphedema Prompts Novel Insights into the Underlying Molecular Pathways
A Multi-Gene Panel to Identify Lipedema-Predisposing Genetic Variants by a Next-Generation Sequencing Strategy
Variant Selection and Interpretation: An Example of Modified VarSome Classifier of ACMG Guidelines in the Diagnostic Setting
Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations
Etiopathogenesis of sacroiliitis: implications for assessment and management
Paraneoplastic Neurological Syndromes: Study of Prevalence in a Province of the Lombardy Region, Italy
Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann–Rautenstrauch syndrome
Genetic contributions to the etiology of anorexia nervosa: New perspectives in molecular diagnosis and treatment
Molecular Aspects of Regional Pain Syndrome
Hydroxytyrosol: A natural compound with promising pharmacological activities
Molecular pathways involved in lymphedema: Hydroxytyrosol as a candidate natural compound for treating the effects of lymph accumulation
A next generation sequencing custom gene panel designed to distinguish isolated polydactyly from syndromic polydactyly during prenatal diagnosis
Genetic tests in lymphatic vascular malformations and lymphedema
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