Academic literature on the topic 'Medical / Laboratory Medicine'
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Journal articles on the topic "Medical / Laboratory Medicine"
Smith, Brian R., Maria Aguero-Rosenfeld, John Anastasi, Beverly Baron, Anders Berg, Jay L. Bock, Sheldon Campbell, et al. "Educating Medical Students in Laboratory Medicine." American Journal of Clinical Pathology 133, no. 4 (April 2010): 533–42. http://dx.doi.org/10.1309/ajcpqct94sferlni.
Full textWilson, Michael L. "Educating Medical Students in Laboratory Medicine." American Journal of Clinical Pathology 133, no. 4 (April 2010): 525–28. http://dx.doi.org/10.1309/ajcpqia4fugmvht8.
Full textArora, DR, and B. Arora. "Ethics in laboratory medicine." Indian Journal of Medical Microbiology 25, no. 3 (2007): 179. http://dx.doi.org/10.4103/0255-0857.34756.
Full textArora, DR, and B. Arora. "ETHICS IN LABORATORY MEDICINE." Indian Journal of Medical Microbiology 25, no. 3 (July 2007): 179–80. http://dx.doi.org/10.1016/s0255-0857(21)02103-4.
Full textSmith, Brian R., Malek Kamoun, and John Hickner. "Laboratory Medicine Education at U.S. Medical Schools." Academic Medicine 91, no. 1 (January 2016): 107–12. http://dx.doi.org/10.1097/acm.0000000000000817.
Full textRodriguez, Fred H. "Why Medical Students Should Study Laboratory Medicine." Critical Values 4, no. 3 (July 1, 2011): 18–21. http://dx.doi.org/10.1093/criticalvalues/4.3.18.
Full textSteiner, M. "Tietz's Applied Laboratory Medicine." LaboratoriumsMedizin 32, no. 2 (January 1, 2008): 118–19. http://dx.doi.org/10.1515/jlm.2008.012i.
Full textMajkić-Singh, Nada. "Laboratory Medicine Management: Leadership Skills for Effective Laboratory." Journal of Medical Biochemistry 36, no. 3 (September 1, 2017): 207–10. http://dx.doi.org/10.1515/jomb-2017-0034.
Full textEngland, J. "Medical Laboratory Haematology." Journal of Clinical Pathology 38, no. 3 (March 1, 1985): 358. http://dx.doi.org/10.1136/jcp.38.3.358-a.
Full textWood, J. "Medical Laboratory Haematology." Journal of Clinical Pathology 44, no. 10 (October 1, 1991): 879–80. http://dx.doi.org/10.1136/jcp.44.10.879-d.
Full textDissertations / Theses on the topic "Medical / Laboratory Medicine"
Suwarno, Neihl Omar 1963. "A computer based data acquisition and analysis system for a cardiovascular research laboratory." Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/558111.
Full textZurgani, Emad K. A. "Documentation of the body transformations during the decomposition process : from the crime scene to the laboratory." Thesis, University of Huddersfield, 2018. http://eprints.hud.ac.uk/id/eprint/34690/.
Full textSmall, Kathy S. "Retention Strategies for Medical Technologists: Addressing the Shortages and Vacancies in the Clinical Laboratory." Digital Commons @ East Tennessee State University, 2013. https://dc.etsu.edu/etd/2299.
Full textO'Connell-Spalla, Joan. "Medical Laboratory Testing Personnel: Perception of Professional Status and Engagement in Professional Development and Career Advocacy." Youngstown State University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1627410209680141.
Full textDe, Beer Corena. "Clinical and laboratory investigation of latex allergy in healthcare workers." Thesis, Stellenbosch : Stellenbosch University, 2004. http://hdl.handle.net/10019.1/49883.
