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Acrocyanosis Acroparaesthesia simple
Acromelalgia
Distal
Erythrocyanosis Erythromelalgia
Erythromelalgia
Erythromelalgia Type II
Erythromelalgia Type III
Fazio-Londe
Gerhardt's disease
Hereditary sensory and autonomic neuropathy type III
Kugelberg-Welander
Mitchell disease
Mitchell's disease
Morquio
Nothnagel's type
Progressive bulbar palsy of childhood
Sanfilippo
Scapuloperoneal form
Schultze's type
Spinal muscular atrophy adult form
Touch type
Type at speed
Type quickly
Typing at speed
Vasomotor
Weir Mitchell's disease

Traduction de «erythromelalgia type iii » (Anglais → Français) :



erythromelalgia | Mitchell disease

acromélalgie | érythromélalgie


acromelalgia | erythromelalgia | Gerhardt's disease | Mitchell's disease | Weir Mitchell's disease

acromélalgie




Acrocyanosis Acroparaesthesia:simple [Schultze's type] | vasomotor [Nothnagel's type] | Erythrocyanosis Erythromelalgia

Acrocyanose Acroparesthésie:simple [type Schultze] | vasomotrice [type Nothnagel] | Erythrocyanose Erythromélalgie




touch type | type quickly | type at speed | typing at speed

taper vite


Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome:Maroteaux-Lamy (mild)(severe) | Morquio(-like)(classic) | Sanfilippo (type B)(type C)(type D)

Carence en bêta-glucoronidase Mucopolysaccharidoses, type III, IV, VI, VII Syndrome de:Maroteaux-Lamy (léger) (sévère) | Morquio (-semblable à) (classique) | Sanfilippo (type B) (type C) (type D)


Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form

Amyotrophie spinale (de):adulte | distale | enfant, type II | forme juvénile, type III [Kugelberg-Welander] | forme scapulo-péronière | Paralysie bulbaire progressive de l'enfant [Fazio-Londe]


Hereditary sensory and autonomic neuropathy type III

dysautonomie familiale




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Date index: 2024-05-19
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