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Books on the topic 'Diagnostic proce'

Author: Grafiati
Published: 9 March 2023
Last updated: 10 March 2023

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1

Corporation, InteLab, ed. U.S. markets for nucleic acid probe-based diagnostic products, 1994-2001. Mission Viejo, CA: InteLab Corporation, 1996.

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2

Krul, Kenneth G. The U.S. market for molecular diagnostics. New York: Kalorama Information, 2001.

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3

Krul, Kenneth G. The U.S. market for molecular diagnostics. Edited by Heffner Steven and Kalorama Information LLC. 2nd ed. New York: Kalorama Information, 2004.

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4

Alekseev, B. V. Zondovyĭ metod diagnostiki plazmy. Moskva: Ėnergoatomizdat, 1988.

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5

Langmuir probe in theory and practice. Boca Raton: BrownWalker Press, 2008.

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6

S, Herrington C., and McGee J. O'D, eds. Diagnostic molecular pathology: A practical approach. Oxford: IRL Press at Oxford University Press, 1992.

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7

Steinwald, Bruce. Medicare physician payment reform: Strategic responses for the medical device and diagnostic industry. [Washington, DC.]: Health Industry Manufacturers Association, 1990.

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8

Ltd, Sigma Chemical Company. Biochemical and organic compounds for research and diagnostic clinical reagents: Price list. Poole: Sigma Chemical Company Ltd., 1988.

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9

Lippincott Williams & Wilkins., ed. Handbook of diagnostic tests. 3rd ed. Philadelphia: Lippincott Williams & Wilkins, 2003.

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10

R, Black Edgar, ed. Diagnostic strategies for common medical problems. 2nd ed. Philadelphia: American College of Physicians, 1999.

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11

Corporation, Market Intelligence Research, ed. Molecular probe markets: Hoffmann-La Roche bids for dominance. Mountain View, CA: Market Intelligence, 1992.

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12

H, Persing David, ed. Diagnostic molecular microbiology: Principles and applications. Washington, D.C: American Society for Microbiology, 1993.

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13

Aldo, Badano, and National Institute of Standards and Technology (U.S.), eds. Characterization of luminance probe for accurate contrast measurements in medical displays. Gaithersburg, Md: U.S. Dept. of Commerce, Technology Administration, National Institute of Standards and Technology, 2003.

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14

Nicolau, Dan V., Daniel L. Farkas, and Robert C. Leif. Imaging, manipulation, and analysis of biomolecules, cells, and tissues X: 21-23 January 2012, San Francisco, California, United States. Bellingham, Wash: SPIE, 2012.

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15

Achilefu, Samuel. Reporters, markers, dyes, nanoparticles, and molecular probes for biomedical applications: 26-29 January 2009, San Jose, California, United States. Bellingham, Wash: SPIE, 2009.

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16

Raghavachari, Ramesh, and Samuel I. Achilefu. Reporters, markers, dyes, nanoparticles, and molecular probes for biomedical applicaitons II: 25-27 January 2010, San Francisco, California, United States. Bellingham, Wash: SPIE, 2010.

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17

Raghavachari, Ramesh, and Samuel Achilefu. Reporters, markers, dyes, nanoparticles, and molecular probes for biomedical applications III: 24-26 January 2011, San Francisco, California, United States. Edited by SPIE (Society). Bellingham, Wash: SPIE, 2011.

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18

(Society), SPIE, ed. Reporters, markers, dyes, nanoparticles, and molecular probes for biomedical applications: 26-29 January 2009, San Jose, California, United States. Bellingham, Wash: SPIE, 2009.

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19

Raghavachari, Ramesh, and Samuel Achilefu. Reporters, markers, dyes, nanoparticles, and molecular probes for biomedical applications V: 4-6 February 2013, San Francisco, Calififornia, United States. Edited by SPIE (Society), SPIE Photonics West (Conference) (2013 : San Francisco, Calif.), and Reporters, Markers, Dyes, Nanoparticles, and Molecular Probes for Biomedical Applications (Conference) (5th : 2013 : San Francisco, Calif.). Bellingham, Washington: SPIE, 2013.

