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AMD
Acid maltase deficiency
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Familia
GSD IV
GSD-II
Gierke's disease
Glycogen disease
Glycogen storage disease
Glycogen storage disease I
Glycogen storage disease type II
Glycogen storage disease type IV
Glycogenosis
Glycogenosis IV
Glycogenosis type II
Hepatorenal glycogenosis
Lipid storage disorders
Lysosomal disease
Lysosomal storage disease
Myopathy in glycogen storage disease
Najjar-Andersen syndrome
Pompe disease
Storage disease
Type 1 glycogenosis
Type I glycogen storage disease
Von Gierke's disease

Traduction de «glycogen storage disease » (Anglais → Français) :

type I glycogen storage disease [ von Gierke's disease | Gierke's disease | type 1 glycogenosis | glycogen storage disease I | hepatorenal glycogenosis ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
maladie de von Gierke [ glycogénose de type I | glycogénose hépato-rénale ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
glycogen storage disease [ glycogen disease | glycogenosis ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
glycogénose
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
A glycogen storage disease of adults with characteristics of progressive upper and lower motor neuron dysfunction, progressive neurogenic bladder and cognitive difficulties that can lead to dementia. The prevalence is unknown. More than 50 cases have
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
maladie des corps de polyglucosane de l'adulte
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
An extremely rare genetic glycogen storage disease reported in one patient to date. Clinical signs included muscle weakness, cardiac arrhythmia associated with accumulation of abnormal storage material in the heart and glycogen depletion in skeletal
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
glycogénose avec cardiomyopathie sévère par déficit en glycogénine
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
acid maltase deficiency | glycogen storage disease type II | glycogenosis type II | Pompe disease | AMD [Abbr.] | GSD-II [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
déficit en maltase acide | glycogénose de type II | maladie de Pompe | GSD II [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Myopathy in:glycogen storage disease (E74.0+) | lipid storage disorders (E75.-+)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Myopathie au cours d'anomalies de stockage (du) (des):glycogène (E74.0+) | lipides (E75.-+)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Andersen's disease [ Andersen disease | Najjar-Andersen syndrome | glycogenosis IV | glycogen storage disease type IV | GSD IV | alpha 1,4-glucan-6-glucosyl transferase deficiency | amylopectinosis brancher deficiency | brancher enzyme deficiency | brancher deficiency | amylopectinosis | familia ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
maladie d'Andersen [ glycogénose musculaire type IV ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
lysosomal disease | lysosomal storage disease
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
déficit du stockage lysosomal | maladie lysosomiale
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
A lysosomal storage disease with clinical characteristics of psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration or strabismus. The disease is rare in the general population but is more prevalent among As
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
mucolipidose type IV
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
storage disease
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
maladie d'entreposage
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]


D'autres ont cherché : andersen disease     andersen's disease     gsd iv     gsd-ii     gierke's disease     najjar-andersen syndrome     pompe disease     acid maltase deficiency     amylopectinosis     amylopectinosis brancher deficiency     brancher deficiency     brancher enzyme deficiency     familia     glycogen disease     glycogen storage disease     glycogen storage disease type ii     glycogen storage disease type iv     glycogenosis     glycogenosis iv     glycogenosis type ii     hepatorenal glycogenosis     lipid storage disorders     lysosomal disease     lysosomal storage disease     storage disease     type 1 glycogenosis     type i glycogen storage disease     von gierke's disease     


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Date index: 2022-11-10
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