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Gierke's disease
Glycogen disease
Glycogen starch synthase
Glycogen storage disease
Glycogen storage disease I
Glycogen synthase
Glycogenosis
Hepatorenal glycogenosis
Liver glycogen
Muscle glycogen
Muscle glycogen depletion
Re-fuelling of glycogen stores
Recovery of glycogen stores
Type 1 glycogenosis
Type I glycogen storage disease
Von Gierke's disease

Vertaling van "Muscle glycogen " (Engels → Frans) :

muscle glycogen depletion

panne de glycogène musculaire




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

glycogénose avec cardiomyopathie sévère par déficit en glycogénine


recovery of glycogen stores | re-fuelling of glycogen stores

restauration de la réserve en glycogène | récupération de la réserve en glycogène


glycogen storage disease [ glycogen disease | glycogenosis ]

glycogénose


type I glycogen storage disease [ von Gierke's disease | Gierke's disease | type 1 glycogenosis | glycogen storage disease I | hepatorenal glycogenosis ]

maladie de von Gierke [ glycogénose de type I | glycogénose hépato-rénale ]


glycogen synthase | glycogen starch synthase

glycogène synthase




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

maladie des corps de polyglucosane de l'adulte


A rare and isolated orofacial defect with manifestation of incomplete median clefts of both the lower lip (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g

fente labiale médiane supérieure et inférieure, forme familiale




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'Muscle glycogen' ->

Date index: 2023-05-09
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