地中海贫血中脾脏和骨髓的储存细胞：一项超微结构研究。 - Suppr

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超能文献

Storage cells of spleen and bone marrow in thalassemia: an ultrastructural study.

作者信息

Beltrami C A, Bearzi I, Fabris G

出版信息

Blood. 1973 Jun;41(6):901-12.

PMID:4351306

Abstract

摘要

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Storage cells of spleen and bone marrow in thalassemia: an ultrastructural study.地中海贫血中脾脏和骨髓的储存细胞：一项超微结构研究。

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引用本文的文献

Gaucher-like Cells in Thalassemia Intermedia: Is It a Challenge?中间型地中海贫血中的戈谢样细胞：这是一项挑战吗？

Diseases. 2023 Nov 6;11(4):161. doi: 10.3390/diseases11040161.

Secondary Sea-Blue Histiocytosis in a Patient with Transfusion Dependent HbE-Beta Thalassaemia and Osteosarcoma.一名依赖输血的血红蛋白E-β地中海贫血和骨肉瘤患者的继发性海蓝色组织细胞增多症

Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):262-6. doi: 10.1007/s12288-015-0582-6. Epub 2015 Aug 29.

Sea blue histiocytosis: a common abnormality of the bone marrow in myelodysplastic syndromes.海蓝色组织细胞增多症：骨髓增生异常综合征中常见的骨髓异常。

J Clin Pathol. 1993 Nov;46(11):1030-2. doi: 10.1136/jcp.46.11.1030.

Circumscribed lytic lesions of the thalassaemic skull.地中海贫血颅骨的局限性溶骨性病变。

Skeletal Radiol. 1988;17(5):344-7. doi: 10.1007/BF00367180.

Sea blue histiocytosis. A clinical cytologic and nosographic study on 23 cases.海蓝色组织细胞增多症。23例临床细胞学及疾病分类学研究。

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

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