Academic literature on the topic 'CDC'

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Journal articles on the topic "CDC"

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Idigbe, Emmanuel Oni, Rosemary A. Audu, Edna O. Iroha, et al. "T-Lymphocyte Subsets in Apparently Healthy Nigerian Children." International Journal of Pediatrics 2010 (2010): 1–7. http://dx.doi.org/10.1155/2010/474380.

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Population studies showed that there are differences in T-lymphocytes subpopulation of normal children in different regions, and reference values in an area might be different from another. This study compared the values in our population with CDC and WHO reference values. Blood samples from 279 healthy, HIV-negative children<12 years of age were analysed for complete blood count, CD3+, CD4+, CD8+ counts and percentages. Except for CD8%, mean values for all parameters measured significantly decreased with age. CD4+ counts were higher in females than males,P<.05. Using the WHO criteria, 1
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Chatila, T. A., and R. S. Geha. "Phosphorylation of T cell membrane proteins by activators of protein kinase C." Journal of Immunology 140, no. 12 (1988): 4308–14. http://dx.doi.org/10.4049/jimmunol.140.12.4308.

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Abstract Activation of the enzyme protein kinase C (PKC) plays an important role in T cell activation. We investigated the phosphorylation of CD2, CD3, CD4, CD5, CD7, CD8, CD28 (Tp44), CD43 (sialophorin, gp115), and LFA-1 after incubation of human PBMC with the (PKC) activator PMA. These proteins were chosen for their role in transmembrane signal transduction (CD2, CD3, CD5, CD28, CD43), cell-cell interaction and adhesion (CD2, CD4, CD8, and LFA-1), or involvement in immunodeficiency states (CD43, CD7). CD5, CD7, CD43, and the alpha-chain of LFA-1 were found to be constitutively phosphorylated
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Raimondi, SC, FG Behm, PK Roberson, et al. "Cytogenetics of childhood T-cell leukemia." Blood 72, no. 5 (1988): 1560–66. http://dx.doi.org/10.1182/blood.v72.5.1560.1560.

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Abstract The karyotypes of 57 cases of childhood T-cell acute lymphoblastic leukemia (ALL) were analyzed to establish the cytogenetic profile in this disease. Three questions were of particular interest. Do the chromosomal changes in T-cell ALL preferentially affect bands where genes encoding the T-cell receptor for antigen (TCR) have been mapped? Do alterations involving the TCR gene regions appear with any notable frequency in B-progenitor ALL? Do chromosomal abnormalities in this disease relate to stage of T-cell ontogeny? A relatively high proportion of cases (65%) had a pseudodiploid kary
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Raimondi, SC, FG Behm, PK Roberson, et al. "Cytogenetics of childhood T-cell leukemia." Blood 72, no. 5 (1988): 1560–66. http://dx.doi.org/10.1182/blood.v72.5.1560.bloodjournal7251560.

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The karyotypes of 57 cases of childhood T-cell acute lymphoblastic leukemia (ALL) were analyzed to establish the cytogenetic profile in this disease. Three questions were of particular interest. Do the chromosomal changes in T-cell ALL preferentially affect bands where genes encoding the T-cell receptor for antigen (TCR) have been mapped? Do alterations involving the TCR gene regions appear with any notable frequency in B-progenitor ALL? Do chromosomal abnormalities in this disease relate to stage of T-cell ontogeny? A relatively high proportion of cases (65%) had a pseudodiploid karyotype at
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Semchenkova, Alexandra, Ekaterina Mikhailova, Irina Demina, et al. "Analysis of Antigen Expression in T-Cell Acute Lymphoblastic Leukemia by Multicolor Flow Cytometry: Implications for the Detection of Measurable Residual Disease." International Journal of Molecular Sciences 26, no. 5 (2025): 2002. https://doi.org/10.3390/ijms26052002.

