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Biochemical follow-up in late-treated nephropathic cystinosis.

作者信息

Vilaseca M A, Camacho J A, Briones P, Farré C, Mas A

机构信息

Servei de Bioquímica, Hospital Universitari Sant Joan de Déu, Barcelona, Spain.

出版信息

J Inherit Metab Dis. 1995;18(2):147-50. doi: 10.1007/BF00711751.

DOI:10.1007/BF00711751
PMID:7564231
Abstract
摘要

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1
Biochemical follow-up in late-treated nephropathic cystinosis.晚发性肾病型胱氨酸病的生化随访
J Inherit Metab Dis. 1995;18(2):147-50. doi: 10.1007/BF00711751.
2
Treatment with recombinant human growth hormone in short children with nephropathic cystinosis: no evidence for increased deterioration rate of renal function. The European Study Group on Growth Hormone Treatment in Short Children with Nephropathic Cystinosis.重组人生长激素治疗肾病型胱氨酸病患儿身材矮小:无肾功能恶化率增加的证据。欧洲肾病型胱氨酸病身材矮小患儿生长激素治疗研究组。
Pediatr Res. 1998 Apr;43(4 Pt 1):484-8. doi: 10.1203/00006450-199804000-00008.
3
Long-term treatment of infantile nephropathic cystinosis with cysteamine.用半胱胺对婴儿肾病性胱氨酸病进行长期治疗。
N Engl J Med. 1985 Dec 5;313(23):1460-3. doi: 10.1056/NEJM198512053132307.
4
Cysteamine therapy in nephropathic cystinosis.
N Engl J Med. 1981 May 7;304(19):1171-3. doi: 10.1056/nejm198105073041915.
5
Predicted reciprocal serum creatinine at age 10 years as a measure of renal function in children with nephropathic cystinosis treated with oral cysteamine.10岁时预测的血清肌酐倒数作为口服半胱胺治疗的肾病性胱氨酸病患儿肾功能的一项指标。
Pediatr Nephrol. 1990 Mar;4(2):129-35. doi: 10.1007/BF00858823.
6
Effects of cysteamine therapy in nephropathic cystinosis.半胱胺治疗肾病性胱氨酸病的效果
N Engl J Med. 1981 Jan 15;304(3):141-5. doi: 10.1056/NEJM198101153040303.
7
Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults.半胱氨酸治疗可延缓晚期青少年和成年患者的囊纤维化肾病进展。
Kidney Int. 2012 Jan;81(2):179-89. doi: 10.1038/ki.2011.277. Epub 2011 Sep 7.
8
Nephropathic cystinosis: ineffectiveness of cysteamine therapy for ocular changes.肾病性胱氨酸病:半胱胺治疗眼部病变无效。
Am J Ophthalmol. 1983 May;95(5):713-4. doi: 10.1016/0002-9394(83)90401-4.
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Progression of chronic renal failure in a historical group of patients with nephropathic cystinosis. European Collaborative Study on Cystinosis.一组患有肾病性胱氨酸病患者的慢性肾衰竭进展情况。欧洲胱氨酸病协作研究。
Pediatr Nephrol. 1994 Aug;8(4):466-71. doi: 10.1007/BF00856532.
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Nephropathic cystinosis: effect of long-term cysteamine therapy.肾性胱氨酸病:长期半胱胺治疗的效果
Clin Nephrol. 1987 Jun;27(6):309-12.

引用本文的文献

1
Cystinosis: the evolution of a treatable disease.胱氨酸病:一种可治疗疾病的演变。
Pediatr Nephrol. 2013 Jan;28(1):51-9. doi: 10.1007/s00467-012-2242-5. Epub 2012 Aug 18.
2
Nephropathic cystinosis: late complications of a multisystemic disease.肾性胱氨酸病:一种多系统疾病的晚期并发症。
Pediatr Nephrol. 2008 Jun;23(6):863-78. doi: 10.1007/s00467-007-0650-8.

本文引用的文献

1
Improved renal function in children with cystinosis treated with cysteamine.用半胱胺治疗的胱氨酸病患儿肾功能改善。
N Engl J Med. 1993 Apr 22;328(16):1157-62. doi: 10.1056/NEJM199304223281604.
2
Muscle carnitine repletion by long-term carnitine supplementation in nephropathic cystinosis.在肾病性胱氨酸病中,通过长期补充肉碱来补充肌肉肉碱。
Pediatr Res. 1993 Aug;34(2):115-9. doi: 10.1203/00006450-199308000-00001.
3
An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.一种影响心肌、骨骼肌和中性粒细胞的X连锁线粒体疾病。
J Neurol Sci. 1983 Dec;62(1-3):327-55. doi: 10.1016/0022-510x(83)90209-5.
4
Cysteamine therapy for children with nephropathic cystinosis.半胱胺治疗肾病型胱氨酸病患儿。
N Engl J Med. 1987 Apr 16;316(16):971-7. doi: 10.1056/NEJM198704163161602.
5
Cystinosis.
Semin Nephrol. 1989 Jun;9(2):147-61.
6
Predicted reciprocal serum creatinine at age 10 years as a measure of renal function in children with nephropathic cystinosis treated with oral cysteamine.10岁时预测的血清肌酐倒数作为口服半胱胺治疗的肾病性胱氨酸病患儿肾功能的一项指标。
Pediatr Nephrol. 1990 Mar;4(2):129-35. doi: 10.1007/BF00858823.
7
Update on nephropathic cystinosis.肾性胱氨酸病的最新进展。
Pediatr Nephrol. 1990 Nov;4(6):645-53. doi: 10.1007/BF00858644.
8
Treatment of cystinosis with cysteamine from early infancy.
J Pediatr. 1991 Sep;119(3):491-3. doi: 10.1016/s0022-3476(05)82072-4.
9
Parenchymal organ cystine depletion with long-term cysteamine therapy.长期使用半胱胺治疗导致实质器官胱氨酸耗竭。
Biochem Med Metab Biol. 1992 Dec;48(3):275-85. doi: 10.1016/0885-4505(92)90074-9.