Full textENGLISH ABSTRACT: Healthcare workers (HCWs) wear latex gloves to protect themselves and their patients against the transmission of microbial, viral and bloodborne diseases. These individuals are primarily exposed to latex via cutaneous (direct contact) and mucocutaneous (inhalation of airborne allergens on glove powder) routes. Repeated exposure leads to the formation of circulating latex-specific IgE and subsequent sensitisation with varying clinical expression. The airconditioning system of the Tygerberg Hospital (TBH) complex was investigated for the presence of aerosolised cornstarch glove powder and proteins. Dust samples were collected from 14 areas with different levels of latex glove usage. Dust samples were spectrophotometrically compared to a calibration graph of pure glove powder. The detection of starch and proteins in all the dust samples confirmed the presence of glove powder and possibly airborne latex allergens in the airconditioning ducts. As expected, the high exposure areas showed the highest concentrations of both starch and proteins. It is possible that other proteins than latex were involved, but the confirmed high level of protein contamination should be a cause for concern. Correlation between starch and protein levels was highly significant (p<0.01) in all instances. A total of 500 questionnaires were circulated for completion by HCWs from TBH. The response rate was 69.8%. After considering specific inclusion criteria, a study group of 152 individuals was compiled (28 males, 124 females). All subjects had current latex exposure and suffered from at least three pre-defined symptoms. Serum was collected from all subjects and dermal fluid from 31 subjects. Total IgE and latex specific IgE analysis were done on all serum and dermal fluid samples. Latex-specific IgE was positive (>0.35 IU/ℓ) in 23 serum and six dermal fluid samples. Skin prick tests (SPTs)for latex were done on 59 subjects with negative serum latex-specific IgE and 34 had positive results. Twelve subjects with negative latex-specific IgE and latex SPTs underwent patch tests with the European Standard Series, a piece of latex glove and glove powder in petrolatum. Three subjects had positive results to one or more of these allergens. Western blot analysis for latex was done on all positive sera and dermal fluid collected from these subjects. Western blot analysis for latex proved to be more sensitive than the capRAST, because it was able to identify specific bands in samples with negative capRAST results. All subjects showed a band for Hev b 1, which has been confirmed as a powder-bound airborne allergen. Hev b 6.01 is associated with HCWs with cutaneous symptoms and this band was recognised by 81% of the subjects. These findings confirmed that airborne and cutaneous routes are the major routes of exposure in HCWs. According to their laboratory results, subjects were divided into the following subgroups and compared statistically: Group A (serum positive, n=23), Group B (SPT positive, n=34) and Group C (negative, n=25). Group D (withdrawn, n=70) could not be used for statistical comparisons, due to incomplete results. An overall latex allergy prevalence of 38% was found. Group A differed significantly from Group B and Group C for most clinical and special investigations. Group A and B were also combined to represent all subjects with positive results (Cohort AB). The Allergy Score and Class were highly significant when Cohort AB was compared to Group C. The selection of clinical symptoms was confirmed to be relevant and work-related deterioration on any of the symptoms should bear a high index of suspicion in the evaluation of latex allergy. Numerical indices and specific symptoms showed high positive predictive values and the Allergy Score produced statistical significance in the positive subgroups when compared to the negative subgroup. Paired statistical significance was confirmed between the Allergy Score and occupational exposure (number of years, hours and pairs per week). The areas with the highest occupational latex exposure in HCWs are the face and hands. Different occupations also have different levels of exposure and two subgroups of HCWs (16 laboratory technologists and 13 theatre staff) were investigated for sebum content on different facial areas and the palms and dorsal areas of both hands. Baseline measurements were done before putting on gloves. In 21 subjects follow up measurements were done following three to four hours of occupational exposure, but before washing their hands. Baseline and follow up values were compared for all the different anatomical regions. Levels on the forehead and cheeks increased over time, while the level on the nose decreased. All hand regions decreased significantly during occupational exposure, suggesting that glove powder contributes to dryness of the skin. In conclusion, the problem posed by latex allergy will not be solved overnight and will probably remain a major occupational hazard for years to come. It is currently not possible to avoid exposure to latex, but it is imperative to institute safety measures to prevent further sensitisation in predisposed individuals and manage those already affected.
