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Apium
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D000077102 |
[A genus comprising several species of flowering plants with global distribution in the family APIACEAE.
, A plant species of the family APIACEAE. The stalks are a food source.
] |
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Chlorophyceae
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D000077105 |
[A class of green algae in the subdivision CHLOROPHYTINA distinguished by its ultrastructural morphology. Some species have distinct arrangement of flagella.
] |
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Epilepsy, Partial, Motor
|
D020938 |
[A disorder characterized by recurrent localized paroxysmal discharges of cerebral neurons that give rise to seizures that have motor manifestations. The majority of partial motor seizures originate in the FRONTAL LOBE (see also EPILEPSY, FRONTAL LOBE). Motor seizures may manifest as tonic or clonic movements involving the face, one limb or one side of the body. A variety of more complex patterns of movement, including abnormal posturing of extremities, may also occur.
] |
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Belladonna Alkaloids
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D03.132.760.180 |
|
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Solanaceous Alkaloids
|
D03.132.760 |
|
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Ginger
|
D020939 |
[Deciduous plant rich in volatile oil (OILS, VOLATILE). It is used as a flavoring agent and has many other uses both internally and topically.
] |
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Congenital Hyperinsulinism
|
D044903 |
[A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8).
] |
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Probiotics
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D019936 |
[Live microbial DIETARY SUPPLEMENTS which beneficially affect the host animal by improving its intestinal microbial balance. Antibiotics and other related compounds are not included in this definition. In humans, lactobacilli are commonly used as probiotics, either as single species or in mixed culture with other bacteria. Other genera that have been used are bifidobacteria and streptococci. (J. Nutr. 1995;125:1401-12)
] |
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Disability Studies
|
D000077109 |
[Interdisciplinary programs of academic study that de-stigmatize disease, illness, and impairment.
] |
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Epilepsy, Benign Neonatal
|
D020936 |
[A condition marked by recurrent seizures that occur during the first 4-6 weeks of life despite an otherwise benign neonatal course. Autosomal dominant familial and sporadic forms have been identified. Seizures generally consist of brief episodes of tonic posturing and other movements, apnea, eye deviations, and blood pressure fluctuations. These tend to remit after the 6th week of life. The risk of developing epilepsy at an older age is moderately increased in the familial form of this disorder. (Neurologia 1996 Feb;11(2):51-5)
] |
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Fat Emulsions, Intravenous
|
D27.720.752.733.500 |
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Parenteral Nutrition Solutions
|
D27.720.752.733 |
|
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Mannosidase Deficiency Diseases
|
D044904 |
[Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.
] |
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Diagnostic Techniques and Procedures
|
D019937 |
[Methods, procedures, and tests performed to diagnose disease, disordered function, or disability.
] |
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Ureteral Obstruction
|
C13.351.968.725.776 |
|
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Epilepsy, Partial, Sensory
|
D020937 |
[A disorder characterized by recurrent focal onset seizures which have sensory (i.e., olfactory, visual, tactile, gustatory, or auditory) manifestations. Partial seizures that feature alterations of consciousness are referred to as complex partial seizures (EPILEPSY, COMPLEX PARTIAL).
] |
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Cardiomyopathy, Hypertrophic
|
C14.280.238.100 |
|
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beta-Mannosidosis
|
D044905 |
[An inborn error of metabolism marked by a defect in the lysosomal isoform of BETA-MANNOSIDASE that results in lysosomal accumulation of mannose-rich intermediate metabolites containing 1,4-beta linkages. The human disease occurs through autosomal recessive inheritance and manifests in the form of a variety of symptoms that depend upon the type of gene mutation.
] |
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Cyclin D1
|
D019938 |
[Protein encoded by the bcl-1 gene which plays a critical role in regulating the cell cycle. Overexpression of cyclin D1 is the result of bcl-1 rearrangement, a t(11;14) translocation, and is implicated in various neoplasms.
] |
|
Gait Analysis
|
D000077107 |
[Determination of the level of functional limitation that may be due to pathology, and evaluating rehabilitative intervention of the way in which the body moves from one point to another. Most often, this is done by walking.
] |
