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Omsk hemorrhagic fever is caused by Omsk hemorrhagic fever virus (OHFV), a member of the Flavivirus family. The current species name is Orthoflavivirus omskense [4] according to International Committee on Taxonomy of Viruses taxonomy standards. The virus was discovered by Mikhail Chumakov and his colleagues between 1945 and 1947 in Omsk, Russia.
Another alternative to oligoclonal bands for MS diagnosis is the MRZ-reaction (MRZR), a polyspecific antiviral immune response against the viruses of measles, rubella and zoster found in 1992. [ 22 ] In some reports the MRZR showed a lower sensitivity than OCB (70% vs. 100%), but a higher specificity (92% vs. 69%) for MS. [ 22 ]
Omsk Giftedness Development Center (or, officially, Multidisciplinary Educational Center for Giftedness Development, Russian: Многопрофильный образовательный центр развития одарённости) is a secondary education institution in Russia, specified in the training for science olympiads in different school subjects, such as mathematics and physics.
MHC class III is a group of proteins belonging the class of major histocompatibility complex (MHC). Unlike other MHC types such as MHC class I and MHC class II, of which their structure and functions in immune response are well defined, MHC class III are poorly defined structurally and functionally.
SD Saint Vitus's dance (see Sydenham chorea) SDD Sensory discrimination disorder SDS Sudden death syndrome SHF Systolic heart failure: SIDS Sudden infant death syndrome: SIRS Systemic inflammatory response syndrome: SIS Shaken infant syndrome: SLE Systemic lupus erythematosus: SM Selective Mutism: SJS Stevens–Johnson syndrome: SMA Spinal ...
Lesions lips, patient with hemorrhagic hereditary telangiectasia. Hereditary hemorrhagic telangiectasia (HHT), also known as Osler–Weber–Rendu disease and Osler–Weber–Rendu syndrome, is a rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver, and brain.
Heřmanský–Pudlák syndrome (often written Hermansky–Pudlak syndrome or abbreviated HPS) is an extremely rare autosomal recessive [1] disorder which results in oculocutaneous albinism (decreased pigmentation), bleeding problems due to a platelet abnormality (platelet storage pool defect), and storage of an abnormal fat-protein compound (lysosomal accumulation of ceroid lipofuscin).
The following other wikis use this file: Usage on af.wikipedia.org Omsk; Usage on ceb.wikipedia.org Omsk (kapital sa lalawigan sa Rusya) Usage on de.wikipedia.org