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1

Swales, John Douglas. Clinical and investigative features of hypertension. Current Medical Literature, 1988.

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Mair, Nicholas S. Yersiniosis: Lab diagnosis : clinical features : epidemiology. Public Health Laboratory Service, 1986.

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Groningen, Rijksuniversiteit te, ed. Clinical and diagnostic features of amyloidosis. [s.n.], 1985.

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C, Sutton George, and Fox Kim M, eds. Clinical and investigative features of cardiac pathology. Current Medical Literature, 1987.

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C, Sutton George, and Fox Kim M, eds. Clinical and investigative features of cardiac pathology. CurrentMedical Literature, 1988.

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C, Sutton George, and Fox Kim M, eds. Clinical and investigative features of cardiac pathology. Current Medical Literature, 1988.

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Friesen, A. Microbiological pharmacological and clinical features of Bactrim. W. Zuckschwerdt, 1989.

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C, Sutton George, Fox Kim M, and Bayliss John, eds. Clinical and investigative features of cardiac pathology. Current Medical Literature, 1988.

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C, Sutton George, and Fox Kim M, eds. Clinical and investigative features of cardiac pathology. Current Medical Literature, 1988.

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10

1946-, Clark Christopher M., and Trojanowski John Q, eds. Neurodegenerative dementias: Clinical features and pathological mechanisms. McGraw-Hill, Health Professions Division, 2000.

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11

Kwiatkowski, David J., Vicky Holets Whittemore, and Elizabeth A. Thiele. Tuberous sclerosis complex: Genes, clinical features and therapeutics. Wiley-VCH, 2010.

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Uliano, Morandi, Moran Cesar, Schoenhuber Rudolf, and SpringerLink (Online service), eds. Thymus Gland Pathology: Clinical, Diagnostic, and Therapeutic Features. Springer Milan, 2008.

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universitet, Københavns, ed. Clinical and prognostic features of advanced ovarian carcinoma. Lægeforeningens Forlag, 1993.

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P, Sharma Om, ed. Atlas of sarcoidosis: Pathogenesis, diagnosis, and clinical features. Springer, 2005.

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15

Kjetil, Søreide, and Søiland Håvard, eds. Clinical, genetic, and molecular precursor features in colorectal neoplasia. Nova Science, 2008.

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Peter, Lance M., ed. Adenomatous polyps of the colon: Pathobiological and clinical features. Springer-Verlag, 1990.

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17

Payton, Antony. HLA associations with clinical features of onchoceriasis in Nigerians. University of Manchester, 1995.

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18

Mosiichuk, V. Self-realization of future clinical psychologists: educational and professional features. East West, 2017.

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19

Neittaanmäki, Heikki. Cold urticaria: Clinical features, histamine release, and effectiveness of treatments. Dept. of Dermatology, University of Kuopio, 1988.

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20

Lester, Rebecca, and John Rex. Fungaemia and disseminated infection. Edited by Christopher C. Kibbler, Richard Barton, Neil A. R. Gow, Susan Howell, Donna M. MacCallum, and Rohini J. Manuel. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198755388.003.0025.

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Invasive fungal disease can present without localization or obvious target organ involvement. These disseminated mycoses occur predominantly in patients who are immunocompromised, particularly from haematological malignancy and HIV. Candidiasis and aspergillosis are the commonest forms of disseminated fungal infection worldwide, but an increasing number of non-Candida yeasts and non-Aspergillus moulds have emerged as important causes of invasive disease in recent years. Endemic fungi such as Histoplasma capsulatum are important causes of invasive disease within limited geographic regions. Feve
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21

Khan, Muhammad Asim. Clinical features. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198734444.003.0011.

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The leading chronic progressive inflammatory disease of the sacroiliac joints and the spinal column, traditionally known as ankylosing spondylitis (AS), is a relatively common but insidious rheumatic disease that can cause progressive limitation of physical function. It is a prototype of related forms of arthritis, grouped under the term spondyloarthritis that is subdivided into predominantly axial and predominantly peripheral forms. This chapter details the clinical features of axial spondyloarthritis, a term that encompasses ankylosing spondylitis. There is a predilection for the inflammatio
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22

Candida And Candidiasis. ASM Press, 2012.

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23

Feist, Eugen, and Gerd-R. Burmester. Rheumatoid arthritis—clinical features. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0111.

