MultiPark: Multidisciplinary research focused on Parkinson´s disease
3281 – 3290 of 3882
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2012
-
Mark
Factitious disorder by proxy in the diagnosis of frontotemporal dementia
2012) International Conference on Frontotemporal Dementias, 2012 In Dementia and Geriatric Cognitive Disorders 33(Supplement 1). p.209-209(
- Contribution to journal › Published meeting abstract
-
Mark
Cometin is a novel neurotrophic factor that promotes neurite outgrowth and neuroblast migration in vitro and supports survival of spiral ganglion neurons in vivo
(
- Contribution to journal › Article
-
Mark
Cerebrospinal Fluid Neurofilament Levels in Neuropathological Subtypes of Frontotemporal Dementia - a Pilot Study
2012) International Conference on Frontotemporal Dementias, 2012 In Dementia and Geriatric Cognitive Disorders 33(Supplement 1). p.101-102(
- Contribution to journal › Published meeting abstract
-
Mark
Progranulin Bridges Energy Homeostasis and Fronto-Temporal Dementia
(
- Contribution to journal › Letter
-
Mark
Inhibition of Microglial Activation Protects Hippocampal Neurogenesis and Improves Cognitive Deficits in a Transgenic Mouse Model for Alzheimer's Disease
(
- Contribution to journal › Article
-
Mark
Psychometric properties of a Swedish version of the Pearlin Mastery Scale in people with mental illness and healthy people.
(
- Contribution to journal › Article
-
Mark
Optimizing nanovial outlet designs for improved solid-phase extraction in the integrated selective enrichment target-ISET.
(
- Contribution to journal › Article
-
Mark
A Pilot Study Examining Associations between DYRK1A and alpha-Synuclein Dementias
(
- Contribution to journal › Article
-
Mark
RNA and DNA Association to Zwitterionic and Charged Monolayers at the Air-Liquid Interface
(
- Contribution to journal › Article
-
Mark
First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutation.
(
- Contribution to journal › Article