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Caption : Accreditation =Accreditation
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    • FRANCE
    • ILE-DE-FRANCE
    • SAINT-OUEN-L'AUMÔNE
    • Accreditation
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria (Cbl C, Cbl D)
    • Laboratoire Cerba
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • NICE
    • Accreditation
    • Biochemical diagnosis of organic acidurias
    • CHU de Nice - Hôpital Pasteur
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • NICE
    • Accreditation
    • Biochemical diagnosis of homocystinuria due to cystathionine betasynthase or cobalamin deficiencies
    • CHU de Nice - Hôpital Pasteur
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Methylmalonicacidemia with Homocystinuria type cblC (MMACHC gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Metabolic Neurodegenerative Disorders (multigene panel; 60 genes)
    • AMC - Academisch Medisch Centrum
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of methylmalonic acidemia with homocystinuria, type cblC, D and F (LMBRD1, MMACHC, MMADHC genes)
    • Centogene AG
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN
    • Accreditation
    • Biochemical diagnosis of Organic acidurias (organic acids, acylcarnitines: by tandem MS in bloodspots & by GC/MS in plasma, urine, CSF)
    • Provinciaal Centrum voor opsporing van Metabole Aandoeningen (PCMA) - Antwerpen
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN
    • Accreditation
    • Biochemical diagnosis of Aminoacidopathies (by aminoacid analysator & tandem MS : serum, urine, CSF)
    • Provinciaal Centrum voor opsporing van Metabole Aandoeningen (PCMA) - Antwerpen
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Biochemical diagnosis of Methylmalonic Acidemia (Analyte: Methylmalonic Acid)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Biochemical diagnosis of Organic Acidurias (Analyte: Organic Acids, quantitative)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Biochemical diagnosis of Amino Acid Metabolism and Transport Defects (Analyte: Amino Acids in plasma (D- and L-Amino Acids), urine and CSF (D- and L-Amino Acids), quantitative)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Biochemical diagnosis of Hyperhomocysteinaemia (Analyte: Total homocysteine)
    • University Hospital of Wales
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Biochemical diagnosis of Methylmalonic acidaemia (Analyte: Methylmalonic acid)
    • University Hospital of Wales
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Biochemical diagnosis of organic aciduria (urinary organic acids with GC/MS)
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Biochemical diagnosis of Amino acid metabolism diseases (amino acid in urine/plasma/liquor)
    • UKE - Universitätsklinikum Hamburg-Eppendorf
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Biochemical diagnosis of the disorders of Amino Acid Metabolism (Analyte: Amino Acids, qualitative and quantitative)
    • St Mary's Hospital
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Biochemical diagnosis of Organic Acidurias (Analyte: Organic acids, qualitative)
    • 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 Hyperhomocysteinaemia (Analyte: Total homocysteine)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Organic acidaemias (Analyte: Qualitative organic acids)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Methylmalonic acidaemia (Analyte: Quantitative methylmalonic acid)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Aminoacidopathies (Analyte: Quantitative and Qualitative amino 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 Aminoacidopathies (Analyte: Quantitative amino acids)
    • Royal Victoria Infirmary
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of Organic acidaemias (Analyte: Organic acid specific quantitation, usually by stable isotope analysis)
    • Royal Victoria Infirmary
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of Organic acidaemias (Analyte: Qualitative organic acids)
    • Royal Victoria Infirmary
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Methylmalonic Aciduria with Homocystinuria, type cblC (MMACHC gene)
    • VUmc - VU 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
    • Strathclyde
    • GLASGOW
    • Accreditation
    • Biochemical diagnosis of Aminoacidopathies (Analyte: Quantitative amino acids)
    • Royal Hospital for Sick Children
    • More information
    • UNITED KINGDOM
    • Strathclyde
    • GLASGOW
    • Accreditation
    • Biochemical diagnosis of Organic acidaemias (Analyte: Qualitative organic acids)
    • Royal Hospital for Sick Children
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Biochemical diagnosis of Hyperhomocysteinaemia (Analyte: Total homocysteine)
    • Bristol Royal Infirmary
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Biochemical diagnosis of Hyperhomocysteinaemia (Analyte: Total homocysteine)
    • Alder Hey Children's Hospital
    • More information
    • UNITED KINGDOM
    • Merseyside
    • LIVERPOOL
    • Accreditation
    • Biochemical diagnosis of Organic acidaemias (Analyte: Qualitative organic acids)
    • Alder Hey Children's Hospital
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Organic Acidurias (Analyte: Acetoacetate, Acylcarnitine, PUFA, 3-Hydroxybutyric Acid, Lactic Acid, Organic Acids and Pyruvic Acid)