AFRIKAANSE OPSOMMING: Gesondheidswerkers dra lateks handskoene om hulleself en hulle pasiënte te beskerm teen die oordrag van mikrobiale, virale en bloed-gedraagde siektes. Die lateks blootstelling vind hier hoofsaaklik plaas via kutane (direkte velkontak) en mukokutane (inaseming van lug-gedraagde allergene op hanskoen poeier) roetes. Herhaalde blootstelling veroorsaak sirkulerende lateksspesifieke IgE en sensitisasie met variërende kliniese beelde. Die lugreëlingstelsel van die Tygerberg hospitaalkompleks is ondersoek vir die teenwoordigheid van handskoenpoeier (stysel) en lateks proteïene. Stofmonsters is versamel in 14 areas wat verskillende blootstellingsvlakke verteenwoordig het. Die stofmonsters is spektrofotometries vergelyk met "n kalibrasiekurwe van suiwer hanskoenpoeier. Stysel en proteïene kon in al die stofmonsters aangetoon word en het die teenwoordigheid van handskoenpoeier en moontlike luggedraagde lateks proteïene in die lugreëlingstelsel bevestig. Soos verwag kon word, het die hoogste stysel en proteïen waardes in hoë blootstellingsareas voorgekom. Hoogs beduidende statistiese korrelasies (p<0.01) tussen die stysel en proteïenvlakke kon aangedui word in alle monsters. "n Totaal van 500 vraelyste is gesirkuleer vir voltooiing deur TBH gesondheidswerkers, waarvan 69.8% voltooide vraelyste terugontvang is. Na evaluering van insluitingskriteria, is "n studiegroep van 152 individue saamgestel (28 mans, 124 vrouens). Almal het huidige lateks blootstelling en ten minste drie het vooraf gedefinieerde simptome gerapporteer. Serum is van die hele groep versamel en dermale vog van 31 proefpersone. Totale IgE en lateks-spesifieke IgE vlakke is op alle serum en dermale vog bepaal. Positiewe resultate (>0.35 IU/ℓ) is verkry in 23 serum en ses dermaIe vog monsters. Velpriktoets vir lateks is op 59 proefpersone uitgevoer en 34 daarvan het positiewe resultate opgelewer. Twaalf proefpersone met negatiewe lateks-spesifieke IgE en velpriktoets resultate het kutane plaktoetse ondergaan met die Europese Standaard Reeks, "n stukkie lateks handskoen en handskoenpoeier in petrolatum. Drie proefpersone het positiewe resultate teen een of meer van die allergene gehad. Westerse kladanalise vir lateks is op alle positiewe serum gedoen, asook die dermale vogte van hierdie proefpersone. Westerse kladanalise vir lateks blyk baie meer sensitief te wees as die capRAST, aangesien dit spesifieke bande kon identifiseer in monsters capRAST resultate. Alle monsters het "n band getoon vir Hev b 1, "n poeier-gebinde, luggedraade allergeen. Hev b 6.01 is geassosieer met gesondheidswerkers met velsimptome en hierdie band is gevind in 81% van die monsters. Hierdie resultate bevestig dat die belangrikste blootstelling aan lateks in gesondheidswerkers deur die vel en inaseming plaasvind. Proefpersone is in die volgende drie groepe verdeel volgens laboratorium resultate en statisties vergelyk: Groep A (positiewe serum, n=23), Groep B (positiewe velpriktoetse, n=34) en Groep C (negatief, n=25). Groep D (onttrek, n=70) kon nie vir betekenisvolle statistiese vergelykings aangewend word nie, as gevolg van onvolledige resultate. 'n Finale lateks allergie prevalensie van 38% is gevind. Groep A het hoogs beduidend verskil van Groep B en C vir die meeste van die kliniese en spesiale laboratoriumondersoeke. Groep A en B is gekombineer om alle proefpersone in te sluit met positiewe resultate (Kohort AB). Die Allergie Telling en Klas van Kohort AB was hoogs beduidend in vergelyking met Groep C. Die gekose simptome is bevestig as relevant en enige werksverwante verergering van simptome moet met 'n hoë mate van agterdog bejeën word in lateks allergie. Numeriese indekse en spesifieke simptome het hoë positiewe voorspellingswaardes gelewer en die Allergie Telling was hoogs beduidend in die positiewe subgroep in vergelyking met die negatiewe subgroep. Gepaarde statistiese beduidenheid is ook gevind tussen die Allergie Telling en beroepsblootstelling (jare van blootstelling, uur en paar handskoene per week). Die meeste beroepsblootstelling aan lateks in gesondheidswerkers vind plaas op die hande en gesig. Verskillende beroepe het ook verskillende blootstellingsvlakke en two subgroepe gesondheidswerkers (16 laboratorium tegnoloë en 13 teater personeel) is ondersoek vir die sebumgehalte op veskillende areas van die gesig en hande. Basislynvlakke is gemeet voordat handskoene aangetrek is en in 21 gevalle is opvolgvlakke gemeet na drie tot vier uur beroepsblootstelling, maar voor die hande gewas is. Basislyn en opvolgvlakke is met mekaar vergelyk vir al die anatomiese areas. Die voorkop en wange het 'n toename in sebumgehalte getoon, terwyl dié van die neus afgeneem het. AI die areas op die hande toon 'n hoogs beduidende afname tydens beroepsblootstelling, wat impliseer dat hanskoenpoeier moontlik bydra tot droogheid van die vel. In samevatting, die lateks allergie probleem sal nie oornag opgelos word nie en sal waarskynlik 'n belangrike beroepsrisiko bly vir die aansienlike toekoms. Totale vermyding van lateks is tans onmoontlik en daarom is dit van uiterste belang om voorsorgmaatreëls in plek te stel om verdere sensitisasie in blootgestelde individue te verhoed en die wat reeds geaffekteer is, effektief te hanteer.
