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

Year Number of Results
1947 3
1948 1
1949 1
1950 1
1951 5
1952 1
1953 4
1954 4
1955 5
1956 2
1957 4
1958 4
1960 5
1961 2
1962 6
1963 8
1964 5
1965 6
1966 2
1967 5
1968 3
1969 2
1970 10
1971 11
1972 8
1973 8
1974 1
1975 10
1976 8
1977 8
1978 4
1979 8
1980 7
1981 7
1982 18
1983 18
1984 7
1985 11
1986 19
1987 23
1988 7
1989 17
1990 13
1991 12
1992 21
1993 34
1994 22
1995 31
1996 30
1997 25
1998 33
1999 34
2000 32
2001 45
2002 50
2003 52
2004 66
2005 58
2006 74
2007 81
2008 58
2009 52
2010 59
2011 75
2012 86
2013 102
2014 96
2015 75
2016 103
2017 119
2018 106
2019 101
2020 106
2021 111
2022 140
2023 125
2024 48

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2,282 results

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The following term was not found in PubMed: Gorkovchuk
Page 1
[Denys-Drash syndrome].
Kohsaka T, Tagawa M, Yamada M. Kohsaka T, et al. Nihon Rinsho. 2006 Sep 28;Suppl 3:457-64. Nihon Rinsho. 2006. PMID: 17022587 Review. Japanese. No abstract available.
The Denys-Drash syndrome.
Mueller RF. Mueller RF. J Med Genet. 1994 Jun;31(6):471-7. doi: 10.1136/jmg.31.6.471. J Med Genet. 1994. PMID: 8071974 Free PMC article. Review. No abstract available.
[Denys-Drash syndrome (DDS)].
Sasaki N. Sasaki N. Nihon Rinsho. 2006 Jun 28;Suppl 2:497-8. Nihon Rinsho. 2006. PMID: 16817450 Review. Japanese. No abstract available.
Denys-Drash syndrome.
Lin HC, Lin SK, Wen MC, Tseng CF, Fu LS, Chi CS. Lin HC, et al. J Formos Med Assoc. 2004 Jan;103(1):71-4. J Formos Med Assoc. 2004. PMID: 15026863
We report a case of Denys-Drash syndrome, a disorder characterized by male pseudohermaphroditism, congenital nephrotic syndrome, and early renal failure. ...
We report a case of Denys-Drash syndrome, a disorder characterized by male pseudohermaphroditism, congenital nephrotic syndrome, and …
Denys-Drash syndrome.
Kucinskas L, Rudaitis S, Pundziene B, Just W. Kucinskas L, et al. Medicina (Kaunas). 2005;41(2):132-4. Medicina (Kaunas). 2005. PMID: 15758579 Free article.
We report on a patient with incomplete Denys-Drash syndrome, which was evident by the clinical data and proved by molecular genetics methods. The patient has the mutation p.R394W in the WT1 gene and clinical symptoms of Denys-Drash syndrome....
We report on a patient with incomplete Denys-Drash syndrome, which was evident by the clinical data and proved by molecular genetics …
Obsessive-compulsive disorder.
Zohar J, Greenberg B, Denys D. Zohar J, et al. Handb Clin Neurol. 2012;106:375-90. doi: 10.1016/B978-0-444-52002-9.00021-8. Handb Clin Neurol. 2012. PMID: 22608632 Review. No abstract available.
Refractory Hypertension in Infantile-Onset Denys-Drash Syndrome.
Nishi K, Kamei K, Ogura M, Sato M, Murakoshi M, Kamae C, Suzuki R, Kanamori T, Nagano C, Nozu K, Ishikura K, Ito S. Nishi K, et al. Tohoku J Exp Med. 2020 Sep;252(1):45-51. doi: 10.1620/tjem.252.45. Tohoku J Exp Med. 2020. PMID: 32863338 Free article.
Denys-Drash syndrome is characterized by progressive nephropathy, gonadal dysgenesis, and Wilms tumor caused by a WT1 gene mutation. ...Severe hypertension is a common complication of infantile-onset Denys-Drash syndrome. The possibility of hypotension after nephrec
Denys-Drash syndrome is characterized by progressive nephropathy, gonadal dysgenesis, and Wilms tumor caused by a WT1 gene mutation.
[Denys-Drash syndrome].
Kohsaka T, Suzuki T, Yamada M. Kohsaka T, et al. Ryoikibetsu Shokogun Shirizu. 1997;(17 Pt 2):599-604. Ryoikibetsu Shokogun Shirizu. 1997. PMID: 9278002 Review. Japanese. No abstract available.
Denys-Drash syndrome (DDS).
Alomari AI, Tham JC. Alomari AI, et al. Pediatr Nephrol. 2006 Sep;21(9):1237-40. doi: 10.1007/s00467-006-0182-7. Epub 2006 Jul 6. Pediatr Nephrol. 2006. PMID: 16823575 No abstract available.
WT1-related disorders: more than Denys-Drash syndrome.
Lopez-Gonzalez M, Ariceta G. Lopez-Gonzalez M, et al. Pediatr Nephrol. 2024 Feb 7. doi: 10.1007/s00467-024-06302-y. Online ahead of print. Pediatr Nephrol. 2024. PMID: 38326647
Historically, specific mutations in WT1 gene have been associated with distinct syndromes based on phenotypic characteristics, including Denys-Drash syndrome (DDS), Frasier syndrome (FS), Meacham syndrome, and WAGR syndrome. ...
Historically, specific mutations in WT1 gene have been associated with distinct syndromes based on phenotypic characteristics, including …
2,282 results