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Caption : Accreditation =Accreditation
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    • FRANCE
    • ILE-DE-FRANCE
    • SAINT-OUEN-L'AUMÔNE
    • Accreditation
    • Biochemical and molecular diagnosis of Tay-Sachs disease (search for mutations in HEXA gene)
    • Laboratoire Cerba
    • More information
    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Ashkenazes carrier screening (ASHPLEX 1, ASHPLEX 2, ASHPLEX Gaucher)
    • Centre Médical Universitaire - CMU
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of GM2 gangliosidosis (GM2A, HEXA and HEXB genes)
    • Ruhr-Universität Bochum
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Ashkenazes carrier screening (ASHPLEX 1, ASHPLEX 2, ASHPLEX Gaucher)
    • Genetica AG
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • GERMANY
    • Hessen
    • BAD NAUHEIM
    • Accreditation
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Centrum für Humangenetik
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Tay-Sachs Disease (HEXA gene)
    • AMC - Academisch Medisch Centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of GM2 gangliosidosis (HEXA and HEXB genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular screening of frequent diseases in Ashkenazi Jewish populations (APEX: ABCC8, AGL, ASPA, BCKDHB, BLM, CFTR, CLRN1, DLD, F11, FANCC, G6PC, GBA, GJB2, HEXA, IKBKAP, LDLR, MCOLN1, MEFV, NEB, PCDH15, SERPINA1, SMPD1, TMEM216 and TOR1A genes)
    • Asper Biotech Ltd.
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Biochemical and molecular diagnosis of Tay-Sachs disease (enzyme assay / HEXA gene)
    • Centogene AG
    • More information
    • GERMANY
    • Baden-Württemberg
    • KARLSRUHE
    • Accreditation
    • Molecular diagnosis of GM2 gangliosidosis (HEXA and HEXB genes)
    • Labor PD Dr. Volkmann und Kollegen
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Accreditation
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Zentrum für Humangenetik
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of GM2 gangliosidosis (GM2A, HEXA and HEXB genes)
    • MVZ Fenner & Krasemann
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Biochemical diagnosis of Tay-Sachs disease
    • UKE - Universitätsklinikum Hamburg-Eppendorf
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Tay-Sachs Disease (HEXA gene: Sequencing of the entire coding region of gene (s) / Targetted mutation analysis (Jewish (Ashkenazi) mutations) / Testing for known mutations in family members
    • Guy's Hospital
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Biochemical diagnosis of Tay-Sachs disease (Analyte: Hexosaminidase A)
    • St Mary's Hospital
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Biochemical diagnosis of Lysosomal Storage disorders (Analyte: Chitotriosidase)
    • St Mary's Hospital
    • More information
    • UNITED KINGDOM
    • Strathclyde
    • GLASGOW
    • Accreditation
    • Biochemical diagnosis of Tay Sachs disease (Analyte: Hexosaminidase A)
    • Royal Hospital for Sick Children
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Biochemical diagnosis of Tay Sachs disease (Analyte: Hexosaminidase A)
    • Birmingham Children's Hospital
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Biochemical diagnosis of Tay Sachs disease (Analyte: Hexosaminidase A)
    • Bristol Royal Infirmary
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Accreditation
    • Molecular and Biochemical diagnosis of Tay Sachs (HEXA, Hexosaminidase A analysis)
    • Hadassah Ein Kerem - Hebrew University Medical Center
    • More information
    • SWEDEN
    • Västra Götalandsregionen
    • GÖTEBORG
    • Accreditation
    • Biochemical diagnosis of Tay-Sachs disease (Hexosaminidase A activity assay)
    • Sahlgrenska university hospital
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of GM2 gangliosidosis (HEXA and HEXB genes: sequencing)
    • CeGaT GmbH
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Biochemical diagnosis of Tay-Sachs disease
    • CHU de Lyon-GH Est - Hospices Civils de Lyon
    • More information
    • FRANCE
    • ALSACE
    • SCHILTIGHEIM
    • Preimplantation genetic diagnosis of Tay-Sachs disease (HEXA gene)
    • Centre Médico-Chirurgical et Obstétrical (CMCO)
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Laboratorio Genoma
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Sistemas Genómicos S.L.
