Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria ( Marchiafava Micheli syndrome) Report of a case with marked thrombocytopenia in a five-year old child

被引：22

作者：

Pierce, PP ^{[1
]}

Aldrich, CA ^{[1
]}

机构：

[1] Childrens Mem Hosp, Chicago, IL USA

来源：

JOURNAL OF PEDIATRICS | 1943年 / 22卷

关键词：

D O I：

10.1016/S0022-3476(43)80138-4

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：30 / 42

页数：13

共 15 条

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Ham, TH .

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[5] Studies on destruction of red blood cells. II. Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria: Certain immunological aspects of the hemolytic mechanism with special reference to serum complement [J].

Ham, TH ;

Dingle, JH .

JOURNAL OF CLINICAL INVESTIGATION, 1939, 18 (06) :657-672

[6] Studies on destruction of red blood cells I Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria - An investigation of the mechanism of hemolysis, with observations on five cases [J].

Ham, TH .

ARCHIVES OF INTERNAL MEDICINE, 1939, 64 (06) :1271-1305

[7] Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria [J].

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Bernnstein, A .

AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1936, 192 :301-316

[8]

KRACKE RR, 1941, DIS BLOOD ATLAS HEMA, P248

[9]

MARCHIAFAVA E, 1931, POLICLINICO M, V38, P105

[10]

MARCHIAFAVA E, 1911, POLICLINICO, V18, P241

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