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Aran-Duchenne disease
CMT
Charcot Marie-Tooth disease
Charcot-Marie-Tooth disease
Cruveilhier disease
Disease Charcot-Marie-Tooth
Déjerine-Sottas
Facioscapulohumeral muscular atrophy
Facioscapulohumeral muscular dystrophy
HMSN
Hereditary motor and sensory neuropathy
Infantile spinal muscular atrophy
Kennedy disease
Kennedy's disease
Landouzy-Dejerine dystrophy
PMA
Peroneal muscular atrophy
Progressive muscular atrophy
Progressive muscular atrophy of infancy
Progressive neuromuscular atrophy
Progressive spinal muscular atrophy
SBMA
SMA
SMA I
SPMA
Severe infantile spinal muscular atrophy
Spinal and bulbar muscular atrophy
Spinal muscular atrophy
Spinal muscular atrophy type I
Spinal progressive muscular atrophy
Spinobulbar muscular atrophy
Werdnig-Hoffman disease
X-linked spinal and bulbar muscular atrophy

Traduction de «Peroneal muscular atrophy » (Anglais → Français) :

peroneal muscular atrophy | Charcot Marie-Tooth disease

amyotrophie péronière | syndrome de Charcot-Marie-Tooth-Hoffmann


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


Charcot-Marie-Tooth Disease Peroneal Muscular Atrophy International Association, Inc.

Charcot-Marie-Tooth Disease Peroneal Muscular Atrophy International Association, Inc.


Charcot-Marie-Tooth disease [ peroneal muscular atrophy ]

maladie de Charcot-Marie-Tooth


Charcot-Marie-Tooth disease | hereditary motor and sensory neuropathy | peroneal muscular atrophy | CMT [Abbr.] | HMSN [Abbr.] | PMA [Abbr.]

amyotrophie péronière de Charcot-Marie-Tooth | CMT | maladie de Charcot-Marie-Tooth | neuropathie héréditaire de Charcot-Marie-Tooth


Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome

Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy


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


Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]

amyotrophie d'Aran-Duchenne | amyotrophie spinale progressive | atrophie de Cruveilhier | atrophie musculaire progressive d'Aran | maladie d'Aran-Duchenne


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


Landouzy-Dejerine dystrophy [ facioscapulohumeral muscular dystrophy | facioscapulohumeral muscular atrophy ]

myopathie facio-scapulo-humérale de Landouzy Déjerine [ myopathie facio-scapulo-humérale | myopathie de Landouzy-Déjerine ]


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