MovDisordV3, Main, Curation, bibRecord, 001797

Atypical juvenile parkinsonism in a consanguineous SPG15 family

Identifieur interne : 001797 ( Main/Curation ); précédent : 001796; suivant : 001798

Atypical juvenile parkinsonism in a consanguineous SPG15 family

Auteurs : Julia Schicks [Allemagne] ; Matthis Synofzik [Allemagne] ; Hjörvar Pétursson [Allemagne] ; Johanna Huttenlocher [Allemagne] ; Matthias Reimold [Allemagne] ; Ludger Schöls [Allemagne] ; Peter Bauer [Allemagne]

Source :

Movement Disorders [ 0885-3185 ] ; 2011-02-15.

RBID : ISTEX:C0F056949BD406B26F1675C9E0FF95222ED92CE7

Descripteurs français

Pascal (Inist)
- Parkinsonisme, Pathologie du système nerveux.

English descriptors

KwdEn :
- Adult, Carrier Proteins (genetics), Consanguinity, Family Health, Fluorine Radioisotopes (diagnostic use), Humans, Magnetic Resonance Imaging (methods), Nervous system diseases, Parkinsonian Disorders (genetics), Parkinsonian Disorders (radionuclide imaging), Parkinsonism, Tomography, Emission-Computed, Single-Photon, Tropanes (diagnostic use), Young Adult.
MESH :
- chemical , diagnostic use : Fluorine Radioisotopes, Tropanes.
- chemical , genetics : Carrier Proteins.
- genetics : Parkinsonian Disorders.
- methods : Magnetic Resonance Imaging.
- radionuclide imaging : Parkinsonian Disorders.
- Adult, Consanguinity, Family Health, Humans, Tomography, Emission-Computed, Single-Photon, Young Adult.

Url:

https://api.istex.fr/document/C0F056949BD406B26F1675C9E0FF95222ED92CE7/fulltext/pdf

DOI: 10.1002/mds.23472

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ISTEX:C0F056949BD406B26F1675C9E0FF95222ED92CE7

Le document en format XML

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	Movement Disorders (revue)
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Movement Disorders (revue)

Atypical juvenile parkinsonism in a consanguineous SPG15 family

Atypical juvenile parkinsonism in a consanguineous SPG15 family

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