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familial hormone production disorder goiter相关文献:
Molecular pathogenesis of nodular goiter.
Paschke R.
Langenbecks Arch Surg. 2011 Dec;396(8):1127-36. doi: 10.1007/s00423-011-0788-5. Epub 2011 Apr 14.
PMID:21487943
Thyroid and Parathyroid Conditions: Hyperthyroidism.
Rhodes MA, Adams CS, Bragg S, Christian N.
FP Essent. 2022 Mar;514:11-17.
PMID:35235281
Autoimmune thyrotoxicosis: diagnostic challenges.
Ponto KA, Kahaly GJ.
Am J Med. 2012 Sep;125(9):S1. doi: 10.1016/j.amjmed.2012.05.011.
PMID:22938935
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities.
Narumi S, Nagasaki K, Kiriya M, Uehara E, Akiba K, Tanase-Nakao K, Shimura K, Abe K, Sugisawa C, Ishii T, Miyako K, Hasegawa Y, Maruo Y, Muroya K, Watanabe N, Nishihara E, Ito Y, Kogai T, Kameyama K, Nakabayashi K, Hata K, Fukami M, Shima H, Kikuchi A, Takayama J, Tamiya G, Hasegawa T.
Nat Genet. 2024 May;56(5):869-876. doi: 10.1038/s41588-024-01735-5. Epub 2024 May 7.
PMID:38714868
Graves' disease: diagnostic and therapeutic challenges (multimedia activity).
Kahaly GJ, Grebe SK, Lupo MA, McDonald N, Sipos JA.
Am J Med. 2011 Jun;124(6):S2-3. doi: 10.1016/j.amjmed.2011.03.001.
PMID:21605717
Novel presentation of the c.1856A > G (p.Asp619Gly) TSHR gene-activating variant: relapsing hyperthyroidism in three subsequent generations manifesting in early childhood and an in vitro functional study.
Bezdicka M, Kleiblova P, Soucek J, Borecka M, El-Lababidi E, Smrz D, Rataj M, Sumnik Z, Malikova J, Soucek O.
Hormones (Athens). 2021 Dec;20(4):803-812. doi: 10.1007/s42000-021-00299-x. Epub 2021 Jun 18.
PMID:34142359
Signal transducer and activator of transcription 3 as a potential therapeutic target for Graves' orbitopathy.
Ko J, Kim JY, Kim BR, Lee EJ, Kikkawa DO, Yoon JS.
Mol Cell Endocrinol. 2021 Aug 20;534:111363. doi: 10.1016/j.mce.2021.111363. Epub 2021 Jun 9.
PMID:34116129
Hyperthyroidism in children and adolescents: Experience in a university hospital in Colombia.
García JS, Sarmiento MP, Bello JD, Zuluaga NA, Forero AC, Niño LF.
Biomedica. 2022 Jun 1;42(2):342-354. doi: 10.7705/biomedica.6244.
PMID:35867926
Nodule-specific NRF2-targeted upregulation in patients with KEAP1 mutations and familial nontoxic multinodular goiter.
Nishihara E, Fukata S, Hirokawa M, Higuchi M, Ito M, Nishikawa M, Miyauchi A, Matsuse M, Mitsutake N, Ito Y, Hishinuma A, Kogai T, Akamizu T.
J Clin Endocrinol Metab. 2024 Oct 7:dgae699. doi: 10.1210/clinem/dgae699. Online ahead of print.
PMID:39373520
Iodine deficiency disorders.
Elliott TC.
Health Technol Dir. 1987;7(1):1-12.
PMID:12343033
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