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Fetal Sex Identification in Maternal Plasma by Means of Short Tandem Repeats on Chromosome X.
Published in:
Annals of the New York Academy of Sciences, 2008, v. 1137, p. 148, doi. 10.1196/annals.1448.038
By:
- Vecchione, Gennaro;
- Tomaiuolo, Michela;
- Sarno, Michelina;
- Colaizzo, Donatella;
- Petraroli, Rosella;
- Matteo, Maria;
- Greco, Pantaleo;
- Grandone, Elvira;
- Margaglione, Maurizio
Publication type:
Article
Recent Italian FFI Cases.
Published in:
Brain Pathology, 1998, v. 8, n. 3, p. 564, doi. 10.1111/j.1750-3639.1998.tb00183.x
By:
- Pocchiari, Maurizio;
- Ladogana, Anna;
- Petraroli, Rosella;
- Cardone, Franco;
- D'Alessandro, Marco
Publication type:
Article
Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: a multi-institutional research study.
Published in:
2018
By:
- Vaughn, Cecily P.;
- Feilotter, Harriet E.;
- Petraroli, Rosella;
- Bagai, Varun;
- Rachiglio, Anna Maria;
- Marino, Federica Zito;
- Tops, Bastiaan;
- Kurth, Henriette M.;
- Sakai, Kazuko;
- Mafficini, Andrea;
- Bastien, Roy R. L.;
- Reiman, Anne;
- Le Corre, Delphine;
- Boag, Alexander;
- Crocker, Susan;
- Bihl, Michel;
- Hirschmann, Astrid;
- Scarpa, Aldo;
- Sheils, Orla;
- Bramlett, Kelli
Publication type:
journal article
A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.
Published in:
Annals of Neurology, 1993, v. 34, n. 6, p. 802, doi. 10.1002/ana.410340608
By:
- Pocchiari, Maurizio;
- Salvatore, Mirella;
- Cutruzzolá, Francesca;
- Genuardi, Maurizio;
- Allocatelli, Carlo Travaglini;
- Masullo, Carlo;
- Macchi, Giorgio;
- Alemá, Giovanni;
- Galgani, Simona;
- Xi, You Geng;
- Petraroli, Rosella;
- Silvestrini, Maria Chiara;
- Brunori, Maurizio
Publication type:
Article

Found: 4

Fetal Sex Identification in Maternal Plasma by Means of Short Tandem Repeats on Chromosome X.

Recent Italian FFI Cases.

Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: a multi-institutional research study.

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.