- ȭǥŰ/Ű ݱ - ESC

 
"progressive spastic spinal paralysis" ˻ Դϴ. ˻ ߿ Tab Ű ø ˻ â õ˴ϴ.
п ˻ ˻ : 15 : 7
  • ѱ
  • juvenile spinal muscular atrophy
    Ҿô()
  • lumbar spinal stenosis
    㸮ô߰(), ô߰()
  • posterior spinal sclerosis
    ôȭ, ôĻȭ
  • spinal
    1. - 2. ô- 3. ô- 4. ô-
  • spinal accessory nerve
    ôνŰ, ôνŰ
  • spinal accessory-facial nerve crossover
    ôξ󱼽Ű汳(), ôξȸŰ汳()
  • spinal anesthesia
    ô, ô߸
  • spinal angiogram
    ô
  • spinal animal
    ô
  • spinal arachnoid
    ôŹ̸, ôָ
  • spinal artery
    ô
  • spinal automatism
    ôڵ
  • spinal canal
    ôְ
  • spinal caries
    ô߰
  • spinal column
    ô
п ˻ ˻ : 15 : 7
  • ѱ
  • spinal anesthesia
    ô
  • spinal angiogram
    ô
  • spinal animal
    ô
  • spinal arachnoid
    ôŹ̸
  • spinal artery
    ô
  • spinal automatism
    ôڵ
  • spinal muscular atrophy
    ô
  • spinal absolute alcohol block
    ڿô
  • concussion of spinal cord
    ô
  • spinal canal
    (vertebral canal) ôְ
  • spinal caries
    ô߰
  • spinal column
    (vertebral) ô
  • spinal cord
    ô
  • spinal acessory-facial nerve crossover
    ôξ󱼽Ű汳
  • spinal disease
    ô
2 п ˻ ˻ : 15 : 7
  • ѱ
  • progressive lenticular degeneration
    ༺ ٺ()(ܨ())
  • progressive lingual hemiatrophy
    ()
  • progressive lingual hemiatrophy
    ༺ ( )
  • progressive lipodystrophy
    ༺ ̿.
  • progressive lipodystrophy
    ༺ ̿( ۸)
  • progressive mean
    (˧̰˻).
  • progressive multifocal leukoencephalopathy
    ༺ ٹ߼ ()
  • progressive multifocal leukoencephalopathy
    ༺ ( ܻ)
  • progressive muscle dystrophy
    ༺ ̿().
  • progressive muscle dystrophy
    ༺ ̿( )
  • progressive myopathy
    ༺ ٺ(ܻ).
  • progressive myopathy
    ༺ ٺ( ܻ)
  • progressive myopia
    ༺ ٽ( ) Ƶ
  • progressive neural muscular atrophy
    ༺ Ű漺 ().
  • progressive neural muscular atrophy
    ༺ Ű漺 ( )
3 п ˻ ˻ : 15 : 7
  • ѱ
  • hereditary progressive mucinous histiocytosis X
    ༺ ׼
  • juvenile progressive muscular atrophy
    Ҽ ༺ ( ).
  • keratosis extremitatum progrediens => progressive diffuse keratoderma
  • leukoencephalopathy,progressive multifocal
    (ܻ)
  • malignant progressive histiocytoma
    Ǽ ༺
  • multiple progressive angioma
    ٹ߼ ༺
  • myopathic progressive muscular atrophy
    ٺ ༺ ()().
  • neural progressive muscular atrophy
    Ű漺 ༺ ().
  • neural progressive muscular atrophy
    Ű漺 ༺ ()( )
  • progressive
  • progressive
    ༺(), ()(())
  • progressive bulbar palsy
    ༺ <>(Ϲ<> ).
  • progressive cardiomyopathic lentiginosis
    ༺ ɱٺ
  • progressive case
    ༺ .
  • progressive deafness
    () û
KMLE о ˻ : 5 : 7
par paraffin; paralysis
PFP peripheral facial paralysis; platelet-free plasma
PIP paralytic infantile paralysis; peak inflation pressure, peak inspiratory pressure; periodic interim ...
RFP recurrent facial paralysis; request for proposal; right frontoposterior [fetal position]
PMF Progressive Massive Fibrosis
  = Silicosis
KMLE ڵ о ˻ : 5 : 7
prcd Progressive rod-cone degeneration
R.P.P. Rapidly Progressive Periodontitis
RPGN Rapidly progressive glomerulonephritis
RCPM Raven Coloured Progressive Matrices
SP Secondary progressive
ϴ ġ ˻ : 15 : 7
  • ѱ
  • diaghragmatic paralysis
    Ⱦݸ
    Ⱦݸ .
  • ephemeral adducter paralysis
    Ͻü
  • Erb-Duchenne paralysis
    -ÿ
    μ 5, 6 Ű ջ ϽŰ μ ħص ʴ Ư¡̴.
  • facial paralysis
    ȸ , ȸŰ
    Bell ó ȸ Ű Ǵ .
  • Felton's paralysis
    뷮 ֱ ٴü ֱ ٴü 鿪АG Ư .
  • functional paralysis
    ɼ
    и Ű漺 ʴ Ͻ .
  • hereditary cerebrospinal paralysis
    ô
    ߳ ʱ⿡ ϴ ȯ Ǵ Ǵ ̳ Ÿ, Ǵ Ư¡̴.
  • hyperkalemic periodic paralysis
    Į ֱ
  • hypoglssal paralysis
    Ű
    Ű Ǵ Ű Ϻ .
  • hypokalemic paralysis
    Į
  • immunological paralysis
    鿪 , 鿪
    ٷ ׿ Ͽ 鿪 ҽǵ .
  • infantile cerebrocerebellar diplegic paralysis
    ҾƳ
    Ʊ⿡ Ͽ ħϿ, ҳ ݵǴ κ ̳ ı ȥ Ÿ.
  • infantile paralysis
    Ҿ , ҾƳ 
    Ǿ=
  • ischemic paralysis
    ̳ ȯ ҿ .
  • Jamaica dogwood ǽõ Ѹ Ĺ.

