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Caption : Accreditation =Accreditation
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    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • NICE
    • Accreditation
    • Molecular diagnosis of mitochondrial oxidative phosphorylation disorder due to a point mutation of mtDNA (MT-ATP6, MT-CO1, MT-CO2, MT-CO3, MT-ND6 genes)
    • CHU de Nice - Hôpital l'Archet 2
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of mitochondriopathies (mtDNA/mtRNA)
    • Medizinisch Genetisches Zentrum München
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Mitochondriopathy (mtDNA; MitoChip)
    • 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
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of NARP/MILS (m.8993T>C/G & m.9176T>C/G in MTATP6, m.13513G>A in MTND5 & m.14459G>A in MTND6 genes)
    • Birmingham Children's Hospital
    • 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 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
    • Molecular diagnosis of Leigh disease (SURF1, SCO2 genes and ADNm)
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • 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
    • BRON
    • Biochemical and molecular diagnosis of Leigh disease (SURF1 and TACO1 genes)
    • CHU de Lyon-GH Est - Hospices Civils de Lyon
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of Leigh disease (SURF1, COX10, COX15, SCO2, MT-ND1, MT-ND5, MT-ND3, MT-ND6, MT-TW, NDUFS8, SLC19A3 genes)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular genetics diagnosis of mitochondrial DNA anomalies (Surveyor and mitochip kits)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of maternally inherited Leigh syndrome (MT-ATP6 gene)
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of Leigh disease (mitochondrial DNA)
    • CHU d'Angers
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular and biochemical diagnosis of mitochondrial diseases (mtDNA)
    • CHU d'Angers
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of ATP synthase deficiency (MT-ATP6, MT-ATP8, ATPAF2, TMEM70 genes)
    • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of maternally-inherited Leigh syndrome (MT-ATP6 gene)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of Maternally-inherited Leigh syndrome (MT-ATP6 gene / mutations T8993C and T8993G)
    • Centro de Análisis Genéticos
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of mitochondrial diseases (mitochondrial genome)
    • Medizinische Universität Wien
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of maternally-inherited Leigh syndrome (MTATP6 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
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of mitochondrial cytopathies: Analysis of the targeted mutations (del4977bp, G3460A, G11778A, T8993C, T8993G, A3271G, A3243G, T8356C, A8344G)
    • CGC Genetics / Centro de Genética Clínica
    • 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
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of Leigh and Leigh-like syndromes (MT-ND5, COX15, MT-TK, MT-TL1 genes by sequencing)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Molecular diagnosis of mitochondriopathies (mtRNA)
    • Technische Universität München
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of mitochondrial diseases (mtDNA/POLG/Twinkle)
    • Karolinska University Hospital - Solna
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of maternally-inherited Leigh syndrome (MTATP6 gene: mutation T8993G)
    • Genetaq
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of maternally-inherited Leigh syndrome (MT-ATP6 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of NARP/MILS syndrome (MT-ATP6 gene)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • SPAIN
    • La Rioja
    • LOGROÑO
    • Molecular diagnosis of maternally-inherited Leigh syndrome (MT-ATP6 gene)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of mitochondrial diseases (sequencing)
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Molecular diagnosis of Leigh syndrome ( MT-TW, MT-TV, MT-ND2, MT-ND3 genes)
    • CHU de Caen - Hôpital de la Côte de Nacre
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of Leigh disease (MT-ATP6 gene)
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of mitochondrial diseases
    • CHU de Bordeaux-GH Pellegrin
    • 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
    • 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
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnosis of Mitocondrial Diseases, mitochondrial DNA
    • Universidad de Zaragoza. Facultad de Veterinaria
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • TRIESTE
    • Molecular diagnosis of mitochondrial diseases, clinically undefinite
    • IRCCS Burlo Garofolo - Istituto per l'Infanzia
    • 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
    • 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
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of Leigh syndrome (MT-ATP6 gene / mutations T8993G and T8993C)
    • Lorgen G.P.
    • 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
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of maternally-inherited Leigh syndrome (MT-ATP6, MT-ND5 and MT-ND6 genes)
    • 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