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Glycinuria, a hereditary disorder associated with nephrolithiasis.

作者信息

DE VRIES A, KOCHWA S, LAZEBNIK J, FRANK M, DJALDETTI M

出版信息

Am J Med. 1957 Sep;23(3):408-15. doi: 10.1016/0002-9343(57)90320-0.

DOI:10.1016/0002-9343(57)90320-0
PMID:13458205
Abstract
摘要

相似文献

1
Glycinuria, a hereditary disorder associated with nephrolithiasis.
Am J Med. 1957 Sep;23(3):408-15. doi: 10.1016/0002-9343(57)90320-0.
2
Ectopic kidney with nephrolithiasis and pyelonephritis.异位肾伴肾结石和肾盂肾炎。
Can Med Assoc J. 1953 Feb;68(2):155-8.
3
Ion-binding properties of electrophoretically homogeneous mucoproteins of urine in normal subjects and in patients with renal calculus disease.
J Urol. 1954 Dec;72(6):1019-31. doi: 10.1016/S0022-5347(17)67711-5.
4
Recurrent nephrolithiasis associated with an unusual tubular defect and hyperchloremic acidosis.复发性肾结石伴异常肾小管缺陷和高氯性酸中毒。
Am J Med. 1958 Oct;25(4):590-9. doi: 10.1016/0002-9343(58)90048-2.
5
Hyperglycinuria with nephrolithiasis.高甘氨酸尿症伴肾结石
Eur J Pediatr. 1978 Apr 20;127(4):279-85. doi: 10.1007/BF00493544.
6
Renal tubular acidosis with recurrent nephrolithiasis and nephrocalcinosis.伴有复发性肾结石和肾钙质沉着症的肾小管性酸中毒。
N Engl J Med. 1957 Aug 29;257(9):399-403. doi: 10.1056/NEJM195708292570903.
7
[ACQUIRED RENAL GLYCINURIA (REPORT OF 2 CASES WITH ARTERIAL HYPERTENSION)].[获得性肾性糖尿(2例合并动脉高血压的报告)]
Rev Clin Esp. 1964 Oct 31;95:72-7.
8
Sodium losing nephropathy in the urological patient: presentation of a case associated with renal calculus disease; differential diagnosis and therapy.
J Urol. 1959 May;81(5):609-11. doi: 10.1016/S0022-5347(17)66079-8.
9
[Surface tension and protective colloid of the urine and their questionable relation to the formation of kidney stones].[尿液的表面张力和保护胶体及其与肾结石形成的可疑关系]
Urol Int. 1957;5(3):149-73. doi: 10.1159/000277307.
10
Nephrolithiasis.肾结石病
Med Clin North Am. 1955 Jul;Cleveland No.:1073-9. doi: 10.1016/s0025-7125(16)34742-3.

引用本文的文献

1
Review of childhood genetic nephrolithiasis and nephrocalcinosis.儿童遗传性肾结石和肾钙质沉着症综述。
Front Genet. 2024 Mar 28;15:1381174. doi: 10.3389/fgene.2024.1381174. eCollection 2024.
2
Hyperglycinuria: diagnosis in middle age.高甘氨酸尿症:中年发病。
BMJ Case Rep. 2022 Mar 2;15(3):e246252. doi: 10.1136/bcr-2021-246252.
3
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.亚氨基甘氨酸尿症和高甘氨酸尿症是由脯氨酸和甘氨酸转运体的复杂突变导致的不同人类表型。
J Clin Invest. 2008 Dec;118(12):3881-92. doi: 10.1172/JCI36625. Epub 2008 Nov 6.
4
[Studies on the metabolism of oxalic acid in a child with oxalosis].[一名草酸尿症患儿草酸代谢的研究]
Klin Wochenschr. 1959 Oct 15;37:1082-6. doi: 10.1007/BF01482917.
5
HYPERGLYCINAEMIA AND HYPERGLYCINURIA IN A NEWBORN INFANT.一名新生儿的高甘氨酸血症和高甘氨酸尿症。
Arch Dis Child. 1964 Aug;39(206):397-402. doi: 10.1136/adc.39.206.397.
6
[ON THE NOMENCLATURE OF CONGENITAL METABOLIC ANOMALIES].[关于先天性代谢异常的命名]
Klin Wochenschr. 1964 Feb 1;42:137-9. doi: 10.1007/BF01479058.
7
RENAL TUBULAR TRANSPORT OF PROLINE, HYDROXYPROLINE, AND GLYCINE IN HEALTH AND IN FAMILIAL HYPERPROLINEMIA.健康及家族性高脯氨酸血症状态下脯氨酸、羟脯氨酸和甘氨酸的肾小管转运
J Clin Invest. 1964 Mar;43(3):374-85. doi: 10.1172/JCI104922.
8
Phenylketonuria with familial hyperglycinuria.苯丙酮尿症伴家族性高甘氨酸尿症。
J Inherit Metab Dis. 1994;17(5):641. doi: 10.1007/BF00711612.
9
Molecular specificity of tubular reabsorption of L-proline. A microperfusion study in rat kidney.L-脯氨酸肾小管重吸收的分子特异性。大鼠肾脏的微灌注研究。
Pflugers Arch. 1980 Sep;387(3):253-9. doi: 10.1007/BF00580978.
10
The prognosis and management of renal tubular disorders.肾小管疾病的预后与管理
Proc R Soc Med. 1967 Nov 1;60(11 Part 1):1149-52. doi: 10.1177/003591576706011P139.