首页 > 按专业查询名词 > 查询PubMed相关文献
名词信息
Pubmed相关的文献
hereditary syndrome associated diabetes 相关文献:
Nephrogenic diabetes insipidus: a comprehensive overview.
Vaz de Castro PAS, Bitencourt L, de Oliveira Campos JL, Fischer BL, Soares de Brito SBC, Soares BS, Drummond JB, Simões E Silva AC.
J Pediatr Endocrinol Metab. 2022 Feb 11;35(4):421-434. doi: 10.1515/jpem-2021-0566. Print 2022 Apr 26.
PMID:35146976
Complexities of the glomerular basement membrane.
Naylor RW, Morais MRPT, Lennon R.
Nat Rev Nephrol. 2021 Feb;17(2):112-127. doi: 10.1038/s41581-020-0329-y. Epub 2020 Aug 24.
PMID:32839582
Breastfeeding and maternal and infant health outcomes in developed countries.
Ip S, Chung M, Raman G, Chew P, Magula N, DeVine D, Trikalinos T, Lau J.
Evid Rep Technol Assess (Full Rep). 2007 Apr;(153):1-186.
PMID:17764214
Epidemiology and Prevention of Prostate Cancer.
Gandaglia G, Leni R, Bray F, Fleshner N, Freedland SJ, Kibel A, Stattin P, Van Poppel H, La Vecchia C.
Eur Urol Oncol. 2021 Dec;4(6):877-892. doi: 10.1016/j.euo.2021.09.006. Epub 2021 Oct 26.
PMID:34716119
Hereditary Paraganglioma-Pheochromocytoma Syndromes.
Else T, Greenberg S, Fishbein L.
2008 May 21 [updated 2023 Sep 21]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
PMID:20301715
Peripheral neuropathies.
Hanewinckel R, Ikram MA, Van Doorn PA.
Handb Clin Neurol. 2016;138:263-82. doi: 10.1016/B978-0-12-802973-2.00015-X.
PMID:27637963
Delineating Wolfram-like syndrome: A systematic review and discussion of the WFS1-associated disease spectrum.
de Muijnck C, Brink JBT, Bergen AA, Boon CJF, van Genderen MM.
Surv Ophthalmol. 2023 Jul-Aug;68(4):641-654. doi: 10.1016/j.survophthal.2023.01.012. Epub 2023 Feb 9.
PMID:36764396
Dermatologic manifestations of endocrine disorders.
Lause M, Kamboj A, Fernandez Faith E.
Transl Pediatr. 2017 Oct;6(4):300-312. doi: 10.21037/tp.2017.09.08.
PMID:29184811
Lynch Syndrome.
Idos G, Valle L.
2004 Feb 5 [updated 2021 Feb 4]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
PMID:20301390
Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment.
Pietrangelo A.
Gastroenterology. 2010 Aug;139(2):393-408, 408.e1-2. doi: 10.1053/j.gastro.2010.06.013. Epub 2010 Jun 11.
PMID:20542038
© Copyright 2021 鸿泰茂源  版权所有All Rights Reserved京ICP备11040441号-3