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Nouvelle revue francaise d'hematologie; blood cells最新文献

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[Treatment of clinical stages I and II of Hodgkin's disease]. [何杰金氏病临床I期和II期的治疗]。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
M Tubiana, G Mathé, M Hayat, J P le Bourgeois, M Henry-Amar, A Laugier
{"title":"[Treatment of clinical stages I and II of Hodgkin's disease].","authors":"M Tubiana, G Mathé, M Hayat, J P le Bourgeois, M Henry-Amar, A Laugier","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 2","pages":"463-72"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12101641","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
[Computer assisted teaching of hematology]. 血液学计算机辅助教学。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
B Varet, J P Lévy
{"title":"[Computer assisted teaching of hematology].","authors":"B Varet, J P Lévy","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 2","pages":"391-400"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11547325","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
[Bernard-Soulier syndrome from the clinical description (1948) to the molecular era (1977) (author's transl)]. [Bernard-Soulier综合征从临床描述(1948)到分子时代(1977)(作者译)]。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
J P Caen, G Tobelem, S Lévy-Tolédano, A Nurden
{"title":"[Bernard-Soulier syndrome from the clinical description (1948) to the molecular era (1977) (author's transl)].","authors":"J P Caen,&nbsp;G Tobelem,&nbsp;S Lévy-Tolédano,&nbsp;A Nurden","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Bernard-Soulier syndrome is a constitutional thrombopathy with an impaired platelet adhesion to the vessel wall. Since the first description in 1948 many works had been reported, and recently a molecular abnormality of the platelet membrane was shown. Interactions between specific membrane sites and platelet functions are now proposed.</p>","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 2","pages":"365-70"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11766515","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
[Congenital recessive methemoglobinemia: a unique disease and variations (proceedings)]. [先天性隐性高铁血红蛋白血症:一种独特的疾病和变异(论文集)]。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
A Leroux, P Beauvais, J C Kaplan
{"title":"[Congenital recessive methemoglobinemia: a unique disease and variations (proceedings)].","authors":"A Leroux,&nbsp;P Beauvais,&nbsp;J C Kaplan","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 1","pages":"217"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12079274","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
[In vitro granulocyte colony formation in children with neuroblastoma (author's transl)]. [神经母细胞瘤患儿体外粒细胞集落形成[作者译]。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
G Tchernia, C Parmentier, S Morel-Brossel, N Morardet, O Schweisguth
{"title":"[In vitro granulocyte colony formation in children with neuroblastoma (author's transl)].","authors":"G Tchernia,&nbsp;C Parmentier,&nbsp;S Morel-Brossel,&nbsp;N Morardet,&nbsp;O Schweisguth","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>In vitro granulocyte colony formation has been studied using the methylcellulose system in 22 children with neuroblastoma, 13 of them having bone marrow invasion. Only one third exhibited normal results. There were various disturbances of granulopoiesis in vitro: colony forming cells were decreased or increased and in the amplification compartment either an ineffective leucopoiesis or an increase in the number of mitosis was present. The abnormalities are not correlated to bone marrow invasion.</p>","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 1","pages":"63-72"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12079287","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
Pluripotential and committed hemopoietic stem cells. A hypothesis. 多能和固定的造血干细胞。一个假设。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
G Brecher
