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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
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Traduction de «Unda maris » (Anglais → Français) :





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 ]


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 ]


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


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


Marie Heim-Vögtlin programme | MHV-subsidies

Programme Marie Heim-Vögtlin | subsides MHV


Autosomal recessive demyelinating Charcot-Marie-Tooth

maladie de Charcot-Marie-Tooth type 4




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Date index: 2021-04-11
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