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"nuclear paralysis"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
  • ¿µ¹®
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  • bulbar paralysis
    ¿¬¼ö¸¶ºñ.
  • capsular paralysis
    ³»Æ÷¼º ¸¶ºñ(¡­Ø«Ýö).
  • convergence paralysis
    ´«¸ðÀ½¸¶ºñ, ÆøÁÖ¸¶ºñ
  • cortical facial paralysis
    ´ë³úÇÇÁú¼º ¾È¸é¸¶ºñ(ÓÞÒàù«òõàõäÔØü Ýö).
  • cortical paralysis
    ´ë³úÇÇÁú¼º ¸¶ºñ(ÓÞÒàù«òõàõ Ýö).
  • crossed paralysis
    ±³Â÷(¼º) ¸¶ºñ(¡­ Ýö).
  • crutch paralysis
    ¸ñ¹ß¸¶ºñ(¡­ Ýö).
  • diaphragm paralysis
    Ⱦ°æ¸·¸¶ºñ
  • diver-s paralysis
    ÀáÇÔº´(Ëö̰ËÓ).
  • divergence paralysis
    ´«¹ú¸²¸¶ºñ, °³»ê¸¶ºñ
  • divergence paralysis
    °³»ê¸¶ºñ(ËÒߤئÝö).
  • ephemeral adducter paralysis
    ÀϽüº ³»Àü±Ù¸¶ºñ(ìéãÁàõÒ®ï®ÐÉØ«Ýö).
  • epidemic infantile paralysis =p. infantills epidemica<³ª>
    À¯Ç༺ ¼Ò¾Æ¸¶ºñ.
  • essential paralysis
    º»Å¼º ¸¶ºñ.
  • extensor paralysis
    °ú½Å±Ù¸¶ºñ(¡­ Ýö).
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HIDA Scan hepato-iminodiacetic acid (lidofenin) [nuclear medicine scan]
HNF hepatocyte nuclear factor
HNF1A hepatocyte nuclear factor-1-alpha
hnRNA heterogeneous nuclear ribonucleic acid
hnRNP heterogeneous nuclear ribonucleoprotein
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EBNA 1 EBV nuclear antigen 1
EBNA 2 EB nuclear antigen 2
EBNA EB-determined nuclear antigen
EBNA EBV)-encoded nuclear antigen
EBER EBV)-encoded small nuclear RNAs
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musculospiral paralysis Paralysis of the muscles of the forearm due to injury of the radial (musculospiral) nerve.
(05 Mar 2000)
coonhound paralysis A polyradiculoneuritis of dogs (especially raccoon-hunting breeds) following a raccoon bite and characterised by weakness, hindlimb hyporeflexia, and a flaccid symmetrical tetraplegia.
(05 Mar 2000)
myogenic paralysis Inflammation of the anterior cornua of the spinal cord; an acute infectious disease caused by the poliomyelitis virus and marked by fever, pains, and gastroenteric disturbances, followed by a flaccid paralysis of one or more muscular groups, and later by atrophy.
Synonym: acute atrophic paralysis, myogenic paralysis.
(05 Mar 2000)
postdiphtheritic paralysis <otolaryngology> Paralysis affecting the uvula most frequently, but also any other muscle, due to toxic neuritis; usually appears in the second or third week following the beginning of the attack of diphtheria.
Synonym: diphtheritic paralysis.
(05 Mar 2000)
crossed paralysis alternating hemiplegia
crutch paralysis A form of pressure paralysis affecting the arm, and caused by compression of the brachial plexus or radial nerve by the crosspiece of a crutch.
Synonym: crutch palsy.
(05 Mar 2000)
posticus paralysis Paralysis of the posterior cricothyroid muscles.
(05 Mar 2000)
Pott's paralysis Paralysis of the lower part of the body and the extremities, due to pressure on the spinal cord as the result of tuberculous spondylitis.
Synonym: Pott's paralysis.
(05 Mar 2000)
pressure paralysis Paralysis due to compression of a nerve, nerve trunk, or spinal cord.
Synonym: pressure palsy.
(05 Mar 2000)
progressive bulbar paralysis Progressive weakness and atrophy of the muscles of the tongue, lips, palate, pharynx, and larynx, usually occurring in later life; most often caused by motor neuron disease.
Synonym: bulbar palsy, bulbar paralysis, Duchenne's disease, Erb disease, glossolabiolaryngeal paralysis, glossolabiopharyngeal paralysis.
(05 Mar 2000)
pseudobulbar paralysis Paralysis of the lips and tongue, simulating progressive bulbar paralysis, but due to supranuclear lesions with bilateral involvement of the upper motor neurons; characterised by speech and swallowing difficulties, emotional instability, and spasmodic, mirthless laughter.
(05 Mar 2000)
sensory paralysis Loss of sensation; anaesthesia.
(05 Mar 2000)
hyperkalaemic periodic paralysis A form of periodic paralysis in which the serum potassium level is elevated during attacks; onset occurs in infancy, attacks are frequent but relatively mild, and myotonia is often present; autosomal dominant inheritance.
(05 Mar 2000)
hypokalaemic periodic paralysis <biochemistry> A rare inherited disorder, affecting men more often than women, characterised by intermittent episodes of muscle weakness or paralysis.
One form, known as hypokalaemic periodic paralysis, is an autosomal recessive disorder that is characterised by bouts of muscle weakness (or paralysis) accompanied by low serum potassium levels.
Inheritance: autosomal recessive.
Incidence: 1 in 100,000.
(11 Jan 1998)
sleep paralysis <neurology, physiology> A condition that occurs in REM stage sleep. There is no movement of the skeletal muscles in this stage of sleep.
See: REM stage sleep.
(27 Sep 1997)
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