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Chronic bee paralysis
Chronic bee-paralysis
Chronic paralysis
DMD
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Enzootic muscular dystrophy
Hairless black syndrome
Infantile spinal muscular atrophy
Kennedy disease
Kennedy's disease
Meryon's disease
Muscle paralysis
Muscular dystrophy
Muscular dystrophy - Duchenne type
Muscular paralysis
Nutritional muscular dystrophy
Paralysis
Paralysis of muscles
Progressive muscular atrophy of infancy
Pseudohypertrophic muscular dystrophy
SBMA
SMA I
Severe infantile spinal muscular atrophy
Spinal and bulbar muscular atrophy
Spinal muscular atrophy type I
Spinobulbar muscular atrophy
Werdnig-Hoffman disease
White muscle disease
X-linked spinal and bulbar muscular atrophy

Vertaling van "muscular paralysis " (Engels → Frans) :

TERMINOLOGIE


paralysis of muscles [ muscle paralysis | muscular paralysis ]

paralysie musculaire


Duchenne muscular dystrophy | Duchenne type muscular dystrophy | Duchenne's muscular dystrophy | Meryon's disease | Muscular dystrophy - Duchenne type | pseudohypertrophic muscular dystrophy | DMD [Abbr.]

dystrophie musculaire de Duchenne | myopathie de Duchenne | myopathie primitive progressive pseudo-hypertrophique type Duchenne-Griesinger | myopathie pseudo-hypertrophique de Duchenne | DMD [Abbr.]


chronic bee paralysis [ chronic bee-paralysis | chronic paralysis | hairless black syndrome | paralysis ]

paralysie chronique de l'abeille [ paralysie chronique | maladie noire ]


A rare genetic motor neuron disease with characteristics of progressive early respiratory failure associated with diaphragm paralysis, distal muscular weakness, joint contractures, and axial hypotonia with preserved antigravity limb movements. The ph

amyotrophie spinale diaphragmatique type 2


A rare autosomal recessive distal hereditary motor neuropathy with characteristics of slowly progressive muscular weakness, hypotonia and atrophy of the lower limbs, more pronounced distally, leading to paralysis, and loss of tendon reflexes. Additio

neuropathie motrice distale héréditaire de l'adulte jeune


muscular dystrophy [ nutritional muscular dystrophy | enzootic muscular dystrophy | white muscle disease ]

maladie du muscle blanc [ maladie des muscles blancs | dystrophie musculaire nutritionnelle | dystrophie musculaire ]


infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]

amyotrophie spinale infantile sévère | amyotrophie spinale progressive de type I | atrophie spinale progressive infantile | maladie de Werdnig-Hoffmann | syndrome de Werdnig-Hoffmann


spinal and bulbar muscular atrophy | SBMA | Kennedy disease | X-linked spinal and bulbar muscular atrophy | spinobulbar muscular atrophy | Kennedy's disease

maladie de Kennedy | atrophie musculaire spinale et bulbaire | atrophie spinale bulbo-musculaire | amyotrophie spinobulbaire | SBMA


A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hyp

myopathie liée à l'X avec atrophie des muscles posturaux
IN-CONTEXT TRANSLATIONS
As the participants at this conference pointed out, and as we heard during our previous debate on the subject, mortality statistics often state as the cause of death the failure of the pulmonary or the cardiovascular system, but do not mention that the primary cause of the pulmonary failure was simply muscular paralysis and that the patient suffocated, or that the cause of the cardiovascular failure was multiple sclerosis.

Ainsi que l’ont souligné les participants à cette conférence et que nous l’avons entendu lors de notre dernier débat sur ce thème, les statistiques sur la mortalité renseignent souvent une défaillance du système pulmonaire ou cardiovasculaire en tant que cause de décès, sans préciser que la cause première de cette défaillance pulmonaire était une paralysie musculaire et que le patient s’est étouffé ou que la défaillance cardiovasculaire avait pour origine une sclérose en plaques.


An attack can damage the eyes and mucous membranes, the lungs, skin and blood-forming organs (2310) Not only did Iraq produce 2,850 tonnes of mustard gas but 210 tonnes of tabun, 795 tonnes of sarin and cyclosarin and 3.9 tonnes of VX. The latter nerve agents can all produce muscular spasms, paralysis and death.

L'exposition à ce gaz peut endommager les yeux et les muqueuses, les poumons, la peau et les organes qui fabriquent le sang (2310) L'Irak a non seulement produit 2 850 tonnes de gaz moutarde mais également 210 tonnes de tabin, 795 tonnes de sarin et de cyclosporine et 3,9 tonnes de DX. Ces derniers agents innervants peuvent tous provoquer des spasmes musculaires, la paralysie et la mort.


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