遗传性肝脾肿大 - Suppr

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超能文献

Hereditary hepatosplenomegaly.

作者信息

Cheng D S, Williams H J, Kitahara M

出版信息

West J Med. 1980 Jan;132(1):70-4.

PMID:7376653

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1271953/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04eb/1271953/7290353c1224/westjmed00233-0080-a.jpg

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本文引用的文献

Cytochemistry of leukocyte alkaline phosphatase. Use of complex naphthol as phosphates in azo dyecoupling technics.白细胞碱性磷酸酶的细胞化学。在偶氮染料偶联技术中使用复合萘酚作为磷酸盐。

Am J Clin Pathol. 1963 May;39:439-49. doi: 10.1093/ajcp/39.5.439.

Generalized lymphohistiocytic infiltration. A familial disease not previously described and different from Letterer-Siwe disease and Chediak-Higashi syndrome.全身性淋巴细胞组织细胞浸润。一种先前未被描述的家族性疾病，不同于勒-雪病和切-希综合征。

Pediatrics. 1961 Jun;27:931-50.

'Non-tropical idiopathic splenomegaly' ('primary hypersplenism'): a review of ten cases and their relationship to malignant lymphomas.“非热带特发性脾肿大”（“原发性脾功能亢进”）：十例病例综述及其与恶性淋巴瘤的关系

Br J Haematol. 1969 Oct;17(4):317-33. doi: 10.1111/j.1365-2141.1969.tb01378.x.

A familial disorder characterized by hepatosplenomegaly presenting as "preleukemia".一种以肝脾肿大为特征的家族性疾病，表现为“白血病前期”。

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An anomaly of neutrophil morphology with impaired function.一种伴有功能受损的中性粒细胞形态异常。

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Primary leucocyte alkaline phosphatase deficiency in an adult with repeated infections.一名反复感染的成年人原发性白细胞碱性磷酸酶缺乏症

Br J Haematol. 1976 Sep;34(1):87-94. doi: 10.1111/j.1365-2141.1976.tb00177.x.

Non-tropical 'idiopathic splenomegaly': a follow-up study of ten patients described in 1969.非热带性“特发性脾肿大”：对1969年描述的10例患者的随访研究

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Overwhelming postsplenectomy infection.

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