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Autosomal dominant Charcot-Marie-Tooth disease type 2K
Autosomal dominant Charcot-Marie-Tooth disease type 2N
CMT
Charcot-Marie-Tooth disease
Disease Charcot-Marie-Tooth
Déjerine-Sottas
HMSN
Hereditary motor and sensory neuropathy
PMA
Peroneal muscular atrophy

Vertaling van "charcot-marie-tooth disease type " (Engels → Nederlands) :

Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso

ziekte van Charcot-Marie-Tooth type 4B2


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

hereditaire motorische en sensorische neuropathie | ziekte van Charcot-Marie-Tooth | HMSN [Abbr.]


Autosomal dominant Charcot-Marie-Tooth disease type 2K

autosomaal dominante ziekte van Charcot-Marie-Tooth type 2K


Autosomal dominant Charcot-Marie-Tooth disease type 2N

autosomaal dominante ziekte van Charcot-Marie-Tooth type 2N


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

hereditaire motorische- en sensorische-neuropathie, type I-IV | infantiele hypertrofische-neuropathie | peroneale spieratrofie (axonaal type)(hypertrofisch type) | syndroom van Roussy-Lévy | ziekte van | Charcot-Marie-Tooth | ziekte van | Déjerine-Sottas




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Date index: 2020-12-30
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