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Familiar ataxia
Friedreich's spinal ataxia
Hereditary spinal ataxia 2.Friedreich's disease
Marie ataxia
Marie's ataxia
Marie's cerebellar ataxia
SCA1
SCA2
SCA7
SCAR2
Spinocerebellar ataxia
Spinocerebellar ataxia 1
Spinocerebellar ataxia 2
Spinocerebellar ataxia 7
Spinocerebellar ataxia II
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 2
Type 1 spinocerebellar ataxia

Translation of "spinocerebellar ataxia ii " (English → French) :

spinocerebellar ataxia 2 | SCA2 | spinocerebellar ataxia type 2 | spinocerebellar ataxia II
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse 2 | SCA2
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
spinocerebellar ataxia 1 | SCA1 | type 1 spinocerebellar ataxia | spinocerebellar ataxia type 1
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse 1 | ataxie spinocérébellaire 1 | ataxie spino-cérébelleuse de type I | ataxie spinocérébelleuse de type 1 | SCA 1
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
spinocerebellar ataxia
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
ataxie spinocérébelleuse
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
SCAR2 (spinocerebellar ataxia autosomal recessive 2)
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ataxie cérébelleuse autosomique récessive type 3
SNOMEDCT-BE (spinocerebellar ataxia autosomal recessive 2) / 715369006
SNOMEDCT-BE (disorder) / 715369006
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
spinocerebellar ataxia
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse
Nervous System | Human Diseases
Système nerveux | Maladies humaines
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
spinocerebellar ataxia 7 | SCA7
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse 7 | SCA 7
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse type 28
SNOMEDCT-BE (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s / 715824008
SNOMEDCT-BE (disorder) / 715824008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Spinocerebellar ataxia type 31 (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense,
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse type 31
SNOMEDCT-BE (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense, / 715826005
SNOMEDCT-BE (disorder) / 715826005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
familiar ataxia | Friedreich's spinal ataxia | hereditary spinal ataxia 2.Friedreich's disease
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
ataxie de Friedreich | ataxie héréditaire | maladie de Friedreich | tabes héréditaire
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Marie ataxia | Marie's ataxia | Marie's cerebellar ataxia
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
hérédo-ataxie cérébelleuse de Pierre Marie
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]


Others have searched : friedreich's spinal ataxia    marie ataxia    marie's ataxia    marie's cerebellar ataxia    familiar ataxia    spinocerebellar ataxia    spinocerebellar ataxia ii    spinocerebellar ataxia type    type 1 spinocerebellar ataxia    


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'spinocerebellar ataxia ii'

Date index:2021-12-08 -

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