Légende
: Accréditation
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- ALLEMAGNE
- Nordrhein-Westfalen
- BOCHUM
- Molecular diagnosis of familial spastic paraplegia SPG3, SPG4, SPG7, SPG10, SPG11, SPG13 and SPG31 (ATL1, HSP60, KIF5A, REEP1, SPAST, SPG7, SPG11 genes)
- Ruhr-Universität Bochum
- Plus d'informations
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- ROYAUME-UNI
- South Yorkshire
- SHEFFIELD
- Molecular diagnosis of Autosomal dominant Spastic Paraplegia type 31 (SPG31; REEP1 gene: DNA sequencing of entire coding region)
- Sheffield Children's NHS Foundation Trust
- Plus d'informations
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- ALLEMAGNE
- Bayern
- REGENSBURG
- Molecular diagnosis of spastic paraplegia (ATL1, CYP7B1, REEP1, SPAST, SPG7, SPG20 genes: sequencing, loci: CYP7B1, SPG7, SPG11, SPG14, SPG20, SPG21, SPG26, ZFYVE26: linkage analysis)
- Universitätsklinikum Regensburg
- Plus d'informations
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- PAYS-BAS
- Limburg
- MAASTRICHT
- Molecular diagnosis of Spastic Paraplegia type 31 (REEP1 gene)
- AZM - Academisch Ziekenhuis Maastricht
- Plus d'informations
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- PAYS-BAS
- Gelderland
- NIJMEGEN
- Molecular diagnosis of Autosomal Dominant Spastic Paraplegia type 3A, 4, 6, 8, 10, 12, 13, 17, 31 and 42 (ATL1, SPAST, NIPA1, KIAA0196, KIF5A, RTN2, HSPD1, BSCL2, REEP1 and SLC33A1 gene)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Plus d'informations
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- Molecular diagnosis of familial spastic paraplegia SPG3A, SPG4 and SPG31 (ATL1, REEP1, SPAST genes)
- Universitätsklinikum Jena
- Plus d'informations
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- ALLEMAGNE
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of spastic paraplegia (genes: ATL1, ACP33, BSCL2, CYP7B1, C12ORF65, FA2H, HSPD1, KIAA0196, KIF5A, L1CAM, NIPA1, PLP1, PNPLA6, REEP1, SLC33A1, SPAST, SPG3A, SPG7, SPG11, SPG20, SPG21, ZFYVE26 and ZFYVE27)
- Institute of Molecular Diagnostics
- Plus d'informations
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- ALLEMAGNE
- Hamburg
- HAMBURG
- Molecular diagnosis of spastic paraplegia (ACP33, BSCL2, CYP7B1, HSPD1, KIAA0196, KIF5A, L1CAM, NIPA1, REEP1, SLC33A1, SPAST, SPG3a, SPG7, SPG11, SPG20, PLP1, ZFYVE26 genes)
- MVZ Fenner & Krasemann
- Plus d'informations
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- Molecular diagnosis of spastic paraplegia (SPAST, SPG3A, REEP1 and SPG7 genes)
- Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
- Plus d'informations
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- Molecular diagnosis of autosomal dominant spastic paraplegia, types 3, 4, 6 and 31 (ATL1 gene / sequence of exons 2-13; NIPA1 and REEP1 genes / mutations; SPAST gene / sequence of exons 1-17)
- Hospital Universitario Central de Asturias
- Plus d'informations
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- ALLEMAGNE
- Niedersachsen
- GÖTTINGEN
- Molecular diagnosis of familial spastic paraplegia (ATL1, SPAST, SPG7, SPG11 and REEP1 genes)
- Universitätsmedizin Göttingen
- Plus d'informations
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- ESPAGNE
- Cataluña
- L'HOSPITALET DE LLOBREGAT
- Molecular diagnosis of autosomal dominant spastic paraplegia type 31. SPG31 gene
- IDIBELL - Instituto de Investigación Biomédica de Bellvitge
- Plus d'informations
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Diagnostic en biologie moléculaire de la paraplégie spastique autosomique dominante de type 31 (gène REEP1)
- CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
- Plus d'informations
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- Molecular diagnosis of Familial dominant spastic paraplegia, SPG3A, SPG4, SPG42, SPG10, SPG31, SPG8, SPG17, SPG6, SPG13 (ALT1, SPAST, SLC33A1, KIF5A, REEP1, KIAA0196, BSCL2, NIPA1 and HSPD1 genes)
- Instituto de Biologia Molecular e Celular
- Plus d'informations
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- Molecular diagnosis of spastic paraplegia (SPG2, 3, 4, and 7, and REEP1 genes)
- Medizinische Universität Wien
- Plus d'informations
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- Molecular diagnosis of Spastic Paraplegia (PLP1, ATL1, SPAST, SPG7, SPG11, and SPG20 genes)
- Praxis für Humangenetik
- Plus d'informations
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- Molecular diagnosis of autosomal dominant spastic paraplegia, type 31 (REEP1 gene)
- Oslo University Hospital, Ullevaal
- Plus d'informations
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- ALLEMAGNE
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of spastic paraplegia (genes: ACP33, BSCL2, CYP7B1, HSPD1, KIAA0196, KIF5A, L1CAM, NIPA1, REEP1, SPAST, SPG3a, SPG7, SPG11(KIAA1840), SPG20, PLP1, ZFYVE26)
- Diagenom GmbH
- Plus d'informations
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- Molecular diagnosis of familial spastic paraplegia (SPAST, ATL1, SPG7, REEP1, BSCL2, CYP7B1 genes)
- Fondazione IRCCS Istituto Neurologico "Carlo Besta"
- Plus d'informations
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- Molecular diagnosis of familial spastic paraplegia (SPAST, ATL1, SPG7 genes)
- CNR
- Plus d'informations
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- Molecular diagnosis of autosomal dominant spastic paraplegia type 31 (REEP1 gene)
- Università degli Studi di Padova
- Plus d'informations
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- ALLEMAGNE
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of familial spastic paraplegia SPG3, SPG4, SPG5, SPG7, SPG11, SPG15 and SPG31 (ATL1, BSCL2, CYP7B1, REEP1, SPAST, SPG7, SPG11, ZFYVE26 genes)
- Hertie-Institut für klinische Hirnforschung
- Plus d'informations
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- ESPAGNE
- Cataluña
- BADALONA
- Molecular diagnosis of autosomal dominant spastic paraplegia type 31 (REEP1 gene)
- Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol
- Plus d'informations
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- ESPAGNE
- Madrid
- SAN SEBASTIÁN DE LOS REYES
- Molecular diagnosis of autosomal dominant pure spastic paraplegia (entire coding sequence of SPAST, ATL1 , REEP1, KIF5A, NIPA1, KIAA0196 and HSPD1 genes / deletions in SPAST and ATL1 genes by MLPA analysis)
- LABORATORIO DE GENÉTICA CLÍNICA S.L.
- Plus d'informations
