intranuclear inclusions
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intranuclear — Within the nucleus of a cell. * * * in·tra·nu·cle·ar n(y)ü klē ər adj situated or occurring within a nucleus <cytomegalic cells with prominent intranuclear inclusions (L. J. Dorfman)> <intranuclear DNA synthesis> * * *… … Medical dictionary
Dentatorubral-pallidoluysian atrophy — Classification and external resources OMIM 125370 DiseasesDB 32909 MeSH … Wikipedia
Inclusion body — Inclusion bodies are nuclear or cytoplasmic aggregates of stainable substances, usually proteins. They typically represent sites of viral multiplication in a bacterium or a eukaryotic cell and usually consist of viral capsid proteins. Inclusion… … Wikipedia
Huntington's disease — Classification and external resources A microscope image of … Wikipedia
Frontotemporal lobar degeneration — Infobox Disease Name = PAGENAME Caption = A human brain showing frontotemporal lobar degeneration causing frontotemporal dementia. DiseasesDB = 10034 ICD10 = ICD9 = ICDO = OMIM = 600274 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID =… … Wikipedia
Progressive multifocal leukoencephalopathy — ] natalizumabcite web |url=http://www.newscientist.com/channel/health/dn8796.html |title=Potential risks of powerful MS drug are weighed health 02 March 2006 New Scientist |accessdate=2008 01 28 |format= |work=] , chemotherapy cite journal… … Wikipedia
Creatine — For the use of creatine to increase athletic performance, see Creatine supplements. Not to be confused with creatinine. Creatine … Wikipedia
Eczema vaccinatum — is a rare severe adverse reaction to smallpox vaccination. It is characterized by serious local or disseminated, umbilicated, vesicular, crusting skin rashes in the face, neck, chest, abdomen, upper limbs and hands, caused by widespread infection … Wikipedia
ATN1 — is a protein found in nervous tissue.It is associated with a form of trinucleotide repeat disorder known as dentatorubral pallidoluysian atrophy or dentatorubropallidoluysian atrophy . PBB Summary section title = summary text = Dentatorubral… … Wikipedia
ATXN2 — Ataxin 2, also known as ATXN2, is a human gene. PBB Summary section title = summary text = Mutations in ATXN2 cause spinocerebellar ataxia type 2 (SCA2). The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of… … Wikipedia
