Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.

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A Personalized Approach to Parkinson's Disease Patients Based on Founder Mutation Analysis Clinical Features of LRRK2 Carriers with Parkinson's Disease.

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Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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Greater improvement in LRRK2 G ...... ared to non-mutation carriers.

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Greater improvement in LRRK2 G ...... ared to non-mutation carriers.

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Greater improvement in LRRK2 G ...... ared to non-mutation carriers.

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Greater improvement in LRRK2 G ...... ared to non-mutation carriers.

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Greater improvement in LRRK2 G ...... ared to non-mutation carriers.

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Greater improvement in LRRK2 G ...... ared to non-mutation carriers.

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P1476

Greater improvement in LRRK2 G ...... ared to non-mutation carriers.

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P2093

Boualem Asselah

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Farida Ferrat

http://www.w3.org/2001/XMLSchema#string

Malika Chaouch

http://www.w3.org/2001/XMLSchema#string

Massiva Sayad

http://www.w3.org/2001/XMLSchema#string

Mohamed Bendini

http://www.w3.org/2001/XMLSchema#string

Mohamed Brahim Errahmani

http://www.w3.org/2001/XMLSchema#string

Mohamed Zouambia

http://www.w3.org/2001/XMLSchema#string

Mustapha Nebbal

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

Association between early-onset Parkinson's disease and mutations in the parkin gene

Deep brain stimulation surgical techniques.

Core assessment program for surgical interventional therapies in Parkinson's disease (CAPSIT-PD).

Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.

LRRK2 mutations in Parkinson's disease: confirmation of a gender effect in the Italian population

P2888

s12868-016-0240-4

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scholarly article

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10.1186/S12868-016-0240-4

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Alexis Brice

Suzanne Lesage

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2016-02-01T00:00:00Z

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1032775659

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26831335

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subthalamic nucleus

deep brain stimulation

P932

4736184

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Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.

about

P2860

P2860

Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.

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