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Acromegaly
Bourneville disease
Bourneville syndrome
Bourneville-Brissaud disease
Bourneville-Pringle syndrome
Bourneville-Pringle's disease
Brissaud-Marie sign
Brissaud-Marie syndrome
CCD
Colony collapse disorder
Debré-Marie syndrome
Disease Charcot-Marie-Tooth
Déjerine-Sottas
Epiloia
Marie's disease
Marie's syndrome
Mary Celeste syndrome
Spontaneous hive collapse
TSC
Tuberous sclerosis
Tuberous sclerosis complex

Translation of "Brissaud-Marie syndrome " (English → French) :

Brissaud-Marie sign | Brissaud-Marie syndrome

diplégie faciale familiale | syndrome de Brissaud et Marie | syndrome de Brissaud-Marie
IATE - Health
IATE - Health


Debré-Marie syndrome

syndrome de Debré-Marie
IATE - Health
IATE - Health


Bourneville disease | Bourneville syndrome | Bourneville-Brissaud disease | Bourneville-Pringle syndrome | Bourneville-Pringle's disease | epiloia | tuberous sclerosis | tuberous sclerosis complex | TSC [Abbr.]

épiloïa | maladie de Bourneville | maladie de Bourneville-Brissaud | phacomatose de Bourneville | sclérose tubéreuse | sclérose tubéreuse de Bourneville | STB [Abbr.]
IATE - Health
IATE - Health


acromegaly [ Marie's disease | Marie's syndrome ]

acromégalie
Symptoms (Medicine)
Symptômes (Médecine)


colony collapse disorder | CCD | spontaneous hive collapse | Mary Celeste syndrome

syndrome d'effondrement des colonies d'abeilles
zootechnie > abeille domestique | écologie | biologie
zootechnie > abeille domestique | écologie | biologie


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
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0


Charcot-Marie-Tooth disease, pyramidal features syndrome

neuropathie sensitivo-motrice héréditaire type 5
SNOMEDCT-BE (disorder) / 771143004
SNOMEDCT-BE (disorder) / 771143004




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'Brissaud-Marie syndrome'

Date index:2021-07-30 -

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