Caption
: Accreditation
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- GERMANY
- Nordrhein-Westfalen
- DORTMUND
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene: codon 304 and 329)
- Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
- More information
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- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCAD gene: K329E)
- Labor Lademannbogen
- More information
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- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Medizinisches Versorgungszentrum Humane Genetik
- More information
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- Molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency (ACADM gene c.985 A>G )
- HUSLAB
- More information
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- UNITED KINGDOM
- Greater Manchester
- MANCHESTER
- Molecular diagnosis of MCAD (MCAD common A985G mutation)
- St Mary's Hospital
- More information
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- Molecular diagnosis of MCAD deficiency (ACADM gene)
- CHU de LIEGE - UniLab Lg
- More information
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- SWITZERLAND
- Suisse Romande
- LAUSANNE
- Molecular diagnosis of Medium Chain Acyl-CoA Deshydrogenase deficiency (MCDA)
- Centre Hospitalier Universitaire Vaudois - CHUV
- More information
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- UNITED KINGDOM
- Merseyside
- LIVERPOOL
- Molecular diagnosis of MCAD deficiency
- Liverpool Women's NHS Foundation Trust
- More information
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- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Molecular diagnosis of Medium Chain Acyl-CoA Dehydrogenase (MCAD) deficiency (Testing for common mutation c.985A>G, p.Lys329Glu and sequencing of coding regions)
- Sheffield Children's NHS Foundation Trust
- More information
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- UNITED KINGDOM
- Tayside
- DUNDEE
- Molecular diagnosis of Medium Chain Acyl-CoA dehydrogenase (MCAD) deficiency (ACADM gene)
- Ninewells Hospital
- More information
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- UNITED KINGDOM
- Greater London
- LONDON
- Molecular diagnosis of Medium chain acyl-CoA dehydrogenase deficiency - MCAD deficiency (ACADM gene)
- Great Ormond Street Hospital NHS Trust
- More information
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- BELGIUM
- HAINAUT
- GOSSELIES
- Molecular diagnosis of MCAD deficiency (MCAD gene, mutation p.K329E)
- Institut de Pathologie et de Génétique - Gosselies
- More information
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- More information
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- NETHERLANDS
- Utrecht
- UTRECHT
- Molecular diagnosis of Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM gene)
- UMC Utrecht - Universitair Medisch Centrum Utrecht
- More information
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- UNITED KINGDOM
- Avon
- BRISTOL
- Molecular diagnosis of Medium Chain Acyl CoA Dehydrogenase Deficiency (MCAD)
- Southmead Hospital
- More information
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- UNITED KINGDOM
- West Midlands
- BIRMINGHAM
- Molecular diagnosis of Medium Chain Acyl CoA Dehydrogenase Deficiency (MCAD, ACADM gene c.985AG -p.Lys329Gln)
- Birmingham Children's Hospital
- More information
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Molecular diagnosis of Medium Chain Acyl CoA Dehydrogenase Deficiency (MCAD)
- International Centre for Life
- More information
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- GERMANY
- Bayern
- MARTINSRIED
- Molecular diagnosis of medium chain Acyl-CoA dehydrogenase deficiency
- Zentrum für Humangenetik und Laboratoriumsmedizin Dr. Klein und Dr. Rost
- More information
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- GERMANY
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Institute of Molecular Diagnostics
- More information
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- GERMANY
- Baden-Württemberg
- HEIDELBERG
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Universitätsklinikum Heidelberg
- More information
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- BELGIUM
- ANTWERPEN
- ANTWERPEN
- Neonatal screening: Biochemical diagnosis of Fatty acid oxidation disorders (acylcarnitines: tandem MS, bloodspots)
- Provinciaal Centrum voor opsporing van Metabole Aandoeningen (PCMA) - Antwerpen
- More information
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- NETHERLANDS
- Utrecht
- UTRECHT
- Biochemical diagnosis of Fatty Acid Oxidation Defects (Analyte: Organic Acids and Acylcarnitines, both quantitative)
- UMC Utrecht - Universitair Medisch Centrum Utrecht
- More information
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- UNITED KINGDOM
- South Glamorgan
- CARDIFF
- Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
- University Hospital of Wales NHS Trust
- More information
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- UNITED KINGDOM
- South Glamorgan
- CARDIFF
- Molecular diagnosis of Medium chain acyl-CoA dehydrogenase deficiency - MCAD (G985A Mutation)
- University Hospital of Wales NHS Trust
- More information
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- Molecular diagnosis of acyl-CoA dehydrogenase deficiency (ACADM, ACADS, ACADVL, ETFA genes)
- MVZ Fenner & Krasemann
- More information
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- Newborn screening : Biochemical diagnosis of medium chain acyl-CoA dehydrogenase deficiency (amino acid and acylcarnitine in dried blood)
- Universitätsklinikum Carl Gustav Carus der TU Dresden
- More information
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- Biochemical diagnosis of fatty acid metabolism disorders (organic acids in urine/liquor, fatty acid analysis)
- Universitätsklinikum Hamburg-Eppendorf
- More information
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- UNITED KINGDOM
- Greater Manchester
- MANCHESTER
- Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
- St Mary's Hospital
- More information
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- GERMANY
- Baden-Württemberg
- SINGEN /HTWL.
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Institut für Laboratoriumsmedizin und Humangenetik
- More information
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- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
- The Sheffield Children's Hospital
- More information
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- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Biochemical diagnosis of Fatty acid oxidation defects (Analyte: Fatty acid oxidation)
- The Sheffield Children's Hospital
- More information
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- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Biochemical diagnosis of MCAD deficiency (Analyte: Medium-chain acyl CoA dehydrogenase)
- The Sheffield Children's Hospital
- More information
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- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Biochemcial diagnosis of MCAD / MADD deficiency (Analyte: Quantitative hexanoylglycine)
- The Sheffield Children's Hospital
- More information
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- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Biochemical diagnosis of disorders of endocrine function / gluconeogenesis / fatty acid oxidation (Analyte: Free fatty acids)
- The Sheffield Children's Hospital
- More information
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- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Biochemical diagnosis of defects of long- and medium-chain fatty acid oxidation (Analyte: Myristate and palmitate oxidation)
- The Sheffield Children's Hospital
- More information
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
- Royal Victoria Infirmary
- More information
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Biochemical diagnosis of MCAD deficiency (Analyte: Medium chain acyl-CoA dehydrogenase)
- Royal Victoria Infirmary
- More information
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Biochemical diagnosis of Fatty acid oxidation defects (Analyte: Fatty acid oxidation)
- Royal Victoria Infirmary
- More information
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Biochemical diagnosis of MCAD deficiency (Analyte: Fatty acids C8-C12)
- Royal Victoria Infirmary
- More information
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- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Biochemical diagnosis of disorders of endocrine function / gluconeogenesis / fatty acid oxidation (Analyte: Free fatty acids)
- Royal Victoria Infirmary
- More information
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- NETHERLANDS
- Noord-Holland
- AMSTERDAM
- Molecular diagnosis of Medium-chain Acyl-CoA Dehydrogenase Deficiency (ACADM gene)
- AMC - Academisch Medisch Centrum
- More information
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- UNITED KINGDOM
- Strathclyde
- GLASGOW
- Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
- Royal Hospital for Sick Children
- More information
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- UNITED KINGDOM
- Avon
- BRISTOL
- Biochemical diagnosis of MCAD deficiency (Analyte: Fatty acids C8-C12)
- Bristol Royal Infirmary
- More information
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- UNITED KINGDOM
- Merseyside
- LIVERPOOL
- Biochemical diagnosis of Fatty acid oxidation disorders and Hyperinsulinism (Analyte: 3-Hydroxybutyrate)
- Alder Hey Children's Hospital
- More information
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- UNITED KINGDOM
- Cambridgeshire
- CAMBRIDGE
- Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
- Addenbrooke's Hospital
- More information
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene: sequencing)
- CeGaT GmbH
- More information
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- NETHERLANDS
- Noord-Holland
- AMSTERDAM
- Biochemical diagnosis of Medium-Chain Acyl-CoA Dehydrogenase Deficiency (Medium-Chain Acyl-CoA Dehydrogenase activity)
- AMC - Academisch Medisch Centrum
- More information
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- NETHERLANDS
- Noord-Holland
- AMSTERDAM
- 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
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- FRANCE
- RHONE-ALPES
- GRENOBLE
- Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- CHU de Grenoble site Nord - Institut de biologie et de pathologie
- More information
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- Biochemical, enzyme and molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- CHU de Lyon-GH Est - Hospices Civils de Lyon
- More information
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- CHU Paris - Hôpital Necker - Enfants Malades
- More information
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- FRANCE
- AQUITAINE
- BORDEAUX
- Molecular diagnosis of MCAD deficiency (ACADM gene)
- CHU de Bordeaux-GH Pellegrin
- More information
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- FRANCE
- ILE-DE-FRANCE
- LE KREMLIN BICETRE
- Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- CHU de Bicêtre
- More information
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- FRANCE
- PAYS DE LA LOIRE
- ANGERS
- Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- CHU d'Angers
- More information
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- FRANCE
- NORD-PAS-DE-CALAIS
- LILLE
- Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- CHRU de Lille - Centre de biologie et pathologie
- More information
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- FRANCE
- NORD-PAS-DE-CALAIS
- LILLE
- Study of beta-oxydation on fibroblasts culture by mass spectrophotometry
- CHRU de Lille - Centre de biologie et pathologie
