Early-onset pathologically proven multiple system atrophy with LRRK2 G2019S mutation

被引：16

作者：

Riboldi, Giulietta Maria ^{[1
]}

Palma, Jose-Alberto ^{[2
]}

Cortes, Etty ^{[3
]}

Iida, Megan A. ^{[3
,4
]}

Sikder, Tamjeed ^{[3
,4
]}

Henderson, Brooklyn ^{[1
]}

Raj, Towfique ^{[4
,5
]}

Walker, Ruth H. ^{[6
,7
]}

Crary, John F. ^{[3
,4
]}

Kaufmann, Horacio ^{[2
]}

Frucht, Steven ^{[1
]}

机构：

[1] NYU, Sch Med, Dept Neurol, Fresco Inst Parkinsons & Movement Disorders, New York, NY USA

[2] NYU, Sch Med, Dept Neurol, Dysauton Ctr, New York, NY USA

[3] Icahn Sch Med Mt Sinai, Dept Pathol, New York, NY 10029 USA

[4] Icahn Sch Med Mt Sinai, Ronald M Loeb Ctr Alzheimers Dis, Friedman Brain Inst, Fishberg Dept Neurosci, New York, NY 10029 USA

[5] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA

[6] James J Peters Vet Affairs Med Ctr, Bronx, NY USA

[7] Icahn Sch Med Mt Sinai, Dept Neurol, New York, NY 10029 USA

来源：

MOVEMENT DISORDERS | 2019年 / 34卷 / 07期

基金：

美国国家卫生研究院;

关键词：

PARKINSONS-DISEASE; RISK; PENETRANCE; VARIANTS;

D O I：

10.1002/mds.27710

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：1080 / 1082

页数：3

共 50 条

[21] Unilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation
Munhoz, R.
Teive, H.
Francisco, A.
PARKINSONISM & RELATED DISORDERS, 2007, 13 : S172 - S172
[22] Unilateral Pallidotomy in a Patient with Parkinsonism and G2019S LRRK2 Mutation
Munhoz, Renato P.
Teive, Helio A.
Francisco, Alexandre N.
Rogaeva, Ekaterina
MOVEMENT DISORDERS, 2009, 24 (05) : 791 - 792
[23] Gait Alterations in Healthy Carriers of the LRRK2 G2019S Mutation
Mirelman, Anat
Gurevich, Tanya
Giladi, Nir
Bar-Shira, Anat
Orr-Urtreger, Avi
Hausdorff, Jeffrey M.
ANNALS OF NEUROLOGY, 2011, 69 (01) : 193 - 197
[24] Clinical findings in presymptomatic LRRK2 G2019S mutation carriers
Aasly, J. O.
MOVEMENT DISORDERS, 2006, 21 : S497 - S498
[25] Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease
Lesage, Suzanne
Leclere, Laurence
Lohmann, Ebba
Borg, Michel
Ruberg, Merle
Duerr, Alexandra
Brice, Alexis
NEURODEGENERATIVE DISEASES, 2007, 4 (2-3) : 195 - 198
[26] LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease
Infante, J
Rodríguez, E
Combarros, O
Mateo, I
Fontalba, A
Pascual, J
Oterino, A
Polo, JM
Leno, C
Berciano, J
NEUROSCIENCE LETTERS, 2006, 395 (03) : 224 - 226
[27] Frequency of the LRRK2 G2019S mutation in late-onset sporadic patients with Parkinson's disease
Chien, Hsin Fen
Figueiredo, Tamires Rocha
Hollaender, Marianna Almeida
Tofoli, Fabiano
Takada, Leonel Tadao
Pereira, Lygia do Veiga
Barbosa, Egberto Reis
ARQUIVOS DE NEURO-PSIQUIATRIA, 2014, 72 (05) : 356 - 359
[28] Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2
Mortiboys, Heather
Johansen, Krisztina K.
Aasly, Jan O.
Bandmann, Oliver
NEUROLOGY, 2010, 75 (22) : 2017 - 2020
[29] Behavioral characteristics of asymptomatic G2019S mutation carriers of the LRRK2 gene
Thaler, A.
Mirelman, A.
Yasinovski, K.
Zalis, M.
Shkedy, A.
Hilel, A.
Marder, K.
Bressman, S.
Orr-Urtreger, A.
Gurevich, T.
Giladi, N.
MOVEMENT DISORDERS, 2013, 28 : S399 - S399
[30] Is the G2019S LRRK2 mutation common in all southern European populations?
Papapetropoulos, Spiridon
Adi, Nikhil
Shehadeh, Lina
Bishopric, Nanette
Singer, Carlos
Argyriou, Andreas A.
Chroni, Elizabeth
JOURNAL OF CLINICAL NEUROSCIENCE, 2008, 15 (09) : 1027 - 1030

← 1 2 3 4 5 →