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Praxis für Humangenetik
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Hexosaminidase A deficiency (HEXA gene): Target mutation analysis - panel of mutation (R178H, R137X, IVS12+1G>C, G269S, V200M, 1VS9+1G>A, R247W)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of GM1and GM2 gangliosidosis (GLB1 3p22.3, GM2A genes: sequencing of entire coding region and prenatal testing)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene / gene sequencing and 1277insTATC, 1421+1G>C, 269S)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Biochemical diagnosis of GM2 - Tay-Sachs (analyte: hexosaminidase A)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Biochemical diagnosis of Tay-Sachs disease
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of Tay-Sachs disease
    • Acibadem healthcare group
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Biochemical diagnosis of Tay-Sachs disease (Hexosaminidase A activity assay)
    • Karolinska University Hospital - Solna
    • More information
    • ISRAEL
    • ISRAEL
    • RAMAT-GAN
    • Molecular diagnosis of Tay Sachs (HEXA, Mutation analysis, Carrier screening, PGD)
    • Sheba Medical Center
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of GM2 gangliosidosis (HEXA and HEXB genes)
    • Diagenom GmbH
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene - c.1274_1277dupTATC, c.1421+1G>C, c.1073+1G>A, p.Gly269Ser, p.Arg247Trp y p.Arg249Trp mutations / entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of Tay-Sachs disease (Hexosaminidase A activity assay)
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • More information
    • FRANCE
    • CHAMPAGNE-ARDENNE
    • REIMS
    • Biochemical diagnosis of Tay-Sachs disease (enzyme assay)
    • CHU de Reims - American Memorial Hospital
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of Tay-Sachs disease (fluorometric determination of beta-hexosaminidase A)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • ITALY
    • FRIULI VENEZIA GIULIA
    • UDINE
    • Biochemical and molecular diagnosis of Tay-Sachs disease (assessment of beta-hexosaminidase A activity and HEXA, GM2A genes)
    • Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Preimplantation genetic diagnosis of Tay-Sachs disease (HEXA gene)
    • CME Barcelona
    • More information
    • CANADA
    • Québec
    • MONTRÉAL
    • Biochemical diagnosis and carrier screening of Tay-Sachs (beta-hexosaminidase assay)
    • Montreal Children's hospital - Hôpital de Montréal pour enfants
    • More information
    • CANADA
    • Québec
    • MONTRÉAL
    • Molecular screening of frequent diseases in Ashkenazi populations (genes ASPA, HEXA, IKBKAP)
    • Montreal Children's hospital - Hôpital de Montréal pour enfants
    • More information
    • CANADA
    • Québec
    • MONTRÉAL
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Montreal Children's hospital - Hôpital de Montréal pour enfants
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Biochemical diagnosis of Tay-Sachs disease
    • CHU de Rouen - Hôpital Charles Nicolle
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Biochemical diagnosis of Tay-Sachs disease (hexosaminidase A activity)
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Biochemical diagnosis of GM1 and GM2/B gangliosidosis
    • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of GM2 gangliosidosis (GM2A gene)
    • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Praxis Dr. med. Ulrike Beudt
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Biochemical and molecular diagnosis of Tay-Sachs disease (enzyme assay / HEXA gene)
    • Labor für molekulare Genetik und metabolische Erkrankungen
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical and molecular diagnosis of Tay-Sachs disease. GM2A and HEXA genes.
    • Hospital Clínic de Barcelona
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Biochemical and molecular diagnosis of Tay-Sachs disease
    • Universitätsmedizin Rostock
    • More information
    • ITALY
    • CALABRIA
    • MANGONE
    • ITALY
    • LAZIO
    • ROMA
    • Biochemical diagnosis of Tay-Sachs disease
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical and molecular diagnosis of gangliosidosis GM1 and GM2 B (Tays-Sachs) and O (Sandhoff) varinates ( GLB1, HEXA and HEX B genes)
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • FINLAND
    • Finland
    • KUOPIO
    • AUSTRIA
    • WIEN
    • WIEN
    • Biochemical diagnosis of GM2-Gangliosidoses
    • Allgemeines Krankenhaus
    • More information
    • ITALY
    • TOSCANA
    • SIENA
    • Biochemical diagnosis of Tay-Sachs disease
    • Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical and molecular diagnosis of Tay-Sachs disease (enzyme assay, complete HEXA gene sequencing)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical diagnosis of Tay-Sachs disease (beta-hexosaminidase A assay)
    • Hospital Universitari Vall d'Hebron. Area Materno Infantil
    • More information
    • ROMANIA
    • CLUJ
    • CLUJ
    • Biochemical diagnosis of Tay-Sachs disease
    • U.M.F. Iuliu Hatieganu Cluj
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Biochemical diagnosis of Tay-Sachs disease (beta-hexosaminidase assay)
    • Institute of Child Health
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Biochemical diagnosis of Tay-Sachs Disease (Analyte: N-acetyl-beta-D-Glucosaminidase A)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • ROTTERDAM
