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Page 1
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.
Kołbuc M, Kołek MF, Motyka R, Bieniaś B, Habbig S, Burgmaier K, Prikhodina L, Papizh S, Tasic V, Okorn C, Szczepańska M, Kiliś-Pstrusińska K, Wasilewska A, Adamczyk P, Tkaczyk M, Pańczyk-Tomaszewska M, Miklaszewska M, Pawlaczyk K, Bukowska-Olech E, Jamsheer A, Jankauskiene A, König J, Cheong HI, Ahn YH, Kaspar S, Sikora P, Beck BB, Zaniew M. Kołbuc M, et al. Among authors: kaspar s. Pediatr Nephrol. 2024 Jun;39(6):1847-1858. doi: 10.1007/s00467-023-06262-9. Epub 2024 Jan 10. Pediatr Nephrol. 2024. PMID: 38196016 Free PMC article. Clinical Trial.
Genetic landscape of pediatric acute liver failure of indeterminate origin.
Lenz D, Schlieben LD, Shimura M, Bianzano A, Smirnov D, Kopajtich R, Berutti R, Adam R, Aldrian D, Baric I, Baumann U, Bozbulut NE, Brugger M, Brunet T, Bufler P, Burnytė B, Calvo PL, Crushell E, Dalgiç B, Das AM, Dezsőfi A, Distelmaier F, Fichtner A, Freisinger P, Garbade SF, Gaspar H, Goujon L, Hadzic N, Hartleif S, Hegen B, Hempel M, Henning S, Hoerning A, Houwen R, Hughes J, Iorio R, Iwanicka-Pronicka K, Jankofsky M, Junge N, Kanavaki I, Kansu A, Kaspar S, Kathemann S, Kelly D, Kirsaçlioğlu CT, Knoppke B, Kohl M, Kölbel H, Kölker S, Konstantopoulou V, Krylova T, Kuloğlu Z, Kuster A, Laass MW, Lainka E, Lurz E, Mandel H, Mayerhanser K, Mayr JA, McKiernan P, McClean P, McLin V, Mention K, Müller H, Pasquier L, Pavlov M, Pechatnikova N, Peters B, Petković Ramadža D, Piekutowska-Abramczuk D, Pilic D, Rajwal S, Rock N, Roetig A, Santer R, Schenk W, Semenova N, Sokollik C, Sturm E, Taylor RW, Tschiedel E, Urbonas V, Urreizti R, Vermehren J, Vockley J, Vogel GF, Wagner M, van der Woerd W, Wortmann SB, Zakharova E, Hoffmann GF, Meitinger T, Murayama K, Staufner C, Prokisch H. Lenz D, et al. Among authors: kaspar s. Hepatology. 2024 May 1;79(5):1075-1087. doi: 10.1097/HEP.0000000000000684. Epub 2023 Nov 16. Hepatology. 2024. PMID: 37976411 Free PMC article.
The retinal phenotype in primary hyperoxaluria type 2 and 3.
Birtel J, Diederen RM, Herrmann P, Kaspar S, Beck BB, Garrelfs SF, Hoppe B, Charbel Issa P. Birtel J, et al. Among authors: kaspar s. Pediatr Nephrol. 2023 May;38(5):1485-1490. doi: 10.1007/s00467-022-05765-1. Epub 2022 Oct 19. Pediatr Nephrol. 2023. PMID: 36260161 Free PMC article.
Mucosal Mast Cell Distribution in the Gastrointestinal Tract of Children: A Preliminary Study for Establishing Reference Values.
Ehrsam C, Rechenauer T, Allabauer I, Siebenlist G, Kaspar S, Rieger D, Schmid M, Rückel A, Woelfle J, Hartmann A, Rieker R, Raithel M, Geppert C, Hoerning A. Ehrsam C, et al. Among authors: kaspar s. J Pediatr Gastroenterol Nutr. 2022 Jan 1;74(1):46-53. doi: 10.1097/MPG.0000000000003338. J Pediatr Gastroenterol Nutr. 2022. PMID: 34694267
Adaptation to mitochondrial stress requires CHOP-directed tuning of ISR.
Kaspar S, Oertlin C, Szczepanowska K, Kukat A, Senft K, Lucas C, Brodesser S, Hatzoglou M, Larsson O, Topisirovic I, Trifunovic A. Kaspar S, et al. Sci Adv. 2021 May 26;7(22):eabf0971. doi: 10.1126/sciadv.abf0971. Print 2021 May. Sci Adv. 2021. PMID: 34039602 Free PMC article.
Chlorhexidine: An Elixir for Periodontics.
Thangavelu A, Kaspar SS, Kathirvelu RP, Srinivasan B, Srinivasan S, Sundram R. Thangavelu A, et al. Among authors: kaspar ss. J Pharm Bioallied Sci. 2020 Aug;12(Suppl 1):S57-S59. doi: 10.4103/jpbs.JPBS_162_20. Epub 2020 Aug 28. J Pharm Bioallied Sci. 2020. PMID: 33149431 Free PMC article. Review.
A salvage pathway maintains highly functional respiratory complex I.
Szczepanowska K, Senft K, Heidler J, Herholz M, Kukat A, Höhne MN, Hofsetz E, Becker C, Kaspar S, Giese H, Zwicker K, Guerrero-Castillo S, Baumann L, Kauppila J, Rumyantseva A, Müller S, Frese CK, Brandt U, Riemer J, Wittig I, Trifunovic A. Szczepanowska K, et al. Among authors: kaspar s. Nat Commun. 2020 Apr 2;11(1):1643. doi: 10.1038/s41467-020-15467-7. Nat Commun. 2020. PMID: 32242014 Free PMC article.
62 results