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Déjerine-Sottas
Hypertrophique de l'enfant
NMM
Neuropathie héréditaire motrice et sensorielle
Neuropathie motrice multifocale
Neuropathie périphérique motrice
Syndrome de Roussy-Lévy

Translation of "neuropathie motrice multifocale " (French → English) :

TERMINOLOGY
see also In-Context Translations below
neuropathie motrice multifocale | NMM [Abbr.]

multifocal motor neuropathy | MMN [Abbr.]
IATE - Health
IATE - Health


neuropathie motrice multifocale avec blocs de conduction

Multifocal motor neuropathy
SNOMEDCT-CA (trouble) / 230591002
SNOMEDCT-CA (trouble) / 230591002


paralysie périodique avec neuropathie motrice distale tardive

A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy.
SNOMEDCT-BE (disorder) / 774154008
SNOMEDCT-BE (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy. / 774154008


neuropathie motrice distale héréditaire de l'adulte jeune

Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006


neuropathie périphérique motrice

peripheral motor neuropathy
IATE - Health
IATE - Health


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

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


Neuropathie héréditaire motrice et sensorielle

Hereditary motor and sensory neuropathy
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
IN-CONTEXT TRANSLATIONS
Immunoglobuline humaine normale (ivig) || Kiovig || 2011 || Extension de l’indication pour inclure le traitement de la neuropathie motrice multifocale et hypogammaglobulinémie après une greffe de cellules souches hématopoïétiques allogéniques chez les adultes et les enfants

Human normal immunoglobulin (ivig) || Kiovig || 2011 || Extension of indication to include treatment of multifocal motor neuropathy and hypogammaglobulinaemia in patients after allogeneic haematopoietic stem cell transplantation in adults and children


Immunoglobuline humaine normale (ivig) || Kiovig || 2011 || Extension de l’indication pour inclure le traitement de la neuropathie motrice multifocale et hypogammaglobulinémie après une greffe de cellules souches hématopoïétiques allogéniques chez les adultes et les enfants

Human normal immunoglobulin (ivig) || Kiovig || 2011 || Extension of indication to include treatment of multifocal motor neuropathy and hypogammaglobulinaemia in patients after allogeneic haematopoietic stem cell transplantation in adults and children




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neuropathie motrice multifocale

Date index:2022-06-11 -

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