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Disease management -- Economic aspects : Investing in strategies to reverse the global incidence of TB / lead authors, Jaap Broekmans, coordinator ; Karen Caines, Joan E. Paluzzi  2005 1
Disease management -- Europe   2
Disease management -- Europe -- Case studies : Managing chronic conditions : experience in eight countries / Ellen Nolte, Cécile Knai, Martin McKee [editors]  2008 1
 

Disease Management Evaluation (Project) -- See DISMEVAL Project


  1
Disease management -- Handbooks, manuals, etc.   3
Disease management -- India : Why India is struggling to cope with Covid-19 / produced by Financial Times  2020 1
Disease management -- Periodicals   3
Disease management -- United States : Population health management in health care organizations / edited by Jennifer L. Hefner, Timothy R. Huerta, Ann Scheck McAlearney, the Ohio State University, Columbus, OH, USA  2014 1
Disease management -- United States -- Periodicals : Medicare disease management (Online)    1
 

Disease Managements -- See Disease Management


A broad approach to appropriate coordination of the entire disease treatment process that often involves shifting away from more expensive inpatient and acute care to areas such as preventive medicine, patient counseling and education, and outpatient care. This concept includes implications of appropriate versus inappropriate therapy on the overall cost and clinical outcome of a particular disease. (From Hosp Pharm 1995 Jul;30(7):596) 		  1
 

Disease Manifestation, Muscle -- See Neuromuscular Manifestations


Signs and symptoms associated with diseases of the muscle, neuromuscular junction, or peripheral nerves 		  1
 

Disease Manifestations, Muscle -- See Neuromuscular Manifestations


Signs and symptoms associated with diseases of the muscle, neuromuscular junction, or peripheral nerves 		  1
 

Disease mapping -- See Medical mapping


  1
 

Disease, Marble Bone -- See Osteopetrosis


Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY) 		  1
 

Disease Medicine, Infectious -- See Infectious Disease Medicine


A branch of internal medicine concerned with the diagnosis and treatment of INFECTIOUS DISEASES 		  1
 

Disease, Meniere -- See Meniere Disease


A disease of the inner ear (LABYRINTH) that is characterized by fluctuating SENSORINEURAL HEARING LOSS; TINNITUS; episodic VERTIGO; and aural fullness. It is the most common form of endolymphatic hydrops 		  1
 

Disease, Meniere's -- See Meniere Disease


A disease of the inner ear (LABYRINTH) that is characterized by fluctuating SENSORINEURAL HEARING LOSS; TINNITUS; episodic VERTIGO; and aural fullness. It is the most common form of endolymphatic hydrops 		  1
Disease [MESH]   2
 

Disease, Metabolic -- See Metabolic Diseases


Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) 		  1
 

Disease, Metabolic Bone -- See Bone Diseases, Metabolic


Diseases that affect the METABOLIC PROCESSES of BONE TISSUE 		  1
 

Disease, Mitochondrial -- See Mitochondrial Diseases


Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes 		  1
 

Disease Model, Animal -- See Disease Models, Animal


Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases 		  1
Disease models. : Toxocara : the enigmatic parasite / edited by Celia V. Holland and Huw V. Smith  2006 1
  Disease models, Animal -- 2 Related Subjects   2
Disease Models, Animal   142
Disease Models, Animals : Models of depressive disorders : psychological, biological, and genetic perspectives / edited by J. John Mann  1989 1
Disease Modesl, Animal : Recent advances on model hosts / Eleftherios Mylonakis [and others], editors  2012 1
 

Disease-Modifying Antirheumatic Drugs -- See Antirheumatic Agents


Drugs that are used to treat RHEUMATOID ARTHRITIS 		  1
 

Disease-Modifying, Antirheumatic Second-Line Drugs -- See Antirheumatic Agents


Drugs that are used to treat RHEUMATOID ARTHRITIS 		  1
 

Disease mortality -- See Mortality


All deaths reported in a given population 		  1
 

Disease, Mouth -- See Mouth Diseases


Diseases involving the MOUTH 		  1
 

Disease, Moya-Moya -- See Moyamoya Disease


A noninflammatory, progressive occlusion of the intracranial CAROTID ARTERIES and the formation of netlike collateral arteries arising from the CIRCLE OF WILLIS. Cerebral angiogram shows the puff-of-smoke (moyamoya) collaterals at the base of the brain. It is characterized by endothelial HYPERPLASIA and FIBROSIS with thickening of arterial walls. This disease primarily affects children but can also occur in adults 		  1
 

Disease, Myelodysplastic-Myeloproliferative -- See Myelodysplastic-Myeloproliferative Diseases


Clonal myeloid disorders that possess both dysplastic and proliferative features but are not properly classified as either MYELODYSPLASTIC SYNDROMES or MYELOPROLIFERATIVE DISORDERS 		  1
 

Disease, Myeloproliferative-Myelodisplastic -- See Myelodysplastic-Myeloproliferative Diseases


Clonal myeloid disorders that possess both dysplastic and proliferative features but are not properly classified as either MYELODYSPLASTIC SYNDROMES or MYELOPROLIFERATIVE DISORDERS 		  1
 

Disease, Myocardial -- See Cardiomyopathies


A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS) 		  1
 

Disease, Nail -- See Nail Diseases


Diseases of the nail plate and tissues surrounding it. The concept is limited to primates 		  1
 

Disease, Nasal -- See Nose Diseases


Disorders of the nose, general or unspecified 		  1
 

Disease, Nasopharyngeal -- See Nasopharyngeal Diseases


Pathological processes involving the NASOPHARYNX 		  1
 

Disease, Neglected -- See Neglected Diseases


Diseases that are underfunded and have low name recognition but are major burdens in less developed countries. The World Health Organization has designated six tropical infectious diseases as being neglected in industrialized countries that are endemic in many developing countries (HELMINTHIASIS; LEPROSY; LYMPHATIC FILARIASIS; ONCHOCERCIASIS; SCHISTOSOMIASIS; and TRACHOMA) 		  1
 

Disease, Neonatal -- See Infant, Newborn, Diseases


Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts 		  1
 

Disease, Nervous System -- See Nervous System Diseases


Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle 		  1
 

Disease, Neurohypophyseal -- See Pituitary Diseases


Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures 		  1
 

Disease, Neuronopathic Gaucher -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement 		  1
 

Disease, Non-Neuronopathic Gaucher -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement 		  1
 

Disease, Nose -- See Nose Diseases


Disorders of the nose, general or unspecified 		  1
 

Disease Notification -- See Also Mandatory Reporting


A legal requirement that designated types of information acquired by professionals or institutions in the course of their work be reported to appropriate authorities 		  1
Disease Notification.   7
Disease Notification -- Methods   2
 

Disease Notifications -- See Disease Notification


Notification or reporting by a physician or other health care provider of the occurrence of specified contagious diseases such as tuberculosis and HIV infections to designated public health agencies. The United States system of reporting notifiable diseases evolved from the Quarantine Act of 1878, which authorized the US Public Health Service to collect morbidity data on cholera, smallpox, and yellow fever; each state in the US has its own list of notifiable diseases and depends largely on reporting by the individual health care provider. (From Segen, Dictionary of Modern Medicine, 1992) 		  1
Disease -- nurses'instruction : Pathophysiology : the biologic basis for disease in adults and children / [edited by] Kathryn L. McCance, Sue E. Huether  1998 1
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