Results 171 to 180 of about 2,784,272 (345)

Interleukin‐6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini   +13 more
wiley   +1 more source

Correlation Between COVID-19 Recovery, Executive Function Decline, and Emotional State. [PDF]

open access: yesPsychol Res Behav Manag
Velásquez Cabrera DM   +4 more
europepmc   +1 more source

Cortical reorganization but no recovery of visual function following an optic nerve injury in mice

open access: gold, 2018
Jacqueline Higgins   +6 more
openalex   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas   +18 more
wiley   +1 more source

Physical rehabilitation approaches for the recovery of function and mobility following stroke. [PDF]

open access: yesCochrane Database Syst Rev
Todhunter-Brown A   +9 more
europepmc   +1 more source

Recovery of Parathyroid Hormone Secretion and Function in Postoperative Hypoparathyroidism: A Case Series [PDF]

open access: bronze, 2013
Natalie E. Cusano   +7 more
openalex   +1 more source

A Comprehensive Overview of the Clinical, Electrophysiological, and Neuroimaging Features of BPAN: Insights From a New Case Series

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Neurodegeneration with brain iron accumulation (NBIA) comprises a genetically and clinically heterogeneous group of rare neurological disorders characterized particularly by iron accumulation in the basal ganglia. To date, 15 genes have been associated with NBIA.
Seda Susgun   +95 more
wiley   +1 more source

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