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Books on the topic 'Tumour'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 September 2023

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1

McGowan, Anthony. Henry Tumour. London: Definitions, 2007.

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2

J, Bicknell R., Lewis Claire E, and Ferrara Napoleone, eds. Tumour angiogenesis. Oxford: Oxford University Press, 1997.

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3

Morrow, Dympna. Is tumour induced anaemia caused by tumour derived cytokines?. [S.l: The Author], 1995.

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4

Lawrence, Toby, and Thorsten Hagemann, eds. Tumour-Associated Macrophages. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-0662-4.

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5

Richard, Coombs, and Friedlaender Gary E, eds. Bone tumour management. London: Butterworths, 1987.

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6

Thorsten, Hagemann, and SpringerLink (Online service), eds. Tumour-Associated Macrophages. New York, NY: Springer Science+Business Media, LLC, 2012.

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7

Hatton, William James. Stereological envmeration of tumour associated macrophages infiltrating human colorectal tumours. [S.l: The Author], 1996.

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8

Walker, Michael D., and David G. T. Thomas, eds. Biology of Brain Tumour. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2297-9.

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9

Gaston, Kevin. Small DNA tumour viruses. Norfolk, UK: Caister Academic Press, 2012.

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10

Károly, Lapis, Eckhardt S, and International Union Against Cancer, eds. Carcinogenesis and tumour progression. Budapest: Akadémiai Kiadó, 1987.

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11

M, Chadwick C., ed. Receptors in tumour biology. Cambridge: Cambridge University Press, 1986.

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12

H, McKee Phillip, and International Union against Cancer, eds. Comprehensive tumour terminology handbook. New York: Wiley, 2001.

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13

1921-, Franks L. M., and Hart I, eds. Tumour progression and metastasis. Oxford: Oxford University Press for the Imperial CancerResearch Fund, 1988.

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14

1938-, Gielen M., ed. Metal-based anti-tumour drugs. London: Freund Pub. House, 1988.

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15

Mulligan, Helen Dawn. Mechanisms of tumour-induced cachexia. Birmingham: Aston University. Department of Pharmaceutical Science, 1991.

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16

Imperial Cancer Research Fund (Great Britain). New approaches to tumour identification. Edited by Britton, K. E. (Keith Eric). Oxford, U.K: Published for the Imperial Cancer Research Fund by Oxford University Press, 1987.

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17

Nicholas, Davies. Octreotide and experimental liver tumour. Edinburgh: University of Edinburgh, 1993.

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18

Gregory, Bock, Marsh Joan, and Ciba Foundation, eds. Genetic analysis of tumour suppression. Chichester: Wiley, 1989.

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19

G, Gallagher, Rees Robert C, and Reynolds Craig W, eds. Tumour immunobiology: A practical approach. Oxford: IRL Press, 1993.

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20

F, Leonard R. C., ed. Serological tumour markers: An introduction. Edinburgh: Churchill Livingstone, 1993.

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21

Hellmen, Eva. Mammary tumours in the female dog: A study of tumour histogenesis and DNA ploidy in relation to histology, prognosis and tumour progression. Uppsala: Sveriges Lantbruksuniversitet, 1989.

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22

Symposium on Tumour Marker (4th 1986 Hamburg, Germany). New tumour markers and their monoclonal antibodies: Actual clinical relevance for diagnosis and therapy of solid tumours: 4th Symposium on Tumour Markers, Hamburg. Stuttgart: Thieme Verlag, 1987.

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23

Higgins, Catherine Ann. Tumour associated macrophages: Tumour infiltrating lymphocytes : apoptotic and mitotic cells in human colorectal cancer. [S.l: The Author], 1998.

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24

O'Keefe, Martina. The role of microvascular pericytes in tumour angiogenesis: Implications for the control of tumour growth. [S.l: The author], 2003.

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25

Giráldez, Fernando, and Miguel A. Herrero, eds. Mathematics, Developmental Biology and Tumour Growth. Providence, Rhode Island: American Mathematical Society, 2009. http://dx.doi.org/10.1090/conm/492.

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26

Ward, Tony Milford, ed. Proteins and Tumour Markers May 1995. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0681-8.

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27

Smith, Kate Louise. Tumour associated proteolysis and protein metabolism. Birmingham: Aston University. Department of Pharmaceutical Sciences, 1992.

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28

1944-, Kanis John A., Russell R. G. G, and Royal Society of Medicine (Great Britain), eds. Tumour-induced hypercalcaemia and its management. London: Royal Society of Medicine Services, 1991.

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29

J, McMichael Andrew, Bodmer W. F. 1936-, and Imperial Cancer Research Fund (Great Britain), eds. A New look at tumour immunology. Plainview, N.Y: Cold Spring Harbor Laboratory Press, 1992.

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30

Gregory, Bock, Marsh Joan, and Symposium on Tumour Necrosis Factor and Related Cytotoxins (1987 : London, England), eds. Tumour necrosis factor and related cytotoxins. Chichester: Wiley, 1987.

