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FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Diagnosis of storage pool platelet disease
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

GERMANY

Baden-Württemberg
MANNHEIM

Accreditation
Molecular diagnosis of gray platelet syndrome (NBEAL2 gene)
Zentrum für Humangenetik Mannheim
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Molecular diagnosis of gray platelet syndrome (NBEAL2 gene)
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Diagnosis of platelets disorders
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular diagnosis of Gray Platelet Syndrome by targetted mutation analysis / DNA sequence analysis (NBEAL2 gene)
St Thomas' Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

NETHERLANDS

Gelderland
NIJMEGEN

Accreditation
Molecular diagnosis of Gray Platelet Syndrome (GFI1B and NBEAL2 gene)
Radboudumc - Radboud universitair medisch centrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

HAUTS-DE-FRANCE
LILLE

Accreditation
Diagnosis of storage pool platelet disease
CHRU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of storage pool platelet disease
Institut Fédératif de Biologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of gray platelet syndrome
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of hemorrhagic disorders due to a constitutional platelet anomaly (Panel)
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

OCCITANIE
MONTPELLIER

Diagnosis of storage pool platelet disease
CHU de Montpellier - Hôpital Saint-Eloi
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

PAYS DE LA LOIRE
LE MANS

Diagnosis of gray platelet syndrome (by flux cytometry)
Centre Hospitalier du Mans
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of storage pool platelet disease
CHU Paris - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of gray platelet syndrome
CHU Paris - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

GRAND-EST
VANDOEUVRE-LÈS-NANCY

Diagnosis of storage pool platelet disease
CHU de Nancy - Hôpitaux de Brabois
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

GRAND-EST
VANDOEUVRE-LÈS-NANCY

Diagnosis of gray platelet syndrome
CHU de Nancy - Hôpitaux de Brabois
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

ITALY

PUGLIA
SAN GIOVANNI ROTONDO

Molecular and biochemical diagnosis of storage pool platelet disease (WAS gene)
IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Biochemical genetics
Objective(s) : Analyte / Enzyme assay

FRANCE

ILE-DE-FRANCE
ARGENTEUIL

Diagnosis of congenital deficiency of coagulation factors
Centre hospitalier Victor Dupouy
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

SERBIA

Serbia
BELGRADE

Diagnosis of inherited bleeding disorders (hemophilia, von Willebrand disease and others rare bleeding disorders)
Blood Transfusion Institute of Serbia
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of thrombocytopenia (Panel)
CHU Paris - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES), Sanger sequencing