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Caption : Accreditation =Accreditation
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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Biochemical diagnosis of tyrosinemia
CHU Paris - Hôpital Robert Debré

FRANCE

ILE-DE-FRANCE
SAINT-OUEN-L'AUMÔNE

FRANCE

PROVENCE-ALPES-COTE D'AZUR
NICE

FRANCE

AUVERGNE-RHONE-ALPES
BRON

UNITED KINGDOM

Tayside
DUNDEE

FRANCE

HAUTS-DE-FRANCE
LILLE

Accreditation
Biochemical diagnosis of tyrosinemia type 1 and 2
CHRU de Lille - Centre de Biologie Pathologie Génétique

NETHERLANDS

Noord-Holland
AMSTERDAM

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Biochemical diagnosis of tyrosinemia type 1, 2 and 3
CHU de Toulouse - Hôpital Purpan

SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Diagnosis of Cardiomyopathies (panel)
Hôpitaux Universitaires de Genève HUG

NETHERLANDS

Gelderland
NIJMEGEN

Accreditation
Molecular diagnosis of Tylosis with Esophageal Cancer (RHBDF2 gene)
Radboudumc - Radboud universitair medisch centrum

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of familial dilated cardiomyopathy (NGS screening panel, 46 genes)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)

NETHERLANDS

Zuid-Holland
ROTTERDAM

NETHERLANDS

Utrecht
UTRECHT

Accreditation
Molecular diagnosis of Cardiomyopathy (gene panel; CAR01v16.1)
UMC Utrecht - Universitair Medisch Centrum Utrecht

GERMANY

Baden-Württemberg
MANNHEIM

Accreditation
Molecular diagnosis of Carvajal syndrome (DSP gene)
Zentrum für Humangenetik Mannheim

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of woolly hair-palmoplantar keratoderma syndrome (KANK2 gene)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of pachyonychia congenita (gene panel)
Reference Laboratory Genetics

FRANCE

ILE-DE-FRANCE
PARIS

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of skin diseases (Panel)
CHU Paris - Hôpital Necker-Enfants Malades

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of cardiomyopathies (Panel)
CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of cardiac rhythm diseases (Panel)
CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière

GERMANY

Bayern
MÜNCHEN

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of tyrosinemia type 2 (TAT gene)
Reference Laboratory Genetics

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Molecular diagnosis of familial dilated cardiomyopathy (NGS panel, 41 genes)
laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen

NETHERLANDS

Noord-Holland
AMSTERDAM

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of tyrosinemia (panel)
Reference Laboratory Genetics

GERMANY

Bayern
MÜNCHEN

UNITED KINGDOM

South Yorkshire
SHEFFIELD

UNITED KINGDOM

Tyne & Wear
NEWCASTLE UPON TYNE

Accreditation
Biochemical diagnosis of PKU and Tyrosinaemia (Analyte: Phenylalanine / Tyrosine)
The Great North Children's Hospita, Royal Victoria Infirmary

UNITED KINGDOM

Strathclyde
GLASGOW

GERMANY

Baden-Württemberg
TÜBINGEN

FRANCE

ILE-DE-FRANCE
PARIS

Biochemical diagnosis of tyrosinemia
CHU Paris - Hôpital Necker-Enfants Malades

ITALY

SARDEGNA
CAGLIARI

Biochemical diagnosis of tyrosinemia type 1 and 2
Ospedale Regionale per le Microcitemie

SPAIN

País Vasco
BARAKALDO

Biochemical diagnosis of tyrosinemia type 1, 2 and 3
Hospital Universitario Cruces - Osakidetza

ITALY

CAMPANIA
NAPOLI

Biochemical diagnosis of tyrosinemia
Biotecnologie Avanzate Srl

GERMANY

Baden-Württemberg
FREIBURG

Molecular diagnosis of tyrosinemia type 2 and 3 (TAT, HPD genes)
Institut für Humangenetik am Universitätsklinikum Freiburg

SPAIN

Madrid
CANTOBLANCO

Biochemical diagnosis of tyrosinemia type 2
Universidad Autónoma de Madrid. Facultad de Ciencias

GERMANY

Baden-Württemberg
FREIBURG

Molecular diagnosis of tyrosinemia type 2 (TAT gene)
Institut für Humangenetik am Universitätsklinikum Freiburg

