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Autosomal recessive demyelinating Charcot-Marie-Tooth
Congenital cerebellar ataxia
MHV-subsidies
Marie Heim-Vögtlin programme
Marie ataxia
Marie disease
Marie's ataxia
Marie's cerebellar ataxia
Marie's disease
Nonne-Marie sydrome
O.M.I.
Oblates Fathers
Oblates of Mary Immaculate
Saint Mary's
Saint Mary's Band
St. Mary's Band
The Missionary Oblates of Mary Immaculate
Unda maris
Voix céleste

Translation of "Unda maris " (English → French) :

unda maris | voix céleste

unda maris | voix céleste
IATE - Culture and religion | Industrial structures and policy
IATE - Culture and religion | Industrial structures and policy


unda maris

unda-maris
Keyboard Instruments | Musicology
Instruments de musique à clavier | Musicologie


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

hérédo-ataxie cérébelleuse
IATE - Health
IATE - Health


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

hérédo-ataxie cérébelleuse de Pierre Marie
IATE - Health
IATE - Health


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

Saint Mary's [ bande Saint Mary's | bande St. Mary's ]
Names of Native Peoples
Noms de peuples autochtones


The Missionary Oblates of Mary Immaculate [ O.M.I. | Oblates of Mary Immaculate | Oblates Fathers | Révérends Pères Oblats de l'Immaculée Conception de Marie ]

Les Missionnaires Oblats de Marie Immaculée [ O.M.I. | Oblats de Marie Immaculée | Pères Oblats | Révérends Pères Oblats de l'Immaculée Conception de Marie ]
International Bodies and Committees | Religion (General)
Organismes et comités internationaux | Religion (Généralités)


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
SNOMEDCT-BE (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 / 715800000
SNOMEDCT-BE (disorder) / 715800000


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
SNOMEDCT-BE (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too / 765746008
SNOMEDCT-BE (disorder) / 765746008


Marie Heim-Vögtlin programme | MHV-subsidies

Programme Marie Heim-Vögtlin | subsides MHV
Insurance
Instituts - compagnies - caisses (Assurance) | Principes généraux de sciences et de culture (Généralités)


Autosomal recessive demyelinating Charcot-Marie-Tooth

maladie de Charcot-Marie-Tooth type 4
SNOMEDCT-BE (disorder) / 715795005
SNOMEDCT-BE (disorder) / 715795005




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'Unda maris'

Date index:2021-11-27 -

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