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Haematologica Latina最新文献

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Haemoglobin A2 in the thalassaemias: hypothesis on the mechanism controlling the synthesis of the chains. 地中海贫血中的血红蛋白A2:控制链合成机制的假说。
Pub Date : 1971-07-01
L Vettore, G Falezza, R Corrocher, G de Sandre
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引用次数: 0
[Relationships of factor VIII (antihemophilic globulin) and its weak inhibitors with the spleen. Effect of adrenaline on splenectomized subjects, on splenomegaly and on patients presenting a weak factor VIII inhibitor]. 因子VIII(抗血友病球蛋白)及其弱抑制剂与脾脏的关系。肾上腺素对脾切除术、脾肿大和弱因子VIII抑制剂患者的影响[j]。
Pub Date : 1971-07-01
G Mayer, V Kalogjera, F Oberling, S Mayer, R Waitz
{"title":"[Relationships of factor VIII (antihemophilic globulin) and its weak inhibitors with the spleen. Effect of adrenaline on splenectomized subjects, on splenomegaly and on patients presenting a weak factor VIII inhibitor].","authors":"G Mayer, V Kalogjera, F Oberling, S Mayer, R Waitz","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":78292,"journal":{"name":"Haematologica Latina","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1971-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16185344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Burning mortality in rats influenced by hematocrit level. Preliminary report. 红细胞压积对大鼠烧伤死亡率的影响。初步报告。
Pub Date : 1971-07-01
E Rewald, F Moscardi
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引用次数: 0
[Multiple myeloma in the dog]. [狗的多发性骨髓瘤]。
Pub Date : 1971-07-01
W C Pires, R B Rojas, H Sechin, C A de Oliveira, R L de Mello
{"title":"[Multiple myeloma in the dog].","authors":"W C Pires, R B Rojas, H Sechin, C A de Oliveira, R L de Mello","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":78292,"journal":{"name":"Haematologica Latina","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1971-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16185348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Further simplification of the method of immunoelectrophoresis]. 【进一步简化免疫电泳方法】。
Pub Date : 1971-07-01
G Caprio, G Parmigiani
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引用次数: 0
Further studies on the abnormal factor X (factor X Friuli) coagulation disorder. A report of another family. 异常因子X(弗留利因子X)凝血障碍的进一步研究。另一个家庭的报告。
Pub Date : 1970-04-01
A Girolami, M Lazzarin, R Scarpa, A Brunetti
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引用次数: 0
[Effect and anti-lymphatic specificity of a combination of cyclophosphamide and vinblastine on normal lymphopoietic tissues in the mouse]. [环磷酰胺与长春碱联合用药对小鼠正常淋巴组织的影响及抗淋巴特异性]。
Pub Date : 1970-04-01
S Tognella, S Conigliaro, G C Scaltrini, P Recalcati, V Grifoni
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引用次数: 0
[Delay of osmotic hemolysis induced by chlorpromazine and chlorpheniramine]. 氯丙嗪和氯苯那敏对渗透性溶血的延缓作用。
Pub Date : 1970-04-01
G Suppa, S Ferri, G Catenazzo
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引用次数: 0
Further studies on the abnormal factor X (factor X Friuli) coagulation disorder. A report of another family. 异常因子X(弗留利因子X)凝血障碍的进一步研究。另一个家庭的报告。
Pub Date : 1970-04-01 DOI: 10.1182/BLOOD.V37.5.534.534
Antonio Girolami, M. Lazzarin, R. Scarpa, A. Brunetti
Another patient with a congenital coagulation disorder due to the presence of an abnormal factor X (factor X Friuli) is presented. The proposita was a 43-yr-old white female who had a bleeding tendency from early childhood (epistaxes, monorrhagias, bleeding after tooth extractions and other surgical procedures, posttraumatic hemarthroses, bleeding from the gums and postpartum hemorrhages). The coagulation work-up demonstrated a prolonged prothrombin time, prolonged partial thromboplastin time, abnormal prothrombin consumption, and abnormal thromboplastin generation corrected by normal serum. Factors II, V, VII, IX, and XII were within normal limits. Platelets, vascular tests and fibrinolysis were normal. Mr. Stuart’s plasma failed to correct the defect of the proposita’s plasma, but a known factor VII deficient plasma was able to correct the abnormality. The factor X assay was low (6-9%) only when tissue thromboplastin, whole or partial, was used. When Factor X was assayed with a Stypven-cephalin mixture, normal or near normal values were observed. Likewise, the Stypven-cephalin clotting time, the Stypven clotting time and the factor II + factor X level using a Stypven-cephalin mixture were normal. The presence of the abnormal factor X was demonstrated immunologically. The defect, like classical factor X deficiency, is transmitted as an autosomal incompletely recessive trait. The mother and the two children of our proposita had factor X levels varying from 38 to 56% of normal and were considered to be heterozygotes.
另一个患者先天性凝血障碍,由于存在异常因子X(因子X弗留利)提出。申请人是一名43岁的白人女性,从小就有出血倾向(鼻出血、出血、拔牙和其他外科手术后出血、创伤后关节出血、牙龈出血和产后出血)。凝血检查显示凝血酶原时间延长,部分凝血活酶时间延长,凝血酶原消耗异常,凝血活酶生成异常被正常血清纠正。因子II、V、VII、IX和XII均在正常范围内。血小板、血管检查和纤溶正常。斯图尔特先生的血浆没能纠正孕妇血浆的缺陷,但一种已知的第七因子缺陷血浆能纠正异常。仅当使用组织凝血活酶(全部或部分)时,因子X测定值较低(6-9%)。当用Stypven-cephalin混合物检测因子X时,观察到正常或接近正常值。Stypven-cephalin凝血时间、Stypven凝血时间及Stypven-cephalin混合液的因子II +因子X水平均正常。免疫学上证实了异常因子X的存在。这种缺陷,像经典的因子X缺乏症一样,是作为常染色体不完全隐性性状遗传的。我们的申请人的母亲和两个孩子的因子X水平从正常的38%到56%不等,被认为是杂合子。
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引用次数: 46
Mycotoxins and their role in oncogenesis, with special reference to blood diseases. 真菌毒素及其在肿瘤发生中的作用,特别涉及血液疾病。
Pub Date : 1970-04-01
J Aleksandrowicz, M Czachor, Z Schiffer, B Smyk
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引用次数: 0
期刊
Haematologica Latina
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