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

Year Number of Results
1964 1
1965 2
1966 2
1967 2
1968 3
1969 4
1970 1
1971 1
1972 2
1973 4
1974 4
1975 7
1976 5
1977 2
1979 8
1980 5
1981 7
1982 10
1983 4
1984 7
1985 4
1986 5
1987 4
1988 7
1989 3
1990 4
1991 2
1992 2
1993 5
1994 7
1995 6
1996 8
1997 11
1998 6
1999 11
2000 12
2001 8
2002 14
2003 12
2004 16
2005 16
2006 21
2007 21
2008 15
2009 33
2010 28
2011 28
2012 35
2013 31
2014 33
2015 50
2016 35
2017 21
2018 29
2019 35
2020 34
2021 34
2022 28
2023 29
2024 17

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697 results

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Page 1
Frailty in older adults: evidence for a phenotype.
Fried LP, Tangen CM, Walston J, Newman AB, Hirsch C, Gottdiener J, Seeman T, Tracy R, Kop WJ, Burke G, McBurnie MA; Cardiovascular Health Study Collaborative Research Group. Fried LP, et al. Among authors: seeman t. J Gerontol A Biol Sci Med Sci. 2001 Mar;56(3):M146-56. doi: 10.1093/gerona/56.3.m146. J Gerontol A Biol Sci Med Sci. 2001. PMID: 11253156
Hypertensive crisis in children and adolescents.
Seeman T, Hamdani G, Mitsnefes M. Seeman T, et al. Pediatr Nephrol. 2019 Dec;34(12):2523-2537. doi: 10.1007/s00467-018-4092-2. Epub 2018 Oct 1. Pediatr Nephrol. 2019. PMID: 30276533 Review.
2016 European Society of Hypertension guidelines for the management of high blood pressure in children and adolescents.
Lurbe E, Agabiti-Rosei E, Cruickshank JK, Dominiczak A, Erdine S, Hirth A, Invitti C, Litwin M, Mancia G, Pall D, Rascher W, Redon J, Schaefer F, Seeman T, Sinha M, Stabouli S, Webb NJ, Wühl E, Zanchetti A. Lurbe E, et al. Among authors: seeman t. J Hypertens. 2016 Oct;34(10):1887-920. doi: 10.1097/HJH.0000000000001039. J Hypertens. 2016. PMID: 27467768 Free article.
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Burgmaier K, Brinker L, Erger F, Beck BB, Benz MR, Bergmann C, Boyer O, Collard L, Dafinger C, Fila M, Kowalewska C, Lange-Sperandio B, Massella L, Mastrangelo A, Mekahli D, Miklaszewska M, Ortiz-Bruechle N, Patzer L, Prikhodina L, Ranchin B, Ranguelov N, Schild R, Seeman T, Sever L, Sikora P, Szczepanska M, Teixeira A, Thumfart J, Uetz B, Weber LT, Wühl E, Zerres K; ESCAPE Study group; GPN study group; Dötsch J, Schaefer F, Liebau MC; ARegPKD consortium. Burgmaier K, et al. Among authors: seeman t. Kidney Int. 2021 Sep;100(3):650-659. doi: 10.1016/j.kint.2021.04.019. Epub 2021 Apr 30. Kidney Int. 2021. PMID: 33940108
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.
Claus LR, Chen C, Stallworth J, Turner JL, Slaats GG, Hawks AL, Mabillard H, Senum SR, Srikanth S, Flanagan-Steet H, Louie RJ, Silver J, Lerner-Ellis J, Morel C, Mighton C, Sleutels F, van Slegtenhorst M, van Ham T, Brooks AS, Dorresteijn EM, Barakat TS, Dahan K, Demoulin N, Goffin EJ, Olinger E; Genomics England Research Consortium; Larsen M, Hertz JM, Lilien MR, Obeidová L, Seeman T, Stone HK, Kerecuk L, Gurgu M, Yousef Yengej FA, Ammerlaan CME, Rookmaaker MB, Hanna C, Rogers RC, Duran K, Peters E, Sayer JA, van Haaften G, Harris PC, Ling K, Mason JM, van Eerde AM, Steet R. Claus LR, et al. Among authors: seeman t. Kidney Int. 2023 Nov;104(5):995-1007. doi: 10.1016/j.kint.2023.07.021. Epub 2023 Aug 19. Kidney Int. 2023. PMID: 37598857 Free PMC article.
Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD).
Bergmann C, Senderek J, Windelen E, Küpper F, Middeldorf I, Schneider F, Dornia C, Rudnik-Schöneborn S, Konrad M, Schmitt CP, Seeman T, Neuhaus TJ, Vester U, Kirfel J, Büttner R, Zerres K; APN (Arbeitsgemeinschaft für Pädiatrische Nephrologie). Bergmann C, et al. Among authors: seeman t. Kidney Int. 2005 Mar;67(3):829-48. doi: 10.1111/j.1523-1755.2005.00148.x. Kidney Int. 2005. PMID: 15698423 Free article.
Hypertension in pediatric kidney transplantation.
Seeman T, Myette RL, Feber J. Seeman T, et al. Pediatr Transplant. 2023 Aug;27(5):e14522. doi: 10.1111/petr.14522. Epub 2023 Apr 28. Pediatr Transplant. 2023. PMID: 37118862 Review.
Bruce McEwen: Colleagues' tribute.
Evans GW, Seeman TE. Evans GW, et al. Among authors: seeman te. Psychoneuroendocrinology. 2023 Jan 31:106047. doi: 10.1016/j.psyneuen.2023.106047. Online ahead of print. Psychoneuroendocrinology. 2023. PMID: 36739211 No abstract available.
697 results