Familial striatal degeneration: New mutation and neuroimaging clues-Reference-Cited by-同舟云学术

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Familial striatal degeneration: New mutation and neuroimaging clues

Published:2015-10-16 Issue:20 Volume:85 Page:1816-1818
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Barsottini Orlando Graziani Povoas,Martins Pedro de Miranda,Chien Hsin Fen,Raskin Salmo,Nunes Renato Hoffmann,da Rocha Antônio José,Pedroso José Luiz

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference7 articles.

1. Autosomal dominant striatal degeneration (ADSD): Clinical description and mapping to 5q13-5q14

2. Autosomal-Dominant Striatal Degeneration Is Caused by a Mutation in the Phosphodiesterase 8B Gene

3. Phosphodiesterases in neurodegenerative disorders

4. Excitotoxicity in Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion

5. The functional connectivity of the human caudate: An application of meta-analytic connectivity modeling with behavioral filtering

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1. A Novel PDE8B Gene Variant Associated with Autosomal Dominant Striatal Degeneration;Movement Disorders Clinical Practice;2024-05-31

2. Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update;Movement Disorders;2022-04-28

3. The Emerging Role of Phosphodiesterases in Movement Disorders;Movement Disorders;2021-06-21

4. Clinical overview and phenomenology of movement disorders;Principles and Practice of Movement Disorders;2021

5. Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disorders;Parkinsonism & Related Disorders;2019-12

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