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Serveur d'exploration autour de Joseph Jankovic - Curation (Ncbi)

Index « Keywords » - entrée « DNA Mutational Analysis »
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DNA Methylation (genetics) < DNA Mutational Analysis < DNA Mutational Analysis (methods)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 14.
Ident.Authors (with country if any)Title
000052 (2003) Wei Le [États-Unis] ; Pingyi Xu ; Joseph Jankovic [États-Unis] ; Hong Jiang ; Stanley. Appel ; Roy. Smith ; Demetrios. VassilatisMutations in NR4A2 associated with familial Parkinson disease.
000078 (2004) Hao Deng ; Weidong Le ; Joseph Jankovic [États-Unis]Premutation alleles associated with Parkinson disease and essential tremor.
000091 (2005) H. Deng [États-Unis] ; W Le ; X. Zhang ; T Pan ; Joseph Jankovic [États-Unis]G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients.
000099 (2005) H. Deng [États-Unis] ; W Le ; Y. Guo ; M Huang ; W Xie ; Joseph Jankovic [États-Unis]Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease.
000108 (2006) Hao Deng [États-Unis] ; Wei Le ; Christine. Hunter ; William. Ondo ; Yi Guo ; Wen Xie ; Joseph Jankovic [États-Unis]Heterogeneous phenotype in a family with compound heterozygous parkin gene mutations.
000130 (2007) Lianna Ishihara [Royaume-Uni] ; Rachel. Gibson ; Liling Warren ; Rim Amouri ; Kelly Lyons ; Catherine Wielinski ; Christine Hunter ; Jina. Swartz ; Ramu Elango ; P Akkari ; David Leppert ; Linda Surh ; Kevin. Reeves ; Siwan Thomas ; Leigh Ragone ; Nobutaka Hattori ; Rajesh Pahwa ; Joseph Jankovic [États-Unis] ; Martha Nance ; Alan Freeman ; Neziha Gouider ; Mounir Kefi ; Mourad Zouari ; Samia Ben ; Samia Ben ; Ghada El ; Lefkos Middleton ; David. Burn ; Ray. Watts ; Faycal HentatiScreening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.
000137 (2007) Hao Deng [États-Unis] ; Wei Le ; Christine. Hunter ; Nicte Mejia ; Wen Xie ; Joseph Jankovic [États-Unis]A family with Parkinson disease, essential tremor, bell palsy, and parkin mutations.
000143 (2007) Hao Deng [États-Unis] ; Weidong Le ; Maosheng Huang ; Wenjie Xie ; Tianghong Pan ; Joseph Jankovic [États-Unis]Genetic analysis of LRRK2 P755L variant in Caucasian patients with Parkinson's disease.
000163 (2008) Hao Deng [États-Unis] ; Weidong Le ; Joohi Shahed ; Wenjie Xie ; Joseph Jankovic [États-Unis]Mutation analysis of the parkin and PINK1 genes in American Caucasian early-onset Parkinson disease families.
000218 (2009) W Nichols ; D Kissell ; N. Pankratz ; M Pauciulo ; V Elsaesser ; K Clark ; C Halter ; A. Rudolph ; J. Wojcieszek ; R Pfeiffer ; T. ForoudVariation in GIGYF2 is not associated with Parkinson disease
000242 (2009) N. Pankratz ; D Kissell ; M Pauciulo ; C Halter ; A. Rudolph ; R Pfeiffer ; K Marder ; T. Foroud ; W NicholsParkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations
000396 (2013) Marina. Svetel [Serbie] ; Gordana Djuric ; Ivana Novakovic ; Valerija Dobricic ; Elka Stefanova ; Nikola Kresojevic ; Aleksandra Tomic ; Milena Jankovic ; Igor Petrovic ; Tatjana Pekmezovic ; Vladimir. KosticA common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia.
000496 (2015) Milena. Jankovi [Serbie] ; Nikola. Kresojevi [Serbie] ; Valerija. Dobri [Serbie] ; Vladana. Markovi [Serbie] ; Igor. Petrovi [Serbie] ; Ivana. Novakovi [Serbie] ; Vladimir. Kosti [Serbie]Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population.
000632 (1998) W Wang [États-Unis] ; M. Khajavi ; B Patel ; J. Beach ; Joseph Jankovic [États-Unis] ; T. AshizawaThe G209A mutation in the alpha-synuclein gene is not detected in familial cases of Parkinson disease in non-Greek and/or Italian populations.

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