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Multicolor flow cytometry (MFC) is a key method for assessing measurable residual disease (MRD) in acute lymphoblastic leukemia (ALL). However, very few approaches were developed for MRD in T-cell ALL (T-ALL). To identify MRD markers suitable for T-ALL, we analyzed the expression of CD2, CD3, CD4, CD5, CD7, CD8, CD10, CD34, CD45, CD48, CD56, CD99, and HLA-DR in T-ALL patients at diagnosis. The median fluorescence intensities (MFIs) of surface CD3, CD4, CD5, CD7, CD8, CD45, CD48, CD99, and CD16+CD56 were also evaluated at Day 15 and the end-of-induction (EOI). The MFC data from 198 pediatric T-
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Amalia, Fatya Alty, Arie Indra Gunawan, and Nono Wibisono. "Citra Destinasi Wisata Halal di Jepang: Wisatawan Dan Non-Wisatawan Muslim Dari Indonesia." Jurnal Bisnis dan Kewirausahaan 17, no. 1 (2021): 1–10. http://dx.doi.org/10.31940/jbk.v17i1.2473.

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Wisata halal merupakan salah satu sektor bisnis halal yang masih berkembang karena banyaknya potensi wisatawan yang masih dapat dimanfaatkan lebih lanjut. Sebagai seorang wisatawan yang memiliki beberapa pilihan destinasi wisata halal, proses pengambilan keputusannya mengenai destinasi yang dipilih dapat sangat dipengaruhi oleh citra destinasi pada atribut wisata halal di destinasi tersebut. Penelitian ini bertujuan untuk mengkaji citra destinasi wisata halal di Jepang dari wisatawan dan non-wisatawan muslim Indonesia. Untuk pendataan dilakukan survey online (Mei-Juni 2020) terhadap umat Islam
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Takamatsu, Hiroyuki, Yoshihiro Yakushijin, Koji Miyazaki, et al. "C-Terminal Defect of CD20 on T-Cell Leukemia/Lymphoma Cells: Implications for Resistance to Rituximab." Blood 112, no. 11 (2008): 5267. http://dx.doi.org/10.1182/blood.v112.11.5267.5267.

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Abstract Rituximab is commonly used for treatment of B-cell leukemia/lymphoma and its efficiency on CD20+ B-cell malignancies has been established. On the other hand, the effect of rituximab on CD20+ T cell leukemia/lymphoma is unclear. Two patients CD20+ T-cell malignancy (1 with T-cell prolymphocytic leukemia (T-PLL) and 1 with peripheral T-cell lymphoma, unspecified (PTCL-u)) were recently treated with rituximab without appreciable effects. The treatment failure prompted a study of the mechanisms underlying the resistance to rituximab therapy using leukemia/lymphoma cells of these patients
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Abbott, Daniel, Steven Kroft, Maria Hintzke, et al. "Immunophenotypic Analysis of Peripheral T-Cell Lymphomas: A Single-Center Retrospective Review of Flow Cytometric Analysis." American Journal of Clinical Pathology 152, Supplement_1 (2019): S109. http://dx.doi.org/10.1093/ajcp/aqz121.012.

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Abstract Background Peripheral T-cell lymphomas (PTCLs) are heterogenous, mature T-cell neoplasms that are a diagnostic challenge, requiring a combination of morphologic assessment and ancillary studies. Flow cytometry (FC) is a tool used routinely in lymphoma diagnosis; however, most analyses are limited to B-cell evaluation and pathologists generally lack experience evaluating for PTCL. We aimed to describe the immunophenotypic aberrancies observed by FC in PTCL. Design PTCLs with FC were collected, excluding primary leukemic processes. Four- and eight-color FC data were reanalyzed with the
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Tjønnfjord, G. E., O. P. Veiby, R. Steen, and T. Egeland. "T lymphocyte differentiation in vitro from adult human prethymic CD34+ bone marrow cells." Journal of Experimental Medicine 177, no. 6 (1993): 1531–39. http://dx.doi.org/10.1084/jem.177.6.1531.

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Pluripotent lymphohematopoietic stem cells are probably confined to bone marrow cells expressing CD34 surface molecules. To investigate the capacity of adult human CD34+ bone marrow cells to differentiate along the T lymphoid lineage, we plated purified CD34+ cells from healthy adults in liquid culture on adherent thymic stromal cells prepared from HLA- or blood group-mismatched postnatal thymic tissue. We show that purified CD34+CD3-CD4-CD8- bone marrow cells contained progenitors with the ability to differentiate into CD4+ and CD8+ T lymphocytes expressing surface (s)CD3 and T cell receptor
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Lukens, Michaël V., Debby Kruijsen, Frank E. J. Coenjaerts, Jan L. L. Kimpen, and Grada M. van Bleek. "Respiratory Syncytial Virus-Induced Activation and Migration of Respiratory Dendritic Cells and Subsequent Antigen Presentation in the Lung-Draining Lymph Node." Journal of Virology 83, no. 14 (2009): 7235–43. http://dx.doi.org/10.1128/jvi.00452-09.

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ABSTRACT In the respiratory tract, different dendritic cell (DC) populations guard a tight balance between tolerance and immunity to infectious or harmless materials to which the airways are continuously exposed. For infectious and noninfectious antigens administered via different routes, different subsets of DC might contribute during the induction of T-cell tolerance and immunity. We studied the impact of primary respiratory syncytial virus (RSV) infection on respiratory DC composition in C57BL/6 mice. We also tracked the migration of respiratory DC to the lymph nodes and studied antigen pre
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Dissertations / Theses on the topic "CDC"

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Hansson, Alexander, and Andreas Petersson. "Mappningsstrategi på IKEA:s CDC-lager i Torsvik." Thesis, Jönköping University, JTH, Industrial Engineering and Management, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-939.

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<p>This study has been assigned by Bengt Hellman who works at the logistic department at IKEA Torsvik just outside of Jönköping. The task has been to develop a new picking strategy for the Oversize area in the CDC-Warehouse. The reason why IKEA wants a new strategy is because they want to minimize the route length for the forklifts when collecting the orders.</p><p>By evaluating the current strategies on other areas in the CDC-storehouse, study literature within this subject and look at restrictions for the storing of goods, we have analyzed how the Oversize area works today. We compared the g
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Ni, Tao. "Structural and functional study of MACPF/CDC superfamily proteins." Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:50793dea-6aa6-4922-b7d8-43c50079639b.

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The thesis mainly focuses on structural study of proteins in membrane attack complex- perforin/cholesterol-dependent cytolysins (MACPF/CDC) superfamily, in particular, Astrotactins from human and perforin-like proteins (PLPs) from Toxoplasma and Plasmodium. Both of these subfamily proteins are implicated in human diseases and structurally uncharacterised before. Astrotactins (ASTNs) have been shown to play a crucial role in enabling neural migration along glial fibres. While ASTN1 directly forms contacts between the neuron and the fibre, ASTN2 is responsible for extracting ASTN1 from contacts
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Patala, Anne Havilah. "Discordance of Drug Susceptibility Test Data between the CDC Mycobacteriology Laboratory and Local Public Health Laboratories Participating in Tuberculosis Clinical Trials, TBTC, CDC." Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/iph_theses/171.

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BACKGROUND: Multi drug resistant Tuberculosis (MDR-TB) is a serious public health concern in many parts of the world. As per the WHO- 2010 global report on Surveillance and response 3.6% of all incident TB cases globally are multidrug resistant. In this regard, there is an increasing demand for timely, reliable and comprehensive drug susceptibility testing (DST) as MDR-TB surveillance is being geared up. The intent of this analysis is to determine whether there is a need to continue routine confirmatory DST testing at CDC in addition to just sending the isolates for genotyping. Analysis is do
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Gordon, Colin B. "Molecular genetics of the cdc 22 gene of Schizosaccharomyces pombe." Thesis, University of Edinburgh, 1985. http://hdl.handle.net/1842/14920.

