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名词信息
中 文 名:
肾小管酸中毒Ⅲ型
英 文 名:
renal tubular acidosis type Ⅲ,mixed renal tubular acidosis
中文又称:
混合型肾小管酸中毒
中文曾称:
名词来源:
所属专业:
肾内科
所属类别:
疾病诊断名词
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Pubmed相关的文献
renal tubular acidosis type Ⅲ,mixed renal tubular acidosis
相关文献:
[Osteomalacia subsequent to mixed type renal tubular acidosis].
PMID:
[A case of renal tubular acidosis type 3 (mixed) with age-related decreased requirement for bicarbonates].
PMID:
Renal Tubular Acidosis.
Mustaqeem R, Arif A.
2023 Jul 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
PMID:30085586
Understanding renal tubular acidosis.
Wang SSY, Tang H, Ho WQJ, Asif S, Li YX, Ekladious A, Javaid MM.
Br J Hosp Med (Lond). 2024 Oct 30;85(10):1-12. doi: 10.12968/hmed.2024.0290. Epub 2024 Oct 14.
PMID:39475030
Familial renal tubular acidosis.
Alper SL.
J Nephrol. 2010 Nov-Dec;23 Suppl 16:S57-76.
PMID:21170890
Transient Type 3 Renal Tubular Acidosis during Cyclic Vomiting Syndrome.
Kumagai N, Kondoh T, Matsumoto Y, Ikezumi Y.
Tohoku J Exp Med. 2022 May 28;257(1):73-76. doi: 10.1620/tjem.2022.J015. Epub 2022 Mar 31.
PMID:35354692
Clinical and laboratory approaches in the diagnosis of renal tubular acidosis.
Santos F, Ordóñez FA, Claramunt-Taberner D, Gil-Peña H.
Pediatr Nephrol. 2015 Dec;30(12):2099-107. doi: 10.1007/s00467-015-3083-9. Epub 2015 Apr 1.
PMID:25823989
Molecular Pathophysiology of Acid-Base Disorders.
Wagner CA, Imenez Silva PH, Bourgeois S.
Semin Nephrol. 2019 Jul;39(4):340-352. doi: 10.1016/j.semnephrol.2019.04.004.
PMID:31300090
An Infant Case of Transient Distal Renal Tubular Acidosis and Fanconi Syndrome Caused by Rotavirus Gastroenteritis.
Kumagai N, Matsuki T, Nakayama M.
Tohoku J Exp Med. 2023 Nov 11;261(3):195-198. doi: 10.1620/tjem.2023.J070. Epub 2023 Aug 25.
PMID:37635062
Genetic diseases of acid-base transporters.
Alper SL.
Annu Rev Physiol. 2002;64:899-923. doi: 10.1146/annurev.physiol.64.092801.141759.
PMID:11826292
[Migraine-induced kidney stones?].
Gerber L, Wüthrich RP, Mohebbi N.
Praxis (Bern 1994). 2012 May 9;101(10):665-8. doi: 10.1024/1661-8157/a000936.
PMID:22565558
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis.
Borthwick KJ, Kandemir N, Topaloglu R, Kornak U, Bakkaloglu A, Yordam N, Ozen S, Mocan H, Shah GN, Sly WS, Karet FE.
J Med Genet. 2003 Feb;40(2):115-21. doi: 10.1136/jmg.40.2.115.
PMID:12566520
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