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Caption : Accreditation =Accreditation
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    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy 2, 7 and 14 (CDKL5-, KCNT1, KCNQ2 genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of SCN1A related epilepsy (SCN1A gene)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Early Infantile Epileptic Encephalopathy type 1, 2, 3, 4, 7, 8, 9, 10, 11 and 12 (ARX, CDKL5, SLC25A22, STXBP1, KCNQ2, ARHGEF9, PCDH19, PNKP, SCN2A and PLCB1 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Benign Neonatal/Infantile Seizures (multigene panel; 5 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Epileptic Encephalopathy (multigene panel; 32 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Generalized Epilepsy with Febrile Seizures plus (multigene panel; 10 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Focal Epilepsy (multigene panel; 9 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy (CDKL5, PLCB1 genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of early infantile epileptic encephalopathy (ARX, CDKL5, KCNQ2, KCNT1, PCDH19, SCN1A, SCN2A, SPTAN1 genes)
    • Praxis Dres. Gencik
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of malignant migrating partial seizures of infancy (SCN1A gene)
    • Genetaq
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ELCHE
    • Molecular diagnosis of epilepsy (genes panel: ARX, CDKL5, CHRNA2, CHRNA4, CHRNB2, GABRG2, KCNQ2, KCNQ3, LGI1, SCN1A, SCN1B, SCN2A, SLC2A1, STXBP1 / sequencing)
    • Bioarray
    • More information