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Fisher, Daniel Leslie. "Molecular characterization of the fission yeast cyclin B homologue, cdc 13." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308658.

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Moissenet, Didier. "Bacille CDC GROUP IVc-2 : caractérisation, phylogénie, épidémiologie, sensibilité aux antibiotiques." Paris 5, 2006. http://www.theses.fr/2006PA05N05S.

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CDC Group IVc-2 est un bacille à Gram négatif, aérobie strict, mobile grâce à une ciliature péritriche, oxydase et catalase positives et non fermentant. Connu depuis les années 80, il a d'abord été rapproché de Bordetella bronchiseptica puis parfaitement différencié biochimiquement de cette espèce en 1986 par Pickett (87). Sa position taxonomique longtemps indéterminée a été précisée en 1999 (74, 83, 116) et nous y avons contribué (74). Bactérie de l'environnement hydrique (7, 63, 82). .<br>Our study of CDC Group IVc-2 began in 1995 with the report of five bacteriema at Trousseau hospital (APH
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Funnell, Tyler. "Transcriptomic consequences of RNA processing disruption via a novel CDC-like kinase inhibitor." Thesis, University of British Columbia, 2014. http://hdl.handle.net/2429/51614.

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RNA splicing is a process by which introns are excised from precursor mRNA. Variations in the segments removed — and the resulting mRNA molecule — may result in gene transcripts with differing and even opposing functions. The mechanisms involved in RNA splicing are tightly regulated, the disruption of which has been implicated in several human diseases including cancer. This presents the RNA splicing machinery as a potential therapeutic target. However, the effects of systematic splicing modulation through pharmaceutical intervention remain under explored. A thorough understanding of splicin
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Fava, Marina Dubois. "Aplicação das normas do CDC aos contratos interempresariais: a disciplina das cláusulas abusivas." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/2/2132/tde-01122010-154105/.

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O presente estudo tem por objetivo demonstrar a necessidade de se tutelar a desigualdade substancial existente nas relações contratuais celebradas entre empresários, quando uma das partes, ainda que profissional, encontrar-se em situação de dependência econômica, favorecendo o abuso da parte contrária na situação concreta. O cerne do trabalho gira em torno do problema das cláusulas abusivas no âmbito dos contratos interempresariais. Busca-se demonstrar que, nas hipóteses em que não for possível repreendê-las por meio da aplicação do Código Civil ou da Lei Antitruste, seria possível equiparar o
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Small, Lawrence Edward. "PAR Proteins Regulate CDC-42-Dependent Myosin Dynamics During C. elegans Zygote Polarization." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1461086954.

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Lai, Man-kit, and 黎文傑. "Junior secondary pupils' learning in the biological concepts included in the CDC science (Forms I-III) syllabus 1986 and prerequisite forthe CDC human biology (Secondary IV-V) syllabus 1987 of Hong Kong." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1988. http://hub.hku.hk/bib/B31955794.

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Books on the topic "CDC"

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Coach Drivers Club of Great Britain. CDC yearbook. CDC, 1999.

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Instruments, Texas. CDC clock-distribution circuits. Texas Instruments, 1994.

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Board, National Institutes of Health (U S. ). Patent Policy. NIH/ADAMHA/CDC technology transfer. The Centers, 1992.

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Centers for Disease Control (U.S.), ed. CDC reports on injury control. Dept. of Health & Human Services, Public Health Service, Centers for Disease Control, 1985.

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Ogden, Horace G. CDC and the smallpox crusade. U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control, 1987.

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Ogden, Horace G. CDC and the smallpox crusade. U.S. DHHS, PHS, Centers for Disease Control, 1987.

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Association, American Public Health, and Center for Disease Control (U.S.), eds. APHA-- CDC recommended minimum housing standards. American Public Health Association, 1986.

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National Center for Injury Prevention and Control (U.S.). CDC injury research agenda: 2009-2018. U.S. Dept. of Health and Human Services, Centers for Disease Control and Prevention, National Center for Injury Prevention and Control, 2009.