Forsgren, Mikael. "The Non-Invasive Liver Biopsy : Determining Hepatic Function in Diffuse and Focal LiverDisease." Doctoral thesis, Linköpings universitet, Avdelningen för radiologiska vetenskaper, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-136545.
Full textMukinda, James Tshikosa. "Acute and chronic toxicity of the flavonoid-containing plant, Artemisia afra in rodents." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&.
Full textLundström, Jonathan, and Joel Skagersten. "Optimering samt implementering av Harts automatiserade färgningsmetod : Ersättning av Verhoeffs manuella elastinfärgning." Thesis, Jönköping University, HHJ, Avd. för naturvetenskap och biomedicin, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-52932.
Full textElastic fibres ensure blood vessels and other tissues flexibility. Elastic staining of tissue is relevant when there is suspicion of melanoma, temporalis arteritis, venous invasion and after operations on blood vessels. The aim of the study was with the help of different tissue samples optimize and implement Hart´s elastic staining method as a substitute for Verhoeff’s at pathology lab at county hospital Ryhov, Jönköping. Colon, kidney, skin, and umbilical cord cross section got stained with Hart´s automated elastic staining method to evaluate the optimal staining procedure. Same region of the tissues was stained with Verhoeff´s manual elastic staining method and Hart´s method. All cross section were assessed and compared with the help of a pathologist doctor. Optimization of Hart´s method resulted in an incubation period of twelve minutes and optimal staining procedure without xylene. Result of comparison between Hart´s staining method and Verhoeff´s staining method showed that Hart´s staining method had a better contrast and background. Conclusions of the study was that Hart´s staining method was better than Verhoeff´s staining method, further studies could include research about a substitution of the blotting step with an extra ethanol bath as an example and liver tissue instead of the umbilical cord.
Prince, Yvonne. "Improving laboratory techniques to detect M. tuberculosis complex and C. neoformans as the causative agents of chronic meningitis in cerebrospinal fluid of adult patients." Thesis, Stellenbosch : University of Stellenbosch, 2010. http://hdl.handle.net/10019.1/4110.
Full textENGLISH ABSTRACT: INTRODUCTION Mycobacterium tuberculosis (MTB) and Cryptococcus neoformans are the most common causes of chronic meningitis in South Africa. Conventional microbiology has limited utility in diagnosing these pathogens due to the paucibacillary nature of cerebrospinal fluid (CSF) and the diagnostic delay associated with culturing methods. This study aimed to evaluate the utility of an in-house polymerase chain reaction (PCR) method for the detection of the etiological agent of chronic meningitis. METHODS CSF samples (where volume exceeded 5ml) were submitted to the Medical Microbiology diagnostic laboratory of the Tygerberg Hospital from patients with suspected tuberculosis meningitis (TBM). Following routine bacteriology, the sample was used to inoculate two mycobacterial growth indicator tubes (MGIT A and B) and subsequently incubated in the BACTEC 960 automated system. MGIT A followed standard operating procedures and the time to culture positivity was noted. Weekly aliquots (up to 6 weeks) were removed from MGIT B. These samples were boiled to inactivate the bacteria and then the DNA was extracted using the Promega Wizard SV Genomic DNA kit. The DNA was then speciated by PCR and high-resolution melting analysis (HRM) by using primers specific to either the RD9 region of MTB complex or primers specific to the partial internal transcribed spacer 1 (ITS1), 5.8S rRNA gene and partial ITS2 sequence of C. neoformans. RESULTS Routine CSF microscopy indicated that 14 of the 78 patients (17.9%) had typical CSF findings of TBM (lymphocytes predominant, increased protein levels and decreased glucose levels). IV Ziehl-Neelsen (ZN) stains were positive for 12 (15.4%) samples, and MTB was cultured from 19 samples (24.4%). Our optimized PCR and HRM method was able to detect M. tuberculosis in 17 of the 19 culture positive specimens with a sensitivity of 89.5% and a specificity of 62.7%. The sensitivity of this method was higher than that of direct microscopy. In all of the PCR positive samples, the time to detection, compared to culture, could be shortened by 1 to 2 weeks. Only one sample was positive for Cryptococcus culture and another sample was positive with a Cryptococcus latex test. PCR for Cryptococcus was positive in 2 cases (n=78), sensitivities and specificities could not be reported due to the low number of positive cases. CONCLUSION We demonstrated that a short culture period and the use of commercial DNA extraction kit on CSF samples increases the sensitivity of molecular tests to diagnose tuberculosis. Furthermore, the molecular techniques could significantly reduce the time to positivity of results, when compared to culture. Due to the low occurrence of Cryptococcus in the samples included in our study, we could not comment on the diagnostic utility of PCR in the diagnosis of Cryptococcal meningitis, when compared to the conventional methods.
