Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 8 (of 8 Records)

Query Trace: Syndrome and LRRK2[original query]
Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.
Neurology 2008 Feb 70 (7): 521-7.
Chen-Plotkin A S, Yuan W, Anderson C, McCarty Wood E, Hurtig H I, Clark C M, Miller B L, Lee V M-Y, Trojanowski J Q, Grossman M, Van Deerlin V
123I-MIBG cardiac uptake and smell identification in parkinsonian patients with LRRK2 mutations.
Journal of neurology 2011 1 258 (6): 1126-32.
Valldeoriola Francesc, Gaig Carles, Muxí Africa, Navales Ignacio, Paredes Pilar, Lomeña Francisco, De la Cerda Andres, Buongiorno Mariateresa, Ezquerra Mario, Santacruz Pilar, Martí Maria Jose, Tolosa Eduar
Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.
JAMA neurology 2013 Nov 70 (11): 1359-66.
Butcher Nancy J, Kiehl Tim-Rasmus, Hazrati Lili-Naz, Chow Eva W C, Rogaeva Ekaterina, Lang Anthony E, Bassett Anne
The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: clinical and demographic characteristics.
Neuroscience letters 2013 Jan .
Mabel GE, Virginia P, Paola CD, José PJ, Cecilia CM, Felix MM, Coro PR
Different Contributions of CDKAL1, KIF21B, and LRRK2/MUC19 Polymorphisms to SAPHO Syndrome, Rheumatoid Arthritis, Ankylosing Spondylitis, and Seronegative Spondyloarthropathy.
Genetic testing and molecular biomarkers 2016 Dec .
Li Nan, Ma Junfen, Li Kai, Guo Changlong, Ming Lia
High Frequency of GBA Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews.
JAMA neurology 2016 Oct .
Shiner Tamara, Mirelman Anat, Gana Weisz Mali, Bar-Shira Anat, Ash Elissa, Cialic Ron, Nevler Naomi, Gurevich Tanya, Bregman Noa, Orr-Urtreger Avi, Giladi N
Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism.
The Indian journal of medical research 2020 Jun 151 (6): 592-597.
Sadhukhan Dipanwita, Biswas Arindam, Bhaduri Arunima, Sarkar Neelanjana, Biswas Atanu, Das Shyamal K, Banerjee Tapas K, Ray Kunal, Ray Jhar
Metabolic syndrome does not influence the phenotype of LRRK2 and GBA related Parkinson's disease.
Scientific reports 2020 6 10 (1): 9329.
Thaler Avner, Shenhar-Tsarfaty Shani, Shaked Yanay, Gurevich Tanya, Omer Nurit, Bar-Shira Anat, Gana-Weisz Mali, Goldstein Orly, Kestenbaum Meir, Cedarbaum Jesse M, Orr-Urtreger Avi, Giladi Nir, Mirelman An
TOP