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Page 1
Clinical spectrum and genetic causes of mitochondrial hepatopathy phenotype in children.
Squires JE, Miethke AG, Valencia CA, Hawthorne K, Henn L, Van Hove JLK, Squires RH, Bove K, Horslen S, Kohli R, Molleston JP, Romero R, Alonso EM, Bezerra JA, Guthery SL, Hsu E, Karpen SJ, Loomes KM, Ng VL, Rosenthal P, Mysore K, Wang KS, Friederich MW, Magee JC, Sokol RJ; Childhood Liver Disease Research Network (ChiLDReN). Squires JE, et al. Among authors: henn l. Hepatol Commun. 2023 May 15;7(6):e0139. doi: 10.1097/HC9.0000000000000139. eCollection 2023 Jun 1. Hepatol Commun. 2023. PMID: 37184518 Free PMC article.
Understanding International Variations in Kidney Failure Incidence and Initiation of Replacement Therapy.
Alencar de Pinho N, Henn L, Raina R, Reichel H, Lopes AA, Combe C, Speyer E, Bieber B, Robinson BM, Stengel B, Pecoits-Filho R; CKDopps investigators. Alencar de Pinho N, et al. Among authors: henn l. Kidney Int Rep. 2022 Sep 5;7(11):2364-2375. doi: 10.1016/j.ekir.2022.08.018. eCollection 2022 Nov. Kidney Int Rep. 2022. PMID: 36531894 Free PMC article.
Serum bile acids as a prognostic biomarker in biliary atresia following Kasai portoenterostomy.
Harpavat S, Hawthorne K, Setchell KDR, Rivas MN, Henn L, Beil CA, Karpen SJ, Ng VL, Alonso EM, Bezerra JA, Guthery SL, Horslen S, Loomes KM, McKiernan P, Magee JC, Merion RM, Molleston JP, Rosenthal P, Thompson RJ, Wang KS, Sokol RJ, Shneider BL; for Childhood Liver Disease Research Network (ChiLDReN). Harpavat S, et al. Among authors: henn l. Hepatology. 2023 Mar 1;77(3):862-873. doi: 10.1002/hep.32800. Epub 2023 Feb 17. Hepatology. 2023. PMID: 36131538 Free PMC article.
52 results