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Fatal granulomatous disease of childhood and benign lymphocytic infiltration of the skin (congenital dysphagocytosis).

作者信息

Macfarlane P S, Speirs A L, Sommerville R G

出版信息

Lancet. 1967 Feb 25;1(7487):408-10. doi: 10.1016/s0140-6736(67)91174-9.

DOI:10.1016/s0140-6736(67)91174-9
PMID:4163887
Abstract
摘要

相似文献

1
Fatal granulomatous disease of childhood and benign lymphocytic infiltration of the skin (congenital dysphagocytosis).儿童致死性肉芽肿病和皮肤良性淋巴细胞浸润(先天性吞咽困难)
Lancet. 1967 Feb 25;1(7487):408-10. doi: 10.1016/s0140-6736(67)91174-9.
2
Fatal (chronic) granulomatous disease of childhood: a hereditary defect of leukocyte function.儿童致死性(慢性)肉芽肿病:一种白细胞功能的遗传性缺陷。
Semin Hematol. 1968 Jul;5(3):215-54.
3
Job's syndrome--a variant of chronic granulomatous disease. Report of a case.乔布综合征——慢性肉芽肿病的一种变异型。病例报告。
J Pediatr. 1969 Aug;75(2):236-42. doi: 10.1016/s0022-3476(69)80394-x.
4
Iodination defect in the leukocytes of a patient with chronic granulomatous disease of childhood.一名患有儿童慢性肉芽肿病患者白细胞中的碘化缺陷。
N Engl J Med. 1969 Feb 27;280(9):460-6. doi: 10.1056/NEJM196902272800902.
5
Congenital dysphagocytosis.
Indian J Pediatr. 1967 Jun;34(233):231-2.
6
[Chronic septic granulomatous disease in two brothers (author's transl)].两兄弟患慢性化脓性肉芽肿病(作者译)
Dtsch Med Wochenschr. 1974 Oct 25;99(43):2172-5. doi: 10.1055/s-0028-1108106.
7
Inheritance of chronic granulomatous disease.慢性肉芽肿病的遗传
Lancet. 1969 Oct 18;2(7625):851.
8
Chronic granulomatous disease: quantitative clinicopathological relationships.慢性肉芽肿病:定量临床病理关系
Arch Dis Child. 1970 Feb;45(239):24-32. doi: 10.1136/adc.45.239.24.
9
Increased lecithin synthesis during phagocytosis by normal leukocytes and by leukocytes of a patient with chronic granulomatous disease.正常白细胞以及慢性肉芽肿病患者的白细胞在吞噬作用过程中卵磷脂合成增加。
N Engl J Med. 1969 Jun 12;280(24):1319-22. doi: 10.1056/NEJM196906122802403.
10
Chronic granulomatous disease of childhood.儿童慢性肉芽肿病
J Kans Med Soc. 1970 Nov;1(11):409-15.

引用本文的文献

1
Noninfectious Manifestations and Complications of Chronic Granulomatous Disease.慢性肉芽肿病的非感染性表现和并发症。
J Pediatric Infect Dis Soc. 2018 May 9;7(suppl_1):S18-S24. doi: 10.1093/jpids/piy014.
2
Cutaneous and other lupus-like symptoms in carriers of X-linked chronic granulomatous disease: incidence and autoimmune serology.X连锁慢性肉芽肿病携带者的皮肤及其他狼疮样症状:发病率及自身免疫血清学
Clin Exp Immunol. 2007 Apr;148(1):79-84. doi: 10.1111/j.1365-2249.2007.03321.x.
3
Chronic Granulomatous Disease; fundamental stages in our understanding of CGD.
慢性肉芽肿病;我们对慢性肉芽肿病理解的基础阶段。
Med Immunol. 2006 Sep 21;5:4. doi: 10.1186/1476-9433-5-4.
4
Relation of monocyte and neutrophil oxidative metabolism to skin and oral lesions in carriers of chronic granulomatous disease.慢性肉芽肿病携带者单核细胞和中性粒细胞氧化代谢与皮肤及口腔病变的关系
Clin Exp Immunol. 1981 Feb;43(2):390-8.
5
Chronic granulomatous disease, a heterogeneous syndrome.慢性肉芽肿病,一种异质性综合征。
Hum Genet. 1983;64(3):207-15. doi: 10.1007/BF00279395.
6
Initiation of the respiratory burst of human neutrophils by influenza virus.流感病毒引发人类中性粒细胞的呼吸爆发。
Infect Immun. 1981 Jun;32(3):1200-5. doi: 10.1128/iai.32.3.1200-1205.1981.
7
The pattern of genetic transmission of the leukocyte defect in fatal granulomatous disease of childhood.儿童致死性肉芽肿病中白细胞缺陷的遗传传递模式。
J Clin Invest. 1968 May;47(5):1026-34. doi: 10.1172/JCI105792.
8
Congenital dysphagocytosis.
Indian J Pediatr. 1967 Jun;34(233):231-2.
9
Correction of metabolic deficiencies in the leukocytes of patients with chronic granulomatous disease.慢性肉芽肿病患者白细胞代谢缺陷的纠正。
J Clin Invest. 1970 May;49(5):865-70. doi: 10.1172/JCI106305.
10
Failure of nitro blue tetrazolium reduction in the phagocytic vacuoles of leukocytes in chronic granulomatous disease.慢性肉芽肿病中白细胞吞噬泡内硝基蓝四氮唑还原失败。
J Clin Invest. 1969 Oct;48(10):1895-904. doi: 10.1172/JCI106156.