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Caption : Accreditation =Accreditation
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    • FRANCE
    • ILE-DE-FRANCE
    • LE KREMLIN-BICÊTRE
    • Accreditation
    • Biochemical diagnosis of multiple acyl-CoA deficiency
    • GHU Paris-Sud - Hôpital de Bicêtre
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of multiple FAD dehydrogenase deficiency (ETFA, ETFB and ETFDH genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Mitochondrial disorders
    • Sheffield Children's NHS Foundation Trust
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of multiple FAD dehydrogenase deficiency (ETFB and ETFDH genes)
    • Centogene AG
    • 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 acyl-CoA dehydrogenase deficiency (ACADM, ACADS, ACADVL, ETFA genes)
    • 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 Glutaryl-CoA dehydrogenase deficiency type 2 and Multiple FAD dehydrogenase deficiency (Analyte: Multiple acyl-CoA dehydrogenase)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Fatty acid oxidation defects (Analyte: Fatty acid oxidation)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemcial diagnosis of MCAD / MADD deficiency (Analyte: Quantitative hexanoylglycine)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Glutaric aciduria / MADD deficiency (Analyte: Quantitative glutaric acid)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of disorders of endocrine function / gluconeogenesis / fatty acid oxidation (Analyte: Free fatty acids)
    • 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
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of Glutaryl-CoA dehydrogenase deficiency type 2 and Multiple FAD dehydrogenase deficiency (Analyte: Multiple acyl-CoA dehydrogenase)
    • Royal Victoria Infirmary
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of Fatty acid oxidation defects (Analyte: Fatty acid oxidation)
    • Royal Victoria Infirmary
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of disorders of endocrine function / gluconeogenesis / fatty acid oxidation (Analyte: Free fatty acids)
    • Royal Victoria Infirmary
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Multiple Acyl-CoA Dehydrogenase Deficiency (ETFDH, ETFA and ETFB gene)
    • AMC - Academisch Medisch Centrum
    • 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
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of acyl-CoA dehydrogenase deficiency (ACADS, ETFA, ETFB and ETFDH genes: sequencing)
    • CeGaT GmbH
    • 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
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Flavin Synthesis and Transport Disorders (Analyte: Flavins)
    • AMC - Academisch Medisch Centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Glutaric Aciduria type 2 (Analyte: Ubiquinon)
    • AMC - Academisch Medisch Centrum
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Biochemical diagnosis of multiple acyl-CoA deficiency
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Molecular, biochemical and enzyme diagnosis of multiple acyl-CoA deficiency (ETFA, ETFB and ETFDH genes)
    • CHU de Lyon-GH Est - Hospices Civils de Lyon
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Biochemical diagnosis of multiple acyl-CoA deficiency (organic acids/ GC-MS, acylcarnitines/MSMS)
    • CHU de Caen - Hôpital de la Côte de Nacre
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Biochemical diagnosis of multiple acyl-CoA deficiency
    • CHU d'Angers
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Biochemical diagnosis of multiple acyl-CoA deficiency
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of glutaric aciduria type 1 and 2
    • Policlinico Umberto I
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Biochemical and molecular diagnosis of glutaric acidemia type 2 (ETFA, ETFB, ETFDH genes)
    • Biotecnologie Avanzate Srl
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical diagnosis of glutaric acidemia type 2
    • Universidad Autónoma de Madrid. Facultad de Ciencias
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Biochemical diagnosis of glutaricaciduria type 2
    • Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Diagnosis of fatty acid oxidation defects : quantitative organic acid analysis (GC/MS)
    • Tartu University Hospital
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of glutaric aciduria type 2B (ETFB gene: sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Multiple acyl-CoA dehydrogenase deficiency (ETFDH gene: sequenciação de toda a região codificante)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of glutaric acidemia type 2 (ETFA, ETFB, ETFDH genes / sequencing)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Biochemical diagnosis of fatty acid oxidation defects and organic acidemias (Analyte: Acylcarnitines by chromatography)
    • CHU de Toulouse - Hôpital Purpan
    • 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
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of glutaric acidemia type 2 (ETFDH gene)
    • Genetaq
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Portuguese National Neonatal Screening Program (Guthrie test)
    • Instituto Nacional de Saúde Dr. Ricardo Jorge - Porto
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Biochemical diagnosis of multiple FAD dehydrogenase deficiency (chromatography of organic acids)
    • CHU de Reims - American Memorial Hospital
    • More information
    • CANADA
    • Québec
    • SHERBROOKE
    • Biochemical analysis of free carnitine and acylcarnitine in serum by LC/MS/MS
    • CHU Sherbrooke - Hôpital Fleurimont
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of multiple acyl-CoA deficiency
    • CHU Paris - Hôpital Robert Debré
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Biochemical diagnosis of multiple FAD dehydrogenase deficiency
    • CHU de Rouen - Hôpital Charles Nicolle
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Biochemical diagnosis of beta-oxidation deficiency (metabolite analysis)
    • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Biochemical diagnosis of multiple acyl-CoA deficiency (glutaricaciduria type 2)
    • Klinikum Schwabing, Städt. Klinikum GmbH
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical and molecular diagnosis of glutaric acidemia type 2 (ETFA, ETFB and ETFDH genes)
    • Hospital Clínic de Barcelona
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Histological diagnosis of Neuromuscular diseases
    • Universitätsklinikum Bonn
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of multiple acyl-CoA deficiency
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical diagnosis of multiple FAD dehydrogenase deficiency
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Biochemical diagnosis of beta-oxidation deficiency
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Biochemical diagnosis of organoacidopathies
    • Medizinische Universität Innsbruck
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of multiple acyl-CoA deficiency
    • CHU Paris - Hôpital Necker-Enfants Malades
    • 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
    • TOSCANA
    • FIRENZE
    • Biochemical diagnosis of glutaric aciduria, type 1, 2 and 3
    • Azienda Ospedaliera Universitaria Anna Meyer
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of glutaric aciduria type II (organic acids in urine, acylcarnitine in dried blood)
    • Universitätsklinikum Heidelberg
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of glutaric aciduria type 1, 2 and 3
    • Ospedale dei Bambini ''Vittore Buzzi"
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LES-NANCY
    • Biochemical diagnostic of glutaric acidemia type 2 (chromatography of organic acids and acylcarnitines)
    • CHU de Nancy
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LES-NANCY
    • Biochemical diagnosis of multiple acyl-CoA dehydrogenase deficiency (chromatography of acylcarnitines)
    • CHU de Nancy
    • 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 glutaric acidemia type 2 (analyte: Urine Glutaric acid, ethilmalonic, dicarboxilic acids)
    • Hospital Universitari Sant Joan de Déu
    • More information
    • ITALY
    • PUGLIA
    • FOGGIA
    • Biochemical diagnosis of glutaric acidemia (tandem mass spectrometry)
    • Azienda Ospedaliero Universitaria di Foggia
    • 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
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Molecular diagnosis of Glutaric acidemia type 2 (ETFA, ETFB, and ETFDH genes)
    • Medizinische Universität Graz
    • 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