伴有低血糖、骨质改变和嗜酸性粒细胞增多的瑞士无丙种球蛋白血症。 - Suppr

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超能文献

Swiss agammaglobulinemia with hypoglycemia, osseous changes and eosinophilia.

作者信息

Duic A, Crozier D N, Lynch M J, McClure P D

出版信息

Can Med Assoc J. 1970 Jul 4;103(1):64-8 passim.

PMID:5424299

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1930334/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/70f35ab46ee9/canmedaj01597-0066-a.jpg

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Swiss agammaglobulinemia with hypoglycemia, osseous changes and eosinophilia.伴有低血糖、骨质改变和嗜酸性粒细胞增多的瑞士无丙种球蛋白血症。

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[Essential lymphocytophthisis; new clinical aspect of infant pathology].[原发性淋巴细胞消耗症；婴儿病理学的新临床方面]

Ann Paediatr. 1950 Jul-Aug;175(1-2):1-32.

Agammaglobulinemia.无丙种球蛋白血症

Pediatrics. 1952 Jun;9(6):722-8.

Alymphocytosis, agammaglobulinaemia, homografts, and delayed hypersen sitivity: study of a case.无淋巴细胞血症、无丙种球蛋白血症、同种移植及迟发型超敏反应：1例研究

Lancet. 1962 Aug 25;2(7252):380-1. doi: 10.1016/s0140-6736(62)90232-5.

[HEREDITARY THYMIC HYPOPLASIA: ITS PLACE AND RESPONSIBILITY IN A CASE OF LYMPHOCYTIC, NORMOPLASMOCYTIC AND NORMOGLOBULINEMIC APLASIA IN AN INFANT].[遗传性胸腺发育不全：在一名婴儿淋巴细胞、正常浆细胞和正常球蛋白血症性再生障碍性贫血病例中的地位及作用]

Arch Fr Pediatr. 1964 Oct;21:897-920.

THE THYMUS AND OTHER LYMPHOID TISSUES IN CONGENITAL AGAMMAGLOBULINEMIA. I. THYMIC ALYMPHOPLASIA AND LYMPHOCYTIC HYPOPLASIA AND THEIR RELATION TO INFECTION.先天性无丙种球蛋白血症中的胸腺及其他淋巴组织。I.胸腺淋巴细胞生成障碍和淋巴细胞发育不全及其与感染的关系。

Pediatrics. 1963 Oct;32:517-30.

Reticular dysgenesia.网状细胞发育不全

Lancet. 1959 Dec 19;2(7112):1123-5. doi: 10.1016/s0140-6736(59)90105-9.

[Agammaglobulinemia & alymphocytosis with atrophy of lymphatic tissue].[无丙种球蛋白血症及淋巴细胞减少伴淋巴组织萎缩]

Helv Paediatr Acta. 1958 Dec;13(6):551-85.

Phagocytosis of mast cell granule by the eosinophilic leukocyte in the rat.大鼠嗜酸性白细胞对肥大细胞颗粒的吞噬作用。

Am J Pathol. 1959 Jan-Feb;35(1):103-11.

[Familial lymphopenia with agammaglobulinemia & severe moniliasis: the essential lymphocytophthisis as a special form of early childhood agammaglobulinemia].[伴有无丙种球蛋白血症和严重念珠菌病的家族性淋巴细胞减少症：作为幼儿期无丙种球蛋白血症一种特殊形式的原发性淋巴细胞消耗症]

Helv Paediatr Acta. 1958 Oct;13(4):313-38.

Thymic dysplasia ("Swiss agammaglobulinemia"). II. Morphologic and functional observations.

J Pediatr. 1967 May;70(5):737-44. doi: 10.1016/s0022-3476(67)80324-x.

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