PIRELLI, ARIANNA
PIRELLI, ARIANNA
Dipartimento di Scienze Cliniche e di Comunità
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Improved Molecular Diagnosis of McCune-Albright Syndrome and Bone Fibrous Dysplasia by Digital PCR
2019 F.M. Elli, L. de Sanctis, M. Bergallo, M.A. Maffini, A. Pirelli, I. Galliano, P. Bordogna, M. Arosio, G. Mantovani
2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance
2019 F.M. Elli, L. de Sanctis, B. Madeo, M.A. Maffini, P. Bordogna, A. Pirelli, M. Arosio, G. Mantovani
Association of GNAS Imprinting Defects and Deletions of Chromosome 2 in Two Patients : Clues Explaining Phenotypic Heterogeneity in Pseudohypoparathyroidism Type 1B/iPPSD3
2019 F.M. Elli, L. Desanctis, M.A. Maffini, P. Bordogna, D. Tessaris, A. Pirelli, M. Arosio, A. Linglart, G. Mantovani
| Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
|---|---|---|---|---|---|
| Improved Molecular Diagnosis of McCune-Albright Syndrome and Bone Fibrous Dysplasia by Digital PCR | 2019 | F. M. ElliM. A. MaffiniA. PirelliM. ArosioG. Mantovani + | Article (author) | - | |
| 2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance | 2019 | F. M. ElliM. A. MaffiniA. PirelliM. ArosioG. Mantovani + | Article (author) | - | |
| Association of GNAS Imprinting Defects and Deletions of Chromosome 2 in Two Patients : Clues Explaining Phenotypic Heterogeneity in Pseudohypoparathyroidism Type 1B/iPPSD3 | 2019 | F. M. ElliM. A. MaffiniA. PirelliM. ArosioG. Mantovani + | Article (author) | - |