Movement Disorders (revue)

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Eléments de l'association

Australie237
Dominic B. Rowe4
Australie Sauf Dominic B. Rowe" 233
Dominic B. Rowe Sauf Australie" 0
Australie Et Dominic B. Rowe 4
Australie Ou Dominic B. Rowe 237
Corpus5903
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List of bibliographic references

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000023 Ainhi D. Ha [Australie] ; Kaitlyn L. Parratt [Australie] ; Nanna D. Rendtorff [Danemark] ; Marianne Lodahl [Danemark] ; Karl Ng [Australie] ; Dominic B. Rowe [Australie] ; Carolyn M. Sue [Australie] ; Michael W. Hayes [Australie] ; Lisbeth Tranebjaerg [Danemark] ; Victor S. C. Fung [Australie]The Phenotypic Spectrum of Dystonia in Mohr-Tranebjaerg Syndrome
000E08 Prachi Mehta [Australie] ; George D. Mellick [Australie] ; Dominic B. Rowe [Australie] ; Glenda M. Halliday [Australie] ; Michael M. Jones [Australie] ; Neil Manwaring [Australie] ; Himesha Vandebona [Australie] ; Peter A. Silbum [Australie] ; JIE JIN WANG [Australie] ; Paul Mitchell [Australie] ; Carolyn M. Sue [Australie]Mitochondrial DNA Haplogroups J and K are not Protective for Parkinson's Disease in the Australian Community
000F11 Greg T. Sutherland [Australie] ; Glenda M. Halliday [Australie] ; Peter A. Silburn [Australie] ; Frank L. Mastaglia [Australie] ; Dominic B. Rowe [Australie] ; Richard S. Boyle [Australie] ; John D. O'Sullivan [Australie] ; Tina Ly [Australie] ; Steve D. Wilton [Australie] ; George D. Mellick [Australie]Do Polymorphisms in the Familial Parkinsonism Genes Contribute to Risk for Sporadic Parkinson's Disease?
001522 YUE HUANG [Australie] ; Glenda M. Halliday [Australie] ; Himesha Vandebona [Australie] ; George D. Mellick [Australie] ; Frank Mastaglia [Australie] ; Julia Stevens [Australie] ; John Kwok [Australie] ; Michael Garlepp [Australie] ; Peter A. Silburn [Australie] ; Malcolm K. Horne [Australie] ; Katya Kotschet [Australie] ; Alison Venn [Australie] ; Dominic B. Rowe [Australie] ; Justin P. Rubio [Australie] ; Carolyn M. Sue [Australie]Prevalence and clinical features of common LRRK2 mutations in australians with Parkinson's disease

Wicri

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