    Jamaica ginger paralysis

    ڸī ߵ
    , Ư μ ڸī Ÿ.
CancerWEB л ˻ : 15 : 7
paralysis, familial periodic An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis).
(12 Dec 1998)
paralysis, obstetric Paralysis of an infant resulting from injury received at birth.
(12 Dec 1998)
ginger paralysis Neuropathy produced by drinking synthetic Jamaican ginger (or "jake" in the vernacular) containing triorthocresylphosphate.
Synonym: ginger paralysis.
(05 Mar 2000)
parturient paralysis A slight elevation of temperature following childbirth, said to be due to the establishment of the secretion of milk, but probably the same as absorption fever, an afebrile metabolic disease, occurring shortly after parturition in dairy cattle, characterised by hypocalcaemia and manifested by loss of consciousness and general paralysis.
Synonym: parturient paralysis, parturient paresis.
(05 Mar 2000)
global paralysis Paralysis of both whole sides of the body; survival is usually of short duration.
Synonym: generalised paralysis.
(05 Mar 2000)
glossolabiolaryngeal 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)
glossopalatolabial paralysis One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles.
Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis.
(05 Mar 2000)
glossopharyngeolabial paralysis One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles.
Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis.
(05 Mar 2000)
vocal cord paralysis Paralysis of one or both of the vocal cords.
(12 Dec 1998)
central paralysis Paralysis due to a lesion in the brain or spinal cord.
(05 Mar 2000)
Chastek paralysis A disease of foxes and mink caused by feeding on raw fish of certain types which contain an enzyme destructive of thiamin; the thiamin deficiency causes loss of appetite, emaciation, and finally paralysis and death.
(05 Mar 2000)
periodic paralysis Term for a group of diseases characterised by recurring episodes of muscular weakness or flaccid paralysis without loss of consciousness, speech, or sensation; attacks begin when the patient is at rest, and there is apparent good health between attacks.
See: hyperkalaemic periodic paralysis, hypokalaemic periodic paralysis, normokalaemic periodic paralysis.
(05 Mar 2000)
peripheral facial paralysis A condition that involves the facial nerve (VII cranial nerve) and results in the paralysis of one side of the face. Bell's (facial nerve palsy) can be differentiated from a central (stroke) deficit by the inability to raise the eyebrow on the affected side.
(27 Sep 1997)
Gubler's paralysis <syndrome> A form of alternating hemiplegia characterised by contralateral hemiplegia and ipsilateral facial paralysis.
Synonym: Gubler's paralysis, Millard-Gubler syndrome.
(05 Mar 2000)
mimetic paralysis Paralysis of the facial muscles.
(05 Mar 2000)
Ʒ ʹ ϴ.
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