Sfoglia per Corso SCIENZE DELLA RIPRODUZIONE E DELLO SVILUPPO
A co-design approach for the development of a mHealth solution to support the first 1000 days of life
2023
Congenital heart defects and placental dysfunction
2018
CORRELATION BETWEEN TISSUE ABNORMALITIES AND MYOCARDIAL DEFORMATION INDICES IN ARRHYTHMOGENIC CARDIOMYOPATHY: A MULTIMODALITY IMAGING STUDY.
2022
DEALING WITH THE MAIN CHALLENGES OF FANCONI ANEMIA MOLECULAR DIAGNOSIS AND THERAPY
2023
DEVELOPMENT OF CUSTOMIZED TESTS FOR THE EARLY DIAGNOSIS OF RELAPSES OF GYNECOLOGICAL TUMORS USING LIQUID BIOPSY
2024
Development of polymeric nanoparticles for the delivery of nucleic acids in the treatment of B-cell malignancies-Targeted production of therapeutic antibodies by Burkitt lymphoma cells
2025
DIAGNOSTIC APPROACH TO MONOGENIC INFLAMMATORY BOWEL DISEASE WITH NEXT-GENERATION SEQUENCING TECHNOLOGIES.
2019
Efficiency and safeness improvement and cost containment strategy in Assisted Reproduction Technique (ART)
2017
EPINICU (Empowering Parents of newborns in the NICU). Progetto multi-paese per identificare modelli di intervento sostenibili in diversi setting: risultati dall'Italia e da 3 revisioni sistematiche.
2024
FUNCTIONAL ANALYSIS OF NEW GENETIC VARIANTS IDENTIFIED IN GENES OF INHERITED THROMBOCYTOPENIA
2021
Hidradenitis suppurativa: identification of the main cellular and molecular pathways involved in immune and cutaneous cell biology.
2021
High throughput sequencing analysis for the molecular diagnosis of Inherited Thrombocytopenias
2019
HIGH-THROUGHPUT DATA ANALYSIS OF HEARING PHENOTYPES ON 9000 SUBJECTS FROM TEN COHORTS AND IN 200.000 INDIVIDUALS FROM UK BIOBANK
2020
IDENTIFICATION OF GENETIC VARIANTS REGULATING FEMALE FERTILITY
2018
Identification of New Hereditary Hearing Loss Genes Using High-Throughput Sequencing Technologies.
2017
Identification of new molecular targets for personalized therapy in pediatric patients with inflammatory bowel disease (IBD)
2018
IDENTIFICAZIONE DI MARCATORI MOLECOLARI DI MALATTIA E DI RISPOSTA ALLA TERAPIA IN PAZIENTI PEDIATRICI AFFETTI DA MALATTIE INFIAMMATORIE CRONICHE INTESTINALI
2021
Identificazione e caratterizzazione funzionale di nuovi geni candidati e varianti associate a Sordità Ereditaria e Presbiacusia
2021
Il ruolo di PACSIN2 come modulatore dell'autofagia e della citotossicità alle tiopurine: studi su modelli linfoidi ed intestinali
2022
In silico identification of predictive markers for precision medicine in pediatric diseases
2025
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