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ALS
Amyotrophic lateral sclerosis
Autosomal recessive demyelinating Charcot-Marie-Tooth
Brissaud-Marie sign
Brissaud-Marie syndrome
Charcot disease
Charcot's disease
Congenital cerebellar ataxia
Lou Gehrig disease
Lou Gehrig's disease
Marie ataxia
Marie disease
Marie's ataxia
Marie's cerebellar ataxia
Marie's disease
Motor neuron disease
Nonne-Marie sydrome
Saint Mary's
Saint Mary's Band
St. Mary's Band

Vertaling van "mary-lou " (Engels → Frans) :

TERMINOLOGIE
Jonathan Mann/Mary-Lou Clements Symposium

Symposium Jonathan Mann/Mary-Lou Clements


amyotrophic lateral sclerosis [ ALS | Lou Gehrig's disease | Lou Gehrig disease | Charcot's disease | Charcot disease ]

sclérose latérale amyotrophique [ SLA | maladie de Lou-Gehrig | maladie de Charcot ]


congenital cerebellar ataxia | Marie disease | Marie's cerebellar ataxia | Marie's disease | Nonne-Marie sydrome

hérédo-ataxie cérébelleuse


Marie ataxia | Marie's ataxia | Marie's cerebellar ataxia

hérédo-ataxie cérébelleuse de Pierre Marie


Saint Mary's [ Saint Mary's Band | St. Mary's Band ]

Saint Mary's [ bande Saint Mary's | bande St. Mary's ]


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

maladie de Charcot-Marie-Tooth type 4B2


Brissaud-Marie sign | Brissaud-Marie syndrome

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


amyotrophic lateral sclerosis | ALS | Charcot disease | motor neuron disease | Lou Gehrig disease

sclérose latérale amyotrophique | SLA | maladie de Charcot | maladie des motoneurones | maladie de Lou Gehrig


A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante C


Autosomal recessive demyelinating Charcot-Marie-Tooth

maladie de Charcot-Marie-Tooth type 4
IN-CONTEXT TRANSLATIONS
Mary-Lou Donnelly, President, Canadian Teachers' Federation: Good morning.

Mary-Lou Donnelly, présidente, Fédération canadienne des enseignantes et des enseignants : Bonjour.


Ms Mary Lou Bird, Policy Analyst, Aboriginal Business Canada, Industry Canada: My name is Mary Lou Bird.

Mme Mary Lou Bird, analyste des politiques, Entreprise autochtone Canada, Industrie Canada: Je m'appelle Mary Lou Bird.


Mary Lou O'Reilly, Executive Director.

Mary Lou O'Reilly, directrice générale.


From the Canadian Teachers' Federation, we have Mary-Lou Donnelly, President.

Nous entendrons également Mary-Lou Donnelly, présidente de la Fédération canadienne des enseignantes et des enseignants.


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CIDA told Mary-Lou Donnelly, President of the Canadian Teachers' Federation, that they were rejected because of a technicality, but the leader is telling us that, in fact, it was not only a technicality; the CIDA officials were wrong when they spoke to Mary-Lou Donnelly.

L'ACDI a dit à Mary-Lou Donnelly, présidente de la Fédération canadienne des enseignantes et des enseignants, que la demande de son organisme avait été rejetée en raison d'un point de détail. Cependant, le leader nous dit qu'en fait, il ne s'agissait pas seulement d'un point de détail.


Mary Lou McDonald (GUE/NGL ), in writing .

Mary Lou McDonald (GUE/NGL ), par écrit .


Bairbre de Brún and Mary Lou McDonald (GUE/NGL), in writing.

Bairbre de Brún et Mary Lou McDonald (GUE/NGL), par écrit.


Bairbre de Brún and Mary Lou McDonald (GUE/NGL ), in writing .

Bairbre de Brún et Mary Lou McDonald (GUE/NGL ), par écrit .


President. Question No. 14 by Mary Lou McDonald (H-0999/05 )

question n° 14 de Mme McDonald (H-0999/05 ):


President. Question No. 14 by Mary Lou McDonald (H-0999/05)

question n° 14 de Mme McDonald (H-0999/05):




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Date index: 2024-12-10
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