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LAF laminar air flow; Latin American female; leukocyte-activating factor; lymphocyte-activating factor
LAFB left anterior fascicular block
LAFR laminar air flow room
LAFU laminar air flow unit
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LAF Laminar Air Flow
LAF Lymphocyte Activating Factor
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  • Lafora body
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  • Lafora body type of myoclonus
    ¶óÆ÷¶ó üÇü ¸¶ÀÌ¿ÀŬ·Î´©½º.
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  • lafora body
    ¶óÆ÷¶ó ¼Òü, Lafora ¼Òü(¡­á³ô÷)
  • laforas disease
    ¶óÆ÷¶ó º´, Lafora º´(¡­Ü»)
  • laforas syndrome
    ¶óÆ÷¶ó ÁõÈıº, Lafora ÁõÈıº(¡­ñøý¦ÏØ)
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  • lymphocyte activating factor (LAF)
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  • Lafora's s.
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  • Lafon's reagent
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  • Lafora syndrome
    ¶óÆ÷¶ó ÁõÈıº
  • Lafora's body
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lafayette <zoology> The dollar fish.
A market fish, the goody, or spot (Liostomus xanthurus), of the southern coast of the United States.
Source: Websters Dictionary
(01 Mar 1998)
Lafora body An intraneural intracytoplasmic inclusion body composed of acid mucopolysaccharides, seen in familial myoclonus epilepsy; a recessive trait.
(05 Mar 2000)
Lafora body disease A form of progressive myoclonus epilepsy beginning from age 6 to 19; characterised by generalised tonic-clonic seizures, resting and action myoclonus, ataxia, dementia, and classic EEG findings, including polyspike and wave discharges; basophilic cytoplasmic inclusion bodies present in portions of the brain, the liver, and skin, as well as the duct cells of the sweat glands. Death usually occurs within 10 years of onset; autosomal recessive inheritance.
Synonym: Lafora's disease.
(05 Mar 2000)
Lafora's disease A form of progressive myoclonus epilepsy beginning from age 6 to 19; characterised by generalised tonic-clonic seizures, resting and action myoclonus, ataxia, dementia, and classic EEG findings, including polyspike and wave discharges; basophilic cytoplasmic inclusion bodies present in portions of the brain, the liver, and skin, as well as the duct cells of the sweat glands. Death usually occurs within 10 years of onset; autosomal recessive inheritance.
Synonym: Lafora's disease.
(05 Mar 2000)
Lafora, Gonzalo Rodriguez <person> Spanish neurologist, 1887-1971.
See: Lafora body, Lafora body disease, Lafora's disease.
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Lafora Disease - »õâ A form of stimulus sensitive myoclonic epilepsy inherited as an autosomal recessive condition. The most common presenting feature is a single seizure in the second decade of life. This is followed by progressive myoclonus, myoclonic seizures, tonic-clonic seizures, focal occipital seizures, intellectual decline, and severe motor and coordination impairments. Most affected individuals do not live past the age of 25 years. Concentric amyloid (Lafora) bodies are found in neurons, liver, skin, bone, and muscle (From Menkes, Textbook of Childhood Neurology, 5th ed, pp111-110)
    Synonyms : Lafora Body Disease, Lafora Body Disease, Late Onset, Lafora Progressive Myoclonic Epilepsy, Lafora Type Progressive Myoclonic Epilepsy, Lafora-Body Disease, Late Onset, Late Onset Lafora Body Disease, Progressive Myoclonic Epilepsy, Lafora, Disease, Lafora
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Lafora's disease myoclonus epilepsy: epilepsy characterized by clonus of muscle groups and progressive mental deterioration and genetic origin
Ãâó: wordnet.princeton.edu/perl/webwn
Lafora's bodies intracytoplasmic inclusions consisting of a complex of glycoprotein and acid mucopolysaccharide; widespread deposits of these bodies are found in Lafora's myoclonus epilepsy.
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
Lafora's sign picking of the nose regarded as an early sign of cerebrospinal meningitis.
Ãâó: www.merckmedicus.com/pp/us/hcp/thcp_dorlands_conte...
Lafora's disease A progressive myoclonic encephalopathy (PME) that is inherited as an autosomal recessive trait. Associated symptoms typically begin in childhood or early adolescence and include frequent seizures characterized by loss of consciousness and rhythmic contraction and relaxation of all muscle groups (generalized tonic-clonic seizures); sudden, involuntary, "shock-like" muscle jerks (myoclonus); and rapidly progressive deterioration of thought processing and acquired intellectual abilities ...
Ãâó: www.dbs-stn.org/glossary2.asp
Lafora's bodies Cytoplasmic inclusion bodies made of acid mucopolysaccharides. They may be found in neuronal tissues taken from patients with familial myoclonic epilepsy.
Ãâó:
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  • Lafayette
    (³²ÀÚÀ̸§)¶óÆÄ¿¹Æ® Marquis de ~(17571834)(ÇÁ¶û½ºÀÇ ±ºÀÎ,Á¤Ä¡°¡,¹Ì±¹ÀÌ µ¶¸³ÀüÀï¿¡ Á¾±ºÇÏ¿´°í ÇÁ¶û½º ´ëÇõ¸í ¶§¿¡µµ Ȱ¾à)
  • LAFTA
    Latin American Free Trade Association ¶óƾ ¾Æ¸Þ¸®Ä« ÀÚÀ¯ ¹«¿ª ¿¬ÇÕ
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LAF a university town in west central Indiana on the Wabash River
LAF a town in south central Louisiana
LAF French soldier who served under George Washington in the American Revolution (1757-1834)
LAF United States economist who proposed the Laffer curve (born in 1940)
LAF a graph purporting to show the relation between tax rates and government income
LAF French pirate who aided the United States in the War of 1812 and received an official pardon for his crimes (1780-1826)
LAF French pirate who aided the United States in the War of 1812 and received an official pardon for his crimes (1780-1826)
LAF epilepsy characterized by clonus of muscle groups and progressive mental deterioration and genetic origin
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  • Lafayette - »õâ
  • Lafayette, Marie Joseph Paul Yves Roch Gilbert du Motier de - »õâ
  • Lafayette, Marquis Marie Joseph Paul Yves Roch Gilbert du Motier de - »õâ
  • Lafcadio Hearn - »õâ
  • Laffer curve - »õâ
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