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FRANCE

PAYS DE LA LOIRE
NANTES

Accreditation
HLA-A and HLA-B genotyping by PCR SSP or PCR SSO
Etablissement Français du Sang - Pays de Loire
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
SAINT-OUEN-L'AUMÔNE

Accreditation
Molecular diagnosis of susceptibility to Behcet's disease (HLA-B gene)
Laboratoire Cerba
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

HAUTS-DE-FRANCE
LILLE

Accreditation
Molecular diagnosis of susceptibility to Behcet disease (search for HLA-B5 (B51) by PCR-SSP)
CHRU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Molecular diagnosis of susceptibility to Behcet disease (HLA-B gene ; LCT)
Établissement Français du Sang Alpes-Méditerranée
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of HLA-B - susceptibility to Behcet's disease, Stevens-Johnson syndrome and ankylosing spondylitis
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

FRANCE

BRETAGNE
RENNES

Accreditation
Molecular diagnosis of predisposition to Behçet disease (HLA-B*51 genotyping)
EFS Bretagne
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing, PCR based techniques

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Autoinflammatory Disease/Recurrent Fever Syndrome NGS Panel and Del/Dup Analysis (17 genes)
The Hospital for Sick Children and University of Toronto
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Array based techniques

FRANCE

ILE-DE-FRANCE
IVRY SUR SEINE

Accreditation
Diagnosis of susceptibility to Behçet disease (HLA-B gene)
Eurofins Biomnis
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

PAYS DE LA LOIRE
ANGERS

Accreditation
Diagnosis of susceptibility to Behçet disease (HLA-B gene)
EFS Angers
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

GRAND-EST
STRASBOURG

Accreditation
Diagnosis of susceptibility to Behçet disease (HLA-B gene)
EFS Alsace
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

BOURGOGNE-FRANCHE-COMTE
BESANÇON

Accreditation
Diagnosis of susceptibility to Behçet disease (lymphotoxicity and HLA-B genotyping)
EFS - Bourgogne/Franche-Comté
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Immunology
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

AUVERGNE-RHONE-ALPES
LYON

Accreditation
Molecular diagnosis of susceptibility to Behcet disease (HLA-B gene)
EFS Rhône-Alpes
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

AUVERGNE-RHONE-ALPES
LA TRONCHE

Accreditation
Molecular diagnosis of susceptibility to Behcet disease (HLA-B gene: PCR-SSO)
EFS Rhône Alpes - Grenoble
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

ITALY

LAZIO
ROMA

Molecular diagnosis of suceptibility to Behçet disease (HLA-B gene)
Azienda Ospedaliera S. Camillo-Forlanini - Ospedale San Camillo
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

CAMPANIA
NAPOLI

Molecular diagnosis of susceptibility to Behcet's disease (HLA-B gene)
Biotecnologie Avanzate Srl
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

PORTUGAL

CENTRO
OEIRAS

Analysis of susceptibility for Behcet disease (HLA-B gene, 51 allele)
Laboratório de Análises Clínicas Dr. Joaquim Chaves
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

PORTUGAL

ILHAS
FUNCHAL

Molecular diagnosis of Behcet disease (HLA-B gene, 51 allele: Sequencing of the exon 2 and 3)
Universidade da Madeira
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of susceptibility to Behçet disease (HLA-B gene: PCR-SSO)
CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Saint-Louis
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

GRAND-EST
REIMS

Diagnosis of predisposition to Behçet disease (HLA-B*51:01 gene)
CHU de Reims - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
MONTPELLIER

Diagnosis of autoinflammatory diseases (Panel)
CHRU de Montpellier - Hôpital Arnaud de Villeneuve
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

FRANCE

BRETAGNE
BREST

Diagnosis of susceptibility to Behcet's disease (HLA-B*51:01)
CHRU de Brest - Hôpital Morvan
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

AUVERGNE-RHONE-ALPES
LYON

HLA-A and HLA-B genotyping by PCR SSP or PCR SSO
Laboratoire Alpigene
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

ITALY

LAZIO
ROMA

Immunological diagnosis of Behçet disease
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE

Diagnosis of vasculitis on nerve and muscle biospy
GHU Paris-Sud - Hôpital de Bicêtre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Pathology

ITALY

EMILIA ROMAGNA
REGGIO EMILIA

Molecular diagnosis of Behçet disease
IRCCS Arcispedale Santa Maria Nuova
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
KIRCHHEIM UNTER TECK

Immunological diagnosis of vasculitides (ANCA, ANA, ACPA, cryoglobulins, lymphocyte phenotyping, BAL)
medius Klinik Kirchheim
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

Molecular diagnosis and serology of susceptibility to Behcet disease (lymphotoxicity and HLA-B51 genotyping)
CHU de Bordeaux-GH Pellegrin
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics, Immunology
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

ITALY

MOLISE
POZZILLI

Molecular diagnosis of susceptibility to Behcet's disease (HLA-B 51 gene)
Istituto Neurologico Mediterraneo - IRCCS Neuromed
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques