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Titel : Accreditatie =Accreditatie
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VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Hereditary Orotic Aciduria (Analyte: Orotic acid)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucolipidosis type 3 (Analyte: multiple lysosomal hydrolases)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Sanfilippo syndrome type C (Analyte: Acetyl-CoA alpha-glucosaminide-N-Acetyltransferase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Cholesteryl ester storage disease and Wolman disease (Analyte: Acid Esterase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 2 (Pompe disease, Analyte: alpha-1,4-glucosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Fucosidosis (alpha-Fucosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Fabry disease (Analyte: alpha-Galactosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Hurler syndrome (Analyte: alpha-Iduronidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of alpha-Mannosidosis (Analyte: alpha-Mannosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 4 (Andersen disease, Analyte: amylo (1,4 : 1,6) transglucosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 3 (Cori disease, analyte: Amylo-1,6-Glucosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical of Metachromatic Leukodystrophy (Analyte: Aryl Sulphatase A)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of beta-Mannosidosis (Analyte: beta-Mannosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucopolysaccharidosis 4B (Morquio disease type B, analyte: beta-Galactosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of GM1 Gangliosidosis (Analyte: beta-Galactosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical of Gaucher disease (Analyte: beta-Glucocerebrosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucopolysaccharidosis type 7 (Sly disease, analyte: beta-Glucuronidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical monitoring of Gaucher disease (Analyte: Chitotriosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Fructose-1,6-bisphosphatase deficiency (Analyte: Fructose-1,6-bisphosphatase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Fructose Intolerance (Analyte: Fructose-1-phosphate aldolase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Krabbe disease (Analyte: Galactocerebrosidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Galactokinase deficiency (Analyte: Galactokinase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 1A (Analyte: Glucose-6-phosphatase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 1B (Analyte: Glucose-6-Translocase T1)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 1C (Analyte: Glucose-6-Translocase T2)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 1D (Analyte: Glucose-6-Translocase T3)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 6B (Hers disease, Analyte: Glycogen Phosphorylase liver)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucopolysaccharidosis types 1, 2, 3, 4, 6, 7 & 9 (Analyte: Glycosaminoglycans qualitative)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Sanfilippo syndrome type A (Analyte: Heparan Sulphamidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Tay Sachs disease (Analyte: Hexosaminidase A)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Sandhoff disease (Analyte: Hexosaminidase A + B)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucopolysaccharidosis type 2 (Hunter syndrome, Analyte: Iduronate sulphatase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 7 (Tarui disease, Analyte: Muscle Phosphofructokinase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease type 5 (McArdle disease, Analyte: Muscle Phosphorylase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Sanfilippo syndrome type B (Analyte: N-Acetyl-alpha-glucosaminidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucopolysaccharidosis type 6 (Analyte: N-acetylgalactosamine-4-sulphatase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucopolysaccharidosis type 4 (Analyte: N-acetylgalactosamine-6-sulphatase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of alpha-N-Acetylgalactosaminidase, NAGA deficiency (Analyte: N-Acetylgalactosaminidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Sanfilippo syndrome type D (Analyte: N-Acetylglucosamine-6-sulphatase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Aspartylglycosaminuria (Analyte: N-aspartyl-beta-glucosaminidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Sialidosis types 1 and 2 (Analyte: Neuraminidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Neuronal Ceroid Lipofuscinosis (Analytes: Palmitoyl-proteine thioesterase & tripeptidyl-peptidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Phenylalanin or Tyrosine metabolism disorder (Analytes: Phenylalanine/Tyrosine)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glucosephosphate isomerase deficiency (Analyte: Phosphoglucosisomerase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Molecular diagnosis of Niemann Pick disease types A & B (Analyte: Sphingomyelinase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Glycogen Storage Disease, type 9 (Analyte: Phosphorylase b Kinase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Peroxisomal disorders (Analyte: Very Long Chain Fatty Acids)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Leucinosis (Analyte: Leucine decarboxylase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucosulfatidosis (Analyte: Multiple sulphatases)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Lathosterolosis (Analyte: Lathosterol)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Congenital disorders of glycosylation type 1b (CGS 1b, Analyte: Phosphomannoisomerase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Congenital disorders of glycosylation type 1a (CGS 1a, Analyte: Phosphomannomutase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Refsum disease (Analyte: Phytanic acid)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of UDP-galactose-4-epimerase deficiency (Analyte: UDP-galactose-4-epimerase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of sulfite oxidase deficiency (Analyte: Sulfite Oxidase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Argininosuccinicaciduria (Analyte: Arginosuccinate Lyase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Citrullinemia (Analyte: Arginosuccinate Synthase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of arginase deficiency (Analyte: Arginase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Cerebrotendinous xanthomatosis (Analyte: Cholestanol)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of carbamoylphosphate synthetase deficiency (Analyte: Carbamoyl Phosphate Synthase)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Smith-Lemli-Opitz syndrome (Analyte: 7-Dehydrocholesterol)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest

VERENIGD KONINKRIJK

Greater London
LONDON

Biochemical diagnosis of Mucolipidosis type 2 (Analyte: multiple lysosomal hydrolases)
University College London Hospitals, NHS Foundation Trust
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Biochemische genetica
Doel : Analyt/Enzymtest