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HHS/CDC-Ethiopia. HHS/CDC-Ethiopia: 2001-2003 report. HHS/CDC-Ethiopia, 2004.

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Pontus, Aspenstrøm, ed. The pombe Cdc 15 homology proteins. Landes Bioscience, 2009.

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Book chapters on the topic "CDC"

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Lackner, K. J., and D. Peetz. "CDC-Referenzmethode." In Springer Reference Medizin. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_696.

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Lackner, K. J., and D. Peetz. "CDC-Referenzmethode." In Lexikon der Medizinischen Laboratoriumsdiagnostik. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-49054-9_696-1.

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Steele, Guy L., Xiaowei Shen, Josep Torrellas, et al. "CDC 6600." In Encyclopedia of Parallel Computing. Springer US, 2011. http://dx.doi.org/10.1007/978-0-387-09766-4_2107.

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Ibbett, R. N., and N. P. Topham. "The CDC Series." In Architecture of High Performance Computers. Springer New York, 1989. http://dx.doi.org/10.1007/978-1-4899-6712-1_9.

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Baumann, Chris, Hume Winzar, and Doris Viengkham. "CDC Over Time." In Confucianism, Discipline, and Competitiveness. Routledge, 2019. http://dx.doi.org/10.4324/9781351062220-4.

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Ibbett, R. N., and N. P. Topham. "The CDC Series." In Architecture of High Performance Computers. Macmillan Education UK, 1989. http://dx.doi.org/10.1007/978-1-349-19757-6_9.

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Schneck, Paul B. "The CDC 6600." In The Kluwer International Series in Engineering and Computer Science. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4615-7957-1_3.

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Knowlton, Christin A., Michelle Kolton Mackay, Tod W. Speer, et al. "Complement-Dependent Cytotoxicity (CDC)." In Encyclopedia of Radiation Oncology. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-540-85516-3_678.

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Churiwala, Sanjay, and Sapan Garg. "Clock Domain Crossing (CDC)." In Principles of VLSI RTL Design. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-9296-3_4.

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Schneck, Paul B. "The CDC STAR-100." In The Kluwer International Series in Engineering and Computer Science. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4615-7957-1_5.

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Conference papers on the topic "CDC"

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Theodoro, Flavia Cristine Medeiros, Luiz Eduardo Nazario Mendes, Lucas de Oliveira Costa, et al. "Identificação dos casos de doenças linfoproliferativas de células T em pacientes de Natal, Rio Grande do Norte, entre 2020 e 2022." In Resumos do 56º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2024. https://doi.org/10.5327/1516-3180.142s1.12275.

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Objetivo: As doenças linfoproliferativas crônicas (DLPC) pertencem a um grupo de neoplasias linfoides caracterizadas pela expansão monoclonal e pelo acúmulo de linfócitos maduros, podendo ser de células B, T e células natural Killer (NK). As doenças linfoproliferativas crônicas de células T (DLPC-T) são menos frequentes e têm o diagnóstico estabelecido pela detecção de fenótipos aberrantes, tais como alterações da relação CD4/CD8, presença de células T CD4+/CD8+ e ausência de antígenos Pam-T, como CD3 e CD7. A caracterização dessas entidades é, na maioria das vezes, mais difícil quando compara
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Borges, JPD, ISMA Sousa, TF Silva, et al. "APLICAÇÃO DA IMUNOFENOTIPAGEM POR CITOMETRIA DE FLUXO NO DIAGNÓSTICO DE DOENÇA LINFOPROLIFERATIVA." In Resumos do 55º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s2.7397.