    • AMC - Academisch Medisch Centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Cobalamin Synthesis and Transport Disorders (Analyte: Methylmalonic Acid and total Homocysteine)
    • AMC - Academisch Medisch Centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Homocystinuria (Analyte: S-adenosylmethionine, S-adenosylhomocysteine and total Homocysteine)
    • AMC - Academisch Medisch Centrum
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria (Cbl C, Cbl D)
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Biochemical diagnosis of methylmalonicacidemia with homocystinuria (Cbl C, Cbl D)
    • CHU de Lyon HCL - GH Est
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Biochemical diagnosis of homocystinuria (Analyte: Total homocysteine)
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria (Cbl C, Cbl D) (organic acids/ GC-MS, acylcarnitines/MSMS, amino acids/HPLC)
    • CHU de Caen - Hôpital de la Côte de Nacre
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria (Cbl C, Cbl D)
    • CHU d'Angers
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of homocystinuria
    • Policlinico Umberto I
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemistry diagnosis of methylglutaconic acidemia (AUH, TAZ, OPA3, DNAJC19 genes)
    • Policlinico Umberto I
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular and biochemical diagnosis of methylmalonic acidemia with homocystinuria (MMACHC gene)
    • Policlinico Umberto I
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Biochemical and molecular diagnosis of methylmalonic acidemia (MUT, MMAA, MMAB, MMACHC genes)
    • Biotecnologie Avanzate Srl
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of methylmalonicacidemia - homocystinuria, type cbl C (MMACHC gene)
    • Laboratorio Genoma
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical and molecular diagnosis of methylmalonic acidemia - homocystinuria (LMBRD1, MMACHC and MMADHC genes)
    • Universidad Autónoma de Madrid. Facultad de Ciencias
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Biochemical diagnosis of methylmalonic acidemia
    • Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Molecular diagnosis of methylmalonic acidemia with homocystinuria, type cblC, D (MMACHC, MMADHC gene: sequencing)
    • Universitätsklinikum Köln
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Diagnosis of organic acidurias : quantitative organic acid analysis (GC/MS)
    • Tartu University Hospital
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Biochemical diagnosis of Homocystinuria and MMA (Homocysteine: HPLC, plasma)
    • CHU Sart Tilman - Liège
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Biochemical diagnosis of Organic acidurias (acylcarnitines: by tandem MS in bloodspots, serum or urine & organic acids by GC/MS in urine)
    • CHU Sart Tilman - Liège
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of methylmalonic acidemia with homocystinuria, type cblC (MMACHC gene / gene and mutation C.271dupA 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
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of methylmalonicacidemia - homocystinuria, type cbl C
    • Karolinska University Hospital - Solna
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular analysis of methylmalonic acuduria and/or homocystinuria, cblD type (MMADHC gene, entire coding region, enzyme assay)
    • Karolinska University Hospital - Solna
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical diagnosis of Aminoacidopathies (Analyte: Quantitative amino acids)
    • St Thomas' Hospital
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical diagnosis of Hyperhomocysteinaemia (Analyte: Total homocysteine)
    • St Thomas' Hospital
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Biochemical diagnosis of organic acidurias (chromatography of organic acids; enzyme assays)
    • CHU de Reims - American Memorial Hospital
    • More information
    • CANADA
    • Québec
    • SHERBROOKE
    • Biochemical diagnosis of methlymalonic acidemia (by GC/MS - quantitative method by stable isotope dilution)
    • CHU Sherbrooke - Hôpital Fleurimont
    • More information
    • CANADA
    • Québec
    • SHERBROOKE
    • Biochemical analysis of organic acids in urine by GC/MS
    • CHU Sherbrooke - Hôpital Fleurimont
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • CRÉTEIL
    • Diagnosis of methylmalonicaciduria with homocystinuria (Cbl C,CblD). Cell cultures; measure synthesis active forms
    • GH Henri Mondor
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical and molecular diagnosis of methylmalonicaciduria with homocystinuria, cbl C and cbl D types (MMACHC and MMADHC genes)
    • CHU Paris - Hôpital Robert Debré
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria
    • CHU de Rouen - Hôpital Charles Nicolle
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Biochemical diagnosis of organic acidemia (metabolite analysis)
    • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of organic aciduria
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria
    • Labor für molekulare Genetik und metabolische Erkrankungen
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical and molecular diagnosis of Methylmalonicacidemia - homocystinuria, type cbl C. MMACHC gene.