AFRIKAANSE OPSOMMING: INLEIDING Mycobacterium tuberculosis (MTB) en Cryptococcus neoformans is die mees algemeenste oorsake van kroniese meningitis in Suid-Afrika. Routine mikroskopie dra beperkte waarde in die diagnose van hierdie patogene as gevolg van die klein hoeveelhede organismes wat in die SSV (serobrospinale vog) voorkom en die lang tyd wat dit benodig om hierdie organisms te kweek. Hierdie studie beoog om die diagnostiese waarde van ‘n polymerase ketting reaksie (PKR) metode wat intern ontwerp is te evalueer vir die identifikasie van patogene verantwoordelik vir kroniese meningitis. METODES SSV monsters (waarvan die volume 5ml oorskry) en waar daar ‘n kliniese vermoede van tuberkulose meningitis (TBM) was, is na die diagnostiese Mediese Mikrobiologie laboratorium van Tygerberg hospitaal gestuur vir roetine bakteriologiese ontleding. Die oorblywende monsters is gebruik om twee mikobakteriële groei-indikasiebuise (MGIT A en B) te innokuleer en hulle is geïnkubeer in ‘n BACTEC 960 geautomatiseerde sisteem. MGIT A is volgens roetine diagnostiese metodes geanaliseer en die tyd tot ‘n positiewe resultaat is aangeteken Weeklikse monsters (tot en met week 6) is uit MGIT B verwyder en die monsters is gekook om sodoende die bakterië te inaktiveer. Die Promega Wizard SV Genomiese DNS ekstraksiemetode is gebruik om die DNS te versuiwer. Spesiëring van die DNS is deur middel van ‘n intern ontwerpte PKR en hoëresolusiesmeltingsmetode (HRS) gedoen met inleiers wat spesifiek is tot die RD9 gedeelte van die MTB kompleks en inleiers spesifiek tot die gedeeltelike interne getranskribeerde spasieerder 1 (ITS1), 5.8S rRNS geen en die gedeeltelike ITS2 DNS volgorde van C. neoformans. VI RESULTATE Roetine SSV mikroskopie het aangedui dat 14 uit 78 (17.9%) pasiënte tipiese SSV bevindings van TBM (oorwegend limfosiete, verhoogde proteïene en verlaagde glukose) gehad het. Ziehl- Neelsen (ZN) kleurings was positief vir 12 (15.4%) monsters, en MTB is gekweek in 19 (24.4%) van hierdie monsters. Ons geoptimaliseerde PKR en HRS metode het daarin geslaag om M. tuberculosis in 17 van die 19 kultuurpositiewe monsters aan te toon met ‘n sensitiviteit van 89.5% en ‘n spesifisitiet van 62.7%. Die sensitiwiteit van die direkte PKR was hoër in vergelyking met mikroskopie. In al die PKR positiewe monsters was die tyd tot aantoning, in vergelyking met kultuur, verkort met 1 tot 2 weke. Slegs een monster het C. neoformans gekweek en ‘n ander monster was positief met die kriptokokkale latekstoets. PKR vir C. neoformans was positief in 2 gevalle (n=78). Die sensitiwiteit en spesifisiteit van die C. neoformans PKR kon nie bepaal word nie weens te min gevalle. GEVOLGTREKKINGS Ons het aangetoon dat ‘n verkorte inkubasieperiode en die gebruik van ‘n kommersiële DNS ekstraksiemetode op SSV monsters die sensitiwiteit van die molekulêre tegniek vir die diagnose van tuberkulose verhoog en dat hierdie metode die tyd na positiwiteit aansienlik verkort in vergelyking met kultuur. Weens die lae getalle van kriptokokkale meningitis in ons studie kon ons nie kommentaar lewer op die akkuraatheid van PKR in die diagnose van kriptokokkale meningitis, in vergelyking met meer konvensionele metodes, nie.
