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Charcot-Marie-Tooth disease
Eichhorst type
Enzootic muscular dystrophy
Erb's disease
Erb-Landouzy disease
Hereditary progressive muscular dystrophy
Idiopathic muscular atrophy
Muscular dystrophy
Myodystrophia
Nutritional muscular dystrophy
Peroneal muscular atrophy
Progressive muscular dystrophy
Progressive muscular dystrophy Eichhorst
Progressive muscular dystrophy of pelvic girdle
Progressive neuromuscular atrophy
White muscle disease

Vertaling van "progressive muscular dystrophy " (Engels → Frans) :

TERMINOLOGIE
progressive muscular dystrophy | Erb-Landouzy disease | Erb's disease | idiopathic muscular atrophy | myodystrophia

myopathie primitive progressive | dystrophie musculaire progressive | myopathie atrophique progressive | amyotrophie primitive progressive | amyotrophie progressive | atrophie musculaire progressive


progressive muscular dystrophy

myopathie primitive progressive


progressive muscular dystrophy of pelvic girdle

syndrome de Duchenne-v.Leyden


progressive muscular dystrophy

dystrophie musculaire progressive


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


Eichhorst type | progressive muscular dystrophy | progressive muscular dystrophy Eichhorst

myopathie primitive progressive type Eichhorst | type d'Eichhorst


Hereditary progressive muscular dystrophy

dystrophie musculaire progressive héréditaire


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

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


Syndrome that is characterized by total color blindness caused by progressive cone dystrophy, degenerative liver disease, and endocrine dysfunction (hypothyroidism, diabetes, repeated abortions or infertility). It has been described in six females fr

syndrome rétino-hépato-endocrinologique


Charcot-Marie-Tooth disease | peroneal muscular atrophy | progressive neuromuscular atrophy

maladie de Charcot-Marie | syndrome de Charcot-Marie | atrophie de Charcot-Marie | atrophie péronière | amyotrophie de Charcot-Marie-Tooth
IN-CONTEXT TRANSLATIONS
Muscular dystrophy is the name of a group of muscle disorders characterized by progressive weakness and wasting of the voluntary muscles that control body movement.

On appelle dystrophie musculaire (DM) un ensemble de maladies musculaires caractérisées par une faiblesse et une atrophie progressive des muscles volontaires qui contrôlent les mouvements du corps.


Stem Cell Research Mrs. Cheryl Gallant (Renfrew—Nipissing—Pembroke, Canadian Alliance): Mr. Speaker, I am pleased to present a petition on behalf of the people of eastern Ontario who state that hundreds of thousands of Canadians suffer from debilitating diseases such as Parkinson's, Alzheimers, diabetes, cancer, muscular dystrophy and spinal cord injury; and that Canadians do support ethical stem cell research, which has already shown encouraging potential cures and therapies for these illnesses; and that non-embryonic stem cells, which are also known as adult stem cells, have shown significant research ...[+++]

La recherche sur les cellules souches Mme Cheryl Gallant (Renfrew—Nipissing—Pembroke, Alliance canadienne): Monsieur le Président, j'ai le plaisir de présenter une pétition au nom d'habitants de l'est de l'Ontario qui font valoir que des centaines de milliers de Canadiens sont atteints de maladies débilitantes telles que la maladie de Parkinson, la maladie d'Alzheimer, le diabète, la dystrophie musculaire et les lésions de la moelle épinière; que les Canadiens sont en faveur de la recherche éthique sur les cellules souches, car celle-ci se révèle prometteuse pour le traitement et la guérison de telles maladies; et que la recherche sur ...[+++]


Canadian medical achievements are numerous, including the discovery of a gene linked to Alzheimer's disease, progress in the understanding of muscular dystrophy, and the development of an innovative approach to reducing the side effects of aspirin.

Je tiens à signaler, parmi les nombreuses réalisations médicales canadiennes, la découverte d'un gène lié à la maladie d'Alzheimer, les progrès accomplis dans la compréhension de la dystrophie musculaire, et l'élaboration d'une approche innovatrice pour réduire les effets secondaires de l'aspirine.




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Date index: 2022-07-20
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