Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Hyperuricemia and HNF1B[original query] |
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Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases. Clinical journal of the American Society of Nephrology : CJASN 2010 Apr . Heidet L, Decramer S, Pawtowski A, Morinière V, Bandin F, Knebelmann B, Lebre AS, Faguer S, Guigonis V, Antignac C, Salomon R |
Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1. American journal of kidney diseases : the official journal of the National Kidney Foundation 2018 5 72 (3): 411-418. Ayasreh Nadia, Bullich Gemma, Miquel Rosa, Furlano Mónica, Ruiz Patricia, Lorente Laura, Valero Oliver, García-González Miguel Angel, Arhda Nisrine, Garin Intza, Martínez Víctor, Pérez-Gómez Vanessa, Fulladosa Xavier, Arroyo David, Martínez-Vea Alberto, Espinosa Mario, Ballarín Jose, Ars Elisabet, Torra Ros |
Clinical characteristics of HNF1B-related disorders in a Japanese population. Clinical and experimental nephrology 2019 5 23 (9): 1119-1129. Nagano China, Morisada Naoya, Nozu Kandai, Kamei Koichi, Tanaka Ryojiro, Kanda Shoichiro, Shiona Shinichi, Araki Yoshinori, Ohara Shinichiro, Matsumura Chieko, Kasahara Katsuaki, Mori Yukiko, Seo Akane, Miura Kenichiro, Washiyama Miki, Sugimoto Keisuke, Harada Ryoko, Tazoe Satoshi, Kourakata Hiroyo, Enseki Mayumi, Aotani Daisuke, Yamada Takeshi, Sakakibara Nana, Yamamura Tomohiko, Minamikawa Shogo, Ishikura Kenji, Ito Shuichi, Hattori Motoshi, Iijima Kazumo |
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry. Pediatric nephrology (Berlin, Germany) 2019 1 34 (6): 1065-1075. Okorn Christine, Goertz Anne, Vester Udo, Beck Bodo B, Bergmann Carsten, Habbig Sandra, König Jens, Konrad Martin, Müller Dominik, Oh Jun, Ortiz-Brüchle Nadina, Patzer Ludwig, Schild Raphael, Seeman Tomas, Staude Hagen, Thumfart Julia, Tönshoff Burkhard, Walden Ulrike, Weber Lutz, Zaniew Marcin, Zappel Hildegard, Hoyer Peter F, Weber Stefan |
Hyperuricemia Is an Early and Relatively Common Feature in Children with HNF1B Nephropathy but Its Utility as a Predictor of the Disease Is Limited. Journal of clinical medicine 2021 8 10 (15): . Ko?buc Marcin, Bienia? Beata, Habbig Sandra, Ko?ek Mateusz F, Szczepa?ska Maria, Kili?-Pstrusi?ska Katarzyna, Wasilewska Anna, Adamczyk Piotr, Motyka Rafa?, Tkaczyk Marcin, Sikora Przemys?aw, Beck Bodo B, Zaniew Marc |
Association of Agenesis of the Dorsal Pancreas With HNF1B Heterozygote Mutation: A Case Report. Frontiers in endocrinology 2021 11 12 640006. Guo Mei, Xu Qinqin, Yu Xuefeng, Yang Qin, Shao Shiyi |
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- Page last updated:Mar 25, 2024
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