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

Year Number of Results
2001 1
2003 2
2004 1
2005 2
2006 3
2007 5
2008 5
2009 9
2010 2
2011 9
2012 8
2013 4
2014 4
2015 7
2016 6
2017 2
2018 10
2019 9
2020 14
2021 14
2022 10
2023 13
2024 1

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111 results

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Page 1
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
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
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.
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
Genetics of hemolytic uremic syndromes.
Malina M, Roumenina LT, Seeman T, Le Quintrec M, Dragon-Durey MA, Schaefer F, Fremeaux-Bacchi V. Malina M, et al. Among authors: seeman t. Presse Med. 2012 Mar;41(3 Pt 2):e105-14. doi: 10.1016/j.lpm.2011.10.028. Epub 2012 Jan 20. Presse Med. 2012. PMID: 22265161 Review.
111 results