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Amyotrophie primitive progressive
Amyotrophie progressive
Atrophie de Duchenne-Friedreich
Atrophie musculaire progressive
Atrophie myotonique
DMD
Dystrophie musculaire
Dystrophie musculaire de Duchenne
Dystrophie musculaire progressive
Dystrophie myotonique
Dystrophie myotonique de Steinert
Maladie de Steinert
Myopathie atrophique avec myotonie
Myopathie atrophique progressive
Myopathie de Duchenne
Myopathie myotonique
Myopathie primitive
Myopathie primitive progressive
Myopathie pseudo-hypertrophique de Duchenne
Myotonie atrophique
Myotonie de Steinert
Myotonie dystrophique
Syndrome de Batten Steinert
Syndrome de Curschmann-Batten-Steinert
Type facio-scapulo-huméral de Landouzy-Déjerine

Translation of "Myopathie atrophique progressive " (French → English) :

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

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


dystrophie myotonique | maladie de Steinert | myotonie dystrophique | myotonie de Steinert | dystrophie myotonique de Steinert | myopathie atrophique avec myotonie | atrophie myotonique | myopathie myotonique | myotonie atrophique | syndrome de Batten Steinert | syndrome de Curschmann-Batten-Steinert

myotonic dystrophy | Steinert's disease | Batten's disease | Batten-Steinert syndrome | Curschmann-Batten-Steinert syndrome | Curschmann-Steinert syndrome | atrophic myotonia
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique


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

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


dystrophie musculaire [ myopathie primitive | myopathie primitive progressive ]

muscular dystrophy
Muscles et tendons
Muscles and Tendons


atrophie de Duchenne-Friedreich | myopathie primitive progressive type pseudo-hypertrophique de Duchenne

Duchenne-Friedreich atrophy
IATE - Health
IATE - Health


myopathie primitive progressive | type facio-scapulo-huméral de Landouzy-Déjerine

facioscapulohumeral progressive muscular dystrophy
IATE - Health
IATE - Health


myopathie primitive progressive

progressive muscular dystrophy
médecine
médecine


syndrome d'ophtalmoplégie externe progressive-myopathie-émaciation

A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with
SNOMEDCT-BE (disorder) / 764733009
SNOMEDCT-BE (disorder) / 764733009


ophtalmoplégie externe progressive chronique de l'adulte avec myopathie mitochondriale

A rare mitochondrial disease with characteristics of adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuro
SNOMEDCT-BE (disorder) / 725464001
SNOMEDCT-BE (e.g. impaired gait, dysarthria) and mild motor peripheral neuro / 725464001




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Myopathie atrophique progressive

Date index:2023-06-17 -

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