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Bone marrow transplantation in Maroteaux-Lamy syndrome (MPS type 6): status 40 months after BMT.

作者信息

McGovern M M, Ludman M D, Short M P, Steinfeld L, Kattan M, Raab E L, Krivit W, Desnick R J

出版信息

Birth Defects Orig Artic Ser. 1986;22(1):41-53.

PMID:3083886
Abstract
摘要

相似文献

1
Bone marrow transplantation in Maroteaux-Lamy syndrome (MPS type 6): status 40 months after BMT.马罗-拉米综合征(黏多糖贮积症6型)的骨髓移植:骨髓移植40个月后的状况
Birth Defects Orig Artic Ser. 1986;22(1):41-53.
2
Bone-marrow transplantation in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI). Biochemical and clinical status 24 months after transplantation.马洛托-拉米综合征(黏多糖贮积症 VI 型)的骨髓移植。移植后 24 个月的生化和临床状况。
N Engl J Med. 1984 Dec 20;311(25):1606-11. doi: 10.1056/NEJM198412203112504.
3
Bone marrow transplantation in the feline model of arylsulfatase B deficiency.芳基硫酸酯酶B缺乏症猫模型中的骨髓移植
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Comparison of enzymatic activity with evidence of engraftment in patients with inborn errors of metabolism receiving allogeneic marrow transplantation.接受异基因骨髓移植的先天性代谢缺陷患者酶活性与植入证据的比较。
Birth Defects Orig Artic Ser. 1986;22(1):135-52.
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Correction of feline arylsulphatase B deficiency (mucopolysaccharidosis VI) by bone marrow transplantation.通过骨髓移植纠正猫的芳基硫酸酯酶B缺乏症(粘多糖贮积症VI型)
Nature. 1984;312(5993):467-9. doi: 10.1038/312467a0.
6
Postnatal and prenatal diagnosis of Maroteaux-Lamy syndrome.马罗-拉米综合征的产后及产前诊断
Acta Anthropogenet. 1985;9(1-3):109-16.
7
[The early diagnosis of Maroteaux-Lamy syndrome with confirmation of arylsulphatase deficiency].[通过确认芳基硫酸酯酶缺乏症对马罗-拉米综合征进行早期诊断]
Arch Fr Pediatr. 1977 Apr;34(4):362-70.
8
Umbilical cord blood transplantation for Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI).
Bone Marrow Transplant. 2000 Aug;26(4):455-8. doi: 10.1038/sj.bmt.1702528.
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[Mucopolysaccharidoses. New therapeutic possibilities increase the need of early diagnosis].[黏多糖贮积症。新的治疗可能性增加了早期诊断的必要性]
Lakartidningen. 2002 Apr 18;99(16):1804-9.
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Allogeneic CD34 selected peripheral stem cell transplant for Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI): rapid haemopoietic and biochemical reconstitution.
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Transplantation as disease modifying therapy in adults with inherited metabolic disorders.将移植作为成人遗传性代谢疾病的疾病修饰治疗。
J Inherit Metab Dis. 2018 Sep;41(5):885-896. doi: 10.1007/s10545-018-0141-z. Epub 2018 Feb 1.
2
Niemann-Pick disease: sixteen-year follow-up of allogeneic bone marrow transplantation in a type B variant.尼曼-匹克病:B型变异型同种异体骨髓移植的16年随访
J Inherit Metab Dis. 2003;26(8):775-85. doi: 10.1023/B:BOLI.0000009950.81514.c8.
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Leukodystrophy and bone marrow transplantation: role of mixed hematopoietic chimerism.
脑白质营养不良与骨髓移植:混合造血嵌合体的作用
Neurochem Res. 1999 Apr;24(4):537-49. doi: 10.1023/a:1022587914079.
4
Bone marrow transplantation for Maroteaux-Lamy syndrome (MPS VI): long-term follow-up.马罗-拉米综合征(MPS VI)的骨髓移植:长期随访
J Inherit Metab Dis. 1999 Feb;22(1):50-62. doi: 10.1023/a:1005447232027.
5
Enzyme replacement therapy from birth in a feline model of mucopolysaccharidosis type VI.在黏多糖贮积症VI型猫模型中从出生起进行酶替代疗法。
J Clin Invest. 1997 Feb 15;99(4):651-62. doi: 10.1172/JCI119208.
6
Arylsulfatase B activities and glycosaminoglycan levels in retrovirally transduced mucopolysaccharidosis type VI cells. Prospects for gene therapy.逆转录病毒转导的VI型黏多糖贮积症细胞中的芳基硫酸酯酶B活性和糖胺聚糖水平。基因治疗的前景。
J Clin Invest. 1996 Jul 15;98(2):497-502. doi: 10.1172/JCI118817.
7
Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome.马罗-拉米综合征猫模型中的酶替代疗法。
J Clin Invest. 1996 Apr 15;97(8):1864-73. doi: 10.1172/JCI118617.
8
Stereological and morphometric analysis of dermal fibroblasts before and after bone marrow transplantation in a case of mucopolysaccharidosis I Scheie phenotype.黏多糖贮积症I型Scheie表型病例中骨髓移植前后真皮成纤维细胞的体视学和形态计量学分析
Acta Neuropathol. 1993;86(1):21-8. doi: 10.1007/BF00454894.
9
Bone marrow transplantation. Part I--Allogeneic.骨髓移植。第一部分——同种异体移植。
West J Med. 1989 Dec;151(6):638-43.
10
Displacement bone marrow transplantation for some inborn errors.
J Inherit Metab Dis. 1990;13(4):572-96. doi: 10.1007/BF01799514.