儿童肝脏疾病：实质性和代谢性疾病中肝脏置换的指征 - Suppr

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超能文献

Liver disorders in children: the indications for liver replacement in parenchymal and metabolic diseases.

作者信息

Mowat A P

出版信息

Transplant Proc. 1987 Aug;19(4):3236-41.

PMID:3303489

Abstract

摘要

相似文献

Liver disorders in children: the indications for liver replacement in parenchymal and metabolic diseases.儿童肝脏疾病：实质性和代谢性疾病中肝脏置换的指征

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引用本文的文献

Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.小儿遗传性代谢疾病的肝移植：适应证、并发症及围手术期管理的考量

Pediatr Transplant. 2016 Sep;20(6):756-69. doi: 10.1111/petr.12741. Epub 2016 Jun 21.

Benign liver tumors in pediatric patients - Review with emphasis on imaging features.小儿患者的肝脏良性肿瘤——重点关注影像特征的综述

World J Gastroenterol. 2015 Jul 28;21(28):8541-61. doi: 10.3748/wjg.v21.i28.8541.

Intrathecal baclofen therapy after liver transplant in a patient with Crigler-Najjar syndrome.肝移植后利鲁唑鞘内治疗克里格勒-纳贾尔综合征患者。

PM R. 2014 Feb;6(2):196-8. doi: 10.1016/j.pmrj.2013.09.004. Epub 2013 Dec 21.

Transplantation immunology: solid organ and bone marrow.移植免疫学：实体器官和骨髓。

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Auxiliary partial orthotopic liver transplantation for Crigler-Najjar syndrome type I.辅助性部分原位肝移植治疗Ⅰ型克里格勒-纳贾尔综合征

Ann Surg. 1999 Apr;229(4):565-9. doi: 10.1097/00000658-199904000-00017.

[Manifestation of Gilbert syndrome (Meulengracht disease) following orthotopic liver transplantation: a rare cause of postoperative hyperbilirubinemia].[原位肝移植后吉尔伯特综合征（梅伦格拉赫特病）的表现：术后高胆红素血症的罕见原因]

Klin Wochenschr. 1988 Jul 1;66(13):596-8. doi: 10.1007/BF01720835.

Organ transplantation in children.

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Visceral pathology of hereditary tyrosinemia type I.I型遗传性酪氨酸血症的内脏病理学

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Arginine remains an essential amino acid after liver transplantation in urea cycle enzyme deficiencies.在尿素循环酶缺乏症患者肝移植后，精氨酸仍然是一种必需氨基酸。

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