Laboratori di Diagnosi

Laboratori di diagnosi

Italia – Costozza di longare
Diagnosi molecolare dell’insonnia familiare fatale (gene PRNP)
B.I.R.D. Foundation

Italia – Troina
Diagnosi molecolare dell’insonnia familiare fatale (gene PRNP)
IRCCS OASI Maria Santissima

Austria – Wien
Molecular diagnosis of prion diseases (PRNP gene)
Allgemeines Krankenhaus

Francia – Paris
Molecular diagnosis of familial fatal insomnia (PRNP gene)
CHU Paris-GH St Louis Lariboisière F.Widal – Hôpital Lariboisière

Francia – Schiltigheim
Preimplantation genetic diagnosis of fatal familial insomnia (PRNP gene)
Centre Médico-Chirurgical et Obstétrical (CMCO)

Germania – Dresden
Molecular diagnosis of human prion diseases (PRNP gene)
Gemeinschaftspraxis Dr. Prager / Dr. Junge / Dr. Hennig / Dr. Linné für Humangenetik

Germania – Dortmund
Molecular diagnosis of human prion diseases (PRNP gene)
Medizinisches Versorgungszentrum (MVZ) Dortmund Dr. Eberhard und Partner

Germania – Göttingen
Clinical diagnosis and epidemiology of spongiforme encephalopathy
Universitätsmedizin Göttingen

Germania – München
Neuropathological, biochemical and molecular diagnosis of spongiforme encephalopathies
Ludwig-Maximilians-Universität München

Germania – Ulm
Molecular diagnosis of human prion diseases (PRNP gene)
Universitätsklinikum Ulm

Germania – Rostock
Molecular diagnosis of human prion diseases (PRNP gene)
Institute of Molecular Diagnostics & Diagenom GmbH

Germania – Tübingen
Molecular diagnosis of human prion diseases (PRNP gene)
CeGaT GmbH

Portogallo – Lisboa
Molecular diagnosis of human prion diseases (PRNP gene)
Instituto Nacional de Saúde Dr. Ricardo Jorge – Lisboa

Spagna – Oviedo
Molecular diagnosis of transmissible spongiform encephalopathies (PRNP gene)
Hospital Universitario Central de Asturias

Spagna – Paterna
Molecular diagnosis of transmissible spongiform encephalopathies (PRNP gene)
IMEGEN – Instituto de Medicina Genómica

Spagna – Tres Cantos (Madrid)
Molecular diagnosis of fatal familial insomnia (PRNP gene)
SECUGEN S. L.