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Objetivo: A síndrome de Sézary (SS) é uma variante leucêmica rara que corresponde a 2% dos casos de linfomas cutâneos de células T. Caracteriza-se por eritrodermia, linfadenopatia periférica e presença de células de Sézary na pele, nos linfonodos e no sangue. As células de Sézary são linfócitos T maduros, de tamanho pequeno a médio, com núcleos convolutos, exibindo fenótipo CD3+, CD4+, CD8-, com perda variável da expressão de CD7(1,2). Este relato objetivou descrever e correlacionar os achados laboratoriais na elucidação de um caso de evolução de micose fungoide para SS. Método: Paciente E. S.
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Наджафова, В. А. к. "Оценка нарушений субпопуляций лимфоцитов у детей с железодефицитной анемией". У General question of world science. Наука России, 2021. http://dx.doi.org/10.18411/gq-31-07-2021-03.

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Статья посвящена проблеме нарушения иммунитета у детей с железодефицитной анемией (ЖДА), проживающих в Азербайджане. Были выявлены более низкие показатели клеточного иммунитета (CD3, CD4, CD8). Относительное количество клеток CD3 в общей группе детей с ЖДА составило 52,7±4,35%, в контрольной группе - 62,6±5,49%, р&lt;0,05. Проведенные исследования выявили положительную корреляцию клеток CD3, CD4, CD8 с гемоглобином и сывороточным железом. Результаты высокой силы связи коэффициента корреляции сывороточного железа с относительным количеством клеток CD3 и CD4 в общих группах детей с ЖДА (r = 0,8)
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Kasteckas, JB, N. Medeiros Junior, AC Carvalho, AR Rinaldi, and RMF Souza. "SÍNDROME DE SÉZARY: RELATO DE CASO EM UM PACIENTE DE HOSPITAL TERCIÁRIO." In Resumos do 54º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2022. http://dx.doi.org/10.5327/1516-3180.140s1.6236.

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Objetivo: Relatar um caso clínico de síndrome de Sézary (SS), destacando a importância do estudo morfológico das células de Sézary. Método: Consulta aos dados clínicos em um prontuário eletrônico; realização de hemograma automatizado e revisão morfológica por microscopia óptica convencional. Caso: M. A. O., 56 anos de idade, sexo feminino, apresentando ao exame físico áreas de eritrodermia com ilhas de pele sã e atrofia em palmas, sendo aventada a hipótese diagnóstica de micose fungoide. Exames complementares: Hb 12,6; Ht 37,6; leucócitos 10190 (neutrófilos 5620 + linfócitos 3780); pesquisa de
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Ni, Fan, Xing Lin, and Song Jiang. "SS-CDC." In SYSTOR '19: The 12th ACM International Systems and Storage Conference. ACM, 2019. http://dx.doi.org/10.1145/3319647.3325834.

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Rana, Seema, and Rajiv Tangri. "Anaplastic large cell lymphoma ALK negative vs. peripheral T cell lymphoma (NOS) - diagnostic dilemma." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685354.

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Middle aged female presented with generalised lymphadenopathy and fever for last one month. Peripheral blood findings were within normal limits. There was no extra nodal involvement. FNAC performed initially from a cervical node suggested possibility of Hodgkin’s lymphoma and a whole node biopsy was performed. Histopathogical examination revealed effaced nodal architecture and a polymorphous population of lymphocytes, plasma cells, neutrophils and scattered large mononuclear cells with prominent nucleolus. An initial panel of CD3, CD20, LCA, CD15, CD30 and PAX5 was performed. The large atypica
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Sousa, I., BL Scarpato, CMR Franzon, AOM Wagner, and ACW Lopes. "RELATO DE CASO: DIAGNÓSTICO DIFERENCIAL ENTRE LINFOMA LINFOBLÁSTICO T E TIMOMA." In Resumos do 54º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2022. http://dx.doi.org/10.5327/1516-3180.140s1.6177.

