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Caption : Accreditation =Accreditation
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    • FRANCE
    • ILE-DE-FRANCE
    • LE KREMLIN-BICÊTRE
    • Accreditation
    • Molecular diagnosis of autosomal dominant progressive external ophthalmoplegia (C10ORF2, SLC25A4 and RRM2B genes)
    • GHU Paris-Sud - Hôpital de Bicêtre
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • NICE
    • Accreditation
    • Molecular diagnosis of autosomal progressive external ophthalmoplegia (POLG, POLG2, C10orf2, SLC25A4, RRM2B genes)
    • CHU de Nice - Hôpital l'Archet 2
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of autosomal progressive external ophthalmoplegia (C10ORF2, POLG, POLG2, RRM2B, SLC25A4 genes)
    • Labor Lademannbogen
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of mitochondriopathies (mtDNA/mtRNA)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of progressive external ophthalmoplegia (C10ORF2, POLG, POLG2, RRM2B, TK2 genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Mitochondrial DNA Disease (Multigene Panel; 37 genes)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Chronic Progressive External Ophthalmoplegia (C10ORF2, POLG and SLC25A4 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
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Accreditation
    • Molecular diagnosis of Mitochondrial DNA Disease (Multigene Panel; 37 genes)
    • The Churchill Hospital
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of progressive external ophthalmoplegia (C10ORF2, POLG, POLG2, RRM2B, SLC25A4, TK2 genes)
    • Centogene AG
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of progressive external ophthalmoplegia (C10ORF2, POLG, POLG2, RRM2B, SLC25A4 genes)
    • MVZ Fenner & Krasemann
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of POLG gene-associated mitochondrial diseases
    • MVZ Fenner & Krasemann
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • BERN
    • Accreditation
    • Molecular diagnosis of mitochondrial diseases (Mitochondrial genom)
    • Inselspital
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of POLG gene-associated mitochondrial diseases (sequencing)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of progressive external ophthalmoplegia (C10ORF2, POLG, SLC25A4 genes: sequencing)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of mitochondriopathies (mtDNA: sequencing)
    • CeGaT GmbH
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Mitochondrial Diseases (Analyte: Lactic Acid, Pyruvic Acid and Ubiquinon)
    • AMC - Academisch Medisch Centrum
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Biochemical and molecular diagnosis of mitochondrial diseases
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Molecular diagnosis of progressive external ophthalmoplegia (POLG & C10ORF2 genes)
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Biochemical and molecular diagnosis of progressive external ophtalmoplegia (MT-TL1, POLG, POLG2, PEO1, SLC25A4 and RRM2B genes)
    • CHU de Lyon HCL - GH Est
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of external ophtalmoplegia (POLG gene)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of autosomal dominant progressive external ophtalmoplegia : search for simple or multiple deletions of POLG1, SLC25A4 and C10ORF2 genes
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Molecular diagnosis of autosomal dominant progressive external ophthalmoplegia (C10orf2, POLG2 and SLC25A4 genes)
    • CHU de Caen - Hôpital de la Côte de Nacre
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of progressive external ophthalmoplegia (POLG and SLC25A4 genes)
    • CHU d'Angers
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of multiple mitochondrial DNA deletion syndrome (mtDNA and POLG, C10ORF2, ANT1, POLG2, RRM2B genes)
    • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of progressive external ophthalmoplegia (POLG, TK2, RRM2B, and C10ORF2 genes)
    • Medizinische Universität Wien
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of mitochondrial diseases (mitochondrial genome)
    • Medizinische Universität Wien
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of autosomal dominant progressive external ophthalmoplegia (POLG gene)
    • Sistemas Genómicos S.L.
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Diagnosis of mitochondrial disorders : quantitative organic acid analysis (GC/MS)
    • Tartu University Hospital
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of progressive external ophthalmoplegia (C10ORF2, POLG genes)
    • Praxis Dres. Gencik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of progressive external ophthalmoplegia (POLG and C10ORF2 genes)
    • Praxis für Humangenetik
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Mitochondrial DNA depletion syndrome (POLG gene: sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Autosomal dominant and autossomal recessive progressive external ophthalmoplegia (POLG 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 progressive external ophthalmoplegia (POLG gene / sequencing)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular screening for Mitochondrial Diseases (mtDNA deletion screen in blood, muscle & liver tissue by southern blot)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of Mitochondrial Diseases (by dHPLC analysis, please contact the lab)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of mitochondrial diseases (mtDNA/POLG/Twinkle)
    • Karolinska University Hospital - Solna
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of progressive external ophtalmoplegia (POLG1, RRM2B, C10ORF2 genes)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of POLG gene-associated mitochondrial diseases (sequencing, MLPA)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of progressive external ophthalmoplegia (C10ORF2, POLG, POLG2, RRM2B, SLC25A4 genes: sequencing, MLPA)
    • Gemeinschaftspraxis für Humangenetik
    • 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
    • ITALY
    • TOSCANA
    • PISA
    • Biochemical diagnosis of mitochondrial diseases
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of POLG related disorders
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Molecular diagnosis of progressive external ophthalmoplegia (mtDNA deletion screeining, C10ORF2, POLG, POLG2, SLC25A4 )
    • Klinikum Schwabing, Städt. Klinikum GmbH
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of POLG related diseases
    • Azienda Ospedaliera di Bologna - Policlinico S. Orsola-Malpighi
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Histological diagnosis of mitochondrial diseases
    • Universitätsklinikum Bonn
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Biochemical diagnosis of respiratory chain multiple deficiences
    • Ospedale Regionale per le Microcitemie
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical and molecular diagnosis of mitochondrial diseases
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • FINLAND
    • Finland
    • TAMPERE
    • Molecular diagnosis of progressive external ophthalmoplegia, mitochondrial recessive ataxia syndrome and Sensory ataxic neuropathy - dysarthria - ophthalmoparesis (POLG gene: sequencing of exons 2, 3, 7, 13)
    • University of Tampere
    • More information
    • FINLAND
    • Finland
    • TAMPERE
    • Molecular diagnosis of Autosomal dominant progressive external ophthalmoplegia 5 (RRM2B gene: sequencing of exon 9)
    • University of Tampere
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of Mitocondrial Diseases, mitochondrial DNA
    • Universidad de Zaragoza. Facultad de Veterinaria
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Molecular diagnosis of POLG gene-associated mitochondrial diseases
    • Charité - Universitätsmedizin Berlin (CVK)
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • TRIESTE
    • Molecular diagnosis of mitochondrial diseases, clinically undefinite
    • IRCCS Burlo Garofolo - Istituto per l'Infanzia
    • More information
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE
    • Molecular diagnosis of Mitochondrial DNA Disease (Multigene Panel; 37 genes)
    • Wellcome Trust Centre for Mitochondrial Research
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of mitochondriopathies (lactate, pyruvate/ free fatty acids/ keton bodies/ amino acids in plasma/ organic acids/ CSF lactate/ amino acids in CSF
    • Universitätsklinikum Heidelberg
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical diagnosis of OXPHOS diseases
    • Fundació Institut de Recerca Hospital Universitari Vall d'Hebron
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Biochemical diagnosis of mitochondrial respiratory chain deficiency (enzyme assay complex I-V)
    • Medizinische Hochschule Hannover
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Biochemical diagnosis of mitochondrial oxidative phosphorylation disorder (enzymatic studies: Citrate synthase, NADH Decylubiquinone oxidoreductase, Succinate-Decylubiquinone dehydrogenase, DBH2 Cytochrome C Oxidoreductase, Cytochrome C Oxidase, NADH-Cytochrome C Reductase, Succinate-Cytochrome C Reductase)
    • Hospital Universitario 12 de Octubre
    • 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