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ABC method
ABC-peroxidase technique
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Avidin-biotin-peroxidase complex method
Avidin-biotin=peroxidase complex technique
Biotin-dependent carboxylase deficiency
Brancher deficiency
Brancher enzyme deficiency
Congenital antithrombin III deficiency
Congenital deficiency of antithrombin III
Cyanocobalamin
Deficiency
Deficiency biotin
Familia
Folate
Folic acid
G-6-p-d deficiency
G6PD deficiency
GCL
GSD IV
Galactocerebrosidase deficiency
Galactosylceramide beta-galactosidase deficiency
Galc deficiency
Globoid cell leukodystrophy
Globoid cell leukoencephalopathy
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Glycogen storage disease type IV
Glycogenosis IV
Haemolytic anaemia secondary to G6PD deficiency
Hemolytic anemia secondary to G6PD deficiency
Hexokinase deficiency
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Krabbe disease
Krabbe's disease
Najjar-Andersen syndrome
PK
Pantothenic acid
Pyruvate kinase
Sulfur deficient
Sulfur-deficient
Sulphur deficient
Sulphur-deficient
Triose-phosphate isomerase deficiency
Vitamin B12

Traduction de «deficiency biotin » (Anglais → Français) :

Deficiency:biotin | cyanocobalamin | folate | folic acid | pantothenic acid | vitamin B12

Carence en:acide folique | acide pantothénique | biotine | cyanocobalamine | folate | vitamine B12


Biotin-dependent carboxylase deficiency

Déficit en carboxylase biotine-dépendante


avidin-biotin-peroxidase complex method [ ABC method | avidin-biotin=peroxidase complex technique | ABC-peroxidase technique ]

méthode utilisant le complexe avidine-biotine peroxydase


haemolytic anaemia secondary to G6PD deficiency | haemolytic anaemia secondary to glucose-6-phosphate dehydrogenase deficiency | hemolytic anemia secondary to G6PD deficiency | hemolytic anemia secondary to glucose-6-phosphate dehydrogenase deficiency

anémie hémolytique par déficit en G6PD


G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency

déficit en G6PD | déficit en glucose-6-phosphate-déshydrogénase


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 ]

maladie d'Andersen [ glycogénose musculaire type IV ]


sulphur deficient [ sulphur-deficient | sulfur-deficient | sulfur deficient ]

déficient en soufre


congenital antithrombin III deficiency | congenital deficiency of antithrombin III | inherited antithrombin III deficiency | inherited deficiency in AT III

déficit congénital en antithrombine III


galactocerebrosidase deficiency | galactosylceramide beta-galactosidase deficiency | Galc deficiency | globoid cell leukodystrophy | globoid cell leukoencephalopathy | Krabbe disease | Krabbe's disease | GCL [Abbr.]

déficit en galactocérébrosidase | leucodystrophie à cellules globoïdes | leucodystrophie de Krabbe | maladie de Krabbe


Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

Anémie (due à):déficit en:hexokinase | pyruvate kinase [PK] | triose-phosphate isomérase | hémolytique non sphérocytaire (héréditaire), type II


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