    • Hospital Clínic de Barcelona
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical diagnosis of cobalamin metabolism disease
    • Hospital Clínic de Barcelona
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of acidemia and methylmalonicaciduria
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria
    • Ospedale Regionale per le Microcitemie
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical diagnosis of methylmalonic aciduria
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical diagnosis of homocystinuria
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Molecular diagnosis of methylmalonicacidemia - homocystinuria, type cbl C (MMACHC gene)
    • Ospedale Regionale per le Microcitemie
    • More information
    • FINLAND
    • Finland
    • HELSINKI
    • Biochemical diagnosis of homocystinuria
    • HUCH - Helsinki University Central Hospital
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of methylmalonicaciduria with homocystinuria (Cbl C, Cbl D)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • UNITED KINGDOM
    • West Yorkshire
    • LEEDS
    • Biochemical diagnosis of Hyperhomocysteinaemia (Analyte: Total homocysteine)
    • St James's University Hospital
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DÜSSELDORF
    • Biochemical diagnosis of Amino acid metabolism diseases
    • Universitätsklinikum Düsseldorf
    • More information
    • HUNGARY
    • Dél-Dunántúl
    • PECS
    • Biochemical diagnosis of methylmalonicaciduria - homocystinuria
    • Department of Paediatrics - Clinical Center - University of Pécs
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Biochemical and molecular diagnosis of methylmalonicaciduria-homocystinuria (MMACHC gene)
    • Azienda Ospedaliera Universitaria Anna Meyer
    • More information
    • SPAIN
    • País Vasco
    • BARAKALDO
    • Biochemical diagnosis of methylmalonicacidemia
    • Hospital Universitario Cruces - Osakidetza
    • More information
    • SPAIN
    • País Vasco
    • BARAKALDO
    • Biochemical diagnosis of organic acidemias (methyl citric acid)
    • Hospital Universitario Cruces - Osakidetza
    • More information
    • ITALY
    • SICILIA
    • CATANIA
    • Molecular and biochemistry diagnosis of methylmalonic acidemia with homocystinuria, type C (defective MMACHC gene) and type G (homocysteine-methyltetrahydrofolate-methyltransferase deficiency)
    • Università degli Studi di Catania
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of homocystinuria
    • Universitätsklinikum Heidelberg
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of methylmalonicaciduria (organic acids in urine, acylcarnitine in dried blood)
    • Universitätsklinikum Heidelberg
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of methylmalonic acidemia with homocystinuria
    • Ospedale dei Bambini ''Vittore Buzzi"
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Biochemical diagnosis of Amino acid metabolism diseases
    • LMU Klinikum der Universität München - Campus Innenstadt
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LÈS-NANCY
    • Biochemical and molecular diagnosis of methylmalonic aciduria CblC type with homcystinuria (MMACHC gene)
    • CHU de Nancy - Hôpital de Brabois
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Biochemical diagnosis of Amino acid metabolism diseases (amino acid in urine/plasma/liquor)
    • Universitätsmedizin Göttingen
    • More information
    • GERMANY
    • Sachsen-Anhalt
    • MAGDEBURG
    • Biochemical diagnosis of organic acidurias
    • Universitätsklinikum Magdeburg A.ö.R
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Biochemical diagnosis of Aminoacidopathies (Analyte: Quantitative amino acids)
    • Royal Hospital for Sick Children
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical diagnosis of Aminoacidopathies (Analyte: Quantitative amino acids)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical diagnosis of Hyperhomocysteinaemia (Analyte: Total homocysteine)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • SPAIN
    • Cataluña
    • ESPLUGUES DE LLOBREGAT
    • Biochemical diagnosis of methylmalonic acidemia with homocystinuria.
    • Hospital Universitari Sant Joan de Déu
    • More information
    • SPAIN
    • Cataluña
    • ESPLUGUES DE LLOBREGAT
    • Biochemical diagnosis of cobalamin metabolism disease.
    • Hospital Universitari Sant Joan de Déu
    • More information
    • SPAIN
    • Cataluña
    • ESPLUGUES DE LLOBREGAT
    • Biochemical diagnosis of methylmalonicacidemia - homocystinuria, type cbl C.
    • Hospital Universitari Sant Joan de Déu
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Biochemical diagnosis of Amino acid metabolism diseases (amino acid in urine/plasma/liquor)
    • Medizinische Hochschule Hannover
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Biochemical diagnosis of organic acidurias
    • Medizinische Hochschule Hannover
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of methylmalonic acidemia - homocystinuria (MMACHC, MMADHC and LMBRD1 genes: entire coding sequence)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Neonatal screening of constitutional megaloblastic anemia due to vitamin B12 metabolism disorder (MS/MS)
    • Genetadi Biotech S.L.
    • More information
    • ITALY
    • MARCHE
    • ANCONA
    • Biochemical diagnosis of organic aciduria (urine organic acid assay and characterization)
    • Ospedali Riuniti "Umberto I - G.M. Lancisi - G. Salesi" - Presidio "G. Salesi"
    • 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 methylmalonic acidemia with homocystinuria, type cblC (MMACHC gene)
    • Igenomix Spain
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Biochemical diagnosis of organic acidurias
    • Klinikum der Johann Wolfgang Goethe-Universität Frankfurt
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Biochemical diagnosis of Amino acid metabolism diseases
    • Klinikum der Johann Wolfgang Goethe-Universität Frankfurt
    • More information