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

Year Number of Results
1890 1
1906 1
1907 1
1909 1
1929 2
1930 1
1932 1
1933 1
1934 3
1935 2
1945 3
1946 1
1947 2
1948 1
1949 1
1950 1
1951 7
1952 5
1953 7
1954 4
1955 6
1956 8
1957 10
1958 7
1959 8
1960 6
1961 14
1962 9
1963 21
1964 30
1965 40
1966 35
1967 43
1968 47
1969 23
1970 49
1971 31
1972 36
1973 34
1974 38
1975 39
1976 32
1977 22
1978 23
1979 32
1980 38
1981 34
1982 25
1983 29
1984 26
1985 18
1986 28
1987 20
1988 27
1989 21
1990 23
1991 24
1992 13
1993 18
1994 25
1995 29
1996 25
1997 17
1998 31
1999 28
2000 34
2001 32
2002 26
2003 36
2004 29
2005 58
2006 32
2007 40
2008 26
2009 21
2010 34
2011 29
2012 22
2013 36
2014 32
2015 41
2016 33
2017 42
2018 38
2019 40
2020 43
2021 17
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1,844 results
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Page 1
Cystinuria: genetic aspects, mouse models, and a new approach to therapy.
Sahota A, Tischfield JA, Goldfarb DS, Ward MD, Hu L. Sahota A, et al. Urolithiasis. 2019 Feb;47(1):57-66. doi: 10.1007/s00240-018-1101-7. Epub 2018 Dec 4. Urolithiasis. 2019. PMID: 30515543 Free PMC article. Review.
Thus, there is a need to reduce or eliminate the risks associated with therapy for cystinuria. Four mouse models for cystinuria have been described and these models provide a resource for evaluating the safety and efficacy of new therapies for cystinuria. ... …
Thus, there is a need to reduce or eliminate the risks associated with therapy for cystinuria. Four mouse models for cystinuria
Metabolic consequences of cystinuria.
Woodard LE, Welch RC, Veach RA, Beckermann TM, Sha F, Weinman EJ, Ikizler TA, Tischfield JA, Sahota A, Wilson MH. Woodard LE, et al. BMC Nephrol. 2019 Jun 20;20(1):227. doi: 10.1186/s12882-019-1417-8. BMC Nephrol. 2019. PMID: 31221135 Free PMC article.
BACKGROUND: Cystinuria is an inherited disorder of renal amino acid transport that causes recurrent nephrolithiasis and significant morbidity in humans. ...Additionally, reduced glutathione may predispose those with cystinuria to injury caused by oxidative stress. W …
BACKGROUND: Cystinuria is an inherited disorder of renal amino acid transport that causes recurrent nephrolithiasis and significant m …
Cystinuria.
Dello Strologo L, Rizzoni G. Dello Strologo L, et al. Acta Paediatr Suppl. 2006 Jul;95(452):31-3. doi: 10.1080/08035320600649473. Acta Paediatr Suppl. 2006. PMID: 16801163 Review.
The two types of cystinuria (A and B) have a similar outcome. A mild renal failure is present in 17% of patients. ...CONCLUSION: Following new achievements in the genetics of cystinuria, a new classification has been proposed. Cystinuria is more severe in mal …
The two types of cystinuria (A and B) have a similar outcome. A mild renal failure is present in 17% of patients. ...CONCLUSION: Foll …
Cystinuria.
Mattoo A, Goldfarb DS. Mattoo A, et al. Semin Nephrol. 2008 Mar;28(2):181-91. doi: 10.1016/j.semnephrol.2008.01.011. Semin Nephrol. 2008. PMID: 18359399 Review.
Cystinuria is an inherited disorder characterized by the impaired reabsorption of cystine in the proximal tubule of the nephron and the gastrointestinal epithelium. ...Thus far, mutations in 2 genes, SLC3A1 and SLC7A9, have been identified as being responsible for most cas
Cystinuria is an inherited disorder characterized by the impaired reabsorption of cystine in the proximal tubule of the nephron and t
[Cystinuria].
Dello Strologo L, Laurenzi C, Emma F. Dello Strologo L, et al. G Ital Nefrol. 2010 Jan-Feb;27(1):30-6. G Ital Nefrol. 2010. PMID: 20191458 Review. Italian.
Cystinuria is an autosomal recessive disorder characterized by impairment of the proximal renal tubules which are unable to reabsorb cystine and dibasic amino acids, leading to the formation of recurrent kidney stones. According to the most recent genetic knowledge, there
Cystinuria is an autosomal recessive disorder characterized by impairment of the proximal renal tubules which are unable to reabsorb
Cystinuria-a urologist's perspective.
Thomas K, Wong K, Withington J, Bultitude M, Doherty A. Thomas K, et al. Nat Rev Urol. 2014 May;11(5):270-7. doi: 10.1038/nrurol.2014.51. Epub 2014 Mar 25. Nat Rev Urol. 2014. PMID: 24662732 Review.
Cystinuria is a genetic disease that leads to frequent formation of stones. In patients with recurrent stone formation, particularly patients <30 years old or those who have siblings with stone disease, urologists should maintain a high index of suspicion of the diagnos
Cystinuria is a genetic disease that leads to frequent formation of stones. In patients with recurrent stone formation, particularly
Cystinuria.
Milliner DS. Milliner DS. Endocrinol Metab Clin North Am. 1990 Dec;19(4):889-907. Endocrinol Metab Clin North Am. 1990. PMID: 2081517 Review.
Cystinuria is an hereditary disorder of renal and intestinal transport characterized by the excessive urinary excretion of cystine, arginine, lysine, and ornithine. ...Urolithiasis with its attendant complications is the sole clinical manifestation of cystinuria and
Cystinuria is an hereditary disorder of renal and intestinal transport characterized by the excessive urinary excretion of cystine, a
Cystinuria.
Feld RD. Feld RD. Crit Rev Clin Lab Sci. 1988;26(3):243-61. doi: 10.3109/10408368809105891. Crit Rev Clin Lab Sci. 1988. PMID: 3077031 Review.
Cystinuria is an inherited metabolic disease resulting in renal stone formation. ...
Cystinuria is an inherited metabolic disease resulting in renal stone formation. ...
[Cystinuria].
Rousaud F, Palacín M, Nunes V. Rousaud F, et al. Nefrologia. 2003;23 Suppl 1:52-9. Nefrologia. 2003. PMID: 12708364 Free article. Review. Spanish. No abstract available.
Cystinuria in association with cataract.
Singh P, Gupta R, Gupta A. Singh P, et al. Indian J Ophthalmol. 2020 Jan;68(1):209. doi: 10.4103/ijo.IJO_1330_19. Indian J Ophthalmol. 2020. PMID: 31856522 Free PMC article. No abstract available.
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