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Results by year

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

Year Number of Results
1965 2
1967 1
1968 1
1969 3
1970 1
1971 2
1972 2
1973 2
1974 8
1975 3
1976 7
1977 5
1978 3
1979 5
1980 3
1981 5
1982 3
1983 1
1984 9
1985 6
1986 12
1987 7
1988 12
1989 6
1990 4
1991 7
1992 4
1993 6
1994 11
1995 6
1996 3
1997 7
1998 12
1999 10
2000 8
2001 6
2002 6
2003 7
2004 3
2005 2
2006 5
2007 5
2008 7
2009 9
2010 7
2011 8
2012 10
2013 10
2014 4
2015 15
2016 8
2017 8
2018 13
2019 10
2020 8
2021 9
2022 8
2023 5
2024 2

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336 results

Results by year

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Page 1
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.
Bedin M, Boyer O, Servais A, Li Y, Villoing-Gaudé L, Tête MJ, Cambier A, Hogan J, Baudouin V, Krid S, Bensman A, Lammens F, Louillet F, Ranchin B, Vigneau C, Bouteau I, Isnard-Bagnis C, Mache CJ, Schäfer T, Pape L, Gödel M, Huber TB, Benz M, Klaus G, Hansen M, Latta K, Gribouval O, Morinière V, Tournant C, Grohmann M, Kuhn E, Wagner T, Bole-Feysot C, Jabot-Hanin F, Nitschké P, Ahluwalia TS, Köttgen A, Andersen CBF, Bergmann C, Antignac C, Simons M. Bedin M, et al. Among authors: klaus g. J Clin Invest. 2020 Jan 2;130(1):335-344. doi: 10.1172/JCI129937. J Clin Invest. 2020. PMID: 31613795 Free PMC article. Clinical Trial.
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Sadowski CE, Lovric S, Ashraf S, Pabst WL, Gee HY, Kohl S, Engelmann S, Vega-Warner V, Fang H, Halbritter J, Somers MJ, Tan W, Shril S, Fessi I, Lifton RP, Bockenhauer D, El-Desoky S, Kari JA, Zenker M, Kemper MJ, Mueller D, Fathy HM, Soliman NA; SRNS Study Group; Hildebrandt F. Sadowski CE, et al. J Am Soc Nephrol. 2015 Jun;26(6):1279-89. doi: 10.1681/ASN.2014050489. Epub 2014 Oct 27. J Am Soc Nephrol. 2015. PMID: 25349199 Free PMC 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. 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
G protein regulation of receptor signalling.
Harnett MM, Klaus GG. Harnett MM, et al. Among authors: klaus gg. Immunol Today. 1988 Oct;9(10):315-20. doi: 10.1016/0167-5699(88)91325-4. Immunol Today. 1988. PMID: 3151244 Review. No abstract available.
Urinalysis in children and adolescents.
Utsch B, Klaus G. Utsch B, et al. Among authors: klaus g. Dtsch Arztebl Int. 2014 Sep 12;111(37):617-25; quiz 626. doi: 10.3238/arztebl.2014.0617. Dtsch Arztebl Int. 2014. PMID: 25283761 Free PMC article. Review.
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA.
Viering D, Schlingmann KP, Hureaux M, Nijenhuis T, Mallett A, Chan MMY, van Beek A, van Eerde AM, Coulibaly JM, Vallet M, Decramer S, Pelletier S, Klaus G, Kömhoff M, Beetz R, Patel C, Shenoy M, Steenbergen EJ, Anderson G, Bongers EMHF, Bergmann C, Panneman D, Rodenburg RJ, Kleta R, Houillier P, Konrad M, Vargas-Poussou R, Knoers NVAM, Bockenhauer D, de Baaij JHF; Genomics England Research Consortium. Viering D, et al. Among authors: klaus g. J Am Soc Nephrol. 2022 Feb;33(2):305-325. doi: 10.1681/ASN.2021050596. Epub 2021 Oct 4. J Am Soc Nephrol. 2022. PMID: 34607911 Free PMC article.
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.
Bedin M, Boyer O, Servais A, Li Y, Villoing-Gaudé L, Tête MJ, Cambier A, Hogan J, Baudouin V, Krid S, Bensman A, Lammens F, Louillet F, Ranchin B, Vigneau C, Bouteau I, Isnard-Bagnis C, Mache CJ, Schäfer T, Pape L, Gödel M, Huber TB, Benz M, Klaus G, Hansen M, Latta K, Gribouval O, Morinière V, Tournant C, Grohmann M, Kuhn E, Wagner T, Bole-Feysot C, Jabot-Hanin F, Nitschké P, Ahluwalia TS, Köttgen A, Andersen CBF, Bergmann C, Antignac C, Simons M. Bedin M, et al. Among authors: klaus g. J Clin Invest. 2022 Jun 1;132(11):e161852. doi: 10.1172/JCI161852. J Clin Invest. 2022. PMID: 35642643 Free PMC article. No abstract available.
Glucocorticoids and growth problems.
Robinson IC, Gabrielsson B, Klaus G, Mauras N, Holmberg C, Mehls O. Robinson IC, et al. Among authors: klaus g. Acta Paediatr Suppl. 1995 Sep;411:81-6. doi: 10.1111/j.1651-2227.1995.tb13870.x. Acta Paediatr Suppl. 1995. PMID: 8563075 Review. No abstract available.
Treat-to-target strategies for the management of familial Mediterranean Fever in children.
Ehlers L, Rolfes E, Lieber M, Müller D, Lainka E, Gohar F, Klaus G, Girschick H, Hörstermann J, Kümmerle-Deschner J, Brunner J, Palm-Beden K, Tenbrock K, von Wrangel L, Faßhauer M, Blank N, Trauzeddel R, von Stuckrad ASL, Higgins S, Welzel T, Lutz T, Hentgen V, Foell D, Wittkowski H, Kallinich T. Ehlers L, et al. Among authors: klaus g. Pediatr Rheumatol Online J. 2023 Sep 26;21(1):108. doi: 10.1186/s12969-023-00875-y. Pediatr Rheumatol Online J. 2023. PMID: 37752496 Free PMC article.
Historical development of root analogue implants: a review of published papers.
Saeidi Pour R, Freitas Rafael C, Engler MLPD, Edelhoff D, Klaus G, Prandtner O, Berthold M, Liebermann A. Saeidi Pour R, et al. Among authors: klaus g. Br J Oral Maxillofac Surg. 2019 Jul;57(6):496-504. doi: 10.1016/j.bjoms.2019.01.021. Epub 2019 May 11. Br J Oral Maxillofac Surg. 2019. PMID: 31085016 Review.
336 results