Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1935 1
1943 1
1946 1
1947 2
1948 2
1949 1
1950 1
1951 1
1953 1
1954 2
1955 4
1957 1
1958 2
1960 1
1961 3
1963 1
1964 2
1965 1
1972 2
1974 1
1976 1
1978 1
1979 1
1980 2
1981 1
1982 6
1983 6
1984 3
1985 2
1986 2
1988 2
1989 1
1991 4
1992 3
1993 2
1994 5
1995 4
1996 3
1997 1
1998 5
1999 2
2000 1
2001 5
2002 1
2003 2
2004 2
2005 2
2006 1
2007 1
2008 3
2009 1
2010 2
2011 3
2012 4
2013 4
2014 9
2015 10
2016 7
2017 4
2018 5
2019 11
2020 9
2021 13
2022 6
2023 10
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

189 results

Results by year

Filters applied: . Clear all
Page 1
Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference.
Guay-Woodford LM, Bissler JJ, Braun MC, Bockenhauer D, Cadnapaphornchai MA, Dell KM, Kerecuk L, Liebau MC, Alonso-Peclet MH, Shneider B, Emre S, Heller T, Kamath BM, Murray KF, Moise K, Eichenwald EE, Evans J, Keller RL, Wilkins-Haug L, Bergmann C, Gunay-Aygun M, Hooper SR, Hardy KK, Hartung EA, Streisand R, Perrone R, Moxey-Mims M. Guay-Woodford LM, et al. Among authors: hartung ea. J Pediatr. 2014 Sep;165(3):611-7. doi: 10.1016/j.jpeds.2014.06.015. Epub 2014 Jul 9. J Pediatr. 2014. PMID: 25015577 Free PMC article.
TBX6 as a cause of a combined skeletal-kidney dysplasia syndrome.
Li G, Strong A, Wang H, Kim JS, Watson D, Zhao S, Vaccaro C, Hartung E, Hakonarson H, Zhang TJ, Giampietro PF, Wu N. Li G, et al. Among authors: hartung e. Am J Med Genet A. 2022 Dec;188(12):3469-3481. doi: 10.1002/ajmg.a.62972. Epub 2022 Sep 26. Am J Med Genet A. 2022. PMID: 36161696 Free PMC article.
OSTEOARTHRITIS.
HARTUNG EF. HARTUNG EF. Arthritis Rheum. 1963 Aug;6:389-97. doi: 10.1002/art.1780060412. Arthritis Rheum. 1963. PMID: 14052862 No abstract available.
State-of-the-Art Renal Imaging in Children.
Viteri B, Calle-Toro JS, Furth S, Darge K, Hartung EA, Otero H. Viteri B, et al. Among authors: hartung ea. Pediatrics. 2020 Feb;145(2):e20190829. doi: 10.1542/peds.2019-0829. Epub 2020 Jan 8. Pediatrics. 2020. PMID: 31915193 Free PMC article.
Circulating Metabolomic Associations with Neurocognitive Outcomes in Pediatric CKD.
Lee AM, Xu Y, Hooper SR, Abraham AG, Hu J, Xiao R, Matheson MB, Brunson C, Rhee EP, Coresh J, Vasan RS, Schrauben S, Kimmel PL, Warady BA, Furth SL, Hartung EA, Denburg MR; CKD Biomarkers Consortium. Lee AM, et al. Among authors: hartung ea. Clin J Am Soc Nephrol. 2023 Oct 23;19(1):13-25. doi: 10.2215/CJN.0000000000000318. Online ahead of print. Clin J Am Soc Nephrol. 2023. PMID: 37871960
Ciliopathies: Coloring outside of the lines.
Strong A, Li D, Mentch F, Bedoukian E, Hartung EA, Meyers K, Skraban C, Wen J, Medne L, Glessner J, Watson D, Krantz I, Hakonarson H. Strong A, et al. Among authors: hartung ea. Am J Med Genet A. 2021 Mar;185(3):687-694. doi: 10.1002/ajmg.a.62013. Epub 2020 Dec 25. Am J Med Genet A. 2021. PMID: 33369054 Free PMC article.
Tuberculous arthritis.
HARTUNG EF. HARTUNG EF. J Am Med Assoc. 1955 Jul 9;158(10):818-21. doi: 10.1001/jama.1955.02960100016004. J Am Med Assoc. 1955. PMID: 14381254 No abstract available.
189 results