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

Year Number of Results
1972 1
1974 7
1975 6
1976 5
1977 4
1979 1
1980 2
1981 4
1982 3
1983 4
1984 5
1985 6
1986 8
1987 6
1988 6
1989 3
1990 3
1991 6
1992 3
1993 2
1994 4
1995 2
1996 4
1997 5
1998 4
1999 4
2000 2
2001 2
2002 4
2003 2
2004 3
2005 1
2006 1
2008 4
2010 2
2011 2
2012 3
2013 1
2014 8
2015 6
2016 4
2017 2
2021 2
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Search Results

151 results
Results by year
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Page 1
Early Volume Expansion and Outcomes of Hemolytic Uremic Syndrome.
Ardissino G, Tel F, Possenti I, Testa S, Consonni D, Paglialonga F, Salardi S, Borsa-Ghiringhelli N, Salice P, Tedeschi S, Castorina P, Colombo RM, Arghittu M, Daprai L, Monzani A, Tozzoli R, Brigotti M, Torresani E. Ardissino G, et al. Among authors: salardi s. Pediatrics. 2016 Jan;137(1). doi: 10.1542/peds.2015-2153. Epub 2015 Dec 7. Pediatrics. 2016. PMID: 26644486
Insulin pump therapy in children and adolescents with type 1 diabetes: the Italian viewpoint.
Pinelli L, Rabbone I, Salardi S, Toni S, Scaramuzza A, Bonfanti R, Cherubini V, Franzese A, Frongia AP, Iafusco D, Sulli N, Tumini S, Curto O, Miassimelli M; Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology. Pinelli L, et al. Among authors: salardi s. Acta Biomed. 2008 Apr;79(1):57-64. Acta Biomed. 2008. PMID: 18551824 Review.
Skin involvement in atypical hemolytic uremic syndrome.
Ardissino G, Tel F, Testa S, Marzano AV, Lazzari R, Salardi S, Edefonti A. Ardissino G, et al. Among authors: salardi s. Am J Kidney Dis. 2014 Apr;63(4):652-5. doi: 10.1053/j.ajkd.2013.09.020. Epub 2013 Nov 27. Am J Kidney Dis. 2014. PMID: 24290245
Neonatal screening for congenital adrenal hyperplasia.
Cacciari E, Balsamo A, Cassio A, Piazzi S, Bernardi F, Salardi S, Cicognani A, Pirazzoli P, Zappulla F, Capelli M, et al. Cacciari E, et al. Among authors: salardi s. Arch Dis Child. 1983 Oct;58(10):803-6. doi: 10.1136/adc.58.10.803. Arch Dis Child. 1983. PMID: 6639129 Free PMC article.
Acquired Complement Regulatory Gene Mutations and Hematopoietic Stem Cell Transplant-Related Thrombotic Microangiopathy.
Ardissino G, Salardi S, Berra S, Colussi G, Cugno M, Zecca M, Giglio F, Peccatori J, Diral E, Tel F, Clivio A, Tedeschi S. Ardissino G, et al. Among authors: salardi s. Biol Blood Marrow Transplant. 2017 Sep;23(9):1580-1582. doi: 10.1016/j.bbmt.2017.05.013. Epub 2017 May 15. Biol Blood Marrow Transplant. 2017. PMID: 28522344 Free article.
Cell membrane abnormalities and genetic hypertension.
Bianchi G, Ferrari P, Cusi D, Guidi E, Salardi S, Torielli L, Tripodi MG, Niutta E, Elli A, Vezzoli G, et al. Bianchi G, et al. Among authors: salardi s. J Clin Hypertens. 1986 Jun;2(2):114-9. J Clin Hypertens. 1986. PMID: 3531412 Review.
Ketoacidosis at diagnosis in childhood-onset diabetes and the risk of retinopathy 20years later.
Salardi S, Porta M, Maltoni G, Cerutti F, Rovere S, Iafusco D, Tumini S, Cauvin V, Zucchini S, Cadario F, d╩żAnnunzio G, Toni S, Salvatoni A, Zedda MA, Schiaffini R; Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED). Salardi S, et al. J Diabetes Complications. 2016 Jan-Feb;30(1):55-60. doi: 10.1016/j.jdiacomp.2015.10.009. Epub 2015 Oct 20. J Diabetes Complications. 2016. PMID: 26598223 Free article.
151 results
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