- More information
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- Molecular and biochemical diagnosis of MCAD deficiency (ACADM gene)
- Policlinico Umberto I
- More information
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- Biochemical and molecular diagnosis of deficiency of acyl-CoA dehydrogenase, medium chain (ACADM gene)
- Biotecnologie Avanzate Srl
- More information
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- Molecular diagnosis of deficiency of acyl-CoA dehydrogenase, medium chain (ACADM gene)
- Laboratorio Genoma
- More information
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- Biochemical and molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Universidad Autónoma de Madrid. Facultad de Ciencias
- More information
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- Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, medium chain
- Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
- More information
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- Biochemical diagnosis of deficiency of short, medium and very long chain Acyl-CoA dehydrogenase
- Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
- More information
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- SPAIN
- Galicia
- SANTIAGO DE COMPOSTELA
- Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- CHUS - Complejo Hospitalario Universitario de Santiago
- More information
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- Molecular diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency (ACADM gene)
- Tartu University Hospital
- More information
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- Diagnosis of fatty acid oxidation defects : quantitative organic acid analysis (GC/MS)
- Tartu University Hospital
- More information
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- GERMANY
- Baden-Württemberg
- STUTTGART
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Klinikum Stuttgart, Standort Olgahospital
- More information
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- Molecular diagnosis of medium chain acyl-Coenzyme A dehydrogenase deficiency (ACADM gene): Target mutation analysis - single mutation (K304E)
- CGC Genetics / Centro de Genética Clínica
- More information
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- BELGIUM
- ARRONDISSEMENT BRUSSELS-CAPITAL
- BRUSSELS
- Molecular diagnosis of MCAD deficiency (ACADM gene)
- Universitair Ziekenhuis Brussel - UZBrussel
- More information
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- 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
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- FRANCE
- MIDI-PYRENEES
- TOULOUSE
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- CHU de Toulouse - Hôpital Purpan
- More information
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- CZECH REPUBLIC
- Capital City Prague
- PRAHA
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Charles University - First faculty of medicine
- More information
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- SWEDEN
- Stockholms läns landsting
- STOCKHOLM
- Molecular diagnosis of MCAD deficiency (ACADM gene)
- Karolinska University Hospital - Solna
- More information
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- Molecular diagnosis of Medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Medizinische Universität Innsbruck
- More information
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- NETHERLANDS
- Brabant
- TILBURG
- Tandem-MS diagnosis of MCAD deficiency (C8-carnitine (C8/C10))
- St. Elisabeth Ziekenhuis
- More information
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- UNITED KINGDOM
- Greater London
- LONDON
- Biochemical diagnosis of Fatty Acid Oxidation disorders (Analyte: Acyl Carnitines by Tandem MS)
- St Thomas' Hospital
- More information
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- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- GENETAQ
- More information
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- Portuguese National Neonatal Screening Program (Guthrie test)
- Instituto Nacional de Saúde Dr. Ricardo Jorge - Porto
- More information
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- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCAD gene: Lys304Glu mutation)
- Nzoz Genomed
- More information
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- FRANCE
- CHAMPAGNE-ARDENNE
- REIMS
- Biochemical diagnosis of medium chain acyl-CoA dehydrogenase deficiency (chromatography of organic acids)
- CHU de Reims - American Memorial Hospital
- More information
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- Biochemical analysis of free carnitine and acylcarnitine in serum by LC/MS/MS
- CHU Sherbrooke - Hôpital Fleurimont
- More information
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- FRANCE
- BASSE-NORMANDIE
- CAEN
- Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- CHU de Caen - Hôpital de la Côte de Nacre
- More information
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- CHU Paris - Hôpital Robert Debré
- More information
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- FRANCE
- HAUTE-NORMANDIE
- ROUEN
- Molecular diagnosis of MCAD deficiency (ACADM gene)
- CHU de Rouen - Hôpital Charles Nicolle
- More information
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- Biochemical diagnosis of beta-oxidation deficiency (metabolite analysis)
- IRCCS Istituto G. Gaslini - Ospedale Pediatrico
- More information
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- Molecular and biochemical diagnosis of metabolic encephalomyopathies (ETFDH, ETF, CPT2, MCAD, VLCAD genes)