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Objetivo: O linfoma linfoblástico T (LBL-T) e o timoma são neoplasias mediastinais primárias distintas que podem ter apresentações clínicas, características morfológicas e imunofenotípicas semelhantes. Um diagnóstico preciso é importante, uma vez que as abordagens de tratamento diferem consideravelmente. O presente estudo relata o caso de uma paciente jovem com massa mediastinal, no qual foi necessário fazer o diagnóstico diferencial entre timoma e LBL-T. Método: Paciente do sexo feminino, 20 anos de idade, com massa mediastinal, tamponamento cardíaco e síndrome de compressão de veia cava. O m
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Theodoro, Flávia Cristine M., Luiz Eduardo Nazario Mendes, Lucas de Oliveira Costa, et al. "Estudo de caso: citometria de fluxo no diagnóstico de leucemia de células vilosas." In Resumos do 56º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2024. https://doi.org/10.5327/1516-3180.142s1.12213.

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Objetivo: A leucemia de células vilosas (LCV), também conhecida como hairy cell leukemia (HCL), compreende uma doença linfoproliferativa maligna de células B maduras, clonal, caracterizada pela presença de linfócitos anômalos com projeções citoplasmáticas semelhantes a fios de cabelo. O comportamento clínico dessa doença está relacionado à infiltração da medula óssea (MO), baço, entre outros tecidos linfoides, podendo acometer o sangue periférico (SP). Os achados laboratoriais da LCV compreendem a citopenia periférica e medular com presença de leucopenia, trombocitopenia e anemia na maioria do
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"Special CDC sessions." In 2008 47th IEEE Conference on Decision and Control. IEEE, 2008. http://dx.doi.org/10.1109/cdc.2008.4738575.

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"CDC 2024 Commentary." In 2024 IEEE 63rd Conference on Decision and Control (CDC). IEEE, 2024. https://doi.org/10.1109/cdc56724.2024.10886665.

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Reports on the topic "CDC"

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Chitanvis, Maneesha Elizabeth. LANL biosurveillance tools at CDC. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1361464.

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Yamada, R., J. Hawtree, K. Kaczar, et al. CDC field mapping device - ''ROTOTRACK''. Office of Scientific and Technical Information (OSTI), 1985. http://dx.doi.org/10.2172/6459052.

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Cohen, Robin, Elizabeth Briones, and Inderbir Sohi. https://stacks.cdc.gov/view/cdc/174610. National Center for Health Statistics (U.S.), 2025. https://doi.org/10.15620/cdc/174610.

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Galea, Sandro, Lawrence Gostin, Alan B. Cohen, and Nicole Lurie. Eight Operational Suggestions for a Renewed CDC. Milbank Memorial Fund, 2021. http://dx.doi.org/10.1599/mqop.2021.0105.

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Menon, Shantanu, Aruna Pandey, Kushagra Merchant, and Satender Rana. Community Development Centre (CDC): A covenant with the Baiga (tribe). Indian School Of Development Management, 2022. http://dx.doi.org/10.58178/2208.1004.

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"This case engages with the journey of Community Development Centre (CDC), a small non-profit organization operating in the Mahakaushal region of Madhya Pradesh for over two decades. The case demonstrates how CDC has created a resilient and responsive organizational culture in a remote and resource-starved environment to address multiple developmental challenges of the region and in particular, of the most marginalized Baiga tribe within it. It underscores the importance of a firm conviction in the cause as a precondition of talent which works in such a context. It draws attention to the persi
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Parsa, Z., and E. Courant. Guide to Accelerator Physics Program Synch - CDC Version. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/1151180.

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Parsa, Zohreh. Guide to VAX, CDC, and IBM 3090 Third Edition. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/1118914.

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Hoerger, Thomas, Joel Segel, Ping Zhang, and Stephen Sorensen. Validation of the CDC-RTI Diabetes Cost-Effectiveness Model. RTI Press, 2009. http://dx.doi.org/10.3768/rtipress.2009.mr.0013.0909.

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Ferron, J. R. User`s manual for the CDC-1 digitizer controller. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10181403.

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Hollander, Attelia. Diagnostic Testing for COVID-19 Bridging Study for CDC EUA assays vs CDC Multiplex N1 FAM, N2 SUN, RNAse P ATTO 647 Assays. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1766983.

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