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20

Raghavachari, Ramesh, and Samuel Achilefu. Reporters, markers, dyes, nanoparticles, and molecular probes for biomedical applications IV: 23-25 January 2012, San Francisco, California, United States. Edited by SPIE (Society). Bellingham, Wash: SPIE, 2012.

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21

Bono, Christopher M., and Charles G. Fisher. Prove it!: Evidence-based analysis of common spine practice. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins, 2010.

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22

The calculation of genetic risks: Worked examples in DNA diagnostics. Baltimore: Johns Hopkins University Press, 1994.

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23

The calculation of genetic risks: Worked examples in DNA diagnostics. 2nd ed. Baltimore: Johns Hopkins University Press, 1997.

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24

Nicolau, Dan V., Daniel L. Farkas, and Robert C. Leif. Imaging, manipulation, and analysis of biomolecules, cells, and tissues IX: 22-25 January 2011, San Francisco, California, United States. Bellingham, Wash: SPIE, 2011.

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25

The proton microprobe: Applications in the biomedical field. Boca Raton, Fla: CRC Press, 1985.

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26

Peter, Ingram, Shelburne John D, and Roggli Victor L, eds. Microprobe analysis in medicine. New York: Hemisphere, 1989.

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27

1956-, Mesko Dusan, and Marks Vincent, eds. Differential diagnosis by laboratory medicine: A quick reference for physicians. Berlin: Springer-Verlag, 2002.

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28

Achilefu, Samuel. Molecular probes for biomedical applications II: 21-22 January 2008, San Jose, California, USA. Edited by SPIE (Society). Bellingham, Wash: SPIE, 2008.

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29

Using eye movements as an experimental probe of brain function: A symposium in honor of Jean Buttner-Ennever. Amsterdam: Elsevier, 2008.

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30

Estridge, Barbara H. Basic medical laboratory techniques. 4th ed. Albany, N.Y: Delmar Publishers, 2000.

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31

Goumegou, Susanne. Schwindend schreiben: Briefe und Tagebücher schwindsüchtiger Frauen im Frankreich des 19. Jahrhunderts. Köln: Böhlau Verlag, 2011.

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32

P, Reynolds Anna, and Walters Norma J, eds. Basic medical laboratory techniques. 4th ed. Albany, N.Y: Delmar Publishers, 2000.

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33

M, Saxe JoAnne, ed. Microscopic procedures for primary care providers. Philadelphia: Lippincott Raven, 1999.

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34

S, Ligler Frances, and Taitt Chris A. Rowe, eds. Optical biosensors: Present and future. Amsterdam: Elsevier, 2002.

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35

Corbett, Jane Vincent. Laboratory Tests and Diagnostic Proced. 3rd ed. Appleton Lange, 1992.

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36

Ghadially. Diagnostic Electron Probe Xray Ana. Butterworth-Heinemann Ltd, 1991.

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37

Ghadially. Diagnostic Electron-Probe X-Ray Analysis. Butterworth-Heinemann Ltd, 1999.

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38

Panzer, Robert J., Edgar R. Black, Donald R. Bordley, and Thomas G. Tape. Diagnostic Strategies for Common Medical Problems (Diagnostic Tools) (Diagnostic Tools) (Diagnostic Tools). 2nd ed. American College of Physicians, 1999.

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39

Global markets for nucleic acid probe diagnostic products, 1997-2004. Mission Viejo, CA: InteLab Corp., 1998.

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40

Poet, Steven E. Development and diagnostic applications of a group-specific caliciviridae cDNA hybridization probe cloned from San Miguel sea lion virus, type 5, a calicivirus of ocean origin. 1994.

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41

Keshav, Satish, and Alexandra Kent. Acute abdominal pain. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0023.

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Acute abdominal pain is pain which is below the chest and above the pelvic brim and which has been present for ≤4 weeks. However, typically, patients present within hours of the onset of pain. The differential diagnosis does not differ much in primary and secondary care, although patients in hospital are probably more likely to be prone to iatrogenic illnesses such as pancreatitis, intestinal ischaemia, and Clostridium difficile-associated colitis. This chapter covers the approach to diagnosis, key diagnostic tests, therapies, prognosis, and dealing with uncertainty.
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42

Boiten, J. C., Ton Brouwer, Marije Bunskoek, Aline van der Feen, Alexandrine Schimmelpenninck van der Oije, and Floor Uilenreef-Tobi. Diagnostiek in de fysiotherapie: Proces en werkwijze. Bohn Stafleu van Loghum, 2017.

