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Caption : Accreditation =Accreditation
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    • UNITED KINGDOM
    • Devon
    • EXETER
    • Accreditation
    • Molecular diagnosis of Persistent hyperinsulinemic hypoglycemia of infancy (HADH gene)
    • Royal Devon and Exeter Hospital - Wonford site
    • More information
    • UNITED KINGDOM
    • Devon
    • EXETER
    • Accreditation
    • Molecular diagnosis of Hyperinsulinemic Hypoglycemia types 1, 2, 3, 4 and 6 (ABCC8, KCNJ11, GCK, HADH, GLUD1 genes)
    • Royal Devon and Exeter Hospital - Wonford site
    • More information
    • GERMANY
    • Sachsen
    • WEIßWASSER
    • Accreditation
    • Molecular diagnosis of hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (HADH gene)
    • Praxis Dr. Mato Nagel
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Persistent Hyperinsulinemic Hypoglycemia (ABCC8, HNF4A, GCK, GLUD1, HADH and KCNJ11 gene)
    • AMC - Academisch Medisch Centrum
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Biochemical diagnosis of fatty acid oxidation defects and organic acidemias (Analyte: Acylcarnitines by chromatography)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular screening of frequent diseases in Ashkenazi Jewish populations (APEX: ABCC8, AGL, ASPA, BCKDHB, BLM, CFTR, CLRN1, DLD, F11, FANCC, G6PC, GBA, GJB2, HEXA, IKBKAP, LDLR, MCOLN1, MEFV, NEB, PCDH15, SERPINA1, SMPD1, TMEM216 and TOR1A genes)
    • Asper Biotech Ltd.
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN
    • Accreditation
    • Neonatal screening: Biochemical diagnosis of Fatty acid oxidation disorders (acylcarnitines: tandem MS, bloodspots)
    • Provinciaal Centrum voor opsporing van Metabole Aandoeningen (PCMA) - Antwerpen
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Biochemical diagnosis of Fatty Acid Oxidation Defects (Analyte: Organic Acids and Acylcarnitines, both quantitative)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
    • University Hospital of Wales
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (HADH gene)
    • MVZ Fenner & Krasemann
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Biochemical diagnosis of fatty acid metabolism disorders (organic acids in urine/liquor, fatty acid analysis)
    • UKE - Universitätsklinikum Hamburg-Eppendorf
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
    • St Mary's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of defects of long- and medium-chain fatty acid oxidation (Analyte: Myristate and palmitate oxidation)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
    • Royal Victoria Infirmary
    • More information
    • UNITED KINGDOM
    • Strathclyde
    • GLASGOW
    • Accreditation
    • Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
    • Royal Hospital for Sick Children
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Biochemical diagnosis of Fatty acid oxidation disorders and Hyperinsulinism (Analyte: 3-Hydroxybutyrate)
    • Alder Hey Children's Hospital
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
    • Addenbrooke's Hospital
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Short-Chain 3-Hydroxy-Acyl-CoA Dehydrogenase Deficiency (Short-Chain 3-Hydroxy-Acyl-CoA Dehydrogenase activity)
    • AMC - Academisch Medisch Centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Fatty Acid Oxidation Disorders (Analyte: Acetoacetate, Acylcarnitine, PUFA, 3-Hydroxybutyric Acid, Lactic Acid and Pyruvic Acid)
    • AMC - Academisch Medisch Centrum
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Biochemical diagnosis of short chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    • CHU de Lyon HCL - GH Est
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemistry diagnosis of 3-hydroxylacyl-CoA dehydrogenase deficiency, medium / short chain (HADHSC gene)
    • Policlinico Umberto I
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Biochemical diagnosis of short chain 3-hydroxyacyl-CoA dehydrogenase deficiency (measurement of amino acids and acylcarnitines by tandem mass spectrometry)
    • Biotecnologie Avanzate Srl
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical diagnosis of short chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    • Universidad Autónoma de Madrid. Facultad de Ciencias
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical and molecular diagnosis of hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (HADH gene)
    • Universidad Autónoma de Madrid. Facultad de Ciencias
