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A large number of diseases affect salivary gland (SG) secretion through different mechanisms, leading to SG dysfunction and associated oral problems. The glands may suffer from viral, bacterial, and, albeit rarely, fungal infections, which may cause painful swelling or obstruction; they could also become the target of an autoimmune attack or may be affected by various benign and malignant tumors which consist of a heterogeneous group of lesions with complex clinical–pathological characteristics. The loss of normal SG function results in widespread deterioration of oral health. This book, entitled “Diseases of Salivary Glands”, provides an overview of recent advances in the field of SG disorders, focusing on the cellular and molecular mechanisms involved in the pathogenesis of SG diseases and on the most innovative investigation techniques that could help to preserve patients’ health, function, and quality of life.

Medicine --- salivary glands --- minor salivary glands --- salivary gland carcinoma --- mucoepidermoid carcinoma --- in situ carcinoma --- intra-cystic carcinoma --- chronic kidney disease --- salivary gland dysfunction --- salivary biomarkers --- oxidative stress --- nitrosative stress --- viral infection --- Epstein-Barr virus --- HTLV-1 --- salivary gland epithelial cell --- Hashimoto’s disease --- saliva --- Sjögren’s syndrome --- autoimmune disease --- physiopathology --- treatment --- diagnosis --- review --- primary Sjögren’s syndrome --- imaging --- salivary gland --- sialography --- salivary gland ultrasonography --- magnetic resonance imaging --- sialendoscopy --- salivary gland scintigraphy --- positron emission tomography --- NF-κB --- inflammation --- autoimmunity --- innate cells --- adaptive cells --- MR sialography --- dynamic --- sublingual gland ducts --- xerostomia --- SGEC --- immortalization --- acinar --- ductal --- spheroid --- n/a --- autoimmune diseases --- Sjögren syndrome --- B-cell lymphoma --- extranodal marginal zone lymphoma --- MALT lymphoma --- primary breast lymphoma --- radiation --- hyposalivation --- purinergic signaling --- bystander effect --- P2 receptors --- radioprotection --- head and neck cancer --- oral candidiasis --- Hashimoto's disease --- Sjögren's syndrome --- primary Sjögren's syndrome --- Sjögren syndrome

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Spinocerebellar Degenerations. --- Ataxia --- Nervous system --- -Neurogenetics --- Early Onset Cerebellar Ataxia --- Familial Spinocerebellar Degenerations --- Garland-Moorhouse Syndrome --- Hereditary Oligophrenic Cerebello-Lental Degeneration --- Hereditary Spinocerebellar Degenerations --- Inherited Spinocerebellar Degenerations --- Late Onset Cerebellar Ataxia --- Marie's Cerebellar Ataxia --- Marinesco-Garland Syndrome --- Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism --- Marinesco-Sjogren Syndrome-Myopathy --- Marinesco-Sjogren-Garland Syndrome --- Marinesco-Sjögren Syndrome --- Spino Cerebellar Degenerations --- Spino-Cerebellar Degenerations --- Spinocerebellar Diseases --- Ataxias, Hereditary --- Cerebellar Ataxia, Early Onset --- Cerebellar Ataxia, Late Onset --- Cerebellar Degenerations, Primary --- Corticostriatal-Spinal Degeneration --- Marie Cerebellar Ataxia --- Marinesco-Sjogren Syndrome --- Spinocerebellar Degeneration --- Ataxia, Hereditary --- Cerebellar Ataxia, Marie --- Cerebellar Ataxia, Marie's --- Cerebellar Degeneration, Primary --- Corticostriatal Spinal Degeneration --- Corticostriatal-Spinal Degenerations --- Degeneration, Corticostriatal-Spinal --- Degeneration, Familial Spinocerebellar --- Degeneration, Hereditary Spinocerebellar --- Degeneration, Inherited Spinocerebellar --- Degeneration, Primary Cerebellar --- Degeneration, Spino Cerebellar --- Degeneration, Spino-Cerebellar --- Degeneration, Spinocerebellar --- Degenerations, Corticostriatal-Spinal --- Degenerations, Familial Spinocerebellar --- Degenerations, Hereditary Spinocerebellar --- Degenerations, Inherited Spinocerebellar --- Degenerations, Primary Cerebellar --- Degenerations, Spino Cerebellar --- Degenerations, Spinocerebellar --- Familial Spinocerebellar Degeneration --- Garland Moorhouse Syndrome --- Hereditary Ataxia --- Hereditary Ataxias --- Hereditary Oligophrenic Cerebello Lental Degeneration --- Hereditary Spinocerebellar Degeneration --- Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic --- Inherited Spinocerebellar Degeneration --- Marinesco Garland Syndrome --- Marinesco Sjogren Garland Syndrome --- Marinesco Sjogren Syndrome --- Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism --- Marinesco Sjogren Syndrome Myopathy --- Marinesco Sjögren Syndrome --- Primary Cerebellar Degeneration --- Primary Cerebellar Degenerations --- Spino Cerebellar Degeneration --- Spino-Cerebellar Degeneration --- Spinocerebellar Degeneration, Familial --- Spinocerebellar Degeneration, Hereditary --- Spinocerebellar Degeneration, Inherited --- Spinocerebellar Degenerations, Familial --- Spinocerebellar Degenerations, Hereditary --- Spinocerebellar Degenerations, Inherited --- Spinocerebellar Disease --- Syndrome, Garland-Moorhouse --- Syndrome, Marinesco-Garland --- Syndrome, Marinesco-Sjogren --- Syndrome, Marinesco-Sjogren-Garland --- Syndrome, Marinesco-Sjögren --- Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren --- Syndrome-Myopathy, Marinesco-Sjogren --- Genetics --- Neurosciences --- Organs (Anatomy) --- Movement disorders --- Diseases --- -Genetic aspects --- Genetic aspects --- Neurogenetics --- Spinocerebellar Degenerations --- Diseases&delete& --- Marinesco-Sjögren Syndrome --- Marinesco Sjögren Syndrome --- Syndrome, Marinesco-Sjögren