Academic literature on the topic 'HISCO'
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Journal articles on the topic "HISCO"
NAYAK, BIBHUTI B., NADIYA BIHARY NAYAK, RAHUL KUMAR MALLIK, and APARNA MONDAL. "SYNTHESIS AND MAGNETIC PROPERTIES OF COBALT FERRITE WITH DIFFERENT MORPHOLOGIES." International Journal of Modern Physics: Conference Series 22 (January 2013): 164–68. http://dx.doi.org/10.1142/s2010194513010064.
Full textBrik, Tymofii. "Social Estates, Occupation, and HISCO: A New Study of Odesa in 1897." East/West: Journal of Ukrainian Studies 9, no. 2 (October 26, 2022): 19–42. http://dx.doi.org/10.21226/ewjus594.
Full textProcanin, B. "Barbara Procanin Sales Engineer, Hisco Registration Committee [EIC Volunteer Profile]." IEEE Electrical Insulation Magazine 22, no. 1 (January 2006): 41. http://dx.doi.org/10.1109/mei.2006.1618971.
Full textDRIBE, MARTIN, and CHRISTER LUNDH. "Partner choice and intergenerational occupational mobility: the case of nineteenth-century rural Sweden." Continuity and Change 24, no. 3 (November 24, 2009): 487–512. http://dx.doi.org/10.1017/s0268416009990178.
Full textFONSECA, HÉLDER ADEGAR, and PAULO EDUARDO GUIMARÃES. "Social mobility in Portugal (1860–1960): operative issues and trends." Continuity and Change 24, no. 3 (November 24, 2009): 513–46. http://dx.doi.org/10.1017/s026841600999018x.
Full textZhao, Jun Xue, Jun Fan, Yuan Ping Chen, and Peng Fei Wang. "Analysis on the Cause of Longitudinal Crack on the Hot-Rolled Ribbed Bar Surface." Advanced Materials Research 295-297 (July 2011): 934–38. http://dx.doi.org/10.4028/www.scientific.net/amr.295-297.934.
Full textKondo, Naru, Kenichiro Uemura, Naoya Nakagawa, Kenjiro Okada, Shintaro Kuroda, Takeshi Sudo, Naoto Hadano, et al. "A Multicenter, Randomized, Controlled Trial Comparing Reinforced Staplers with Bare Staplers During Distal Pancreatectomy (HiSCO-07 Trial)." Annals of Surgical Oncology 26, no. 5 (February 19, 2019): 1519–27. http://dx.doi.org/10.1245/s10434-019-07222-0.
Full textGoh, Brian K. P. "A Multicenter, Randomized, Controlled Trial Comparing Reinforced Staplers with Bare Staplers During Distal Pancreatectomy (HiSCO-07 Trial)." Annals of Surgical Oncology 27, S3 (March 27, 2020): 948–49. http://dx.doi.org/10.1245/s10434-020-08401-0.
Full textShimomura, Manabu, Satoshi Ikeda, Masahiro Nakahara, Tomohiro Adachi, Yasufumi Saitoh, Yosuke Shimizu, Kazuhiro Toyota, et al. "Prospective cohort study of patients with stage III colorectal cancer aged ≥ 80 years who underwent curative resection: The HiSCO-04 study." Journal of Clinical Oncology 41, no. 4_suppl (February 1, 2023): 102. http://dx.doi.org/10.1200/jco.2023.41.4_suppl.102.
Full textWestberg, Annika, Elisabeth Engberg, and Sören Edvinsson. "A Unique Source for Innovative Longitudinal Research: The POPLINK Database." Historical Life Course Studies 3 (March 15, 2016): 20–31. http://dx.doi.org/10.51964/hlcs9351.
Full textDissertations / Theses on the topic "HISCO"
Buchs, Jean-Paul. "Das ABO-Histo-Blutgruppensystem /." Bern, 1991. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.
Full textLe, Bars Pierre. "Etude histo-immunologique de la stomatite prothetique." Nantes, 2000. http://www.theses.fr/2000NANT23VS.
Full textBarbé, Laure. "Spécificité d’attachement sur les glycannes, vers une amélioration des vaccins rotavirus." Thesis, Nantes, 2018. http://www.theses.fr/2018NANT1017/document.