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31

György, Fekete. Congenital chromosome aberrations and tumour predisposition. Budapest: Adadémiai Kiadó, 1990.

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32

Beck, Susan Anne. Catabolic factors in tumour-induced cachexia. Birmingham: Aston University. Department of Pharmaceutical Sciences, 1989.

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33

The oncogene and tumour suppressor gene factsbook. 2nd ed. San Diego, Calif: Academic Press, 1997.

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34

Anees, Mohammad. Tumour cell surface proteases and their inhibitors. Manchester: University of Manchester, 1995.

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35

Winograd, Benjamin, Michael Peckham, and Herbert Michael Pinedo, eds. Human Tumour Xenografts in Anticancer Drug Development. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73252-2.

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36

Zurita, Maria Trinidad. Tumour necrosis factor inhibitory drugs in meningitis. Birmingham: University of Birmingham, 1994.

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37

Jondle, Donita. Wanted Brain Tumour : Understanding Brain Tumors: Dipg Brain Tumour. Independently Published, 2021.

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38

Coronado, Jamison. Wanted Brain Tumour : Understanding Brain Tumors: Russell Watson Brain Tumour. Independently Published, 2021.

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39

Tumour. Oolichan Books, 2015.

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40

Aston, Derek. Benign Brain Tumour : Warning Signs of Brain Tumor : : The Wanted Singer Brain Tumour. Independently Published, 2021.

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41

Tumour Viruses. MDPI, 2016. http://dx.doi.org/10.3390/books978-3-03842-152-8.

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42

Lewis, Claire E., Napoleone Ferrara, and Roy Bicknell. Tumour Angiogenesis. Oxford University Press, 1997.

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43

Moles, Rob. Tumour Humour. Independently Published, 2018.

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44

Henry Tumour. Random House Childre, 2006.

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45

Komor, Zoltan. Tumour-Djinn. MorbidbookS, 2014.

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46

Gikas, Panagiotis D., and Timothy W. R. Briggs. Choice of surgery for tumour: Staging and surgical margins. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.002001.

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Abstract:
♦ Bone and soft tissue tumours are rare and should therefore be assessed and treated in specialized centres♦ Clinical staging and pathological grading is used to classify the extent of a tumour♦ Clinical staging uses various imaging techniques, pathological grading requires tumour biopsy following clinical staging♦ The Enneking system is commonly used for surgical staging of bone and soft tissue tumours♦ Surgery is the mainstay of treatment for musculoskeletal tumours♦ The surgical margin describes the extent of the procedure♦ Intralesional margins describe a procedure that removes the tumour alone, radical margins may require removal of entire bone♦ Open incisional biopsy is the gold standard method for obtaining a representative specimen of tumour♦ Careful planning and good collaboration between surgeons, radiologists, and pathologists is crucial to avoid unnecessary or dangerous biopsy procedures.
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47

Lawrence, Toby, and Thorsten Hagemann. Tumour-Associated Macrophages. Springer, 2011.

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48

Lawrence, Toby, and Thorsten Hagemann. Tumour-Associated Macrophages. Springer, 2014.

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49

Miller-Hodges, Eve, and Christopher Mitchell. The patient with Wilms tumour. Edited by Giuseppe Remuzzi. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0173_update_001.

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Abstract:
Wilms tumour is the most common renal tumour in childhood. It is most commonly identified as a large abdominal mass. Treatment by surgical removal and chemotherapy, and radiotherapy in more advanced stages, is curative in most patients. Five year survival is over 90%. Survivors may be at some risk from long term complications including the effects of radiotherapy on the remaining kidney.A small minority of Wilms tumours occur in individuals with an underlying mutation in the WT1 gene. WT1 mutations may also cause developmental abnormalities of the genitourinary system, and renal disease including steroid-resistant nephrotic syndrome / focal segmental glomerulosclerosis.
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50

Plotkin, Scott R., Jaclyn A. Biegel, David Malkin, Robert Martuza, and D. Gareth Evans. Familial tumour syndromes: neurofibromatosis, schwannomatosis, rhabdoid tumour predisposition, Li–Fraumeni syndrome, Turcot syndrome, Gorlin syndrome, and Cowden syndrome. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199651870.003.0015.

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Abstract:
‘Familial tumour syndromes’ reviews some of the genetic syndromes associated with an increased incidence of nervous system tumours, including neurofibromatosis 1, neurofibromatosis 2, schwannomatosis, rhabdoid tumour predisposition, Li–Fraumeni syndrome, Turcot syndrome, Gorlin syndrome, and Cowden syndrome. The chapter reviews the epidemiology of these rare conditions with discussion of current diagnostic criteria. It reviews the genetic basis and pathogenesis of the conditions as well as the availability of genetic testing. It covers the clinical aspects of these conditions, including clinical presentation, associated nervous system tumours, and recommended management of these syndromes with a discussion of the role of imaging. The review is written for the practising neuro-oncologist and other specialists who care for patients with genetic syndromes affecting the nervous system.
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