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1

Ogbureke, Kalu U. E. Oral cancer. Rijeka, Croatia: InTech Europe, 2012.

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2

Harris, Michael K. Oral cancer: Causes, diagnosis, and treatment. Hauppauge, N.Y: Nova Science Publishers, 2010.

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3

S, Avery B., ed. Oral cancer: A synopsis of pathology and management. Oxford: Wright, 1998.

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4

Consensus Development Conference on Oral Complications of Cancer Therapies-- Diagnosis, Prevention, and Treatment (1989 Bethesda, Md.). Consensus Development Conference on Oral Complications of Cancer Therapies: Diagnosis, prevention and treatment. Bethesda, MD: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Cancer Institute, 1990.

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5

Kirita, Tadaaki, and Ken Omura. Oral Cancer: Diagnosis and Therapy. Springer, 2015.

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6

Kirita, Tadaaki, and Ken Omura. Oral Cancer: Diagnosis and Therapy. Springer, 2015.

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7

Kirita, Tadaaki, and Ken Omura. Oral Cancer: Diagnosis and Therapy. Springer, 2016.

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8

1926-, Silverman Sol, and American Cancer Society, eds. Oral cancer. 5th ed. Hamilton, ON: B.C. Decker, 2003.

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9

Oral Cancer: Diagnosis, Management, and Rehabilitation. Thieme Medical Pub, 2007.

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10

Oral cancer: Diagnosis, management, and rehabilitation. New York: Thieme, 2007.

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11

Oral cancer: Diagnosis, management, and rehabilitation. New York, NY: Thieme Medical Publishers, 2006.

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12

Greenspan, John S., and Saman Warnakulasuriya. Textbook of Oral Cancer: Prevention, Diagnosis and Management. Springer, 2020.

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13

Managing The Oral Effects Of Cancer Treatment Diagnosis To Survivorship. Oncology Nursing Society, 2011.

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14

A, Ord Robert, and Blanchaert Remy H, eds. Oral cancer: The dentist's role in diagnosis, management, rehabilitation, and prevention. Chicago: Quintessence, 1999.

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15

(Editor), Robert A. Ord, and Remy H. Blanchaert (Editor), eds. Oral Cancer: The Dentist's Role in Diagnosis, Management, Rehabilitation, and Prevention. Quintessence Publishing (IL), 2000.

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16

Diagnosis and Management of Skin Cancer, An Issue of Oral and Maxillofacial Surgery Clinics (The Clinics: Surgery). Saunders, 2005.

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17

Powers, David B. Wound Ballistics and Management: An Issue of Oral and Maxillofacial Surgery Clinics. Saunders, 2005.

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18

W, Johnson Newell, and Royal Society of Medicine (Great Britain). Section of Odontology., eds. Risk markers for oral diseases. Cambridge: Cambridge University Press, 1991.

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19

Robinson, Max, Keith Hunter, Michael Pemberton, and Philip Sloan. Soames' & Southam's Oral Pathology. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199697786.001.0001.

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A sound understanding of clinical oral pathology is essential if a dental clinician is to navigate successfully through clinical guidelines, make timely referrals to specialists, and provide good care for patients. This new edition of Soames' & Southam's Oral Pathology provides a clear and friendly guide for students, practitioners, and the whole dental team. Thoroughly updated for today's clinical practice, this textbook covers 'must-know' oral pathology and integrates key aspects of oral medicine. It begins by explaining the principles of clinical assessment, the synthesis of a differential diagnosis, and the selection of further investigations including laboratory tests. Ten chapters bring this theory to life by looking at the clinical and pathological features of a wide range of common oral diseases including oral cancer, salivary gland disorders, and diseases of the jaws. Two new chapters address skin diseases affecting the oro-facial region and neck lumps. A final chapter highlights the importance of clinical oral pathology in the context of systemic human disease. New radiology content includes examples of cross-sectional imaging. Photomicrographs have been replaced with carefully selected images to illustrate key pathological features. Each chapter includes key points boxes and tables to aid learning. Written by experts in both oral pathology and oral medicine, this new edition is a must-have for dentistry students, and those working in the field, providing current and trustworthy information.
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20

Murphy, Barbara A., Lauren A. Zatarain, Anthony J. Cmelak, Steven Bayles, Ellie Dowling, Cheryl R. Billante, Sheila Ridner, et al. Palliative issues in the care of patients with cancer of the head and neck. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656097.003.0145.