{"title":"Pluripotential and committed hemopoietic stem cells. A hypothesis.","authors":"G Brecher","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The hypothesis is proposed that regulation of hemopoiesis is largely accomplished by expansion or contraction of the committed stem cell compartments and that pluripotential stem cells are normally not involved or in cycle. The thesis appears supported by the fact that erythropoietin affects the committed red cell precursors, that 98% of marrow mitoses have been shown to occur in cells clearly recognizable as red or white cell precursors (while the pluripotential stem cells by definition are not so recognizable), and that it has been shown (by the spleen nodule assay) that the pluripotential stem cell compartment in the marrow cannot be readily expanded. The major objection to the proposed hypothesis are tritiated thymidine suicide data, which suggest that up to 20% of pluripotential stem cells may be constantly in cycle in some stains of mice. Preliminary experimental evidence supporting the hypothesis has been obtained: normal pluripotential stem cells which transfused into normal isologous mice are not lost as has been assumed but proliferate after irradiation, suggesting that it takes a special stimulus to \"turn-on\" the normally quiescent pluripotential stem cells.</p>","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 2","pages":"285-91"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11547324","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
[The quantification of surface immunoglobulins in lymphoproliferative syndromes]. [淋巴增生性综合征的表面免疫球蛋白定量]。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
G Dighiero, J Y Follezou, J P Roisin, D Charron, E Bouvet, T Ternyck, J L Binet
{"title":"[The quantification of surface immunoglobulins in lymphoproliferative syndromes].","authors":"G Dighiero,&nbsp;J Y Follezou,&nbsp;J P Roisin,&nbsp;D Charron,&nbsp;E Bouvet,&nbsp;T Ternyck,&nbsp;J L Binet","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 1","pages":"180-1"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11615049","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
[Mouse rosettes in normal subjects and in hyperlymphocytosis]. [正常受试者和淋巴细胞增多症小鼠的玫瑰结]。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
A Moutte
{"title":"[Mouse rosettes in normal subjects and in hyperlymphocytosis].","authors":"A Moutte","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 1","pages":"255-6"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11543645","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
[Double erythrocyte enzymopathy. Acquired pyruvate kinase and inherited glucose-6-phosphate dehydrogenase deficiencies]. 双红细胞酶病。获得性丙酮酸激酶和遗传性葡萄糖-6-磷酸脱氢酶缺乏症]。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
R Herbeuval, C Vigneron, J P Aymard, P Lederlin, F Witz, O Guerci, G Thibaut
{"title":"[Double erythrocyte enzymopathy. Acquired pyruvate kinase and inherited glucose-6-phosphate dehydrogenase deficiencies].","authors":"R Herbeuval,&nbsp;C Vigneron,&nbsp;J P Aymard,&nbsp;P Lederlin,&nbsp;F Witz,&nbsp;O Guerci,&nbsp;G Thibaut","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 1","pages":"232-4"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12079280","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
[Erythrocyte membrane protein abnormalities in hereditary hemolytic anemias]. [遗传性溶血性贫血的红细胞膜蛋白异常]。
Nouvelle revue francaise d'hematologie; blood cells Pub Date : 1977-01-01
P Boivin, C Galand
{"title":"[Erythrocyte membrane protein abnormalities in hereditary hemolytic anemias].","authors":"P Boivin,&nbsp;C Galand","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The structural and functional abnormalities of erythrocyte membrane proteins in hereditary hemolytic anemias are reviewed. The authors stress the problems of protein solubilization and the artefacts of the sodium dodecylsulphate polyacrylamide gel electrophoresis; protein abnormalities observed with that method are inconstant and non-specific. Abnormal \"spectrin\" has been reported in hereditary spherocytosis: however analysis of purified spectrin peptides by isoelectric focusing in 8M urea did not reveal any difference between normal and hereditary spherocytosis spectrin. Deficient autophosphorylation of erythrocyte membrane proteins by endogenous membrane protein-kinases 3'5-cyclic-AMP dependent and independent was pointed out in hereditary spherocytosis and stomatocytosis: the authors' experience was contrary to such results: quantitatively and qualitatively normal activity of membrane protein-kinase was found in five cases of hereditary spherocytosis. The authenticity, frequency and specificity of the various membrane protein abnormalities reported so far, are not firmly established. Many insufficiently verified results published prematurely have been later denied. To date no membrane protein anomaly may be considered as a biochemical cause of any type of hereditary hemolytic anemia.</p>","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 1","pages":"95-116"},"PeriodicalIF":0.0,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11413822","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
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