Van, Vuuren Petra J. "The effects of physical and psychological stress on the behaviour and neurochemistry of rats." Thesis, Link to the online version, 2005. http://hdl.handle.net/10019/1274.
Full textBooks on the topic "Medical / Laboratory Medicine"
Cheesbrough, Monica. Medical laboratory manual for tropical countries. 2nd ed. [Dottington, Cambridgeshire, England]: Tropical Health Technology, 1991.
Find full textCheesbrough, Monica. Medical laboratory manual for tropical countries. 2nd ed. [Dottington, Cambridgeshire, England]: Tropical Health Technology, 1987.
Find full textBiomedical sciences: Essential laboratory medicine. Chichester, West Sussex, UK: John Wiley & Sons Ltd, 2011.
Find full textDirckx, John H. Laboratory tests and diagnostic procedures in medicine. Modesto, CA: Health Professions Institute, 2004.
Find full textQueen Elizabeth Hospital (Charlottetown, P.E.I.). Q. E. H. Department of Laboratory medicine Provincial clinical Laboratory. Charlottetown: Queen Elizabeth Hospital, 1990.
Find full textCheesbrough, Monica. Medical laboratory manual for tropical countries. 2nd ed. London: Butterworth - Vol.11, 1985.
Find full textW, Harvey John, ed. Veterinary laboratory medicine: Interpretation & diagnosis. 2nd ed. Philadelphia: W.B. Saunders, 1998.
Find full textW, Harvey John, ed. Veterinary laboratory medicine: Interpretation & diagnosis. 3rd ed. St. Louis, Mo: Saunders, 2004.
Find full textRainer, Haeckel, ed. Evaluation methods in laboratory medicine. Weinheim: VCH, 1993.
Find full textEstridge, Barbara H. Basic medical laboratory techniques. 4th ed. Albany, N.Y: Delmar Publishers, 2000.
Find full textBook chapters on the topic "Medical / Laboratory Medicine"
Wood, W. G. "In Vitro Diagnosis in the Nuclear Medical Laboratory." In Nuklearmedizin / Nuclear Medicine, 363–405. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-82225-4_2.
Full textWorboys, Michael. "Vaccine Therapy and Laboratory Medicine in Edwardian Britain." In Medical Innovations in Historical Perspective, 84–103. London: Palgrave Macmillan UK, 1992. http://dx.doi.org/10.1007/978-1-349-22078-6_5.
Full textBoran, G., P. Eldridge, J. Nolan, P. Brosnan, and R. O’Moore. "A Decision Support Tool for Laboratory Medicine Based on Automatic Knowledge Acquisition." In Medical Informatics Europe ’90, 329–33. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-51659-7_63.
Full textMarchevsky, Alberto M., and Ruta Gupta. "Development of Evidence-Based Diagnostic Criteria and Prognostic/Predictive Models: Experience at Cedars Sinai Medical Center." In Evidence Based Pathology and Laboratory Medicine, 213–34. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-1030-1_13.
Full textPradella, M., R. Dorizzi, D. Giavarina, A. Camerotto, and F. Rigolin. "Electrolyte and Haemostasis Test Interpretation by Expert Systems on Microcomputer in Medical Laboratory." In Expert Systems and Decision Support in Medicine, 240–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-48706-4_37.
Full textGuarnieri, Patrizia. "Theatre and Laboratory: Medical Attitudes to Animal Magnetism in Late-Nineteenth-Century Italy." In Studies in the History of Alternative Medicine, 118–39. London: Palgrave Macmillan UK, 1988. http://dx.doi.org/10.1007/978-1-349-19606-7_7.
Full textEdy, V., and M. Gamlen. "Chapter 29. Good Manufacturing Practice for Investigational Medicinal Products." In Good Clinical, Laboratory and Manufacturing Practices, 407–18. Cambridge: Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557728-00407.
Full textAroor, AR. "Chapter-41 Biochemical Investigations in Laboratory Medicine." In Medical Biochemistry, 888–94. Jaypee Brothers Medical Publishers (P) Ltd., 2011. http://dx.doi.org/10.5005/jp/books/11450_41.