Full textHuman strains of rotavirus A (RVAs) recognize fucosylated glycans of the histo-blood group family (HBGAs) as well as gangliosides through the VP8* protein of their capsid. Interaction with gangliosides is essential for cell entry and lack of fucosylated ligands due to HBGAs genetic polymorphism is associated with resistance to RVA gastroenteritis. Our goals are to delineate the contribution of HBGAs and gangliosides in the infection process and to explore the consequences of HBGAs polymorphisms on the virus transmission and efficacy of the available live vaccines. This study highlighted the concordance between the glycan specificity of P[8] VP8*, the most common genotype in France, and the HBGA-dependant susceptibility to RVA gastroenteritis. The recognition of HBGAs by human RVA strains therefore appears essential to the infection. Yet, our results suggest that HBGA binding corresponds to an early event since it is not required for infection of poorly differentiated cells by cell culture-adapted P[8] strains. The contribution of GM1a on infection remains unclear. Finally, we showed that HBGA recognition is conserved between recent and older P[8] strains, suggesting that HBGAs polymorphism may contribute to explain the low efficacy of vaccines in areas where the frequency of individuals who do not express fucosylated ligands is high
Miola, Marcos Paulo. "Resolução de discrepâncias do Sistema histo-sanguíneo ABO." Faculdade de Medicina de São José do Rio Preto, 2017. http://hdl.handle.net/tede/392.
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Introduction. ABO histo-blood group system is the most important transfusional system and the identification of its phenotypes is often performed by means of direct and reverse typing, which must always present concordant results. However, some genetic factors such as natural chimerisms and point mutations in the ABO gene may affect the expression of the antigens and antibodies of this system, contributing to the discrepancy in the phenotyping, requiring investigations to define the correct phenotype of receptors and blood donors. Objectives. The main objective of this study was to investigate the variations in the expression of the antigens of the ABO histo-blood group system. Its specific objectives were: 1. Selection of recipients and blood donors that presented discrepancies between the results of the direct and reverse phenotyping of the ABO histo-blood group system; 2. Investigation, using serological and molecular methods, of the causes of phenotypic changes and discrepancies between the results of direct and reverse phenotypes in the ABO histo-blood group system in the recipients and donors of blood. Material and Methods. Samples of recipients (n = 2) and blood donors (n = 7) presenting discrepancies between the direct and reverse phenotyping were selected. Phenotyping were performed using conventional and modified hemagglutination methods in tubes and gel columns with commercial antisera and lectins. Molecular investigations were performed using PCR-RFLP method and sequencing of exons 6 and 7 of the ABO gene and exon 2 of the FUT2 gene. Results. Four cases with poor expression of antigen A and absence of expected antibody, observed in hemagglutination, were identified as A2B, Ael and Aw. Four cases without antigenic alteration but carrying an irregular antibody anti-A1 or absence of expected antibody were characterized as AB, A1 and O and presented common ABO alleles. A case of non-dizygotic twins, phenotyped as AB and with double red blood cell population was characterized as hematopoietic chimera after extensive family analysis. The DNA extracted from buccal swab revealed the ABO (A101/B101) and FUT2 (SE*25.01.01/SE*25.01.01) genotypes in the male twin and the ABO (O01/O02) and FUT2 (SE*01.04.01/SE*01.06.03) genotypes in the female twin. Sequences of two new ABO (ABO*Aw.38; KT906366.1) and FUT2 (SE*01.06.03; KX550421) allele sequences were deposited on GenBank. Conclusions. Our results demonstrate that the use of serum and salivary serological assays combined with molecular methods are good tools to solving discrepancies between the direct and reverse phenotyping of the ABO histo-blood group system as well as elucidate cases of twin chimerism in humans, with a double population of red blood cells. In addition, they contribute to the identification of new alleles of the ABO and FUT2 genes.
