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Sabine Leh

Explore the profile of Sabine Leh including associated specialties, affiliations and a list of published articles. Areas
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Articles 69
Citations 612
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Recent Articles
1.
Ovrehus M, Asbjorn K, Langlo R, Leh S, Eikrem O, Romundstad S, et al.
BMC Nephrol . 2025 Feb; 26(1):76. PMID: 39948520
Background: Biobanks that hold blood, urine and kidney tissue are key for translational nephrology research but are few and have limited availability. We describe the organization, baseline characteristics, and generalizability...
2.
Montezuma D, Oliveira S, Tolkach Y, Boor P, Haragan A, Carvalho R, et al.
Lab Invest . 2024 Nov; 105(3):102203. PMID: 39615882
Integrating digital pathology and artificial intelligence (AI) algorithms can potentially improve diagnostic practice and precision medicine. Developing reliable, generalizable, and comparable AI algorithms depends on access to meticulously annotated data....
3.
Rivedal M, Mikkelsen H, Marti H, Liu L, Kiryluk K, Knoop T, et al.
Kidney Int . 2023 Dec; 105(4):717-730. PMID: 38154557
Some patients diagnosed with benign IgA nephropathy (IgAN) develop a progressive clinical course, not predictable by known clinical or histopathological parameters. To assess if gene expression can differentiate between progressors...
4.
Nordbo O, Landolt L, Eikrem O, Scherer A, Leh S, Furriol J, et al.
Physiol Rep . 2023 Oct; 11(19):e15825. PMID: 37813528
Hypertensive nephrosclerosis (HN) and Type 2 diabetic nephropathy (T2DN) are the leading causes of chronic kidney disease (CKD). To explore shared pathogenetic mechanisms, we analyzed transcriptomes of kidney biopsies from...
5.
Kipp A, Marti H, Babickova J, Nakken S, Leh S, Halden T, et al.
BMC Nephrol . 2023 Aug; 24(1):254. PMID: 37626301
Background: Diabetes mellitus (DM), either preexisting or developing after transplantation, remains a crucial clinical problem in kidney transplantation. To obtain insights into the molecular mechanisms underlying PTDM development and early...
6.
OKeeffe M, Oterhals A, Weishaupt H, Leh S, Ulvik A, Ueland P, et al.
Eur J Nutr . 2023 Aug; 62(8):3227-3240. PMID: 37550593
Purpose: The obese black and tan, brachyuric (BTBR) ob/ob mouse spontaneously develops features comparable to human diabetic nephropathy. The primary aim of the present study was to investigate if a...
7.
Delaleu N, Marti H, Strauss P, Sekulic M, Osman T, Tondel C, et al.
Kidney Int . 2023 Jul; 104(4):803-819. PMID: 37419447
Fabry disease is a rare disorder caused by variations in the alpha-galactosidase gene. To a degree, Fabry disease is manageable via enzyme replacement therapy (ERT). By understanding the molecular basis...
8.
Vildmyren I, Oterhals A, Leh S, Samuelsen T, Halstensen A, Marti H, et al.
Food Nutr Res . 2022 Nov; 66. PMID: 36340918
Background: Documentation of health effects of residuals after fish filleting may motivate both consumers and producers to increase the use of this under-utilised protein source. Objectives: The primary objective of...
9.
Gjerstad A, Skrunes R, Tondel C, Asberg A, Leh S, Klingenberg C, et al.
Pediatr Nephrol . 2022 Aug; 38(4):1249-1256. PMID: 35994104
Background: There is scarce information on biopsy-verified kidney disease in childhood and its progression to chronic kidney disease stage 5 (CKD 5). This study aims to review biopsy findings in...
10.
Krendel M, Leh S, Garone M, Edwards-Richards A, Lin J, Brackman D, et al.
Pediatr Nephrol . 2022 Jun; 38(2):439-449. PMID: 35723736
Background: Pathogenic mutations in the non-muscle single-headed myosin, myosin 1E (Myo1e), are a rare cause of pediatric focal segmental glomerulosclerosis (FSGS). These mutations are biallelic, to date only reported as...