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80 Result(s)

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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis (C9ORF72, FUS, SOD1, TARDB, VAPB genes)
    • Universitätsklinikum Ulm
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis 1 (SOD1 gene)
    • Medizinische Universität Graz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • STEIERMARK
    • GRAZ
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis type 1, 4, 6, 9, 10 and 14 (SOD1, SETX, FUS, ANG, TARDBP and VCP gene)
    • AMC - Academisch Medisch Centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, CHGB, FIG4, FUS, OPTN, SOD1, TARDBP, UBQLN2, VAPB genes)
    • Centogene AG
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis type 1 (SOD1 gene)
    • Sheffield Children's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of ALS, amyotrophic lateral sclerosis (SOD1, TDP43, FUS, ANG genes)
    • University Hospitals Leuven - Gasthuisberg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis type 1, 2, 4, 6, 8, 9, 10, 11, 14 and 15 (SOD1, ALS2, SETX, FUS, VAPB, ANG, TARDBP, FIG4, VCP and UBQLN2 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis type 4 and 5 (SETX and SPG11 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis (TARDBP gene: exon 6 sequencing)
    • Sheffield Children's NHS Foundation Trust
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, CHCHD10, CHMP2B, FUS, OPTN, PFN1, SOD1, TARDBP, TBK1, UBQLN2, VAPB, VCP genes: sequencing)
    • CeGaT GmbH
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of familial amyotrophic lateral sclerosis (SOD1 gene)
    • Paxis und Labor Dr. med Karl Mehnert
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • NEU-ULM
    • Accreditation
    • Molecular diagnosis of juvenile amyotrophic lateral sclerosis 4 (SETX gene)
    • Ruhr-Universität Bochum
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, CHCHD10, C9ORF72, FIG4, FUS, SOD1, UBQLN2, TARDB, VAPB genes)
    • Medizinisch Genetisches Zentrum München
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of Amyotrophic lateral sclerosis type 4 - ALS4 (SETX gene, by MLPA and seq)
    • Institut de Pathologie et de Génétique - Gosselies
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis, dominant (SOD1, SETX, FUS, VAPB, ANG, TARDBP genes): sequencing of the entire coding region for all genes and deletion/duplication analysis of SETX gene
    • Instituto de Biologia Molecular e Celular
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, DCTN1, FIG4, TARDBP, VAPB)
    • MVZ Fenner & Krasemann
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis - ALS (C9orf72 gene)
    • Sheffield Children's NHS Foundation Trust
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • South Yorkshire
    • SHEFFIELD
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis/Frontotemporal Dementia (C9orf72 gene)
    • National Hospital for Neurology and Neurosurgery
    • Purpose(s) : Somatic genetics
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, CFIG4, C9ORF72, OPTN, SOD1, TARDBP, VABP genes)
    • Praxis für Humangenetik Freiburg
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia (ALS and FTD, C9ORF72 gene: Molecular diagnosis through gene expansion analysis)
    • University Hospital of Wales
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis
    • Technical procedure(s) : PCR based techniques
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis type 14 (VCP gene)
    • Ruhr-Universität Bochum
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BOCHUM
    • Accreditation
    • Molecular diagnosis of Dementia (NGS panel for MAPT, PGRN, VCP, PRNP, SCNA, SNCB, CHMP2B, FUS, TARDBP, PSEN1, PSEN2, APOE, APP genes: Sequencing of the entire coding region)
    • Instituto de Biologia Molecular e Celular
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Accreditation
    • Molecular diagnosis of motor neuron diseases related to CHCHD10 gene (complete coding sequence)
    • CHU de Nice - Hôpital l'Archet 2
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • NICE
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, ANG, TARDBP, FUS, FIG4 genes)
    • Reference Laboratory Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Accreditation
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, FIG4, FUS, OPTN, SOD1, TARDBP, VAPB genes: sequencing)
    • Pränatalmedizin München
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis type 1 (SOD1 gene)