Full textLemos, Carlos. "Innovation in Laboratory Medicine." In Advances in Business Strategy and Competitive Advantage, 117–37. IGI Global, 2019. http://dx.doi.org/10.4018/978-1-5225-7265-7.ch007.
Full textProvan, Drew. "Nuclear medicine." In Oxford Handbook of Clinical and Laboratory Investigation, edited by Drew Provan, 865–956. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198766537.003.0014.
Full textConference papers on the topic "Medical / Laboratory Medicine"
Pattichis, C. S., M. Fredj, C. N. Schizas, G. Gabriel, K. Panayides, A. Drousiotou, R. R. Livesay, and L. T. Middleton. "An integrated system for medical diagnosis: Laboratory findings." In 1992 14th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 1992. http://dx.doi.org/10.1109/iembs.1992.5761345.
Full textPattichis, Fredj, Schizas, Gabriel, Panayides, Drousiotou, Lnesa, and Middleton. "An Integrated System For Medical Diagnosis: Laboratory Findings." In Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 1992. http://dx.doi.org/10.1109/iembs.1992.594687.
Full textZhao, Yundong, Limei Liu, Mingcheng Li, Ailin Wang, and Liyuan Sun. "Construction of a System of Experiment Assessment of Medical Laboratory Technologies." In 2016 8th International Conference on Information Technology in Medicine and Education (ITME). IEEE, 2016. http://dx.doi.org/10.1109/itme.2016.0110.
Full textPatil, Meru A., Sandip Bhaumik, Soubhik Paul, Swarupananda Bissoyi, Raj Roy, and Seungwoo Ryu. "Estimating personalized risk ranking using laboratory test and medical knowledge (UMLS)." In 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2013. http://dx.doi.org/10.1109/embc.2013.6609740.
Full textMacri, S., L. Mainetti, L. Patrono, S. Pieretti, A. Secco, and I. Sergi. "A tracking system for laboratory mice to support medical researchers in behavioral analysis." In 2015 37th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2015. http://dx.doi.org/10.1109/embc.2015.7319501.
Full textCiorap, Radu, Catalina Luca, and Doru Andritoi. "REALISTIC PATIENT SIMULATORS FOR EDUCATION IN MEDICINE AND BIOENGINEERING." In eLSE 2018. Carol I National Defence University Publishing House, 2018. http://dx.doi.org/10.12753/2066-026x-18-200.
Full textZavrel, Erik A., and Ana C. Krieger. "An Inter-Device Accuracy Comparison of Consumer Sleep Trackers." In 2019 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/dmd2019-3205.
Full textFranco-Clark, D., A. B. Pimentel-Aguilar, and R. Rodríguez-Vera. "Design of a Medical And Laboratory Equipment Management Program for the new standards certification achievement in Mexico." In 2010 32nd Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC 2010). IEEE, 2010. http://dx.doi.org/10.1109/iembs.2010.5626427.
Full textLupu, Vasile Valeriu, Ingrith Miron, Anamaria Ciubara, Valeriu Lupu, Anca Lavinia Cianga, Iuliana Magdalena Starcea, Stefan Lucian Burlea, Alexandru Bogdan Ciubara, and Ancuta Lupu. "SARS-COV 2 PANDEMIC AND THE PRINCIPLES OF MEDICAL ETHICS." In The European Conference of Psychiatry and Mental Health "Galatia". Archiv Euromedica, 2023. http://dx.doi.org/10.35630/2022/12/psy.ro.2.
Full textAndreeva, A. D., P. A. Shagalova, and E. S. Sokolova. "Development of an Interface for Intelligent Medical Research in Microscopy." In 32nd International Conference on Computer Graphics and Vision. Keldysh Institute of Applied Mathematics, 2022. http://dx.doi.org/10.20948/graphicon-2022-1165-1174.
Full textReports on the topic "Medical / Laboratory Medicine"
López Núñez, Álvaro José. Anatomía ósea para estudiantes. Ediciones Universidad Cooperativa de Colombia, November 2021. http://dx.doi.org/10.16925/gcgp.34.
Full textDodel, Matías, and Leticia Brandino. Competencias digitales: cómo se definen, entienden y miden. Grupo de Trabajo en Ciudadanía Digital (Uruguay), December 2021. http://dx.doi.org/10.22235/cd/md.lb/2021.
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