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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 2
1982 3
1983 1
1984 2
1985 1
1986 2
1987 5
1988 1
1989 4
1990 1
1991 3
1992 3
1993 4
1994 1
1995 1
1996 1
1998 1
1999 2
2000 1
2001 2
2002 1
2004 6
2005 9
2006 7
2007 9
2008 15
2009 10
2010 14
2011 10
2012 9
2013 18
2014 13
2015 14
2016 9
2017 12
2018 9
2019 9
2020 7
2021 5
2022 1
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Search Results

199 results
Results by year
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Page 1
C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia.
Savarirayan R, Irving M, Bacino CA, Bostwick B, Charrow J, Cormier-Daire V, Le Quan Sang KH, Dickson P, Harmatz P, Phillips J, Owen N, Cherukuri A, Jayaram K, Jeha GS, Larimore K, Chan ML, Huntsman Labed A, Day J, Hoover-Fong J. Savarirayan R, et al. Among authors: harmatz p. N Engl J Med. 2019 Jul 4;381(1):25-35. doi: 10.1056/NEJMoa1813446. Epub 2019 Jun 18. N Engl J Med. 2019. PMID: 31269546 Clinical Trial.
Once-daily, subcutaneous vosoritide therapy in children with achondroplasia: a randomised, double-blind, phase 3, placebo-controlled, multicentre trial.
Savarirayan R, Tofts L, Irving M, Wilcox W, Bacino CA, Hoover-Fong J, Ullot Font R, Harmatz P, Rutsch F, Bober MB, Polgreen LE, Ginebreda I, Mohnike K, Charrow J, Hoernschemeyer D, Ozono K, Alanay Y, Arundel P, Kagami S, Yasui N, White KK, Saal HM, Leiva-Gea A, Luna-González F, Mochizuki H, Basel D, Porco DM, Jayaram K, Fisheleva E, Huntsman-Labed A, Day J. Savarirayan R, et al. Among authors: harmatz p. Lancet. 2020 Sep 5;396(10252):684-692. doi: 10.1016/S0140-6736(20)31541-5. Lancet. 2020. PMID: 32891212 Clinical Trial.
Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa.
Kishnani PS, Rush ET, Arundel P, Bishop N, Dahir K, Fraser W, Harmatz P, Linglart A, Munns CF, Nunes ME, Saal HM, Seefried L, Ozono K. Kishnani PS, et al. Among authors: harmatz p. Mol Genet Metab. 2017 Sep;122(1-2):4-17. doi: 10.1016/j.ymgme.2017.07.010. Epub 2017 Jul 25. Mol Genet Metab. 2017. PMID: 28888853 Free article. Review.
Mucopolysaccharidosis VI.
Valayannopoulos V, Nicely H, Harmatz P, Turbeville S. Valayannopoulos V, et al. Among authors: harmatz p. Orphanet J Rare Dis. 2010 Apr 12;5:5. doi: 10.1186/1750-1172-5-5. Orphanet J Rare Dis. 2010. PMID: 20385007 Free PMC article. Review.
Iron chelation therapy in thalassemia major: a systematic review with meta-analyses of 1520 patients included on randomized clinical trials.
Maggio A, Filosa A, Vitrano A, Aloj G, Kattamis A, Ceci A, Fucharoen S, Cianciulli P, Grady RW, Prossomariti L, Porter JB, Iacono A, Cappellini MD, Bonifazi F, Cassarà F, Harmatz P, Wood J, Gluud C. Maggio A, et al. Among authors: harmatz p. Blood Cells Mol Dis. 2011 Oct 15;47(3):166-75. doi: 10.1016/j.bcmd.2011.07.002. Epub 2011 Aug 16. Blood Cells Mol Dis. 2011. PMID: 21843958 Review.
Management guidelines for mucopolysaccharidosis VI.
Giugliani R, Harmatz P, Wraith JE. Giugliani R, et al. Among authors: harmatz p. Pediatrics. 2007 Aug;120(2):405-18. doi: 10.1542/peds.2006-2184. Pediatrics. 2007. PMID: 17671068 Review.
Anaesthesia and airway management in mucopolysaccharidosis.
Walker R, Belani KG, Braunlin EA, Bruce IA, Hack H, Harmatz PR, Jones S, Rowe R, Solanki GA, Valdemarsson B. Walker R, et al. Among authors: harmatz pr. J Inherit Metab Dis. 2013 Mar;36(2):211-9. doi: 10.1007/s10545-012-9563-1. Epub 2012 Nov 30. J Inherit Metab Dis. 2013. PMID: 23197104 Free PMC article. Review.
199 results