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    Year Entries
  Dysnomia -- See Anomia
A language dysfunction characterized by the inability to name people and objects that are correctly perceived. The individual is able to describe the object in question, but cannot provide the name. This condition is associated with lesions of the dominant hemisphere involving the language areas, in particular the TEMPORAL LOBE. (From Adams et al., Principles of Neurology, 6th ed, p484)
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Dyspareunia : Clinical management of vulvodynia : tips and tricks / Alessandra Graziottin, Filippo Murina.  2011 1
Dyspepsia Diagnosis : Dyspepsia in clinical practice / edited by Marko Duvnjak.  2011 1
Dyspepsia Therapy : Dyspepsia in clinical practice / edited by Marko Duvnjak.  2011 1
  Dysphagia -- See Deglutition Disorders
Difficulty in SWALLOWING which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the PHARYNX and UPPER ESOPHAGEAL SPHINCTER; and esophageal dysphagia due to malfunction of the ESOPHAGUS.
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  Dysphasia -- See Aphasia
A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia.
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  Dysphasia Broca -- See Aphasia, Broca
An aphasia characterized by impairment of expressive LANGUAGE (speech, writing, signs) and relative preservation of receptive language abilities (i.e., comprehension). This condition is caused by lesions of the motor association cortex in the FRONTAL LOBE (BROCA AREA and adjacent cortical and white matter regions).
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Dyspnea Therapy   2
  Dyspraxia -- See Apraxias
A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7)
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  Dyssocial Behavior -- See Antisocial Personality Disorder
A personality disorder whose essential feature is a pervasive pattern of disregard for, and violation of, the rights of others that begins in childhood or early adolescence and continues into adulthood. The individual must be at least age 18 and must have a history of some symptoms of CONDUCT DISORDER before age 15. (From DSM-IV, 1994)
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Dyssomnias   2
Dyssomnias Therapy : Curing insomnia naturally with Chinese medicine / Bob Flaws.  1997 1
  Dysthymia -- See Dysthymic Disorder
Chronically depressed mood that occurs for most of the day more days than not for at least 2 years. The required minimum duration in children to make this diagnosis is 1 year. During periods of depressed mood, at least 2 of the following additional symptoms are present: poor appetite or overeating, insomnia or hypersomnia, low energy or fatigue, low self esteem, poor concentration or difficulty making decisions, and feelings of hopelessness. (DSM-IV)
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Dysthymic Disorder : Beating the blues : new approaches to overcoming dysthymia and chronic mild depression / Michael E. Thase and Susan S. Lang.  2004 1
Dysthymic Disorder Rehabilitation : Beating the blues : new approaches to overcoming dysthymia and chronic mild depression / Michael E. Thase and Susan S. Lang.  2004 1
Dystocia Diagnosis : Shoulder dystocia and birth injury : prevention and treatment / James A. O'Leary, editor.  2009 1
Dystocia Therapy : Shoulder dystocia and birth injury : prevention and treatment / James A. O'Leary, editor.  2009 1
  Dystonia -- 2 Related Mesh   2
Dystonia   3
Dystonia Drug Therapy : Techniques of botulinum toxin injections in the head and neck / Michael S. Benninger, P. Daniel Knott.  2012 1
Dystonia Musculorum Deformans   2
Dystonia Psychology : The dystonia patient : a guide to practical management / [edited by] Michael S. Okun.  2009 1
Dystonia Therapy   2
Dystonic Disorders   4
  Dystrophia Myotonica -- See Myotonic Dystrophy
Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2.
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  Dystrophin -- See Also Muscular Dystrophy, Duchenne
An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
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  E B Virus -- See Herpesvirus 4, Human
The type species of LYMPHOCRYPTOVIRUS, subfamily GAMMAHERPESVIRINAE, infecting B-cells in humans. It is thought to be the causative agent of INFECTIOUS MONONUCLEOSIS and is strongly associated with oral hairy leukoplakia (LEUKOPLAKIA, HAIRY;), BURKITT LYMPHOMA; and other malignancies.
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  E Cig -- See Electronic Nicotine Delivery Systems
Devices or objects designed to provide NICOTINE in the form of an inhaled aerosol.
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  E Cigarette -- See Electronic Nicotine Delivery Systems
Devices or objects designed to provide NICOTINE in the form of an inhaled aerosol.
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  E Coli -- See Escherichia coli
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
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  E Coli O157 -- See Escherichia coli O157
A verocytotoxin-producing serogroup belonging to the O subfamily of Escherichia coli which has been shown to cause severe food-borne disease. A strain from this serogroup, serotype H7, which produces SHIGA TOXINS, has been linked to human disease outbreaks resulting from contamination of foods by E. coli O157 from bovine origin.
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  E Coli O157 H7 -- See Escherichia coli O157
A verocytotoxin-producing serogroup belonging to the O subfamily of Escherichia coli which has been shown to cause severe food-borne disease. A strain from this serogroup, serotype H7, which produces SHIGA TOXINS, has been linked to human disease outbreaks resulting from contamination of foods by E. coli O157 from bovine origin.
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  E Mail -- See Electronic Mail
Messages between computer users via COMPUTER COMMUNICATION NETWORKS. This feature duplicates most of the features of paper mail, such as forwarding, multiple copies, and attachments of images and other file types, but with a speed advantage. The term also refers to an individual message sent in this way.
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  E2f Transcription Factor -- See E2F Transcription Factors
A family of basic helix-loop-helix transcription factors that control expression of a variety of GENES involved in CELL CYCLE regulation. E2F transcription factors typically form heterodimeric complexes with TRANSCRIPTION FACTOR DP1 or transcription factor DP2, and they have N-terminal DNA binding and dimerization domains. E2F transcription factors can act as mediators of transcriptional repression or transcriptional activation.
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E2f Transcription Factors : Rb and tumorigenesis / [edited by] Maurizio Fanciulli.  2006 1
  Eaggec -- See Escherichia coli
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
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Eagles : DDT wars : rescuing our national bird, preventing cancer, and creating EDF / Charles F. Wurster.  2015 1
Ear   4
Ear Anatomy And Histology   5
Ear Auricle : Prop├Ądeutik der Ohrakupunktur. English  2017 1
Ear Canal : The human ear canal / Bopanna B. Ballachanda ; contributions from Richard T. Miyamoto, R. Christopher Miyamoto, Brian Taylor.  2013 1
Ear Cartilage Abnormalities : Auricular reconstruction / [edited by] Francoise Firmin, Joseph Dusseldorp, Alexandre Marchac.  2017 1
Ear Cartilage Surgery : Auricular reconstruction / [edited by] Francoise Firmin, Joseph Dusseldorp, Alexandre Marchac.  2017 1
Ear Deformities Acquired Surgery   2
Ear Diseases   12
Ear Diseases Diagnosis   3
Ear Diseases History : Ophthalmology and otolaryngology / editor-in-chief, John Boyd Coates Jr. ; editor for ophthalmology, M. Elliott Randolph ; editor for otolaryngology, Norton Canfield ; associate editor, Elizabeth M. McFetridge.  1957 1
Ear Diseases Physiopathology : Middle ear diseases and surgery viewed from the physiology of pressure regulation / Haruo Takahashi.  2017 1
Ear Diseases Surgery   5
Ear Diseases Surgery Congresses : Cholesteatoma and ear surgery : an update.  2013 1
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