GERMANY

Nordrhein-Westfalen
BONN

SPAIN

Comunidad Valenciana
PATERNA

GERMANY

Baden-Württemberg
FREIBURG

Molecular diagnosis of pachyonychia congenita (KRT6A, KRT6B, KRT16, KRT17 genes)
Institut für Humangenetik am Universitätsklinikum Freiburg

FRANCE

AUVERGNE-RHONE-ALPES
BRON

Diagnosis of cardiomyopathies (Panel)
CHU de Lyon HCL - GH Est

SPAIN

País Vasco
SAN SEBASTIÁN

GERMANY

Sachsen
DRESDEN

Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Carl Gustav Carus an der TU Dresden

GERMANY

Baden-Württemberg
FREIBURG

Molecular diagnosis of palmoplantar keratoderma-esophageal carcinoma syndrome (RHBDF2 gene)
Institut für Humangenetik am Universitätsklinikum Freiburg

GERMANY

Baden-Württemberg
FREIBURG

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

Diagnosis of palmoplantar keratoderma (Panel)
CHU de Bordeaux-GH Pellegrin

GERMANY

Baden-Württemberg
FREIBURG

Molecular diagnosis of diseases with associated palmoplantar keratoderma (NGS panel, 15 genes)
Institut für Humangenetik am Universitätsklinikum Freiburg

ITALY

VENETO
PADOVA

Molecular diagnosis of familial cardiomyopathy [panel of genes]
Research&Innovation S.r.l. (R&I Genetics)

SPAIN

Madrid
MADRID

Diagnosis of hereditary cancer (panel)
Fundación Jiménez Díaz

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

ITALY

LIGURIA
GENOVA

Biochemical diagnosis of aminoacidopathies (metabolite analysis)
IRCCS Istituto G. Gaslini - Ospedale Pediatrico

SPAIN

Cataluña
BARCELONA

Diagnosis of tyrosinemia types 1, 2 and 3
Hospital Clínic de Barcelona

ITALY

LAZIO
ROMA

Biochemical diagnosis of tyrosinemia type 1, 2 and 3
IRCCS Ospedale Pediatrico Bambino Gesù - SEDE SAN PAOLO

PORTUGAL

NORTE
PORTO

Biochemical diagnosis of tyrosinemia, types I, II and III
CGMJM - Centro de Genética Médica Jacinto Magalhães

FINLAND

Finland
HELSINKI

Biochemical diagnosis of tyrosinemia
Clinical Research Institute HUCH Ltd

ESTONIA

Tartu
TARTU

Diagnosis of amino acid disorders: quantitative amino acid analysis (HPLC)
Tartu University Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Biochemical genetics
Objective(s) : Analyte / Enzyme assay

ITALY

TOSCANA
FIRENZE

Biochemical diagnosis of tyrosinemia type 1 and 2
Azienda Ospedaliera Universitaria Anna Meyer

FRANCE

NOUVELLE AQUITAINE
BORDEAUX

LITHUANIA

DZUKIJA
VILNIUS

ITALY

LOMBARDIA
MILANO

Biochemical diagnosis of tyrosinemia type 2
Ospedale dei Bambini ''Vittore Buzzi"

PORTUGAL

NORTE
PORTO

Portuguese National Neonatal Screening Program (Guthrie test)
Instituto Nacional de Saúde Dr. Ricardo Jorge - Porto

SPAIN

Cataluña
ESPLUGUES DE LLOBREGAT

Diagnosis of tyrosinemia type 2 (UHPLC/MS_MS analysis)
Hospital Sant Joan de Déu Barcelona

ITALY

VENETO
PADOVA

Biochemical diagnosis of tyrosinemia type 2
Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano

ITALY

PUGLIA
FOGGIA

Biochemical diagnosis of tyrosinemia type 1 and 2 (tandem mass spectrometry)
Azienda Ospedaliero Universitaria di Foggia - Ospedali Riuniti

FRANCE

GRAND-EST
REIMS

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of pachyonychia congenita (KRT6A, KRT16, KRT6B, KRT6C and KRT17 genes)
LabGenetics - Laboratorio de Genética Clínica, S.L.

FRANCE

GRAND-EST
VANDOEUVRE-LÈS-NANCY

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of palmoplantar keratoderma-esophageal carcinoma syndrome (RHBDF2 gene)
LabGenetics - Laboratorio de Genética Clínica, S.L.

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of tyrosinemia (FAH, TAT, HPD genes)
LabGenetics - Laboratorio de Genética Clínica, S.L.

AUSTRIA

STEIERMARK
GRAZ