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Caption : Accreditation =Accreditation
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    • FRANCE
    • ILE-DE-FRANCE
    • LE KREMLIN-BICÊTRE
    • Accreditation
    • Biochemical and molecular diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene)
    • GHU Paris-Sud - Hôpital de Bicêtre
    • More information
    • FINLAND
    • Finland
    • HELSINKI
    • Accreditation
    • Molecular diagnosis of long chain fatty acid 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene c.1528G>C)
    • HUCH - Helsinki University Central Hospital
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency - LCHAD (HADHA gene: 1528G>C)
    • St Mary's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Long Chain Acyl-CoA Dehydrogenase deficiency - LCHAD (HADHA gene: testing for common mutation c.1528G>C, p.Glu510Gln)
    • Sheffield Children's NHS Foundation Trust
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency - LCHAD deficiency (HADHA gene)
    • Great Ormond Street Hospital for Children, York House
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of LCHAD deficiency (LCHAD gene, p.E510Q mutation)
    • 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
    • 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
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency - LCHAD (HADHA gene c.1528GC -p.Glu510Gln)
    • Birmingham Children's Hospital NHS Foundation Trust
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene)
    • Centogene AG
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Accreditation
    • Molecular diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene: E510Q)
    • Institut für Humangenetik am Universitätsklinikum Heidelberg
    • 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
    • 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
    • GERMANY
    • Baden-Württemberg
    • SINGEN /HTWL.
    • Accreditation
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA 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 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 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
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of LCHAD deficiency (Analyte: Long-chain-3-hydroxyacyl CoA dehydrogenase)
    • Royal Victoria Infirmary
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of Mitochondrial trifunctional protein deficiency & LCHAD deficiency (Analyte: Mitochondrial trifunctional protein)
    • Royal Victoria Infirmary
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of LCHAD Deficiency (HADHA gene; G1528C mutation)
    • 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
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Long-Chain 3-Hydroxy-Acyl-CoA Dehydrogenase Deficiency (Long-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
    • AUSTRALIA
    • New South Wales
    • WESTMEAD
    • Accreditation
    • Biochemical diagnosis of LCHAD deficiency (Long-chain-3-hydroxyacyl CoA dehydrogenase activity)
    • The Children's Hospital
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Biochemical diagnosis of long chain fatty acid 3-hydroxyacyl-CoA dehydrogenase deficiency
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Biochemical diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    • CHU de Lyon HCL - GH Est
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of LCHAD deficiency (HADHA gene)
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Biochemical diagnosis of long chain fatty acid 3-hydroxyacyl-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 long chain fatty acid 3-hydroxyacyl-CoA dehydrogenase deficiency
    • CHU d'Angers
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Biochemical diagnosis of 3-hydroxyacyl-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
    • LOMBARDIA
    • CREMONA
    • Molecular diagnosis of LCHAD deficiency (HADHA gene)
    • Azienda Ospedaliera Istituti Ospitalieri di Cremona
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular and biochemical diagnosis of LCHAD deficiency (HDHA gene)
    • Policlinico Umberto I
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Biochemical and molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene)
    • Biotecnologie Avanzate Srl
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical and molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA 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
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Biochemical and molecular diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency. HADHA gene
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency (HADHA 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
    • PORTUGAL
    • NORTE
    • PORTO
    • Prenatal and postnatal molecular diagnosis of Long Chain 3-Hydroxyacyl-CoA dehydrogenase deficiency (HADHA: sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of LCHAD deficiency (HADHA gene)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of LCHAD deficiency (HADHA gene)
    • Karolinska University Hospital - Solna
    • More information
    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Molecular diagnosis of Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene)
    • Medizinische Universität Innsbruck
    • More information
    • NETHERLANDS
    • Brabant
    • TILBURG
    • Tandem-MS diagnosis of LCHAD deficiency (C16OH-carnitine)
    • 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
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene: analysis of coding regions)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Portuguese National Neonatal Screening Program (Guthrie test)
    • Instituto Nacional de Saúde Dr. Ricardo Jorge - Porto
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene - p.Glu510Gln mutation / entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Biochemical diagnosis of LCHAD 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
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene / sequencing)
    • GenoClinics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency
    • CHU Paris - Hôpital Robert Debré
    • 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
    • Biochemical diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    • Klinikum Schwabing, Städt. Klinikum GmbH
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical and molecular diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency
    • Hospital Clínic de Barcelona
    • 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
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical and molecular diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of 3-hydroxyacyl-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
    • ITALY
    • TOSCANA
    • FIRENZE
    • Biochemical and molecular diagnosis of LCHAD deficiency (HADHA gene)
    • Azienda Ospedaliera Universitaria Anna Meyer
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene)
    • Charles University - First faculty of medicine
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Newborn screening : Biochemical diagnosis of VLCAD/LCHAD deficiency
    • Dietmar-Hopp-Stoffwechselzentrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (acylcarnitine in dried blood and plasma)
    • Dietmar-Hopp-Stoffwechselzentrum
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of deficiency of 3-hydroxyacyl-CoA dehydrogenase, long 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
    • NETHERLANDS
    • Zuid-Holland
    • CAPELLE AAN DEN IJSSEL
    • Tandem-MS diagnosis of LCHAD deficiency (C16OH-carnitine)
    • IJsselland Ziekenhuis
    • More information
    • NETHERLANDS
    • Overijsel
    • ZWOLLE
    • Tandem-MS screening of LCHAD deficiency (C16OH-carnitine)
    • Isala Klinieken, locatie Sophia
    • More information
    • NETHERLANDS
    • Utrecht
    • BILTHOVEN
    • Newborn screening: Tandem-MS diagnosis of Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (Analyte: C16OH)
    • 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
    • More information
    • SPAIN
    • Cataluña
    • ESPLUGUES DE LLOBREGAT
    • Biochemical diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (analyte: Urine Dicarboxilic acids)
    • Hospital Universitari Sant Joan de Déu
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of LCHAD deficiency (HADHA gene)
    • The Children's Memorial Health Institute CMHI (IP-CZD)
    • More information
    • ITALY
    • PUGLIA
    • FOGGIA
    • Biochemical diagnosis of deficiency of 3-hydroxyacyl-CoA dehydrogenase, long chain (tandem mass spectrometry)
    • Azienda Ospedaliero Universitaria di Foggia - Ospedali Riuniti
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene: entire coding sequence/E474Q and Q342X mutations)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Neonatal screening of long 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
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Preimplantation genetic diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene)
    • Igenomix Spain
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Molecular diagnosis of long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (HADHA gene)
    • 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