Results 151 to 160 of about 1,027,501 (383)
Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy
S. Bodine +15 more
semanticscholar +1 more source
ABSTRACT Pathogenic variants in KIF1C cause Spastic Paraplegia 58 (SPG58), typically presenting with cerebellar ataxia and spastic paraparesis. We report two unrelated patients with spastic paraparesis, cerebellar ataxia, and tremor. Whole‐exome sequence analysis identified novel homozygous variants in the motor domain of KIF1C (NM_006612.6): c.921G>A (
Akihiko Mitsutake +12 more
wiley +1 more source
Background and Objectives: One of the major problems during aging is sarcopenia, which one of its important involved mechanisms is loss of motor neurons.
Zeinab Sadat Geramian +3 more
doaj
JoAnn V, Pinkerton, Richard J, Santen
openaire +2 more sources
Identification and characterization of a spinal muscular atrophy-determining gene
S. Lefebvre +15 more
semanticscholar +1 more source
Discriminating α-synuclein strains in Parkinson’s disease and multiple system atrophy
M. Shahnawaz +14 more
semanticscholar +1 more source
Chapter Five. Systematic review results by biomarker classifications [PDF]
5.1 Markers of Absorption and Permeability Overview 5.2 Markers of Absorption 5.3 Markers of Permeability 5.4 Markers of Digestion 5.5 Markers of Intestinal Inflammation and Intestinal Immune Activation 5.6 Markers of Systemic Inflammation and Systemic ...
Denno, Donna M +4 more
core +1 more source
ABSTRACT Objective This study aims to identify both fluid and neuroimaging biomarkers for CSF1R‐RD that can inform the optimal timing of treatment administration to maximize therapeutic benefit, while also providing sensitive quantitative measurements to monitor disease progression.
Tomasz Chmiela +13 more
wiley +1 more source
Second consensus statement on the diagnosis of multiple system atrophy
S. Gilman +19 more
semanticscholar +1 more source