Introdução. O sistema histo-sanguíneo ABO é o de maior importância transfusional e a identificação de seus fenótipos é frequentemente realizada por meios das tipagens direta e reversa as quais sempre devem apresentar resultados concordantes. Entretanto, alguns fatores genéticos como quimerismos naturais e mutações pontuais no gene ABO, podem afetar a expressão dos antígenos e anticorpos deste sistema, contribuindo com a discrepância nas fenotipagens, requerendo investigações para se definir o correto fenótipo de receptores e doadores de sangue. Objetivos. O objetivo geral deste estudo foi investigar as variações na expressão dos antígenos do sistema histo-sanguíneo ABO. Seus objetivos específicos compreenderam: 1. Seleção de receptores e doadores de sangue que apresentaram discrepâncias entre os resultados das fenotipagens direta e reversa do sistema histo-sanguíneo ABO; 2. Investigação, com o uso de métodos sorológicos e moleculares, das causas das alterações fenotípicas e discrepâncias entre os resultados das fenotipagens direta e reversa no sistema histo-sanguíneo ABO nos receptores e doadores de sangue. Material e Método. Foram selecionadas amostras de receptores (n=2) e doadores (n=7) de sangue com discrepâncias entre as fenotipagens direta e reversa. As fenotipagens foram realizadas com o uso dos métodos de hemaglutinação convencional e modificada, em tubos e colunas de gel, com antissoros comerciais e lectinas. As investigações moleculares foram realizadas com o uso dos métodos PCR-RFLP e sequenciamento dos exons 6 e 7 do gene ABO e do exon 2 do gene FUT2. Resultados: Quatro casos com fraca expressão do antígeno A e ausência do anticorpo esperado, observados na hemaglutinação, foram identificados como A2B, Ael e Aw. Quatro casos sem alteração antigênica, mas com presença de anticorpo irregular ou ausência do anticorpo esperado, foram caracterizados como AB, A1 e O e apresentaram alelos comuns. Um caso de gêmeos não dizigóticos, fenotipados como AB e com dupla população de hemácias foi caracterizado como quimera hematopoiética, após extensa análise familiar. O DNA extraído de swab bucal revelou os genótipos ABO (A101/B101) e FUT2 (SE*25.01.01/SE*25.01.01) no gêmeo masculino e os genótipos ABO (O01/O02) e FUT2 (SE*01.04.01/SE*01.06.03) no gêmeo feminino. As sequências de dois novos alelos dos genes ABO (ABO*Aw.38; KT906366.1) e FUT2 (SE*01.06.03; KX550421) foram depositadas no GenBank. Conclusões: Nossos resultados demonstram que o uso de análises sorológicas eritrocitárias e salivares combinadas a métodos moleculares são fundamentais na resolução de discrepâncias entre as fenotipagens direta e reversa do sistema histo-sanguíneo ABO bem como no esclarecimento de casos de quimerismo gemelar em humanos, contendo dupla população de hemácias. Além disso, contribuem para a identificação de novos alelos dos genes ABO e FUT2.
Becker, Philippe. "Etude histo-enzymologique du muscle oculaire droit interne." Nancy 1, 1988. http://www.theses.fr/1988NAN11283.
Full textVaglio, Giovanna. "Analyse histo-morphométrique des vaisseaux sanguins du ligament parodontal bovin /." Genève : [s.n.], 2008. http://opac.nebis.ch/cgi-bin/showAbstract.pl?sys=000253997.
Full textBrückner, Stella. "Histo- und cytochemische Untersuchung der Zwischenwirbelscheibe des Rhesusaffen (Macaca mulatta)." Diss., lmu, 2004. http://nbn-resolving.de/urn:nbn:de:bvb:19-18952.
Full textLuciene, Della Libera Miguel. "Associação entre o sistema histo-sanguíneo ABO e mucosite oral." Faculdade de Medicina de São José do Rio Preto, 2016. http://hdl.handle.net/tede/405.
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Introduction: Oral mucositis is one of the most frequent diseases resulting from the side effects of Chemotherapy and Radiotherapy. In addition to compromising the quality of life, it increases the risk of infections, especially in patients undergoing bone marrow transplantation. However, genetic risk factors related to the susceptibility to this disease have not been fully clarified. Objectives: The aim of this study was to verify whether there is an association between ABO blood group phenotyping and oral mucositis. Methods: Data were selected from two hundred twenty nine records of patients undergoing HSCT in the Unit of Bone Marrow Transplantation of Hospital de Base São José do Rio Preto; out from the underlying disease between March 2006 and March 2012. Group 1 (G1) comprised data from patients with mucositis demonstrations after HSCT; Group 2 (G2) comprised patients without data mucositis demonstrations after HSCT. The Chi-Square and Fisher Exact tests were used for comparison of proportions between patients with and without oral mucositis and other risk factors. The mean of ages was calculated using the t test. The values of Odds Ratio (OR) and confidence intervals (CI) of 95% were also calculated (p <0.05). Results: No statistically significant differences were observed in the frequency of erythrocyte phenotypes of the ABO blood group in patients with and without oral mucositis (χ2: 2.654, p = 0.448, DF = 3). Statistically significant differences were found between the frequencies of the ABO blood group phenotypes when comparisons were related to the type of transplantation, conditioning and degree of oral mucositis. Conclusion: ABO blood group is not associated to the occurrence of oral mucositis in patients undergoing bone marrow transplantation.
Introdução: Mucosite oral é uma das mais frequentes doenças resultantes dos efeitos colaterais de quimioterápicos e radioterápicos. Além de comprometer a qualidade de vida, aumenta os riscos de infecções, especialmente em pacientes submetidos ao transplante de medula óssea. Contudo, fatores de risco genéticos envolvidos na suscetibilidade a esta doença ainda não foram totalmente esclarecidos. Objetivos: O objetivo geral deste estudo foi verificar se há associação entre os fenótipos eritrocitários do sistema histo-sanguíneo ABO e a mucosite oral. Casuística e Método: Foram selecionados dados de duzentos e vinte nove prontuários de pacientes submetidos ao TCPH na Unidade de Transplante de Medula Óssea do Hospital de Base de São José do Rio Preto, independente da doença de base, entre Março de 2006 e Março de 2012. O grupo 1 (G1) compreendeu dados de pacientes com manifestações de mucosite, após o TCPH; o grupo 2 (G2) compreendeu dados de pacientes sem manifestações de mucosite, após o TCPH. Os testes exato de Fisher e qui-quadrado foram utilizados para comparação das proporções entre pacientes com e sem mucosite oral e outros fatores de risco. As médias de idade foram calculadas com o uso do teste t. Os valores de Odds Ratio (OR) e de intervalos de confiança (IC) a 95% também foram calculados (p<0,05). Resultados: Não foram observadas diferenças estatisticamente significantes nas frequências dos fenótipos eritrocitários do sistema histo-sanguíneo ABO em pacientes com e sem mucosite oral (χ2: 2.654, p = 0.448, GL = 3). Também não foram observadas diferenças estatisticamente significantes entre as frequências dos fenótipos eritrocitários ABO quando as comparações compreenderam tipo de transplante, condicionamento e graus de mucosite oral. Conclusão: O sistema histo-sanguíneo ABO não está associado à ocorrência de mucosite oral em pacientes submetidos ao transplante de medula óssea.
Fernandes, Sandra Regina Muchinechi 1954. "Poliarterite nodosa : contribuição ao estudo clinico, laboratorial, histo-patologico e angiografico." [s.n.], 1993. http://repositorio.unicamp.br/jspui/handle/REPOSIP/310426.
Full textTese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciencias Medicas
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Resumo: Foram estudados 20 casos de Poliarterite Nodosa (PAN), quanto à freqüência das manifestações clínicas, alterações laboratoriais e dados histopatológicos e arteriográficos. A PAN sistêmica foi caracterizada em 16 casos e a PAN cutânea benigna em quatro. Em relação aos sintomas gerais na PAN sistêmica oito tiveram febre e 11 emagrecimento, sugerindo doença sistêmica, em oposição aos quatro restantes que não tinham essas evidências, mas apresentavam microaneurismas em artérias renais. Artralgia ou artrite esteve presente em oito casos e neuropatia periférica em seis. Envolvimento renal foi constatado em oito casos, sendo hipertensão arterial em sete, hematúria em cinco, proteinúria em quatro e insuficiência renal em três. Manifestações pulmonares, cardíacas e do sistema nervoso central foram infrequentes. A idade de inicio superior a 50 anos, a presença de manifestações musculares, gastrointestinais e hematúria foram elementos significativos nos casos que evoluiram ao óbito. No laboratório, os dados hematológicos foram inespecíficos revelando leucocitose, anemia e VHS elevado. De oito casos investigados dois apresentaram antígeno HBsAg. ANCA resultou negativo em todos os sete investigados. Cinco em seis biopsiados na pele evidencia~am dados histopatológicos de vasculite necrosante, sugerindo que este procedimento é importante para nortear o diagnóstico da PAN sistêmica, embora sem distingui-Ia da PAN cutânea. A biópsia muscular, revelou-se positiva apenas em dois de um total de cinco examinados. A histopatologia renal, foi a mais marcante, visto que todos os casos examinados revelaram vasculite necrosante extraglomerular não deixando dúvida quanto ao diagnóstico. Seis em onze casos apresentaram alterações à arteriografia renal, cinco com microaneurismas e um com diminuição do lume vascular. Não obstante este achado, três tinham cifras pressóricas normais e quatro sem evidências de alterações renais pela analise do sedimento urinário. A arteriografia renal foi o procedimento diagnóstico em três casos. A PAN cutânea revelou-se de evolução e prognóstico benignos nos quatro casos estudados. Nestes, os dados laboratoriais, sejam da doença ou das complicações viscerais apresentaram-se constantemente normais ou ausentes. Numa escala de valores de procedimentos diagnósticos, lado dos dados clínicos que, em sua maioria, se assemelhavam aos da literatura, a biópsia de pele lesada revelou-se o dado mais marcante seguida pela arteriografia renal
Abstract: Twenty patients with polyarteritis nodosa (PAN) were studied to determine the clinical, laboratorial, histologic and renal arteriogram features. Sixteen patients presented the systemic subset and four had the characteristics of cutaneous PAN. Constitutional symptoms such as fever and weight lass was observed in eight and 11 patients with systemic PAN respectively. Four patients didn't present these manifestations but had aneurysms in renal arteriograms. Joint involvement and peripheral neuropathy were common. Renal manifestations were observed in eight cases, seven of them with hypertension, urinary protein in four, hematuria in five and renal insufficiency in three. Pulmonary, cardiac and cerebrovascular involvement were rarely seem. Age of onset the disease superior to 50 years, gut involvement, hematuria and muscle manifestations were associated with a worse prognosis. Leukocytosis, anemia and elevated ESR were often detected, but were not diagnostic. Serum hepatitis B surface antigen determinations were performed in eight cases and in two were positive. ANCA was negative in alI seven performed. Six clinically involved skin was biopsied, and it revealed necrotizing vasculitis in alI but one. This procedure was important to make the diagnosis of a systemic PAN, although this histologic features is the same of cutaneous PAN. Skeletal muscle was biopsied in five cases and revealed vasculitis in only two. AlI renal samples showed extraglomerular necrotizing vasculitis. Renal arteriograms were performed in 11 patients and revealed aneurysms in five and reduced lume in another. Of these six cases, three didn't had hypertension and four had a normal urine sediment Renal arteriograms defined a diagnosis of systemic PAN in three cases. The cases of cutaneous PAN had a benign course, with exacerbations and remissions that never showed systemic involvement. The laboratorial findings were essentially normal
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Bulut, Murat. "Kinetics of methane adsorption on HiPco purified single-walled carbon nanotubes /." Available to subscribers only, 2008. http://proquest.umi.com/pqdweb?did=1594488051&sid=1&Fmt=2&clientId=1509&RQT=309&VName=PQD.
Full textBooks on the topic "HISCO"
1964-, Maas I., and Miles Andrew 1961-, eds. HISCO: Historical international standard classification of occupations. Leuven, Bilgium: Leuven University Press, 2002.
Find full textMarco H.D. van Leeuwen. HISCO: Historical International Standard Classification of Occupations. Leuven: Leuven University Press, 1998.
Find full textIse, Akifumi. Daigishi hisho no himitsu: Yūnōna hisho damena hisho no miwakekata. Tōkyō: Ēru Shuppansha, 1999.
Find full textDōmoto, Hisao. Dōmoto Hisao Ten: Hisao Domoto, retrospective. [Kyoto]: Kyōto Kokuritsu Kindai Bijutsukan, 2005.
Find full textŌsaka Shōsen Mitsui Senpaku Kabushiki Kaisha., ed. Tsuisōroku Fukuda Hisao. Tōkyō: Ōsaka Shōsen Mitsui Senpaku Kabushiki Kaisha, 1985.
Find full textBook chapters on the topic "HISCO"
Webb, Benjamin L. J., David Holmes, Chun Li, Jin Z. Zhang, and Matthew T. Lloyd. "High-Pressure Carbon Monoxide (HiPCO)." In Encyclopedia of Nanotechnology, 1022. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-9751-4_100297.
Full textShirato, Haruko. "Norovirus and Histo-Blood Group Antigens." In Glycoscience: Biology and Medicine, 1–5. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54836-2_146-1.
Full textShirato, Haruko. "Norovirus and Histo-Blood Group Antigens." In Glycoscience: Biology and Medicine, 731–35. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54841-6_146.
Full textGlick, David. "Principles of Enzymic Histo- and Cytochemistry." In Advances in Enzymology - and Related Areas of Molecular Biology, 585–611. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/9780470122549.ch10.
Full textGreiner, Rasmus. "Introduction." In Cinematic Histospheres, 1–16. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-70590-9_1.
