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- Molecular diagnosis of mitochondriopathies (mtDNA/mtRNA)
- Medizinisch Genetisches Zentrum München
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- SWITZERLAND
- Suisse Alémanique
- BERN
- Molecular diagnosis of mitochondrial diseases (Mitochondrial genom)
- Inselspital
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis of Combined Oxidative Phosphorylation Deficiency (C10ORF2, GFM1, MRPS16 and PUS1 gene)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
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- Enzyme diagnosis of mitochondrial respiratory chain deficiency (complex I-IV) in fibroblast cell culture and muscle tissue
- Universitätsklinikum Hamburg-Eppendorf
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of mitochondriopathies (mtDNA: sequencing)
- CeGaT GmbH
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- NETHERLANDS
- Noord-Holland
- AMSTERDAM
- Biochemical diagnosis of Mitochondrial Diseases (Analyte: Lactic Acid, Pyruvic Acid and Ubiquinon)
- AMC - Academisch Medisch Centrum
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- FRANCE
- RHONE-ALPES
- GRENOBLE
- Biochemical and molecular diagnosis of mitochondrial diseases
- CHU de Grenoble site Nord - Institut de biologie et de pathologie
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Molecular diagnosis of mitochondrial diseases
- CHU Paris - Hôpital Necker - Enfants Malades
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Biochemical diagnosis of respiratory chain multiple deficiencies
- CHU Paris - Hôpital Necker - Enfants Malades
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- FRANCE
- PROVENCE-ALPES-COTE D'AZUR
- NICE
- Biochemical diagnosis of respiratory chain deficiencies
- CHU de Nice - Hôpital l'Archet 2
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- FRANCE
- PAYS DE LA LOIRE
- ANGERS
- Molecular and biochemical diagnosis of mitochondrial diseases (mtDNA)
- CHU d'Angers
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- FRANCE
- NORD-PAS-DE-CALAIS
- LILLE
- Diagnosis of enzymatic deficiency of respiratory chain on muscular biopsy
- CHRU de Lille - Centre de biologie et pathologie
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- Molecular diagnosis of mitochondrial diseases (mitochondrial genome)
- Medizinische Universität Wien
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- Diagnosis of mitochondrial disorders : quantitative organic acid analysis (GC/MS)
- Tartu University Hospital
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- 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
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- BELGIUM
- ARRONDISSEMENT BRUSSELS-CAPITAL
- BRUSSELS
- Molecular diagnosis of Mitochondrial Diseases (by dHPLC analysis, please contact the lab)
- Universitair Ziekenhuis Brussel - UZBrussel
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- Molecular diagnosis of mitochondrial respiratory chain deficiency (BCS1L, COX10, COX15, MTCYB, SDHA, SCO1, SCO2, SDHAF1, SURF1, TMEM70 and UQCRB genes)
- Technische Universität München
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- SWEDEN
- Stockholms läns landsting
- STOCKHOLM
- Molecular diagnosis of mitochondrial diseases (mtDNA/POLG/Twinkle)
- Karolinska University Hospital - Solna
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Molecular diagnosis of mitochondrial diseases (sequencing)
- CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
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- FRANCE
- BASSE-NORMANDIE
- CAEN
- Molecular diagnosis of mitochondrial diseases (mtDNA)
- CHU de Caen - Hôpital de la Côte de Nacre
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- FRANCE
- AQUITAINE
- BORDEAUX
- Molecular diagnosis of mitochondrial diseases
- CHU de Bordeaux-GH Pellegrin
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- Biochemical diagnosis of beta-oxidation deficiency (metabolite analysis)
- IRCCS Istituto G. Gaslini - Ospedale Pediatrico
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- Molecular and biochemical diagnosis of metabolic encephalomyopathies (ETFDH, ETF, CPT2, MCAD, VLCAD genes)
- Fondazione IRCCS Istituto Neurologico "Carlo Besta"
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- Biochemical diagnosis of mitochondrial diseases
- Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
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- Biochemical diagnosis of mitochondrial respiratory chain deficiency (complex I-IV)
- Labor für molekulare Genetik und metabolische Erkrankungen
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- Biochemical diagnosis of mitochondrial respiratory chain defects
- Hospital Clínico de Barcelona (Edificio Helios III)
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- GERMANY
- Nordrhein-Westfalen
- BONN
- Histological diagnosis of mitochondrial diseases
- Universitätsklinikum Bonn
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- Biochemical diagnosis of respiratory chain defects and mitochondrial ATP synthesis
- IRCCS Ospedale Pediatrico Bambino Gesù
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- Biochemical diagnosis of respiratory chain multiple deficiences
- Ospedale Regionale per le Microcitemie
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- Biochemical and molecular diagnosis of mitochondrial diseases
- CGMJM - Centro de Genética Médica Jacinto Magalhães
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- Molecular diagnosis of Mitocondrial Diseases, mitochondrial DNA
- Universidad de Zaragoza. Facultad de Veterinaria
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- ITALY
- FRIULI VENEZIA GIULIA
- TRIESTE
- Molecular diagnosis of mitochondrial diseases, clinically undefinite
- IRCCS Burlo Garofolo - Istituto per l'Infanzia
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- GERMANY
- Rheinland-Pfalz
- LUDWIGSHAFEN
- Biochemical and molecular diagnosis of mitochondrial respiratory chain deficiency complex I (NDUFV1, NDUFV2, NDUFS1, NDUFS2, NDUFS4, NDUFS7, NDUFS8, NDUFAF2 genes)
- Klinikum der Stadt Ludwigshafen gGmbH
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- GERMANY
- Rheinland-Pfalz
- LUDWIGSHAFEN
- Biochemical and molecular diagnosis of mitochondrial respiratory chain deficiency complex IV (MTCO1, MTCO2, MTCO3, COX10, COX15, MTTS1, SCO1, SCO2, SURF1 genes)
- Klinikum der Stadt Ludwigshafen gGmbH
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- GERMANY
- Rheinland-Pfalz
- LUDWIGSHAFEN
- Biochemical and molecular diagnosis of mitochondrial respiratory chain deficiency complex III (BCS1L gene)
- Klinikum der Stadt Ludwigshafen gGmbH
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- 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
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- Biochemical diagnosis of respiratory chain deficiencies (complex I-V muscle enzymatic test)
- Hadassah Ein Kerem - Hebrew University Medical Center
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- Biochemical diagnosis of OXPHOS diseases
- Institut de Recerca Hospital Universitari Vall d'Hebron
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- GERMANY
- Niedersachsen
- HANNOVER
- Biochemical diagnosis of mitochondrial respiratory chain deficiency (enzyme assay complex I-V)
- Medizinische Hochschule Hannover
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- 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
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- Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
- Medizinische Universität Wien
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