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Biochemical diagnosis of deficiency of 3-hydroxyacyl-CoA dehydrogenase, long and short chain
    • Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
    • More information
    • DENMARK
    • Fyn
    • ODENSE
    • Molecular diagnosis of persistent hyperinsulinemic hypoglycemia of infancy
    • Odense University hospital
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (HADH gene)
    • Praxis Dres. Gencik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Hyperinsulinism due to HADH deficiency (HADH gene)
    • Praxis für Humangenetik
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of persistent hyperinsulinemic hypoglycemia (ABCC8, HNF1A, HNF4A, GCK, GLUD1, HADH and KCNJ11 genes)
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of 3-hydroxylacyl-CoA dehydrogenase deficiency
    • Karolinska University Hospital - Solna
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of persistent hyperinsulinemic hypoglycemia of infancy (HADH gene)
    • Karolinska University Hospital - Solna
    • More information
    • ITALY
    • VENETO
    • VERONA
    • Molecular diagnosis of 3-hydroxylacyl-CoA dehydrogenase deficiency, medium / short chain (HADH gene)
    • Azienda Ospedaliera Universitaria Integrata di Verona - Ospedale Borgo Roma
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
    • St Thomas' Hospital
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (HADH gene: sequencing)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • CANADA
    • Québec
    • SHERBROOKE
    • Biochemical analysis of free carnitine and acylcarnitine in serum by LC/MS/MS
    • CHU Sherbrooke - Hôpital Fleurimont
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of deficiency of 3-hydroxyacyl-CoA dehydrogenase, long and short chain
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Biochemical diagnosis of deficiency of 3-hydroxyacyl-CoA dehydrogenase, short and long chain
    • Ospedale Regionale per le Microcitemie
    • More information
    • UNITED KINGDOM
    • West Yorkshire
    • LEEDS
    • Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
    • St James's University Hospital
    • More information
    • BULGARIA
    •  South-West region
    • SOFIA
    • Biochemical diagnosis of fatty acid oxydation disorders using GCMS analysis
    • University hospital of Obstetrics and Gynecology
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of deficiency of 3-hydroxyacyl-CoA dehydrogenase, short chain
    • Ospedale dei Bambini ''Vittore Buzzi"
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of deficiency of 3-hydroxyacyl-CoA dehydrogenase, short chain
    • Ospedale dei Bambini ''Vittore Buzzi"
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LÈS-NANCY
    • Biochemical diagnostic of 3-hydroxyacyl-CoA dehydrogenase deficiency (chromatography of acylcarnitines and organic acids)
    • CHU de Nancy - Hôpital de Brabois
    • More information
    • GERMANY
    • Sachsen-Anhalt
    • MAGDEBURG
    • Biochemical diagnosis of fatty acid metabolism disorders
    • Universitätsklinikum Magdeburg A.ö.R
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Biochemical diagnosis of Fatty acid oxidation (Palmitate and Myristate oxidation)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • SPAIN
    • Cataluña
    • ESPLUGUES DE LLOBREGAT
    • Biochemical diagnosis of persistent hyperinsulinemic hypoglycemia of infancy.
    • Hospital Universitari Sant Joan de Déu
    • More information
    • SPAIN
    • Cataluña
    • ESPLUGUES DE LLOBREGAT
    • Biochemical diagnosis of 3-hydroxyacyl-CoA dehydrogenase, short chain, deficiency
    • Hospital Universitari Sant Joan de Déu
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of HAD deficiency (HADH gene)
    • Medgene s.r.o.
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Neonatal screening of short chain 3-hydroxyacyl-CoA dehydrogenase deficiency (MS/MS)
    • Genetadi Biotech S.L.
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
    • Medizinische Universität Wien
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Biochemical diagnosis of fatty acid oxidation defects (analyte: free fatty acids, free carnitine, GC/MS analysis of organic acids in urine)
    • University Hospital Bratislava - Stare mesto
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Biochemical diagnosis of fatty acid metabolism disorders
    • Klinikum der Johann Wolfgang Goethe-Universität Frankfurt
    • More information