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Traduction de «Neurogenic atrophy » (Anglais → Français) :

neurogenic atrophy

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

atrophie neurogène

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high

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neuropathie sensitivo-motrice héréditaire type Okinawa

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neurogenic acro-osteolysis | neuropathic neurotrophic osseous atrophy

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acro-ostéolyse progressive

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

dentatorubral pallidolusyian atrophy | DRPLA | dentato-rubro-pallidolusian atrophy | dentatorubropallidoluysian atrophy | dentatorubral-pallidoluysian atrophy

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

diabète insipide central | DIC | diabète insipide neurogène

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

maladie de Kennedy | atrophie musculaire spinale et bulbaire | atrophie spinale bulbo-musculaire | amyotrophie spinobulbaire | SBMA

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

amyotrophie spinale infantile sévère | amyotrophie spinale progressive de type I | atrophie spinale progressive infantile | maladie de Werdnig-Hoffmann | syndrome de Werdnig-Hoffmann

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

maladie de Duchenne de Boulogne

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hyp

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myopathie liée à l'X avec atrophie des muscles posturaux

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A rare endocrine disease with characteristics of the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy

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syndrome de Wolfram-like

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D'autres ont cherché : duchenne disease duchenne dystrophy duchenne muscular dystrophy duchenne type muscular dystrophy duchenne-griesinger disease erb atrophy erb dystrophy kennedy disease kennedy's disease werdnig-hoffman disease zimmerlin atrophy central di central diabetes insipidus dentatorubral pallidolusyian atrophy hyopthalamic diabetes insipidus hypothalamic di infantile spinal muscular atrophy neurogenic di neurogenic acro-osteolysis neurogenic atrophy neurogenic diabetes insipidus neuropathic neurotrophic osseous atrophy progressive muscular atrophy of infancy severe infantile spinal muscular atrophy spinal and bulbar muscular atrophy spinal muscular atrophy type spinobulbar muscular atrophy Neurogenic atrophy

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'Neurogenic atrophy' ->

Date index: 2024-02-06