Results 161 to 170 of about 95,803 (361)

Luchoelmis : a new genus of Elmidae (Coleoptera) from Chile and Argentina [PDF]

open access: yes, 2002
Luchoelmis New Genus is described with four new species: aequalis, magallanensis, and penai from Chile and cekalovici from Argentina and Chile. Luchoelmis penai is designated as the type species of the genus.
Spangler, P. J., Staines, Charles L.
core  

Association of Corticospinal Tract Asymmetry With Ambulatory Ability After Intracerebral Hemorrhage

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Ambulatory ability after intracerebral hemorrhage (ICH) is important to patients. We tested whether asymmetry between ipsi‐ and contra‐lesional corticospinal tracts (CSTs) assessed by diffusion tensor imaging (DTI) is associated with post‐ICH ambulation.
Yasmin N. Aziz   +25 more
wiley   +1 more source

Sense-checking the approach to quantitative sensory testing to detect chemotherapy-induced peripheral neuropathy. [PDF]

open access: yesPLoS One
Dujmović M   +15 more
europepmc   +2 more sources

Functional Connectivity Linked to Cognitive Recovery After Minor Stroke

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Patients with minor stroke exhibit slowed processing speed and generalized alterations in functional connectivity involving frontoparietal cortex (FPC). The pattern of connectivity evolves over time. In this study, we examine the relationship of functional connectivity patterns to cognitive performance, to determine ...
Vrishab Commuri   +7 more
wiley   +1 more source

Chondroid Syringoma of Dorsum of the Nose

open access: yesBengal Journal of Otolaryngology and Head Neck Surgery, 2018
IntroductionChondroid syrigomas are rare, usually benign tumors occurring predominantly in the head and neck area. These are also known as mixed tumors of skin.
Netra Aniruddha Pathak   +2 more
doaj  

Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian   +9 more
wiley   +1 more source

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