Légende
: Accréditation
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- SUISSE
- Suisse Romande
- GENÈVE
- Diagnostic moléculaire de la dystonie dopa-sensible autosomique récessive (gène GCH1)
- Centre Médical Universitaire - CMU
- Plus d'informations
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- DANEMARK
- Sjælland
- GLOSTRUP
- Prenatal and postnatal molecular diagnosis of doparesponsive dystonia (TH, GCH1 and SPR genes: mutation screening ; carrier screening)
- Kennedy Center
- Plus d'informations
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- ROYAUME-UNI
- South Yorkshire
- SHEFFIELD
- Molecular diagnosis of Autosomal Recessive Dopa-responsive Dystonia (TH gene: DNA sequencing of entire coding region)
- Sheffield Children's NHS Foundation Trust
- Plus d'informations
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- PAYS-BAS
- Gelderland
- NIJMEGEN
- Molecular diagnosis of Autosomal Recessive Dopa Responsive Dystonia due to Tyrosine Hydroxylase Deficiency (TH gene)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Plus d'informations
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- PAYS-BAS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Movement Disorders (exome sequencing)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Plus d'informations
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- PAYS-BAS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Plus d'informations
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- ALLEMAGNE
- Baden-Württemberg
- FREIBURG
- Molecular diagnosis of dopa-responsive dystonia (GCH1, TH genes)
- Praxis für Humangenetik / Center for Human Genetics Freiburg
- Plus d'informations
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- SUISSE
- Suisse Alémanique
- ZÜRICH
- Biochemical and molecular diagnosis of dopa-reponsive dystonia (GCH1 gene)
- Universitäts-Kinderspital
- Plus d'informations
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- SUISSE
- Suisse Alémanique
- ZÜRICH
- Biochemical and molecular diagnosis of Segawa syndrome, autosomal recessive (TH gene)
- Universitäts-Kinderspital
- Plus d'informations
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- PAYS-BAS
- Noord-Holland
- AMSTERDAM
- Molecular diagnosis of Tyrosine Hydroxylase Deficiency (TH gene)
- AMC - Academisch Medisch Centrum
- Plus d'informations
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- ALLEMAGNE
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of dopa-responsive dystonia (GCH1, TH genes: sequencing)
- CeGaT GmbH
- Plus d'informations
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- PAYS-BAS
- Noord-Holland
- AMSTERDAM
- Biochemical diagnosis of Neurotransmission Anomalies (Analyte: Free Catecholamines, Metanephrines, MHPG and Phenolic Acids)
- AMC - Academisch Medisch Centrum
- Plus d'informations
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- PAYS-BAS
- Noord-Holland
- AMSTERDAM
- Biochemical diagnosis of Biogenic Amine Metabolism Disorders (Analyte: Pterins)
- AMC - Academisch Medisch Centrum
- Plus d'informations
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- Biochemical and molecular diagnosis of neurotransmitter biosynthesis deficiency (TH gene)
- Policlinico Umberto I
- Plus d'informations
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- ESPAGNE
- Madrid
- CANTOBLANCO
- Molecular and biochemical diagnosis of dopa-responsive dystonia autosomal recessive (TH gene)
- Universidad Autónoma de Madrid. Facultad de Ciencias
- Plus d'informations
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- Biochemical diagnosis of biogenic amine metabolism disorder
- Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
- Plus d'informations
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Diagnostic en biologie moléculaire de la dystonie dopa-sensible autosomique récessive (gène TH)
- CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
- Plus d'informations
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- Molecular diagnosis of autosomal recessive dopa-responsive dystonia (TH gene) by sequencing of entire coding region and delection/duplication analysis by MLPA
- Instituto de Biologia Molecular e Celular
- Plus d'informations
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- Molecular diagnosis of dopa-responsive dystonia (GCH1 and TH gene)
- Praxis für Humangenetik
- Plus d'informations
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- ALLEMAGNE
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of dystonias (ATP1A3, GCH1, MR1(PNKD), PRKRA, SGCE, TH, THAP1, TOR1A genes)
- Diagenom GmbH
- Plus d'informations
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- Molecular diagnosis of dystonia, dopa-responsive, autosomal recessive. TH gene.
- GENETAQ
- Plus d'informations
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- ESPAGNE
- Comunidad Valenciana
- PATERNA
- Molecular diagnosis of autosomal recessive dopa-responsive dystonia (TH gene - entire coding sequence)
- IMEGEN - Instituto de Medicina Genómica
- Plus d'informations
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- ALLEMAGNE
- Sachsen
- DRESDEN
- Molecular diagnosis of dopa-responsive dystonia (GCH1, TH genes: sequencing, MLPA)
- Gemeinschaftspraxis für Humangenetik
- Plus d'informations
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- Biochemical diagnosis of tyrosine hydroxylase deficiency
- Ospedale Regionale per le Microcitemie
- Plus d'informations
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- Biochemical diagnosis of tyrosine hydroxylase deficiency
- CGMJM - Centro de Genética Médica Jacinto Magalhães
- Plus d'informations
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- Biochemical diagnosis of Segawa syndrome
- CGMJM - Centro de Genética Médica Jacinto Magalhães
- Plus d'informations
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- PAYS-BAS
- Gelderland
- NIJMEGEN
- Molecular and biochemical diagnosis of autosomal recessive dopa-responsive dystonia (TH gene; Analyte: tyrosine hydroxylase)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Plus d'informations
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- ESPAGNE
- Cataluña
- ESPLUGUES DE LLOBREGAT
- Biochemical and molecular diagnosis of autosomal recessive dopa-responsive dystonia (TH gene)
- Hospital Universitari Sant Joan de Déu
- Plus d'informations
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- ESPAGNE
- Cataluña
- ESPLUGUES DE LLOBREGAT
- Biochemical diagnosis of dystonia, dopa-responsive, autosomal recessive
- Hospital Universitari Sant Joan de Déu
- Plus d'informations
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- ALLEMAGNE
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of dopa-responsive dystonias (GCH1, TH, SPR genes)
- Hertie-Institut für klinische Hirnforschung
- Plus d'informations
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- Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
- Medizinische Universität Wien
- Plus d'informations
