BUCOSSI, SERENA
BUCOSSI, SERENA
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Microduplication encompassing CCL2 segregates in a family with recurrent anencephaly and dorsal dermal sinus: a possible link between chemokine and neural tube defects?
2025-01-01 Mastromoro, G; Darelli, D; Mariani, S; Colantoni, F; Bucossi, S; Canestrelli, M; Dello Russo, C; Squitti, R; Micalizzi, A; Zumpano, A; Pizzuti, A; Rongioletti, Mca
Non-ceruloplasmin copper identifies a subtype of Alzheimer's disease (CuAD): characterization of the cognitive profile and case of a CuAD patient carrying an RGS7 stop-loss variant
2023-01-01 Squitti, Rosanna; Catalli, Claudio; Gigante, Laura; Marianetti, Massimo; Rosari, Mattia; Mariani, Stefania; Bucossi, Serena; Mastromoro, Gioia; Ventriglia, Mariacarla; Simonelli, Ilaria; Tondolo, Vincenzo; Singh, Parminder; Kumar, Ashok; Pal, Amit; Rongioletti, Mauro
NUAK2 Pathogenic Variants are Definitively Associated with Neural Tube Defects in Humans: New Genotype-Phenotype Correlation and Review of the Literature
2025-01-01 Mastromoro, G; Dello Russo, C; Mariani, S; Bucossi, S; Riccardi, R; Pal, A; Squitti, R; Dangi, M; Pizzuti, A; Rongioletti, Mca
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Microduplication encompassing CCL2 segregates in a family with recurrent anencephaly and dorsal dermal sinus: a possible link between chemokine and neural tube defects? | 1-gen-2025 | Mastromoro, G; Darelli, D; Mariani, S; Colantoni, F; Bucossi, S; Canestrelli, M; Dello Russo, C; Squitti, R; Micalizzi, A; Zumpano, A; Pizzuti, A; Rongioletti, Mca | |
| Non-ceruloplasmin copper identifies a subtype of Alzheimer's disease (CuAD): characterization of the cognitive profile and case of a CuAD patient carrying an RGS7 stop-loss variant | 1-gen-2023 | Squitti, Rosanna; Catalli, Claudio; Gigante, Laura; Marianetti, Massimo; Rosari, Mattia; Mariani, Stefania; Bucossi, Serena; Mastromoro, Gioia; Ventriglia, Mariacarla; Simonelli, Ilaria; Tondolo, Vincenzo; Singh, Parminder; Kumar, Ashok; Pal, Amit; Rongioletti, Mauro | |
| NUAK2 Pathogenic Variants are Definitively Associated with Neural Tube Defects in Humans: New Genotype-Phenotype Correlation and Review of the Literature | 1-gen-2025 | Mastromoro, G; Dello Russo, C; Mariani, S; Bucossi, S; Riccardi, R; Pal, A; Squitti, R; Dangi, M; Pizzuti, A; Rongioletti, Mca |