Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Lawrence E. Pierce"'
Autor:
Clara S. P. Chan, James B. Peter, Susan B. Wormsley, Lawrence E. Pierce, Geraldine P. Schechter
Publikováno v:
American Journal of Hematology. 33:101-109
Dual-parameter flow cytometric analysis of B-cell antigens and DNA content was used to determine the phenotypes of proliferating tumor cells (S-phase cells) from 30 patients with multiple myeloma. B4 (CD19), J5 (CALLA, CD10), B1 (CD20), and monotypic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07b5cfdc3e6288e10229c40ac5efcd26
https://doi.org/10.1002/ajh.2830330206
https://doi.org/10.1002/ajh.2830330206
Publikováno v:
29th Aerospace Sciences Meeting.
This paper describes a surface grid generation tool called S3D. It is the result of integrating a robust and widely applicable interpolation technique with the latest in workstation technology. Employing the use of a highly efficient and user-friendl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebfff63fde658c5ebe4b7f5345e43028
https://doi.org/10.2514/6.1991-796
https://doi.org/10.2514/6.1991-796
Publikováno v:
Cancer. 51:844-850
Pure red cell aplasia (PRCA) represents selective failure of erythropoiesis in the absence of abnormalities in leukopoiesis or thrombocytopoiesis. Acquired PRCA has occurred uncommonly in chronic lymphocytic leukemia (CLL). We report six patients wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::618892452376626c20b3bf2335474858
https://doi.org/10.1002/1097-0142(19830301)51:5<844::aid-cncr2820510517>3.0.co
https://doi.org/10.1002/1097-0142(19830301)51:5<844::aid-cncr2820510517>3.0.co
Publikováno v:
Blood. 29:540-549
A patient with disseminated eosinophilic collagen disease as reported in the Scandanavian and European literature and perhaps described under various titles—such as eosinophilic leukemia, Loeffler’s syndrome, parietal endocarditis,16 and allergic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa219b53999fd9fca67de694d933830a
https://doi.org/10.1182/blood.v29.4.540.540
https://doi.org/10.1182/blood.v29.4.540.540
Publikováno v:
Blood. 23:200-205
Measurement of various lipid moieties of the nonsickled erythrocytes of patients with sickle cell disease demonstrate an increased concentration of all lipid fractions when compared to a normal similarly aged population of erythrocytes. Highly signif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eaada1db42036b305f4f2350d9758aa8
https://doi.org/10.1182/blood.v23.2.200.200
https://doi.org/10.1182/blood.v23.2.200.200
Autor:
Lawrence E. Pierce, Charles E. Rath
Publikováno v:
Blood. 20:19-32
Two cases are presented of sickle cell anemia demonstrating evidence of folic acid deficiency during a period of anemic crisis. One patient had acute hypoplastic crisis associated with megaloblastic erythropoiesis not in conjunction with acute infect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5aea4a720d8ffa3a6893464f0e54bff6
https://doi.org/10.1182/blood.v20.1.19.19
https://doi.org/10.1182/blood.v20.1.19.19
Publikováno v:
New England Journal of Medicine. 266:505-507
VACUOLIZATION of primitive rubriblasts in the bone marrow has been found to be a feature of early chloramphenicol bone-marrow toxicity.1 , 2 These changes have not previously been observed in other...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d719fe3f7bf32de080fdb28bdcef093
https://doi.org/10.1056/nejm196203082661008
https://doi.org/10.1056/nejm196203082661008
Publikováno v:
Blood; February 1964, Vol. 23 Issue: 2 p200-205, 6p
Autor:
Nicholas P. Anagnou, Entezam A. Sahovic, Alan N. Schechter, Lawrence E. Pierce, Constance Tom Noguchi, Griffin P. Rodgers
Publikováno v:
The American journal of medicine. 80(4)
An 86-year-old black woman admitted for an elective cataract extraction was found to have moderate hypochromic microcytic anemia. Hematologic evaluation disclosed the presence of hemoglobin SC disease and heterozygous alpha-thalassemia-2 (alpha alpha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b0fd6399e30310d42d6bc536bc040f6
https://pubmed.ncbi.nlm.nih.gov/3963052
https://pubmed.ncbi.nlm.nih.gov/3963052
Publikováno v:
The New England journal of medicine. 268
THE red-cell sickling tendency of certain persons has long been a matter of great interest. Study of this problem by Pauling and his associates1 led to the suggestion of a genetic change in hemoglobin formation that resulted in synthesis of different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cfb5a79b12a2dd7b2fe03ac532943f4
https://pubmed.ncbi.nlm.nih.gov/13943409
https://pubmed.ncbi.nlm.nih.gov/13943409