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FRANCE

OCCITANIE
MONTPELLIER

Accreditation
Diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
CHU de Montpellier - Hôpital Saint-Eloi
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
ARGENTEUIL

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

GERMANY

Rheinland-Pfalz
INGELHEIM AM RHEIN

Accreditation
Diagnosis of congential plasminogen activator inhibitor type 1 deficiency
Bioscientia Institut für Medizinische Diagnostik GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

GERMANY

Hessen
FRANKFURT AM MAIN

Accreditation
Diagnosis of congential plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
bio.logis Zentrum für Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

GREECE

ATTIKI
ATHENS

Accreditation
Molecular diagnosis of congenital PAI-1 deficiency (4G/5G allele)
BioAnalytica-GenoType SA
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Italienne
LUGANO

Accreditation
Molecular diagnosis of Thrombophilia (PAI1 gene)
Procrea Lab SA - Laboratorio di Genetica Molecolare
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Alémanique
AARAU

Accreditation
Molecular diagnosis of plasminogen activator inhibitor-1 deficiency (SERPINE1 gene sequencing and deletion analysis)
Kantonsspital Aarau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis

GERMANY

Niedersachsen
HANNOVER

Accreditation
Diagnosis of PAI-1 deficiency (SERPINE1 gene)
amedes genetics im MVZ wagnerstibbe
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
Diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 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

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Diagnosis of PAI-1 deficiency (SERPINE1 gene)
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

GERMANY

Bayern
MÜNCHEN

Accreditation
Diagnosis of PAI-1 deficiency (SERPINE1 gene)
Pränatalmedizin München
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
Institut Fédératif de Biologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

GERMANY

Nordrhein-Westfalen
MÖNCHENGLADBACH

Accreditation
Diagnosis of congenital plasminogen activator inhibitor type 1 deficiency
MVZ Dr. Stein + Kollegen Mönchengladbach
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Biochemical genetics
Objective(s) : Analyte / Enzyme assay

CZECH REPUBLIC

Capital City Prague
PRAHA

Accreditation
Molecular diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency (SERPINE1 gene)
Motol university hospital - 2nd Medical School Charles University Prague
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
HEIDELBERG

Accreditation
Diagnosis of PAI-1 deficiency (SERPINE1 gene)
Zentrallabor des Universitätsklinikums Heidelberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

CZECH REPUBLIC

South Moravia
HODONIN

Accreditation
Molecular diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
Chemila, spol. s r.o.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

TURKEY

TURKEY
ISTANBUL

Molecular diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency (SERPINE1 gene)
Acibadem healthcare group
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (PAI1 gene)
Centogene AG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

ITALY

CAMPANIA
NAPOLI

Diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
Biotecnologie Avanzate Srl
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

SPAIN

Comunidad Valenciana
PATERNA

Diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
IMEGEN - Delegación Valencia
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

SPAIN

La Rioja
LOGROÑO

Diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
Fundación Rioja Salud - Centro de Investigación Biomédica de La Rioja
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
LabGenetics - Laboratorio de Genética Clínica, S.L.
Purpose(s) : Antenatal diagnosis, 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

AUSTRIA

WIEN
WIEN

Molecular diagnosis of congenital Plasminogen activator inhibitor-1 deficiency (SERPINE1 gene)
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

HAUTS-DE-FRANCE
AMIENS

Diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
CHU Amiens-Picardie - Site Sud
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

OCCITANIE
TOULOUSE

Diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
CHU de Toulouse - Hôpital Rangueil
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

GRAND-EST
VANDOEUVRE-LÈS-NANCY

Diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
CHU de Nancy - Hôpitaux de Brabois
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

AUVERGNE-RHONE-ALPES
CLERMONT-FERRAND

Diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
CHU de Clermont-Ferrand - Hôpital d'Estaing
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

PORTUGAL

SUL
LISBOA

Analysis of thrombosis predisposition genetic factors (MTHFR C667T and A1298C, PAI-1 -675G>A; F5: 1691 G>A; F2: 20210 G>A)
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

BULGARIA

 South-West region
SOFIA

Molecular diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency
University hospital of Obstetrics and Gynecology
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Moravia-Silesia
OSTRAVA

Molecular diagnosis of congenital plasminogen activitor inhibitor type 1 deficiency (SERPINE1 gene)
CGB laboratory Ltd.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

MARCHE
JESI

Molecular diagnosis of plasminogen activitor inhibitor type 1 congenital deficiency (SERPINE1 gene)
BIOAESIS
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

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

PORTUGAL

NORTE
PORTO

PAI1 deficiency
CGC Genetics / Centro de Genética Clínica
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

CZECH REPUBLIC

Olomouc
OLOMOUC

Molecular diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
University hospital Olomouc
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Liberec
LIBEREC

Molecular diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
Regional Hospital Liberec, Krajska nemocnice Liberec
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Plzen
PLZEN - BORY

Molecular diagnosis of congenital plasminogen activator inhibitor type 1 deficiency (SERPINE1 gene)
Pilsen University Hospital, Fakultni nemocnice Plzen - areal Bory
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

AUSTRIA

WIEN
WIEN

Molecular diagnosis of congenital Plasminogen activator inhibitor-1 deficiency (SERPINE1 gene)
Praxis für Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

PORTUGAL

ILHAS
FUNCHAL

Molecular diagnosis of congenital PAI-1 deficiency (PAI1 gene: Analysis of nucleotide 675 - single base deletion 4G/5G - by sequencing)
Universidade da Madeira
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis

PORTUGAL

NORTE
PORTO

Diagnosis of PAI1 deficiency (SERPINE1 gene)
CGC Genetics / Centro de Genética Clínica
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing