Found: 12
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Incidence Trends for SARS-CoV-2 Alpha and Beta Variants, Finland, Spring 2021.
- Published in:
- Emerging Infectious Diseases, 2021, v. 27, n. 12, p. 3137, doi. 10.3201/eid2712.211631
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- Article
Sindbis virus outbreak and evidence for geographical expansion in Finland, 2021.
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- Eurosurveillance (15607917), 2022, v. 27, n. 31, p. 11, doi. 10.2807/1560-7917.ES.2022.27.31.2200580
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- Article
Predicting Spatial Patterns of Sindbis Virus (SINV) Infection Risk in Finland Using Vector, Host and Environmental Data.
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- International Journal of Environmental Research & Public Health, 2021, v. 18, n. 13, p. 7064, doi. 10.3390/ijerph18137064
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- Article
Pathogenic Variant Spectrum in Breast Cancer Risk Genes in Finnish Patients.
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- Cancers, 2022, v. 14, n. 24, p. 6158, doi. 10.3390/cancers14246158
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- Article
SNPs in lncRNA Regions and Breast Cancer Risk.
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- Frontiers in Genetics, 2020, v. 11, p. 1, doi. 10.3389/fgene.2020.00550
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- Article
A novel negevirus isolated from Aedes vexans mosquitoes in Finland.
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- Archives of Virology, 2020, v. 165, n. 12, p. 2989, doi. 10.1007/s00705-020-04810-4
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- Article
Characterisation of the RNA Virome of Nine Ochlerotatus Species in Finland.
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- Viruses (1999-4915), 2022, v. 14, n. 7, p. N.PAG, doi. 10.3390/v14071489
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- Article
Clinical features and outcome of childhood minimal change nephrotic syndrome: is genetics involved?
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- Pediatric Nephrology, 2005, v. 20, n. 8, p. 1073, doi. 10.1007/s00467-005-1965-y
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- Article
Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.
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- Clinical & Experimental Nephrology, 2017, v. 21, n. 4, p. 677, doi. 10.1007/s10157-016-1331-3
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- Article
Podocyte proteins in congenital and minimal change nephrotic syndrome.
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- Clinical & Experimental Nephrology, 2015, v. 19, n. 3, p. 481, doi. 10.1007/s10157-014-1020-z
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- Article
Single Nucleotide Polymorphisms in Pediatric Idiopathic Nephrotic Syndrome.
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- International Journal of Nephrology, 2016, p. 1, doi. 10.1155/2016/1417456
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- Article
NTHL1 is a recessive cancer susceptibility gene.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-47441-w
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- Article