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Caption : Accreditation =Accreditation
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    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Heterozygote screening by NGS Inherited Disease Panel (Kingsmore)
    • Pränatalmedizin München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of cerebral folate transport deficiency (FOLR1 gene)
    • Medizinisch Genetisches Zentrum München
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Metabolic Disease with Epilepsy (multigene panel; 24 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Biochemical and molecular diagnosis of neurodegenerative syndrome due to cerebral folate transport deficiency (FOLR1 gene analysis, 5MTHF in CSF)
    • Universitäts-Kinderspital
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Neurodegenerative Syndrome due to Cerebral Folate Transport Deficiency (FOLR1 gene)
    • VUmc - VU medisch centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of Leukodystrophy and Leukencephalopathy (ABCD1, ADAR, AIMP1, ARSA, ASPA, CLCN2, EARS2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, FAM126A, FOLR1, GALC, GFAP, GJC2, HEPACAM, HSPD1, L2HGDH, MLC1, NOTCH3, PLP1, POLR3A, POLR3B, PSAP, RNASEH2A, RNASEH2B, RNASEH2C, RNASET2, SAMHD1, SOX10, SUMF1, TREX1, TUBB4A genes: Brain Development Disorders Panel)
    • CeGaT GmbH
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Folate Transport Disorders (Analyte: Methyltetrahydrofolate and Pyridoxal Phosphate)
    • AMC - Academisch Medisch Centrum
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of neurodegenerative syndrome due to cerebral folate transport deficiency (FOLR1 gene)
    • Policlinico Umberto I
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of central folate deficiency (5-MTHF assay in CSF)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of neurodegenerative syndrome due to cerebral folate transport deficiency (FOLR1 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of neurodegenerative syndrome due to cerebral folate transport deficiency (FOLR1 gene)
    • CHU Paris - Hôpital Robert Debré
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LÈS-NANCY
    • Molecular diagnosis of neurodegenerative syndrome due to cerebral folate transport deficiency (FOLR1 gene)
    • CHU de Nancy - Hôpital de Brabois
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Molecular diagnosis of cerebral folate transport deficiency (FOLR1 gene)
    • Universitätsmedizin Göttingen
    • More information
    • SPAIN
    • Cataluña
    • ESPLUGUES DE LLOBREGAT
    • Biochemical diagnosis of neurodegenerative syndrome due to cerebral folate transport deficiency (analyte: 5-methyltetrahydrofolate in cerebrospinal fluid and folate in serum)
    • Hospital Universitari Sant Joan de Déu
    • 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