| Rossi PI, Vaccari CM, Terracciano A, et al.
The metabotropic glutamate receptor 1, GRM1: evaluation as a candidate gene for inherited forms of cerebellar ataxia. [JOURNAL ARTICLE]
J Neurol 2009 Nov 19.
Abstract | Full Citation | | Hartung HP, Aktas O, Kieseier B, et al.
Development of oral cladribine for the treatment of multiple sclerosis. [JOURNAL ARTICLE]
J Neurol 2009 Nov 18.
Abstract | Full Citation | | Jongen PJ, Sindic C, Carton H, et al.
Improvement of health-related quality of life in relapsing remitting multiple sclerosis patients after 2 years of treatment with intramuscular interferon-beta-1a. [JOURNAL ARTICLE]
J Neurol 2009 Nov 18.
Abstract | Full Citation | | Romito LM, Contarino FM, Albanese A
Transient gender-related effects in Parkinson's disease patients with subthalamic stimulation. [JOURNAL ARTICLE]
J Neurol 2009 Nov 18.
Abstract | Full Citation | Find Related Articles | | Scheurich A, Urban PP, Koch-Khoury N, et al.
CSF phospho-tau is independent of age, cognitive status and gender of neurological patients. [JOURNAL ARTICLE]
J Neurol 2009 Nov 17.
Abstract | Full Citation | Find Related Articles | | Strupp M
Parkinson's disease I: glucocerebrosidase mutations, family history of melanoma and questionable effects of rasagiline. [JOURNAL ARTICLE]
J Neurol 2009 Nov 17.
Full Citation | Find Related Articles | | Wittstock M, Grossmann A, Kunesch E, et al.
Altered callosal function in cerebral microangiopathy. [JOURNAL ARTICLE]
J Neurol 2009 Nov 16.
Abstract | Full Citation | Find Related Articles | | Resnick AS, Foote KD, Rodriguez RL, et al.
Erratum to: The number and nature of emergency department encounters in patients with deep brain stimulators. [JOURNAL ARTICLE]
J Neurol 2009 Nov 14.
Full Citation | Publisher Full Text | Find Related Articles | | Kambe T, Motoi Y, Ishii K, et al.
Posterior cortical atrophy with [(11)C] Pittsburgh compound B accumulation in the primary visual cortex. [JOURNAL ARTICLE]
J Neurol 2009 Nov 14.
Full Citation | Find Related Articles | | Pollazzon M, Suominen T, Penttilä S, et al.
The first Italian family with tibial muscular dystrophy caused by a novel titin mutation. [JOURNAL ARTICLE]
J Neurol 2009 Nov 13.
Abstract | Full Citation |   |
|
| | Enter
www.unboundmedicine.com/medline
in your iPhone browser
or View our
Unbound MEDLINE
iPhone demo
Advertise on this site.
|
