伴有酸性磷酸酶血症的家族性海蓝色组织细胞增多症。一种类似戈谢病的综合征：刘易斯变异型。 - Suppr | 超能文献

Familial sea-blue histiocytes with acid phosphatemia. A syndrome resembling Gaucher disease: the Lewis variant.

作者信息

Blankenship R M, Greenburg B R, Lucas R N, Reynolds R D, Beutler E

出版信息

JAMA. 1973 Jul 2;225(1):54-6.

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

Familial sea-blue histiocytes with acid phosphatemia. A syndrome resembling Gaucher disease: the Lewis variant.伴有酸性磷酸酶血症的家族性海蓝色组织细胞增多症。一种类似戈谢病的综合征：刘易斯变异型。

JAMA. 1973 Jul 2;225(1):54-6.

2

Marrow storage cells: an ultrastructural study.

J Reticuloendothel Soc. 1976 Feb;19(2):109-19.

3

Acquired lipidosis of marrow macrophages: birefringent blue crystals and Gaucher-like cells, sea-blue histiocytes, and grey-green crystals.

J Clin Pathol. 1979 May;32(5):420-8. doi: 10.1136/jcp.32.5.420.

4

Acute neuronopathic (infantile) and chronic nonneuronopathic (adult) Gaucher disease in full siblings.全同胞中的急性神经元病变型（婴儿型）和慢性非神经元病变型（成人型）戈谢病。

J Pediatr. 1982 Feb;100(2):252-4. doi: 10.1016/s0022-3476(82)80650-1.

5

Sea-blue histiocytes.海蓝色组织细胞

Lancet. 1970 Feb 28;1(7644):459-60.

6

[Comparative cytochemical studies of "Gaucher's-cells" and phagocytizing reticulum cells in the bone marrow of healthy subjects].

Wien Klin Wochenschr. 1969 May 30;81(22):416-8.

7

Syndrome of the sea-blue histiocyte--the first case report in Japan and review of the literature--.

Acta Pathol Jpn. 1979 Jan;29(1):73-97. doi: 10.1111/j.1440-1827.1979.tb01294.x.

8

Sea-blue histiocytes in a patient with lymphoma.淋巴瘤患者中的海蓝色组织细胞。

Am J Med. 1978 Mar;64(3):515-8. doi: 10.1016/0002-9343(78)90245-0.

9

[Sea-blue histiocytosis. Histochemical study of a case with splenic localization].[海蓝色组织细胞增生症。脾脏定位病例的组织化学研究]

Minerva Med. 1975 Jul 11;66(50):2464-7.

10

[Comparative study of 3 types sphingolipidosis: Gaucher's disease, Niemann-Pick disease and the "sea-blue" histiocyte syndrome: cytology, ultrastructure and cytochemistry].

Arch Inst Pasteur Tunis. 1982 Jun-Sep;59(2-3):283-301.

引用本文的文献

1

Niemann-Pick disease (variation in the sphingomyelinase deficient group). Neurovisceral phenotype (A) with an abnormally protracted clinical course and variable expression of neurological symptomatology in three siblings.尼曼-匹克病（鞘磷脂酶缺乏组的变异型）。三名兄弟姐妹出现神经内脏表型（A），临床病程异常迁延，神经症状表现多样。

Eur J Pediatr. 1983 Sep;140(4):323-8. doi: 10.1007/BF00442673.

2

Sea blue histiocytosis. A clinical cytologic and nosographic study on 23 cases.

Klin Wochenschr. 1978 Jan 1;56(1):17-30. doi: 10.1007/BF01476739.

3

A new form of Niemann-Pick disease characterised by temperature-labile sphingomyelinase.一种以温度不稳定的鞘磷脂酶为特征的新型尼曼-匹克病。

J Med Genet. 1978 Oct;15(5):370-4. doi: 10.1136/jmg.15.5.370.