- Fondazione IRCCS Istituto Neurologico "Carlo Besta"
- More information
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- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Labor für molekulare Genetik und metabolische Erkrankungen
- More information
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- Biochemical and molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency
- Klinikum Schwabing, Städt. Klinikum GmbH
- More information
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- Biochemical and molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- Hospital Clínico de Barcelona (Edificio Helios III)
- More information
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- ITALY
- EMILIA ROMAGNA
- BOLOGNA
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Azienda Ospedaliera di Bologna - Policlinico S. Orsola-Malpighi
- More information
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- Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, short, medium and very long chain
- IRCCS Ospedale Pediatrico Bambino Gesù
- More information
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- Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, medium, short and very long chain
- Ospedale Regionale per le Microcitemie
- More information
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- Biochemical and molecular diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency
- CGMJM - Centro de Genética Médica Jacinto Magalhães
- More information
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- FRANCE
- AQUITAINE
- BORDEAUX
- Biochemical diagnosis of medium chain Acyl-CoA dehydrogenase deficiency
- CHU de Bordeaux-GH Pellegrin
- More information
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
- CHU Paris - Hôpital Necker - Enfants Malades
- More information
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- 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
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- BULGARIA
- South-West region
- SOFIA
- Biochemical diagnosis of fatty acid oxydation disorders using GCMS analysis
- University hospital of Obstetrics and Gynecology
- More information
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- Biochemical and molecular diagnosis of SCAD and MCAD deficiency (ACADS and ACADM genes)
- Azienda Ospedaliera Universitaria Anna Meyer
- More information
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- GERMANY
- Baden-Württemberg
- HEIDELBERG
- Newborn screening : Biochemical diagnosis of medium chain acyl-CoA dehydrogenase deficiency
- Universitätsklinikum Heidelberg
- More information
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- GERMANY
- Baden-Württemberg
- HEIDELBERG
- Biochemical diagnosis of medium chain acyl-CoA dehydrogenase deficiency (acylcarnitine in dried blood and plasma)
- Universitätsklinikum Heidelberg
- More information
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- Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, medium chain
- Ospedale dei Bambini ''Vittore Buzzi"
- More information
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- NETHERLANDS
- Zuid-Holland
- CAPELLE AAN DEN IJSSEL
- Tandem-MS diagnosis of MCAD deficiency (C8-carnitine (C8/C10))
- IJsselland Ziekenhuis
- More information
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- NETHERLANDS
- Overijsel
- ZWOLLE
- Tandem-MS screening of MCAD deficiency (C8-carnitine (C8/C10))
- Isala Klinieken, locatie Sophia
- More information
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- NETHERLANDS
- Utrecht
- BILTHOVEN
- Newborn screening: Tandem-MS diagnosis of Medium Chain Acyl-CoA Dehydrogenase Deficiency (Analyte: C8 and ratio C8/C10)
- RIVM - Rijksinstituut voor Volksgezondheid en Milieu
- More information
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- GERMANY
- Sachsen-Anhalt
- MAGDEBURG
- Biochemical diagnosis of fatty acid metabolism disorders
- Universitätsklinikum Magdeburg A.ö.R
- More information
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- Biochemical diagnosis of Fatty acid oxidation (Palmitate and Myristate oxidation)
- Hadassah Ein Kerem - Hebrew University Medical Center
- More information
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- 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
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- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- The Children's Memorial Health Institute CMHI (IP-CZD)
- More information
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- Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, short, medium and very long chain(tandem mass spectrometry)
- Azienda Ospedaliero Universitaria di Foggia
- More information
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- Biochemical diagnosis of MCAD deficiency (tandem mass spectrometry)
- Azienda Ospedaliero Universitaria di Foggia
- More information
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- SPAIN
- Madrid
- SAN SEBASTIÁN DE LOS REYES
- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene: entire coding sequence/K304E mutation)
- LABORATORIO DE GENÉTICA CLÍNICA S.L.
- More information
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- Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
- Medizinische Universität Wien
- More information
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- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
- Medizinische Universität Graz
- More information
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- Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCAD gene: Lys304Glu mutation)
- MEDGEN
- More information