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43

Molecular probe markets for human diagnostics: Emergence of expanding markets. Mountain View, CA, USA: Market Intelligence Research Co., 1989.

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44

Bunch, Chris. Diagnosis and investigation in haematology. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0278.

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This chapter addresses the interpretation of the full blood count, blood film, bone marrow examination, and related tests in the diagnosis of haematological disorders. Examination of a stained blood film, which should always be requested if a blood count abnormality cannot readily be explained by the clinical context, may give clues to the cause of the abnormality or prove diagnostic. Examination of the bone marrow is essential to the proper evaluation and diagnosis of many haematological disorders. The simplest form of marrow examination involves needle aspiration of marrow cells from the posterior iliac crest; smears are made and stained in the same way as a blood film. Bone marrow can also be biopsied for histological examination, at the same time as marrow aspiration.
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45

Sobey, Christopher. Orofacial Pain. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190217518.003.0023.

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Management of orofacial pain in the general population can be a challenging and demanding undertaking due to the complex neurological anatomy and close proximity to vital structures. Differentiating various syndromes and origins of pain can prove difficult; thus, specific emphasis on establishing the correct diagnosis is of the utmost importance in formatting a successful treatment plan. The questions in this chapter delve into the presentations, physical exam findings, diagnostic testing, psychological effects, and evidence-based medical and interventional treatment algorithms of both common and less common craniofacial pain disorders. This chapter covers pathophysiology of the neurological, biomechanical, and central causes of facial pain.
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46

Ophthalmic diagnostics using a new dynamic light scattering fiber optic probe. [Washington, DC]: National Aeronautics and Space Administration, 1995.

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47

Lakowicz, Joseph R. Topics in Fluorescence Spectroscopy: Volume 4: Probe Design and Chemical Sensing (Topics in Fluorescence Spectroscopy). Springer, 1994.

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48

Clinical Dermatology 5Ed Spl Price. John Wiley(Exclusive), 2015.

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49

Read, Jennifer S., and Mark R. Schleiss, eds. Congenital and Perinatal Infections. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190604813.001.0001.

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Congenital and perinatal infections are commonly encountered in clinical practice. This book provides a summation of the data regarding infections transmitted from mother to child during the antepartum, intrapartum, or postnatal period, with the goal of providing a complete and critical review of the literature regarding the prevention, diagnosis, and management of congenital and perinatal infections. Emphasis is placed on epidemiology, clinical manifestations, key diagnostic studies, and therapeutic interventions. Individual chapters elucidate the pathogenesis of these infections, as well as high-priority areas for future research. This text will prove useful to medical students and residents, fellows, and practicing physicians in obstetrics and pediatrics, as well as family-practice physicians and specialists who care for pregnant women and newborns.
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50

Todd, Stacy, and Nick Beeching. Fungal infection. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0315.

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Fungi, comprising yeasts, moulds, and higher fungi, have a worldwide distribution and are uncommon causes of disease in healthy individuals. However, over the last 20 years, invasive fungal disease (IFD) has become an increasing cause of morbidity and mortality. This is probably due to the increasing numbers of patients with underlying host conditions, which predispose to opportunistic IFD (e.g. transplant and anti-tumour necrosis factor immunosuppression, HIV, or chronic lung disease), and to increased recognition of endemic IFD (e.g. histoplasmosis), which cause disease in both immunocompetent and immunocompromised hosts in selected geographic locations. Diagnosis of IFD remains a challenge. Symptoms are often non-specific, and a definite diagnosis requires invasive sampling with appropriate laboratory testing of these samples. Non-invasive tests are being developed, but their positive and negative predictive values still need validation. Diagnostic criteria (‘proven, probable, and possible’) established primarily for use in research and clinical trials can also prove useful in clinical environments. However, the most important step in identifying patients with IFD is to consider the diagnosis in those at risk. This chapter will focus on the commonest causes of IFD (Candida spp., Aspergillus spp., Cryptococcus spp., and histoplasmosis).
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