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Caption : Accreditation =Accreditation
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    • FRANCE
    • ILE-DE-FRANCE
    • LE KREMLIN-BICÊTRE
    • Accreditation
    • Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
    • GHU Paris-Sud - Hôpital de Bicêtre
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene: codon 304 and 329)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCAD gene: K329E)
    • Labor Lademannbogen
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene: sequencing)
    • Pränatalmedizin München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Medizinisches Versorgungszentrum Humane Genetik
    • More information
    • FINLAND
    • Finland
    • HELSINKI
    • Accreditation
    • Molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency (ACADM gene c.985 A>G )
    • HUCH - Helsinki University Central Hospital
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of medium chain Acyl-CoA Dehydrogenase defficiency (ACADM common A985G mutation)
    • St Mary's Hospital
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Accreditation
    • Molecular diagnosis of MCAD deficiency (ACADM gene)
    • CHU de LIEGE - UniLab Lg
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of Medium Chain Acyl-CoA Deshydrogenase deficiency (MCDA)
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of MCAD deficiency (gene: ACADM)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Molecular diagnosis of Medium Chain Acyl-CoA Dehydrogenase Deficiency by Targeted mutation analysis (p.K329E, ACADM gene)
    • Liverpool Women's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • 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
    • UNITED KINGDOM
    • Tayside
    • DUNDEE
    • Accreditation
    • Molecular diagnosis of Medium Chain Acyl-CoA dehydrogenase (MCAD) deficiency (ACADM gene)
    • Ninewells Hospital
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Medium chain acyl-CoA dehydrogenase deficiency - MCAD deficiency (ACADM gene)
    • Great Ormond Street Hospital for Children, York House
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of MCAD deficiency (MCAD gene, mutation p.K329E)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Praxis für Humangenetik Freiburg
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Molecular diagnosis of Medium Chain Acyl CoA Dehydrogenase Deficiency (MCAD)
    • Southmead Hospital
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Molecular diagnosis of Medium Chain Acyl-CoA Dehydrogenase Deficiency by Targeted mutation analysis (ACADM gene)
    • Southmead Hospital
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Medium Chain Acyl CoA Dehydrogenase Deficiency (MCAD, ACADM gene c.985AG -p.Lys329Gln)
    • Birmingham Children's Hospital NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Medium Chain Acyl CoA Dehydrogenase Deficiency (MCAD)
    • International Centre for Life
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Molecular diagnosis of Medium chain Acyl-CoA Dehydrogenase Deficiency (ACADM gene: Targetted mutation analysis / Testing for known mutations in family members)
    • International Centre for Life
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Zentrum für Humangenetik und Laboratoriumsmedizin Dr. Klein und Dr. Rost
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Centogene AG
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Universitätsklinikum Heidelberg
    • More information
    • GERMANY
    • Baden-Württemberg
    • KARLSRUHE
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Labor PD Dr. Volkmann und Kollegen
    • 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
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Medium chain acyl-CoA dehydrogenase deficiency - MCAD (G985A Mutation)
    • 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
    • Sachsen
    • DRESDEN
    • Accreditation
    • Newborn screening : Biochemical diagnosis of medium chain acyl-CoA dehydrogenase deficiency (amino acid and acylcarnitine in dried blood)
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • More information
    • NORWAY
    • Østlandet
    • OSLO
    • Accreditation
    • Molecular diagnosis of Medium chain acyl-CoA dehydrogenase deficiency (ACADM gene: c.985 A>G; p.Lys329Glu and c.199T>C; p.Tyr67His)
    • Oslo University Hospital, Rikshospitalet
    • 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 London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Medium chain Acyl-CoA Dehydrogenase Deficiency (ACADM gene: Targetted mutation analysis c.985A>G common mutation / Sequencing of the entire coding region of gene (s))
    • Guy's Hospital
    • 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
    • GERMANY
    • Baden-Württemberg
    • SINGEN /HTWL.
    • Accreditation
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Institut für Laboratoriumsmedizin und Humangenetik
    • 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 Fatty acid oxidation defects (Analyte: Fatty acid oxidation)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of MCAD deficiency (Analyte: Medium-chain acyl CoA dehydrogenase)
    • 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 disorders of endocrine function / gluconeogenesis / fatty acid oxidation (Analyte: Free fatty acids)
    • 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
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of MCAD deficiency (Analyte: Medium chain 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 MCAD deficiency (Analyte: Fatty acids C8-C12)
    • 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 Medium-chain Acyl-CoA Dehydrogenase Deficiency (ACADM 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
    • Avon
    • BRISTOL
    • Accreditation
    • Biochemical diagnosis of MCAD deficiency (Analyte: Fatty acids C8-C12)
    • Bristol Royal Infirmary
    • 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 Medium-Chain Acyl-CoA Dehydrogenase Deficiency (Medium-Chain 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
    • GRENOBLE
    • Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Biochemical, enzyme and molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • CHU de Lyon HCL - GH Est
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of MCAD deficiency (ACADM gene)
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase 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 medium-chain acyl-CoA dehydrogenase deficiency
    • CHU d'Angers
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Study of beta-oxydation on fibroblasts culture by mass spectrophotometry
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular and biochemical diagnosis of MCAD deficiency (ACADM gene)
    • Policlinico Umberto I
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Biochemical and molecular diagnosis of deficiency of acyl-CoA dehydrogenase, medium chain (ACADM gene)
    • Biotecnologie Avanzate Srl
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of deficiency of acyl-CoA dehydrogenase, medium chain (ACADM gene)
    • Laboratorio Genoma
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical and molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Universidad Autónoma de Madrid. Facultad de Ciencias
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, medium chain
    • Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • 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
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Molecular diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency (ACADM gene)
    • Tartu University Hospital
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Diagnosis of fatty acid oxidation defects : quantitative organic acid analysis (GC/MS)
    • Tartu University Hospital
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Klinikum Stuttgart - Standort Olgahospital
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of medium chain acyl-Coenzyme A dehydrogenase deficiency (ACADM gene: Sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene / gene and MUT.K302E sequencing)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of MCAD deficiency (ACADM gene)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • 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
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of MCAD deficiency (ACADM gene)
    • Karolinska University Hospital - Solna
    • More information
    • ITALY
    • VENETO
    • VERONA
    • Molecular diagnosis of SCAD and MCAD deficiency (ACADS and ACADM genes)
    • Azienda Ospedaliera Universitaria Integrata di Verona - Ospedale Borgo Roma
    • More information
    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Molecular diagnosis of Medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Medizinische Universität Innsbruck
    • More information
    • NETHERLANDS
    • Brabant
    • TILBURG
    • Tandem-MS diagnosis of MCAD deficiency (C8-carnitine (C8/C10))
    • St. Elisabeth Ziekenhuis
    • 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 medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Genetaq
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Portuguese National Neonatal Screening Program (Guthrie test)
    • Instituto Nacional de Saúde Dr. Ricardo Jorge - Porto
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCAD gene: Lys304Glu mutation)
    • Nzoz Genomed
    • More information
    • 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
    • CANADA
    • Québec
    • SHERBROOKE
    • Biochemical analysis of free carnitine and acylcarnitine in serum by LC/MS/MS
    • CHU Sherbrooke - Hôpital Fleurimont
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCAD gene: Lys304Glu mutation)
    • MEDGEN
    • More information
    • CANADA
    • Québec
    • MONTRÉAL
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency; MCAD (ACADM gene / mutation K304E)
    • Montreal Children's hospital - Hôpital de Montréal pour enfants
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
    • CHU Paris - Hôpital Robert Debré
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Molecular diagnosis of MCAD deficiency (ACADM gene: common mutations)
    • 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
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular and biochemical diagnosis of metabolic encephalomyopathies (ETFDH, ETF, CPT2, MCAD, VLCAD genes)
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Labor für molekulare Genetik und metabolische Erkrankungen
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Biochemical and molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency
    • Klinikum Schwabing, Städt. Klinikum GmbH
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical and molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
    • Hospital Clínic de Barcelona
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Policlinico S. Orsola-Malpighi - Area S. Orsola
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, short, medium and very long chain
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, medium, short and very long chain
    • Ospedale Regionale per le Microcitemie
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical and molecular diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Biochemical diagnosis of medium chain Acyl-CoA dehydrogenase deficiency
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of medium-chain acyl-CoA dehydrogenase 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 and molecular diagnosis of SCAD and MCAD deficiency (ACADS and ACADM genes)
    • Azienda Ospedaliera Universitaria Anna Meyer
    • More information
    • 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
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Newborn screening : Biochemical diagnosis of medium chain acyl-CoA dehydrogenase deficiency
    • Universitätsklinikum Heidelberg
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of medium chain acyl-CoA dehydrogenase deficiency (acylcarnitine in dried blood and plasma)
    • Universitätsklinikum Heidelberg
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, medium chain
    • Ospedale dei Bambini ''Vittore Buzzi"
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • CAPELLE AAN DEN IJSSEL
    • Tandem-MS diagnosis of MCAD deficiency (C8-carnitine (C8/C10))
    • IJsselland Ziekenhuis
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    • NETHERLANDS
    • Overijsel
    • ZWOLLE
    • Tandem-MS screening of MCAD deficiency (C8-carnitine (C8/C10))
    • Isala Klinieken, locatie Sophia
    • More information
    • 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
    • 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
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    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • The Children's Memorial Health Institute CMHI (IP-CZD)
    • More information
    • ITALY
    • PUGLIA
    • FOGGIA
    • Biochemical diagnosis of deficiency of acyl-CoA dehydrogenase, short, medium and very long chain(tandem mass spectrometry)
    • Azienda Ospedaliero Universitaria di Foggia
    • More information
    • ITALY
    • PUGLIA
    • FOGGIA
    • Biochemical diagnosis of MCAD deficiency (tandem mass spectrometry)
    • Azienda Ospedaliero Universitaria di Foggia
    • More information
    • 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
    • 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 medium chain acyl-CoA dehydrogenase deficiency (ACADM gene)
    • Medizinische Universität Graz
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    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of medium chain acyl-CoA dehydrogenase deficiency (ACADM gene / real-time PCR)
    • GenoClinics
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    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency (mutations c.985A>C, c.199T>C and sequencing analysis of ACADM gene)
    • University Hospital Bratislava - Stare mesto
    • 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
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