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Rheumatoid arthritis (RA) presents with variable clinical features, making this most frequent chronic systemic autoimmune disease with characteristic joint involvement a diagnostic and therapeutic challenge. This chapter describes in detail the different clinical, laboratory and imaging findings in patients with RA. In addition to the characteristic arthritic involvement, which can lead to severe joint changes with progressive destruction and loss of function, other systemic disease manifestations as well as an increased risk for cardiovascular events and non-Hodgkin's lymphoma with relevance
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Bowman, Simon, John Hamburger, Elizabeth Price, and Saaeha Rauz. Sjögren’s syndrome—clinical features. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0127.

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Sjögren's syndrome is a chronic, immune-mediated, condition of unknown aetiology characterized by focal lymphocytic infiltration of exocrine glands associated with dry mouth and eyes. It occurs in its own right (primary Sjögren's syndrome, pSS), or as a late feature of other rheumatic diseases such as rheumatoid arthritis, systemic lupus erythematosus or scleroderma (secondary Sjögren's syndrome). There is a strong female bias. pSS typically affects women in their middle years with an estimated prevalence of 0.1–0.6%. 75% of patients have anti-Ro and/or anti-La antibodies, often with raised im
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Bowman, Simon, John Hamburger, Elizabeth Price, and Saaeha Rauz. Sjögren’s syndrome—clinical features. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0127_update_001.

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Sjögren’s syndrome is a chronic, immune-mediated, condition of unknown aetiology characterized by focal lymphocytic infiltration of exocrine glands associated with dry mouth and eyes. It occurs in its own right (primary Sjögren’s syndrome, pSS), or as a late feature of other rheumatic diseases such as rheumatoid arthritis, systemic lupus erythematosus or scleroderma (secondary Sjögren’s syndrome). There is a strong female bias. pSS typically affects women in their middle years with an estimated prevalence of 0.1–0.6%. 75% of patients have anti-Ro and/or anti-La antibodies, often with raised im
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Dalbeth, Nicola. Clinical features of gout. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198748311.003.0005.

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About 60% of the variance in serum urate levels can be explained by inherited genetic factors, but the extent of the contribution of genetic factors to gout in the presence of hyperuricaemia is not known. Genome-wide association studies in Europeans have identified 28 loci controlling serum urate levels, although the molecular basis of the majority of these genetic associations is currently unknown. The SLC2A9 and ABCG2 renal and gut uric acid transporters have very strong effects on urate levels and the risk of gout. Other uric acid transporters (e.g. SLC22A11/OAT478, SLC22A12/URAT1) and a gl
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27

Lam, Raymond W. Clinical features and diagnosis. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199692736.003.0004.

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• Depression is associated with a number of physical, emotional, and cognitive symptoms.• Sub-typing of major depressive disorder has implications for treatment choice and selection.• The differential diagnosis of depression includes bereavement, bipolar disorder, and other medical or substance-induced conditions.Depression is associated with many different types of symptoms which can result to a variable presentation in any given person. The features of depression can be physical (sleep, energy, appetite, libido), emotional (low mood, anxiety, crying) or cognitive (guilt, pessimism, suicidal
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Sobel, Jack D. Clinical Perspectives: Terconazole, an Advance in Vulvovaginal Candidiasis Therapy. McGraw, 1988.

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29

Surlin, Petra. Periodontology: Fundamentals and Clinical Features. IntechOpen, 2022.

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Gross, Wolfgang L., and Julia U. Holle. Clinical features of ANCA-associated vasculitis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0131.

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The primary ANCA-associated vasculitides are granulomatosis with polyangiitis (Wegener's, GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA, Churg-Strauss syndrome, CSS). They predominantly affect small (and medium-sized) vessels and share a variable association with ANCA (anti-neutrophil cytoplasm antibody) directed against neutrophil proteinase 3 (PR3, mainly in GPA) and myeloperoxidase (MPO, mainly in MPA and CSS). Crescentic necrotizing glomerulonephritis and alveolar haemorrhage due to pulmonary capillaritis represent classical (vasculitic) orga
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31

Rhodes, Ben, and Caroline Gordon. Clinical features of systemic lupus erythematosus. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198739180.003.0004.

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Systemic lupus erythematosus is characterized by diverse clinical features that reflect underlying multisystem inflammation. This chapter discusses the range of these clinical presentations, including common problems such as arthritis, serositis, and cutaneous lupus, along with rarer manifestations such as neuropsychiatric lupus, and gastrointestinal and cardiac disease. It highlights both the diagnostic features that are an essential part of disease classification, and also less specific, but common, clinical features such as fatigue. Recognized organ-specific classification systems for lupus
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Haddad, Fuad Sami, Oreste de Divitiis, and Mehmet Turgut. Neurobrucellosis: Clinical, Diagnostic and Therapeutic Features. Springer London, Limited, 2016.