    • Guy's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Amyotrophic Lateral Sclerosis 6 and 10 (FUS, TARDBP genes: Sequencing of the entire coding region of gene (s) / Testing for known mutations in family members)
    • Guy's Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Molecular diagnosis of amyotrophic lateral sclerosis
    • A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of amyotrophic lateral sclerosis (FUS, SOD1, TARDB genes)
    • Institut für Humangenetik des UKGM am Standort Gießen
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Hessen
    • GIEßEN
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, TARDBP, FUS, C9ORF72 genes)
    • IRCCS AOU San Martino - IST - DIMI
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of amyotrophic lateral sclerosis (ALS2, FUS, SOD1, TARDBP genes)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene)
    • Turku University Hospital
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene)
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene)
    • A.O.U. di Ferrara - Polo Chimico-Bio-Medico
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • FERRARA
    • 'Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, FUS, TARDBP, UBQLN2, OPTN, ANG genes: exons and flanking intronic regions sequencing ; C9ORF72 gene: hexanucleotide GGGGCC repeats)'
    • CHRU de Tours - Hôpital Bretonneau
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • FRANCE
    • CENTRE
    • TOURS
    • Molecular diagnosis of amyotrophic lateral sclerosis (FUS, SOD1, TARDBP, VAPB genes)
    • Institut für Humangenetik am Universitätsklinikum Köln
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 smd SETX genes)
    • B.I.R.D. Foundation
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene)
    • Oslo University Hospital, Ullevaal
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NORWAY
    • Østlandet
    • OSLO
    • Molecular diagnosis of ALS (FUS, SOD1, TARDBP, VCP genes; C9ORF72 repeat)
    • University of Antwerp - UA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene)
    • Laboratorio Genoma
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, C9ORF72, FIG4, FUS, OPTN, SOD1, VAPB, VCP genes)
    • Praxis Dres. Gencik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of amyotrophic lateral sclerosis (ALS2, ANG, FIG4, FUS, OPTN, SETX, SOD1, TARDBP, VAPB, VCP genes)
    • Genetaq
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of Amyotrophic lateral sclerosis (SOD1, FUS and TARDBP genes): sequencing of the entire coding region.
    • Faculdade de Medicina da Universidade de Lisboa
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene)
    • Hospital Universitario Virgen del Rocío
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular diagnosis of amyotrophic lateral sclerosis (FUS, SOD1, C9ORF72, TARDBP genes)
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, ANG, C9ORF72, FUS, TARDBP genes)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, FIG4, FUS, SOD1, TARDBP, VAPB genes: sequencing)
    • Gemeinschaftspraxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, ALS2, VAPB, and VCP genes)
    • Medizinische Universität Wien
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Amyotrophic lateral sclerosis (SOD1, ALS2, SETX, FUS, VAPB, ANG, TARDBP, FIG4, OPTN, and VCP genes)
    • Praxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of amyotrophic lateral sclerosis (FUS, SOD1 genes)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • La Rioja
    • LOGROÑO
    • Molecular diagnosis of amyotrophic lateral sclerosis (SETX, FUS, FIG4 genes)
    • Sistemas Genómicos S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, TARDBP, C9ORF72 genes)
    • Consorzio per la Genetica Molecolare Umana
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MONZA
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, FUS, ANG, TARDBP, FIG4, C9ORF72 genes)
    • IDIBELL - Instituto de Investigación Biomédica de Bellvitge
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene / sequencing)
    • Centro Inmunológico de Alicante (CIALAB)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular Diagnosis of Amyotrophic Lateral Sclerosis (SOD1 sequence analysis)
    • University of Alberta
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • CANADA
    • Alberta
    • EDMONTON
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, ALS2, SETX, FUS, VAPB, ANG, TDP43, FIG4 genes)
    • Fondazione IRCCS Istituto Neurologico "Carlo Besta"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1,ANG, DCTN, PGN, TARBDP, FUS, SETX, ALS2, VCP, C9ORF72 genes)
    • Ospedale Niguarda Ca' Granda
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene)
    • Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • TOSCANA
    • PISA
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 gene)
    • CNR
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • CALABRIA
    • MANGONE
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, TARDBP, FUA, C9ORF72 genes)
    • Ospedale "R. Binaghi"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • SARDEGNA
    • CAGLIARI
    • Molecular diagnosis of amyotrophic lateral sclerosis 1 (SOD1 gene)
    • Allgemeines Krankenhaus der Stadt Wien
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of amyotrophic lateral sclerosis
    • Policlinico S. Orsola-Malpighi - Area S. Orsola
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of amytrophic lateral sclerosis (ALS2 gene)
    • IRCCS "E. Medea"
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • BOSISIO PARINI
    • Molecular diagnosis of amyotrophic lateral sclerosis, ALS1 (SOD1, sequencing analysis, PGD)
    • Wolfson Medical Center
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ISRAEL
    • ISRAEL
    • HOLON
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, FUS, OPTN, UBQLN2, C9ORF72, ATXN2, VCP, TARDBP, EPHA4 and CHCHD10 genes)
    • CHU de Nîmes - Hôpital Caremeau
    • Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • NÎMES
    • Molecular diagnosis of amyotrophic lateral sclerosis. TARDBP gene
    • Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BADALONA
    • Molecular diagnosis of amyotrophic lateral sclerosis (C9orf72 gene: mutation analysis; SOD1, TARDBP, VAPB genes: complete sequencing)
    • University of Tampere
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • FINLAND
    • Finland
    • TAMPERE
    • Molecular diagnosis of amyotrophic lateral sclerosis (ANG, UBQLN2, C9orf72 genes)
    • Fondazione Istituto Neurologico "C. Mondino" - IRCCS
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • PAVIA
    • Molecular diagnosis of amyotrophic lateral sclerosis (entire coding sequence of SOD1, ANG, TARDBP, FUS and SETX genes)
    • Laboratorio de Genética Clínica, S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Reference Centre for neuromuscular diseases: neuropathological, molecular analysis and electronic microscopy of muscle, nerv and skin biopsies
    • Universitätsklinikum Aachen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics, Biochemical genetics, Immunology, Pathology
    • Objective(s) : Analyte / Enzyme assay
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • AACHEN
    • Histological diagnosis of Neuromuscular diseases
    • Universitätsklinikum Bonn
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Pathology
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, SETX, TARDBP, ANG and FUS genes)
    • Instituto de Investigación Hospital 12 de Octubre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Postnatal molecular diagnosis of amyotrophic lateral sclerosis (sequence analysis of the entire coding region of VAPB, SOD1, SETX genes)
    • Università degli Studi di Padova- Polo A.Vallisneri
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Molecular diagnosis of amyotrophic lateral sclerosis (ATXN2 gene)
    • Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BADALONA
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1, TARDBP genes)
    • Azienda Ospedaliero Universitaria Careggi - NEUROFARBA
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • TOSCANA
    • FIRENZE
    • Molecular diagnosis of amyotrophic lateral sclerosis (SOD1 and C9ORF genes)
    • Istituto Neurologico Mediterraneo - IRCCS Neuromed
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • MOLISE
    • POZZILLI
    • Molecular diagnosis of Paget disease of bone (PDB) and amyotrophic lateral sclerosis 17 (ALS17) (SQSTM1 gene: sequencing of the coding region)
    • University of Tampere
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FINLAND
    • Finland
    • TAMPERE
    • Molecular diagnosis of familial amyotrophic lateral sclerosis (C9ORF72, SOD1, FUS genes)
    • Centro de estudios genéticos ATG Medical
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • TRES CANTOS
    • Diagnostic of amyotrophic lateral sclerosis (FIG4 gene)
    • Centro de Investigación Príncipe Felipe (CIPF)
    • Purpose(s) : Post-natal diagnosis, Somatic genetics
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Diagnosis of amyotrophic lateral sclerosis (ANG, C9ORF72, SOD1, TARDBP genes)
    • Bioarray
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ELCHE