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Caption : Accreditation =Accreditation
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    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of Zellweger syndrome (PEX1 gene: sequencing)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Peroxisome biogenesis disorders (PEX1, PEX6, PEX10, PEX12 and PEX26 genes: analysis of common mutations and sequencing)
    • Sheffield Children's NHS Foundation Trust
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of Zellweger syndrome (PEX1, PEX2, PEX3, PEX6, PEX10, PEX12, PEX26 genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Biochemical diagnosis of Zellweger syndrome
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Biochemical diagnosis of Zellweger syndrome
    • Universitäts-Kinderspital
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of peroxisomal disorders (PEX1-3, PEX5-7, PEX10-14, PEX16, PEX19, PEX26 genes)
    • Centogene AG
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Biochemical diagnosis of Peroxisomal Disorders (Analyte: Pristanic Acid, Phytanic Acid, Pipecolic Acid and Very Long Chain Fatty Acids)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of peroxisomal disorders (PEX1, PEX2, PEX3, PEX5, PEX6, PEX12, PEX14, PEX26 genes)
    • MVZ Fenner & Krasemann
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Biochemical diagnosis of Peroxisomal disorders (Analytes: plasmalogens, pristanic acid, phytanate and VLCFA)
    • St Mary's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Peroxisomal biogenesis disorders & Peroxisomal single enzyme defects (Analyte: Fatty acids very-long-chain)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Adult Refsum disease / Peroxisomal disorders (Analyte: Phytanic acid)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Peroxisomal disorders (Analytes: Pristanic acid, plasmalogens, pipecolic acid & Very Long Chain Fatty acids)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Biochemical diagnosis of Peroxisomal biogenesis disorders/ Zellweger spectrum (by Di-hydroxyacetonephosphate Acyltansferase (DHAP-AT) & Catalase staining in fibroblasts)
    • The Sheffield Children's Hospital
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of Peroxisomal disorders (Analyte: Very Long Chain Fatty Acids)
    • Royal Victoria Infirmary
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • Accreditation
    • Biochemical diagnosis of Peroxisomal disorders (Analyte: Pristanic acid)
    • Royal Victoria Infirmary
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Zellweger Spectrum Disorders (PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX 19 and PEX26 gene)
    • AMC - Academisch Medisch Centrum
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Biochemical diagnosis of Pipecolic acidemia (Analyte: Pipecolic acid)
    • Bristol Royal Infirmary
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Biochemical diagnosis of Peroxisomal disorders (Analyte: Very Long Chain Fatty Acids - VLCFA)
    • Addenbrooke's Hospital
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of peroxisomal disorders (PEX1, PEX2, PEX3, PEX5, PEX6, PEX12, PEX14, PEX26 genes)
    • CeGaT GmbH
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Zellweger Spectrum Disorders (DHAPAT activity, Plasmalogen levels, immunoblotting of ACOX1 and Peroxisomal Thiolase and Complementation Analysis)
    • AMC - Academisch Medisch Centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Immunofluorescent diagnosis of Zellweger Spectrum Disorders (Catalase and ALDP)
    • AMC - Academisch Medisch Centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Peroxisomal Disorders (Analyte: Bile Acids, PUFA, Phytanic, Pristanic and Pipecolic Acid, Plasmalogens and Very Long-Chain Fatty Acids)
    • AMC - Academisch Medisch Centrum
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Biochemical diagnosis of pipecolic acidemia
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Biochemical and molecular diagnosis of peroxisome biogenesis disorder (PEX1, PEX2, PEX6, PEX10, PEX12 and PEX26 genes)
    • CHU de Lyon HCL - GH Est
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Biochemical diagnosis of Zellweger syndrome
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Biochemical diagnosis of pipecolic acidemia
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical diagnosis of Zellweger syndrome
    • Universidad Autónoma de Madrid. Facultad de Ciencias
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical and molecular diagnosis of peroxisome biogenesis disorder (PEX1, PEX6, PEX12, PEX26 genes)
    • Universidad Autónoma de Madrid. Facultad de Ciencias
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Biochemical diagnosis of Zellweger syndrome
    • Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Biochemical diagnosis of pipecolic acidemia
    • Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Diagnosis of peroxisomal metabolism disorders : very long chain fatty acid analysis (GC/MS)
    • Tartu University Hospital
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of Zellweger syndrome (PEX1, PEX6, PEX10 ,PEX12, PEX26 genes)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of peroxisomal disorders (PEX2 gene)
    • Klinikum Stuttgart - Standort Olgahospital
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Zellweger syndrome (PEX1 gene)
    • Praxis für Humangenetik
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Biochemical diagnosis of Peroxisomial Disorders (VLCFA, Phytanic and Pristanic Acid by GCMSMS: serum)
    • CHU Sart Tilman - Liège
    • More information
    • NORWAY
    • Østlandet
    • OSLO
    • Molecular diagnosis of Zellweger syndrome (PEX1 gene)
    • Oslo University Hospital, Ullevaal
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Zellweger syndrome (PEX1, PEX6, PEX26, PEX10 and PEX12 genes)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of peroxisomal diseases (very long chain fatty acids assay in plasma; phytanic and pristanic acids assays)
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Biochemical diagnosis of pipecolic acidemia (chromatography of aminoacids)
    • CHU de Reims - American Memorial Hospital
    • More information
    • CANADA
    • Québec
    • SHERBROOKE
    • Biochemical analysis of phytanic acid and very long chain fatty acids in serum by GC/MS
    • CHU Sherbrooke - Hôpital Fleurimont
    • More information
    • CANADA
    • Québec
    • SHERBROOKE
    • Biochemical analysis of pipecolic acid by LC/MS
    • CHU Sherbrooke - Hôpital Fleurimont
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Mass spectometry diagnosis of Zellweger syndrome (Analytes: phytanic acid, very long chain C22-C26 fatty acids and plasmalogen phospholipids)
    • Faculté de Médecine Pierre et Marie Curie - Hôpital Saint-Antoine
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • MONTPELLIER
    • Biochemical diagnosis of Zellweger syndrome (dosage by GC/MS)
    • CHRU de Montpellier - Hôpital Lapeyronie
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Biochemical diagnosis of peroxisomal diseases (metabolite analysis)
    • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of Zellweger syndrome
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical diagnosis of Zellweger syndrome
    • Hospital Clínic de Barcelona
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of Zellweger syndrome
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Biochemical diagnosis of Zellweger syndrome
    • Ospedale Regionale per le Microcitemie
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical diagnosis of Zellweger syndrome
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical diagnosis of pipecolic acidemia
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Biochemical diagnosis of peroxisomal diseases
    • Allgemeines Krankenhaus der Stadt Wien
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of pipecolic acidemia
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of Zellweger syndrome
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Peroxysomal diseases testing
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • HUNGARY
    • Dél-Dunántúl
    • PECS
    • Biochemical diagnosis of Zellweger syndrome
    • Department of Paediatrics - Clinical Center - University of Pécs
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Biochemical diagnosis of Zellweger syndrome : quantitation of very long chain fatty acids, plasmalogens, phytanate and pristanate
    • Institute of Child Health
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Biochemical diagnosis of Zellweger syndrome
    • Azienda Ospedaliera Universitaria Anna Meyer
    • More information
    • SPAIN
    • País Vasco
    • BARAKALDO
    • Biochemical diagnosis of peroxisoma diseases (long chain fatty acids)
    • Hospital Universitario Cruces - Osakidetza
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of peroxisomal disorders (very long chain fatty acids, phytanic acid, pipecolic acid in plasma, erythrocyte plasmalogen levels, bile acids in urine)
    • Dietmar-Hopp-Stoffwechselzentrum
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LÈS-NANCY
    • Biochemical diagnostic of peroxisome biogenesis disorder-Zellweger syndrome spectrum (chromatography of organic acids and amino acids)
    • CHU de Nancy - Hôpital de Brabois
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Molecular diagnosis of peroxisomal disorders (PEX1, PEX2, PEX3, PEX5, PEX6, PEX7, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX26 genes)
    • Universitätsmedizin Göttingen
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Biochemical diagnosis of peroxisomal disorders (metabolite profile)
    • Universitätsmedizin Göttingen
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUXELLES
    • Biochemical analysis of phytanic acid and VLCFA in plasma by GC-MS
    • Université Libre de Bruxelles - ULB
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical diagnosis of Peroxisomal disorders (Analyte: Very Long Chain Fatty Acids)
    • Great Ormond Street Hospital for Children, NHS Foundation Trust
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of Zellweger syndrome
    • CHU Paris Centre - Hôpital Cochin
    • 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 peroxisome biogenesis disorder-Zellweger syndrome spectrum (PEX1 gene)
    • Igenomix Spain
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Biochemical and molecular diagnosis of peroxisomal diseases (PEX1, PEX2, PEX3, PEX5, PEX6, PEX7, PEX10, PEX11, PEX12, PEX13, PEX14, PEX16, PEX19 and PEX26 genes)
    • Medizinische Universität Graz
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Biochemical diagnosis of peroxisomal disorders (analyte: very long chain fatty acid, pipecolic acid, phytanic acid, plasmalogens)
    • University Hospital Bratislava - Stare mesto
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Biochemicka diagnostika peroxizomovych ochoreni (analyt: mastne kyseliny s velmi dlhym retazcom, kyseliny pristanovej, fytanovej, pipekolovej a plazmalogenov)
    • University Hospital Bratislava - Stare mesto
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • Molecular diagnosis of peroxisome biogenesis disorders - analysis of common mutations (PEX1 - c.2528GA and c.2097ins7 - exons 13 and 15, hotspot in exon 18; PEX2 - hotspot in exon 4; PEX6 - hotspot in exon 1; PEX10 - hotspot in exons 3, 4, 5; PEX12 - hotpost in exons 2, 3; PEX26 - hotspots in exons 1, 2; in case of no finding, sequencing analysis of 24 exons of PEX1 gene)
    • University Hospital Bratislava - Stare mesto
    • More information