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33

Murrell, Dédée F. Blistering Diseases: Clinical Features, Pathogenesis, Treatment. Springer London, Limited, 2015.

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Murrell, Dédée F. Blistering Diseases: Clinical Features, Pathogenesis, Treatment. Springer, 2015.

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Haddad, Fuad Sami, Oreste de Divitiis, and Mehmet Turgut. Neurobrucellosis: Clinical, Diagnostic and Therapeutic Features. Springer, 2019.

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Murrell, Dedee. Blistering Diseases: Clinical Features, Pathogenesis, Treatment. Springer Berlin / Heidelberg, 2016.

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Haddad, Fuad Sami, Oreste de Divitiis, and Mehmet Turgut. Neurobrucellosis: Clinical, Diagnostic and Therapeutic Features. Springer, 2015.

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38

Dystonia: Etiology, Clinical Features, and Treatment. Lippincott Williams & Wilkins, 2004.

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39

Epidermolysis Bullosa: Pathogenesis and Clinical Features. Elsevier - Health Sciences Division, 2010.

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40

Gordon, Caroline. Systemic lupus erythematosus—clinical features and aetiopathogenesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0117.

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Systemic lupus erythematosus (SLE or lupus) is a multisystem, autoimmune disease associated with the formation of autoantibodies that form pathological immune complexes and activate a number of inflammatory pathways. The disease is characterized by remissions and relapses (flares) that can present with a variety of clinical manifestations. The symptoms and signs may range from mild features that can be treated easily to organ and even life threatening manifestations requiring potent immunosuppression. This chapter will review the epidemiology and pathology of lupus, then the clinical features
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41

Misbah, Siraj. Clinical features and diagnosis of immunological disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0294.

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Immunological disease can be broadly defined as a spectrum of problems ranging from failure of the immune system (primary or secondary immunodeficiency) to the clinical consequences of an overzealous immune system, manifesting clinically as autoimmunity, allergy, or, rarely, as an autoinflammatory syndrome. This chapter addresses the clinical features and diagnosis of immunological disease.
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42

ME/CFS: Causes, Clinical Features and Diagnosis. MDPI, 2022. http://dx.doi.org/10.3390/books978-3-0365-2438-2.

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Abhishek, Abhishek, and Michael Doherty. Clinical features of calcium pyrophosphate crystal deposition. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199668847.003.0050.

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Calcium pyrophosphate deposition (CPPD) occurs in the elderly, and is commonly asymptomatic. However, it can cause acute calcium pyrophosphate (CPP) crystal arthritis, chronic CPP crystal inflammatory arthritis, and is frequently present in joints with osteoarthritis (OA). Acute CPP crystal arthritis presents with rapid onset of acute synovitis, which frequently affects the knees, wrists, shoulders, and elbows. It can mimic sepsis in the elderly, and may require hospital admission. Patients with CPPD plus OA may have more inflammatory signs and symptoms (e.g. joint swelling, stiffness) than th
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44

Periodontology - Fundamentals and Clinical Features [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.87277.

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Murillo-Rodríguez, Eric, Emmanuel S. Onaivi, Nissar A. Darmani, and Edward Wagner, eds. Endocannabinoids: Molecular, Pharmacological, Behavioral and Clinical Features. BENTHAM SCIENCE PUBLISHERS, 2013. http://dx.doi.org/10.2174/97816080502841130101.

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Pesci, A., Giorgia Dalpiaz, R. Polverosi, Mario Maffessanti, and M. Zompatori. Diffuse Lung Diseases: Clinical Features, Pathology, HRCT. Springer London, Limited, 2007.

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Aguilar, Keith. Facial Paralysis: Clinical Features, Management and Outcomes. Nova Science Publishers, Incorporated, 2016.

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Lewis, R. A. Sickle Stages Clinical Features in West Africans. Panther House, 2000.

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(Contributor), R. Polverosi, M. Zompatori (Contributor), A. Pesci (Contributor), A. Cancellieri (Contributor), Mario Maffessanti (Editor), and Giorgia Dalpiaz (Editor), eds. Diffuse Lung Diseases: Clinical Features, Pathology, HRCT. Springer, 2006.

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Khamidov, O. A., Z. N. Nurmurzaev, D. Zh Yakubov, S. O. Gaybullaev, and M. S. Usarov. Clinical and Sonic Features of Cervical Cancer. Primedia eLaunch LLC, 2023.

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