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Head and neck cancer (HNC) refers to tumours arising from the epithelial lining of the upper aerodigestive track, including the oral cavity, larynx, pharynx, paranasal sinuses, and salivary glands. There are 50,000 cases of HNC diagnosed annually within the United States. The majority of tumours (> 90%) are squamous cell carcinomas. Risk factors include tobacco, alcohol, and areca nuts; human papilloma virus (HPV) or Epstein-Barr virus; and mucosal irritation. Previously considered to be a disease of older adults, the epidemic of HPV-associated oropharyngeal cancers has led to a striking increase in HNC among middle-aged adults. Symptoms are usually present at the time of diagnosis and remain problematic through the terminal phase. For those patients who are cured, long-term biopsychosocial sequelae may persist for years. Thus, assessment and treatment of palliative issues is an intrinsic and vital component of care for the HNC patient.
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21

Singh, Surya P., and Arja M. Kullaa. Diagnosis of Oral Cancers: An Optical Perspective. SPIE PRESS, 2016. http://dx.doi.org/10.1117/3.2235415.

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22

Tworoger, Shelley S., Amy L. Shafrir, and Susan E. Hankinson. Ovarian Cancer. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0046.

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Worldwide, ovarian cancer is the seventh most commonly diagnosed cancer and the eighth most common cause of death from cancer. In 2012, 239,000 women were diagnosed with ovarian cancer and 152,000 women died of the disease worldwide. In the United States in 2015, an estimated 21,290 women were newly diagnosed with ovarian cancer and 14,180 died from the disease. Both incidence and mortality have decreased over time in the United States, with a 1.6% and 2.1% annual decrease, respectively, from 2003 to 2012. Ovarian cancers can arise from epithelial, germ, or stromal cells, although about 90% are epithelial in origin. Risk factors best confirmed to increase risk of ovarian cancer include age and a family history of ovarian cancer, while parity, oral contraceptive use, and tubal ligation decrease risk. Several etiologic pathways, including hormonal and inflammatory pathways, have garnered substantial support from both epidemiologic and laboratory studies, although many questions remain.
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23

Sagher, Oren, Emily Levin, and Julie Pilitsis, eds. Pain Neurosurgery. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780190887674.001.0001.

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Part of the Neurosurgery by Example series, this volume on pain neurosurgery presents exemplary cases in which renowned authors guide readers through the assessment and planning, decision making, surgical procedure, after care, and complication management of common and uncommon disorders. The cases explore the spectrum of clinical diversity and complexity within pain neurosurgery, including trigeminal neuralgia, postherpetic neuralgia, occipital neuralgia, percutaneous cordotomy for cancer-associated pain, chronic lumbar radiculopathy, and more. Each chapter also contains ‘pivot points’ that illuminate changes required to manage patients in alternate or atypical situations, and pearls for accurate diagnosis, successful treatment, and effective complication management. Containing a focused review of medical evidence and expected outcomes, Pain Neurosurgery is appropriate for neurosurgeons who wish to learn more about a subspecialty, and those preparing for the American Board of Neurological Surgery oral examination.
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24

Hollak, Carla E. M. Gaucher Disease. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0047.

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Gaucher disease is frequently diagnosed in adulthood and may manifest at any age. Chronic neuronopathic forms are rarely seen but may come to the attention of the adult physician. Nonneuronopathic or type 1 disease is extremely variable. Main symptoms are cytopenia, hepatosplenomegaly and bone disease. The majority of patients diagnosed in adulthood present with thrombocytopenia and splenomegaly. In moderate to severe disease, treatment with intravenous enzyme replacement is highly effective. Substrate reduction therapy with miglustat or eliglustat is an oral alternative for some. Awareness of a number of severe complications and associated conditions, including irreversible bone disease, rare cancers and Parkinson's disease, is of importance.
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