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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 26, 2023. (Total: 221463Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Cysts and HNF1B[original query]
HNF1B deletions in patients with young-onset diabetes but no known renal disease.
Diabetic medicine : a journal of the British Diabetic Association 2013 Jan 30 (1): 114-7.
Edghill E L, Stals K, Oram R A, Shepherd M H, Hattersley A T, Ellard
Searching for mutations in the HNF1B gene in a Brazilian cohort with renal cysts and hyperglycemia.
Archives of endocrinology and metabolism 2019 5 63 (3): 250-257.
Dotto Renata P, Santana Lucas Santos de, Lindsey Susan C, Caetano Lilian Araújo, Franco Luciana F, Moisés Regina Célia M S, Sa João R, Nishiura José Luiz, Teles Milena Gurgel, Heilberg Ita P, Dias-da-Silva Magnus R, Giuffrida Fernando M A, Reis André
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
Genotype and Phenotype Analyses in Pediatric Patients with HNF1B Mutations.
Journal of clinical medicine 2020 7 9 (7): .
Lim Seon Hee, Kim Ji Hyun, Han Kyoung Hee, Ahn Yo Han, Kang Hee Gyung, Ha Il-Soo, Cheong Hae
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