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Acute autoimmune neuropathy
Acute inflammatory polyradiculoneuropathy
Acute motor axonal neuropathy
CMT
Charcot-Marie-Tooth disease
Chinese paralytic syndrome
Disease Charcot-Marie-Tooth
Distal hereditary motor neuropathy type 7
Déjerine-Sottas
Guillain-Barre syndrome
Guillaine-Barre syndrome
HMSN
Hereditary motor and sensory neuropathy
Landry-Guillain-Barre syndrome
MMN
Multifocal motor neuropathy
PMA
Peripheral motor neuropathy
Peroneal muscular atrophy

Traduction de «Multifocal motor neuropathy » (Anglais → Français) :

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous
multifocal motor neuropathy | MMN [Abbr.]

neuropathie motrice multifocale | NMM [Abbr.]


peripheral motor neuropathy

neuropathie périphérique motrice


Distal hereditary motor neuropathy type 7

neuropathie motrice distale héréditaire type 7


A rare syndrome with the association of congenital hypertrichosis in the anterior cervical region, peripheral sensory and motor neuropathy. It has been described in three members of the same family and in one unrelated boy. Associated features in the

syndrome d'hypertrichose cervicale-neuropathie périphérique


A rare distal hereditary motor neuropathy with characteristics of slowly progressive atrophy and weakness of distal muscles of hands and feet with normal deep tendon reflexes or absent ankle reflexes and minimal or no sensory loss, sometimes mild pro

atrophie musculaire spinale distale liée à l'X type 3


Guillain-Barre syndrome [ Guillaine-Barre syndrome | Landry-Guillain-Barre syndrome | acute autoimmune neuropathy | acute inflammatory demyelinating polyradiculoneuropathy | acute inflammatory polyradiculoneuropathy | Chinese paralytic syndrome | acute motor axonal neuropathy ]

syndrome de Guillain-Barré


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


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


Hereditary motor and sensory neuropathy

Neuropathie héréditaire motrice et sensorielle
TRADUCTIONS EN CONTEXTE
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

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




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Date index: 2021-12-14
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