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Year Number of Results
1999 1
2001 2
2002 1
2003 2
2004 1
2005 1
2007 1
2008 1
2014 1
2024 0

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Page 1
Primary ciliary dyskinesia: diagnostic and phenotypic features.
Noone PG, Leigh MW, Sannuti A, Minnix SL, Carson JL, Hazucha M, Zariwala MA, Knowles MR. Noone PG, et al. Among authors: sannuti a. Am J Respir Crit Care Med. 2004 Feb 15;169(4):459-67. doi: 10.1164/rccm.200303-365OC. Epub 2003 Dec 4. Am J Respir Crit Care Med. 2004. PMID: 14656747
Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype.
Knowles MR, Ostrowski LE, Leigh MW, Sears PR, Davis SD, Wolf WE, Hazucha MJ, Carson JL, Olivier KN, Sagel SD, Rosenfeld M, Ferkol TW, Dell SD, Milla CE, Randell SH, Yin W, Sannuti A, Metjian HM, Noone PG, Noone PJ, Olson CA, Patrone MV, Dang H, Lee HS, Hurd TW, Gee HY, Otto EA, Halbritter J, Kohl S, Kircher M, Krischer J, Bamshad MJ, Nickerson DA, Hildebrandt F, Shendure J, Zariwala MA. Knowles MR, et al. Among authors: sannuti a. Am J Respir Crit Care Med. 2014 Mar 15;189(6):707-17. doi: 10.1164/rccm.201311-2047OC. Am J Respir Crit Care Med. 2014. PMID: 24568568 Free PMC article.
Mutations in DNAI1 (IC78) cause primary ciliary dyskinesia.
Noone PG, Zariwala M, Sannuti A, Minnix S, Leigh MW, Carson J, Knowles MR. Noone PG, et al. Among authors: sannuti a. Chest. 2002 Mar;121(3 Suppl):97S. Chest. 2002. PMID: 11893720 No abstract available.
Histoplasmosis after treatment with anti-tumor necrosis factor-alpha therapy.
Wood KL, Hage CA, Knox KS, Kleiman MB, Sannuti A, Day RB, Wheat LJ, Twigg HL 3rd. Wood KL, et al. Among authors: sannuti a. Am J Respir Crit Care Med. 2003 May 1;167(9):1279-82. doi: 10.1164/rccm.200206-563OC. Epub 2003 Feb 13. Am J Respir Crit Care Med. 2003. PMID: 12615627
Discordant organ laterality in monozygotic twins with primary ciliary dyskinesia.
Noone PG, Bali D, Carson JL, Sannuti A, Gipson CL, Ostrowski LE, Bromberg PA, Boucher RC, Knowles MR. Noone PG, et al. Among authors: sannuti a. Am J Med Genet. 1999 Jan 15;82(2):155-60. doi: 10.1002/(sici)1096-8628(19990115)82:2<155::aid-ajmg11>3.0.co;2-t. Am J Med Genet. 1999. PMID: 9934981