Full textLe Pendu, Jacques. "Histo-Blood Group Antigen and Human Milk Oligosaccharides." In Advances in Experimental Medicine and Biology, 135–43. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4757-4242-8_13.
Full textLeuther, Joachim. "Ziele, Management, Erfahrungen strategischer Wertschöpfungspartnerschaften — das Beispiel Hiscox." In Strategische Kooperationen in der Versicherungsbranche, 35–50. Wiesbaden: Gabler Verlag, 2004. http://dx.doi.org/10.1007/978-3-663-01567-3_2.
Full textMilton, Leanne Wiberg. "The Hico Impact Structure of North-Central Texas." In Research in Terrestrial Impact Structures, 131–40. Wiesbaden: Vieweg+Teubner Verlag, 1987. http://dx.doi.org/10.1007/978-3-663-01889-6_7.
Full textHakomori, Sen-itiroh, and Monica Palcic. "Histo-Blood Group A Variants, O Variants, and Their Alleles." In Handbook of Glycosyltransferases and Related Genes, 479–93. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54240-7_159.
Full textKatthagen, B. D., and H. Mittelmeier. "Histo-morphometrische Untersuchung der Knochenregeneration unter dem Einfluß verschiedener Knochenersatzmaterialien." In Aktuelle Ergebnisse der Osteologie, edited by P. Dietsch, E. Keck, H. P. Kruse, and F. Kuhlencordt, 277–81. Berlin, Boston: De Gruyter, 1986. http://dx.doi.org/10.1515/9783110853247-048.
Full textConference papers on the topic "HISCO"
Gayen, Avijit, and Nilotpal Chakraborty. "HISC NEMO." In MobiCom '18: The 24th Annual International Conference on Mobile Computing and Networking. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3241539.3267767.
Full textBartels, Peter H., and James Ranger-Moore. "Quantitative Histo- and Cytopathology." In Frontiers in Optics. Washington, D.C.: OSA, 2005. http://dx.doi.org/10.1364/fio.2005.ftuu5.
Full textHinze, Ralf, and Nicolas Wu. "Histo- and dynamorphisms revisited." In the 9th ACM SIGPLAN workshop. New York, New York, USA: ACM Press, 2013. http://dx.doi.org/10.1145/2502488.2502496.
Full textKnobloch, Pascal, K. Schmalstieg, Martin Koch, E. Rehberg, F. Vauti, and K. Donhuijsen. "THz imaging of histo-pathological samples." In European Conference on Biomedical Optics, edited by Albert-Claude Boccara and Alexander A. Oraevsky. SPIE, 2001. http://dx.doi.org/10.1117/12.446686.
Full textKnobloch, P., K. Schmalstieg, M. Koch, E. Rehberg, F. Vauti, and K. Donhuijsen. "THz imaging of histo-pathological samples." In European Conference on Biomedical Optics. Washington, D.C.: Optica Publishing Group, 2001. http://dx.doi.org/10.1364/ecbo.2001.4434_239.
Full textTufillaro, Nicholas B., and Curtiss O. Davis. "Derivative spectroscopy with HICO^®." In Optical Remote Sensing of the Environment. Washington, D.C.: OSA, 2012. http://dx.doi.org/10.1364/orse.2012.rtu2e.5.
Full textDaum, Rainer, Andreas Achtermann, and Rainer Uhl. "Automated Slide-Screening Platform for Histo/Pathology." In European Conference on Biomedical Optics. Washington, D.C.: OSA, 2007. http://dx.doi.org/10.1364/ecbo.2007.6631_51.
Full textDaum, Rainer, Andreas Achtermann, and Rainer Uhl. "Automated slide-screening platform for histo/pathology." In European Conference on Biomedical Optics, edited by Christian D. Depeursinge. SPIE, 2007. http://dx.doi.org/10.1117/12.729554.
Full textLutkiewicz, Przemyslaw. "Designing and Optimising Duplex/Superduplex Compact Flanges to Negate HISC in Subsea Applications." In ASME 2021 Pressure Vessels & Piping Conference. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/pvp2021-61347.
Full textLockey, Aaron, Andy Young, Tim Turner, and Brendan Kelly. "HISC in Onshore Pipelines: Design Considerations." In 2016 11th International Pipeline Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/ipc2016-64310.
Full textReports on the topic "HISCO"
Corson, Michael R. Hyperspectral Imager for the Coastal Oecan (HICO). Fort Belvoir, VA: Defense Technical Information Center, September 2009. http://dx.doi.org/10.21236/ada531718.
Full text