A salt wasting syndrome in infancy.
作者信息
CHEEK D B, PERRY J W
出版信息
Arch Dis Child. 1958 Jun;33(169):252-6. doi: 10.1136/adc.33.169.252.
Abstract
摘要
相似文献
1
A salt wasting syndrome in infancy.婴儿期的盐耗竭综合征。
Arch Dis Child. 1958 Jun;33(169):252-6. doi: 10.1136/adc.33.169.252.
2
The low salt syndrome.低盐综合征
Heart Bull. 1960 Nov-Dec;9:105-7.
3
The low salt syndrome.低盐综合征
Mod Concepts Cardiovasc Dis. 1955 Jul;24(7):283-5.
4
Cortisone treatment of the low-salt syndrome.可的松治疗低盐综合征。
Br Med J. 1956 Apr 7;1(4970):778-9. doi: 10.1136/bmj.1.4970.778.
5
[Salt depletion syndrome].[盐耗竭综合征]
Pediatr Prat. 1956 Nov;27(11):381-6.
6
[Postoperative & posttraumatic salt deficiency syndrome].[术后及创伤后盐缺乏综合征]
Langenbecks Arch Klin Chir Ver Dtsch Z Chir. 1959;290(3):310-4.
7
[Scarlatina; Marchand-Waterhouse-Friderichsen syndrome; and hypotonic dehydration or salt depletion].[猩红热；华-佛综合征；以及低渗性脱水或缺盐]
Rev Sanid Milit Argent. 1959 Jul-Sep;58:240-2.
8
Presence of an aldosterone stimulating substance in the urine of rats deprived of salt.缺盐大鼠尿液中醛固酮刺激物质的存在。
Am J Physiol. 1957 Nov;191(2):323-8. doi: 10.1152/ajplegacy.1957.191.2.323.
9
Time relation of renal and sweat gland adjustments to salt deficiency in men.男性肾脏和汗腺对缺盐适应的时间关系。
J Appl Physiol. 1955 Sep;8(2):159-65. doi: 10.1152/jappl.1955.8.2.159.
10
Salt-losing nephritis.失盐性肾炎
AMA J Dis Child. 1958 Aug;96(2):191-6. doi: 10.1001/archpedi.1958.02060060193010.
引用本文的文献
1
Clinical and Biochemical Characteristics of Pseudohypoaldosteronism Type 1 with and Without Genetic Mutations: A Literature Review.伴有和不伴有基因突变的1型假性醛固酮减少症的临床和生化特征：文献综述
J Clin Med. 2025 Jun 20;14(13):4408. doi: 10.3390/jcm14134408.
2
Case Report: Autoimmune hepatitis in a patient with pseudohypoaldosteronism type 1-insights into a rare co-occurrence.病例报告：1型假性醛固酮减少症患者合并自身免疫性肝炎——对一种罕见共病情况的深入了解
Front Pediatr. 2025 Apr 15;13:1558179. doi: 10.3389/fped.2025.1558179. eCollection 2025.
3
Genetics of Hypertension: From Monogenic Analysis to GETomics.高血压的遗传学：从单基因分析到基因组学
J Cardiovasc Dev Dis. 2024 May 18;11(5):154. doi: 10.3390/jcdd11050154.
4
Autosomal Dominant Pseudohypoaldosteronism Type 1 in a Newborn With Failure to Thrive.1型常染色体显性遗传性假性醛固酮增多症在一名发育不良的新生儿中的病例报告
Cureus. 2024 Apr 30;16(4):e59356. doi: 10.7759/cureus.59356. eCollection 2024 Apr.
5
Pseudohypoaldosteronism type 1b in fraternal twins of a Chinese family: report of two cases and literature review.1b 型假性醛固酮减少症在一个华人家族的双胞胎兄弟中：两例报告及文献复习。
Arch Endocrinol Metab. 2023 May 12;67(4):e000620. doi: 10.20945/2359-3997000000620.
6
Systemic Pseudohypoaldosteronism Type 1 Due to a Novel Mutation in SCNN1B Gene: A Case Report.因SCNN1B基因新突变导致的1型全身性假性醛固酮减少症：一例报告
EJIFCC. 2022 Oct 28;33(3):268-273. eCollection 2022 Oct.
7
Neonatal Pseudohypoaldosteronism Type-1 in Japan.日本的1型新生儿假性醛固酮减少症
J Clin Med. 2022 Aug 31;11(17):5135. doi: 10.3390/jcm11175135.
8
Mechanistic insights into the primary and secondary alterations of renal ion and water transport in the distal nephron.深入了解远曲小管中肾脏离子和水转运的原发性和继发性改变的机制。
J Intern Med. 2023 Jan;293(1):4-22. doi: 10.1111/joim.13552. Epub 2022 Aug 21.
9
Challenges of Diagnosing Pseudohypoaldosteronism (PHA) in an Infant.诊断婴儿假性醛固酮减少症（PHA）的挑战
Case Rep Endocrinol. 2022 Jul 11;2022:9921003. doi: 10.1155/2022/9921003. eCollection 2022.
10
Pseudohypoaldosteronism Type 1: The Presentation and Management of a Neonate With a Novel Mutation of the SCNN1B Gene Found in Two Hispanic Siblings.1型假性醛固酮减少症：在两名西班牙裔兄弟姐妹中发现携带SCNN1B基因新突变的新生儿的临床表现及管理
Cureus. 2022 Apr 7;14(4):e23918. doi: 10.7759/cureus.23918. eCollection 2022 Apr.
本文引用的文献
1
OBSERVATIONS ON SODIUM CHLORIDE RESTRICTION AND UREA CLEARANCE IN RENAL INSUFFICIENCY.关于肾功能不全时氯化钠限制与尿素清除率的观察
J Clin Invest. 1935 Sep;14(5):525-41. doi: 10.1172/JCI100703.
2
The metabolic response of infants to heat stress.婴儿对热应激的代谢反应。
Yale J Biol Med. 1950 Jan;22(3):227-49.
3
A photoelectric flame photometer.一台光电火焰光度计。
Biochem J. 1949;45(4):400-8.
4
A modified Conway unit for microdiffusion analysis.用于微扩散分析的改良康威装置。
Biochem J. 1955 Jan;59(1):134-6. doi: 10.1042/bj0590134.
5
The regulation of aldosterone secretion in man: the role of fluid volume.人体中醛固酮分泌的调节：体液量的作用。
J Clin Invest. 1956 Nov;35(11):1306-15. doi: 10.1172/JCI103386.
6
A simple method for collection and analysis of sweat for chloride.一种用于收集和分析汗液中氯化物的简单方法。
AMA J Dis Child. 1956 Aug;92(2):160-3. doi: 10.1001/archpedi.1956.02060030154009.
7
An appraisal of methods of tissue chloride analysis: the total carcass chloride, exchangeable chloride, potassium and water of the rat.组织氯分析方法的评估：大鼠的全尸氯、可交换氯、钾和水
J Clin Invest. 1955 Dec;34(12):1744-55. doi: 10.1172/JCI103229.
8
Modification of the Reddy-Jenkins-Thorn method for the estimation of 17-hydroxycorticoids in urine.用于估算尿中17-羟皮质类固醇的雷迪-詹金斯-索恩方法的改良
Metabolism. 1954 Nov;3(6):489-92.
9
Inborn defects of the renal tubule.肾小管先天性缺陷
Postgrad Med J. 1954 Sep;30(347):476-84. doi: 10.1136/pgmj.30.347.476.
10
Observations on total body chloride in children.关于儿童全身氯化物的观察
Pediatrics. 1954 Jul;14(1):5-10.
Zotero 插件