    • Biochemical diagnosis of GM2 Gangliosidosis (Analyte: beta-Hexosaminidase A and B)
    • Erasmus MC, Faculteitsgebouw
    • More information
    • BULGARIA
    •  South-West region
    • SOFIA
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • University hospital of Obstetrics and Gynecology
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Biochemical diagnosis of Tay-Sachs disease
    • Azienda Ospedaliera Universitaria Anna Meyer
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of Tay-Sachs disease (enzyme activity assay, oligosaccharide TLC)
    • Universitätsklinikum Heidelberg
    • More information
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LES-NANCY
    • Biochemical diagnostic of Tay-Sachs disease (enzymatic dosage of hexosaminidase A)
    • CHU de Nancy
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Biochemical diagnosis of GM2-gangliosides (metabolite profile / enzyme assay)
    • Universitätsmedizin Göttingen
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of Tay-Sachs disease caused by GM2 activator deficiency (sequencing of whole gene)
    • Istanbul University
    • More information
    • ISRAEL
    • ISRAEL
    • BEER YAAKOV
    • Molecular diagnosis of Tay-Sachs (HEXA, Mutation analysis, Carrier screening)
    • Assaf Harofeh Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • HAIFA
    • Molecular diagnosis of Tay Sachs (HEXA, Mutation analysis, Carrier screening)
    • Carmel Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • HAIFA
    • Molecular diagnosis of Tay Sachs (HEXA, Mutation analysis, Carrier screening)
    • The Bnai Zion Medical Center, Technion-Rappaport Faculty of Medicine
    • More information
    • ISRAEL
    • ISRAEL
    • REHOVOT
    • Molecular diagnosis of Tay Sachs (HEXA, Mutation analysis, Carrier screening)
    • Kaplan Medical Center
    • More information
    • ISRAEL
    • ISRAEL
    • JERUSALEM
    • Molecular diagnosis of Tay Sachs (HEXA A, Linkage analysis, PGD)
    • Shaare Zedek Medical Center
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Biochemical diagnosis of Tay-Sachs disease (beta-hexosaminidase A)
    • Ghent University Hospital - UZGent
    • More information
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Biochemical diagnosis of Tay-Sachs disease (N-acetyl-beta-hexosaminidase iso-enzymes in WBC)
    • Ghent University Hospital - UZGent
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Biochemical diagnosis of Tay-Sachs disease (beta-hexosaminidase A)
    • University Hospitals Leuven - Gasthuisberg
    • More information
    • UNITED KINGDOM
    • County Antrim
    • BELFAST
    • Biochemical diagnosis of Tay Sachs disease (Analyte: Hexosaminidase A)
    • Royal Group of Hospitals Belfast
    • More information
    • UNITED KINGDOM
    • Lothian
    • EDINBURGH
    • Biochemical diagnosis of Tay Sachs disease (Analyte: Hexosaminidase A)
    • Royal Hospital for Sick Children
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical and Molecular diagnosis of Tay-Sachs disease (Hexosaminidase A)
    • Guy's Hospital
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Biochemical diagnosis of Tay Sachs disease (Analyte: Hexosaminidase A)
    • Great Ormond Street Hospital NHS Foundation Trust
    • More information
    • NETHERLANDS
    • Limburg
    • MAASTRICHT
    • Biochemical marker for Lysosomal Storage Diseases (Analyte: Chitotriosidase)
    • AZM - Academisch Ziekenhuis Maastricht
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Biochemical diagnosis of Tay-Sachs disease (thermolabile beta-hexosaminidase A enzyme assay)
    • Instytut Psychiatrii i Neurologii - Institute of Psychiatry and Neurology
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Biochemical diagnosis of Tay-Sachs Disease (Analyte: N-acetyl-beta-D-glucosaminidase A)
    • AMC - Academisch Medisch Centrum
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of Tay-Sachs disease (entire coding sequence of HEXA gene / mutations 1277insTATC, 1421+1G>C, G269S)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of Tay-Sachs disease (HEXA and GM2A genes: entire coding sequence)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical and molecular diagnosis of sphingolipidosis (GMI, GMII, Sandhoff disorder, Metachromatic leukodystrophy, Fabry disorder, Gaucher disorder, ARSA, GBA, GLA, GLB1, HEXA, HEXB genes)
    • Instituto de Biologia Molecular e Celular
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of Tay-Sachs disease (entire coding sequence of HEXA gene / mutations 1277insTATC, 1421+1G>C and G269S)
    • Lorgen G.P.
    • More information
    • SPAIN
    • Madrid
    • MAJADAHONDA
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Genyca Innova
    • More information
    • ITALY
    • MARCHE
    • ANCONA
    • Biochemical diagnosis of Tay-Sachs disease (beta-D-N-acetilglucosaminidase and esosaminidase total assay in leucocytes)
    • Ospedali Riuniti "Umberto I - G.M. Lancisi - G. Salesi" - Presidio "G. Salesi"
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
    • Medizinische Universität Wien
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Biochemical and molecular diagnosis of Tay-Sachs disease (HEXA gene)
    • Medizinische Universität Graz
    • More information
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of Tay-Sachs disease (HEXA gene / sequencing)
    • GenoClinics
    • More information