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12 Result(s)

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(12)
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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Accreditation
    • Molecular diagnosis of immunodeficiency due to complement deficiency (C5, C6, C7 genes)
    • Pränatalmedizin München
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Diagnosis of predisposition to meningococcal infections : protein of complement common final pathway deficiency and properdin deficiency (C5, C6, C7, CFP, C8A, C8B, C8G genes)
    • CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
    • Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Accreditation
    • Diagnosis of specific complement deficiencies (C3, C4, functional hemolytic test for the classical and alternative pathways (CH50 and AP50 test), serum titers of MBL) (only with blood drawn on site)
    • Ghent University Hospital - UZGent
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Immunology
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Genetic diagnosis and immunological analysis of the C5 levels in the complement component 5 deficiency (C5 gene)
    • Hospital Universitario La Paz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Immunology
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Immunological diagnosis of the C6 levels in the complement component 6 deficiency
    • Hospital Universitario La Paz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Immunology
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Immunological diagnosis of the C7 levels in the complement component 7 deficiency
    • Hospital Universitario La Paz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Immunology
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Immunological diagnosis of the C8 levels in the complement component 8 deficiency
    • Hospital Universitario La Paz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Immunology
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of immunodeficiency due to a late component of complements deficiency (C5 gene)
    • Sistemas Genómicos S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Diagnosis of complement proteins in recurring meningococcal meningitis : complement proteins common final pathway deficiency (C5, C6, C7, C8, C9) and properdine deficiency
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Immunology
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Immunological diagnosis of primary immunodeficiencies (PID) - Immunophenotyping including adhesion molecules
    • Klinik für Kinder- und Jugendmedizin des Universitätsklinikums Ulm
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Immunology
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Immunochemical diagnosis of TLR signaling defect (cytokine production IL6, IL1beta, IL10 upon stimulation with TLR ligands)
    • Ghent University Hospital - UZGent
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Biochemical genetics
    • Objective(s) : Protein expression
    • Technical procedure(s) : Immunohistochemistry
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Diagnosis of hereditary immune deficiencies (Panel)
    • Université Paris 7 - Bâtiment Lamarck
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS