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Page 1
Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).
Carrera P, Calzavara S, Magistroni R, den Dunnen JT, Rigo F, Stenirri S, Testa F, Messa P, Cerutti R, Scolari F, Izzi C, Edefonti A, Negrisolo S, Benetti E, Alibrandi MT, Manunta P, Boletta A, Ferrari M. Carrera P, et al. Among authors: stenirri s. Sci Rep. 2016 Aug 8;6:30850. doi: 10.1038/srep30850. Sci Rep. 2016. PMID: 27499327 Free PMC article.
2. Post-Natal Molecular Diagnosis of Inherited Diseases.
Ferrari M, Cremonesi L, Stenirri S. Ferrari M, et al. Among authors: stenirri s. EJIFCC. 2008 Apr 3;19(1):7-12. eCollection 2008 Apr. EJIFCC. 2008. PMID: 27683285 Free PMC article. No abstract available.
Molecular diagnostics by microelectronic microchips.
Ferrari M, Stenirri S, Bonini P, Cremonesi L. Ferrari M, et al. Among authors: stenirri s. Clin Chem Lab Med. 2003 Apr;41(4):462-7. doi: 10.1515/CCLM.2003.069. Clin Chem Lab Med. 2003. PMID: 12747587 Review.
Familial hemiplegic migraine: a ion channel disorder.
Carrera P, Stenirri S, Ferrari M, Battistini S. Carrera P, et al. Among authors: stenirri s. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):239-41. doi: 10.1016/s0361-9230(01)00570-6. Brain Res Bull. 2001. PMID: 11719257 Review.
Molecular diagnostics by microelectronic microchips.
Ferrari M, Cremonesi L, Bonini P, Stenirri S, Foglieni B. Ferrari M, et al. Among authors: stenirri s. Expert Rev Mol Diagn. 2005 Mar;5(2):183-92. doi: 10.1586/14737159.5.2.183. Expert Rev Mol Diagn. 2005. PMID: 15833048 Review.
Denaturing HPLC analysis of DNA deletions and insertions.
Cremonesi L, Stenirri S, Fermo I, Paroni R, Ferrari M, Cazzola M, Arosio P. Cremonesi L, et al. Among authors: stenirri s. Hum Mutat. 2003 Jul;22(1):98-102. doi: 10.1002/humu.10234. Hum Mutat. 2003. PMID: 12815600
23 results