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

Year Number of Results
1951 1
1957 1
1968 2
1970 1
1973 1
1974 2
1975 1
1976 1
1980 2
1988 1
1997 1
1999 1
2000 1
2005 2
2009 1
2010 2
2011 4
2012 4
2013 3
2014 2
2015 3
2016 3
2017 6
2018 6
2019 7
2020 4
2021 1
2022 3
2023 6
2024 0

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62 results

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Page 1
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.
Gribouval O, Morinière V, Pawtowski A, Arrondel C, Sallinen SL, Saloranta C, Clericuzio C, Viot G, Tantau J, Blesson S, Cloarec S, Machet MC, Chitayat D, Thauvin C, Laurent N, Sampson JR, Bernstein JA, Clemenson A, Prieur F, Daniel L, Levy-Mozziconacci A, Lachlan K, Alessandri JL, Cartault F, Rivière JP, Picard N, Baumann C, Delezoide AL, Belar Ortega M, Chassaing N, Labrune P, Yu S, Firth H, Wellesley D, Bitzan M, Alfares A, Braverman N, Krogh L, Tolmie J, Gaspar H, Doray B, Majore S, Bonneau D, Triau S, Loirat C, David A, Bartholdi D, Peleg A, Brackman D, Stone R, DeBerardinis R, Corvol P, Michaud A, Antignac C, Gubler MC. Gribouval O, et al. Among authors: krogh l. Hum Mutat. 2012 Feb;33(2):316-26. doi: 10.1002/humu.21661. Epub 2011 Dec 22. Hum Mutat. 2012. PMID: 22095942 Review.
Is MED13L-related intellectual disability a recognizable syndrome?
Tørring PM, Larsen MJ, Brasch-Andersen C, Krogh LN, Kibæk M, Laulund L, Illum N, Dunkhase-Heinl U, Wiesener A, Popp B, Marangi G, Hjortshøj TD, Ek J, Vogel I, Becher N, Roos L, Zollino M, Fagerberg CR. Tørring PM, et al. Among authors: krogh ln. Eur J Med Genet. 2019 Feb;62(2):129-136. doi: 10.1016/j.ejmg.2018.06.014. Epub 2018 Jun 27. Eur J Med Genet. 2019. PMID: 29959045
Effects of endogenous GIP in patients with type 2 diabetes.
Stensen S, Gasbjerg LS, Krogh LL, Skov-Jeppesen K, Sparre-Ulrich AH, Jensen MH, Dela F, Hartmann B, Vilsbøll T, Holst JJ, Rosenkilde MM, Christensen MB, Knop FK. Stensen S, et al. Among authors: krogh ll. Eur J Endocrinol. 2021 May 21;185(1):33-45. doi: 10.1530/EJE-21-0135. Eur J Endocrinol. 2021. PMID: 33886495
Exploring the hereditary background of renal cancer in Denmark.
Christensen MB, Wadt K, Jensen UB, Lautrup CK, Bojesen A, Krogh LN, Overeem Hansen TV, Gerdes AM. Christensen MB, et al. Among authors: krogh ln. PLoS One. 2019 Apr 29;14(4):e0215725. doi: 10.1371/journal.pone.0215725. eCollection 2019. PLoS One. 2019. PMID: 31034483 Free PMC article.
62 results