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CMT
Charcot-Marie-Tooth disease
Disease Charcot-Marie-Tooth
Déjerine-Sottas
HMSN
Hereditary motor and sensory neuropathy
Hereditary sensory and autonomic neuropathy type 1B
Hereditary sensory and autonomic neuropathy type I
Hereditary sensory and autonomic neuropathy type III
PMA
Peroneal muscular atrophy

Traduction de «Hereditary sensory and autonomic neuropathy type III » (Anglais → Français) :

Hereditary sensory and autonomic neuropathy type III

dysautonomie familiale


Hereditary sensory and autonomic neuropathy type I

neuropathie héréditaire sensitive et autonomique type 1


Hereditary sensory and autonomic neuropathy type 1B

neuropathie héréditaire sensitive et autonomique type 1B


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




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'Hereditary sensory and autonomic neuropathy type III' ->

Date index: 2022-08-17
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