Results 171 to 180 of about 925,078 (312)

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

Elevated autistic features in Parkinson's disease and other motor disorders. [PDF]

open access: yesAutism
Dey I   +6 more
europepmc   +1 more source

Similar Cognitive Skill Impairment in Children with Upper Limb Motor Disorders Due to Arthrogryposis Multiplex Congenita and Obstetrical Brachial Plexus Palsy. [PDF]

open access: yesInt J Environ Res Public Health, 2023
Blagovechtchenski E   +7 more
europepmc   +1 more source

The MMP‐9/TIMP‐1 Ratio and Concentrations of Osteopontin Are Elevated in Cerebrospinal Fluid of People With Multiple Sclerosis and Decrease After Autologous Hematopoietic Stem Cell Transplantation

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives To evaluate the utility of cerebrospinal fluid (CSF) biomarkers—matrix metalloproteinase‐9 (MMP‐9), tissue inhibitor of metalloproteinases‐1 (TIMP‐1), the MMP‐9/TIMP‐1 ratio, and osteopontin (OPN)—as indicators of blood–brain barrier (BBB) integrity and disease activity in people with relapsing–remitting multiple sclerosis (pwMS ...
Ivan Pavlovic   +6 more
wiley   +1 more source

Response to Fortin-Bédard et al. “User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study”

open access: yesNeurological Research and Practice
Susanne Spittel   +18 more
doaj   +1 more source

Aberrant Auditory and Visual Memory Development of Children with Upper Limb Motor Disorders. [PDF]

open access: yesBrain Sci, 2021
Koriakina M   +13 more
europepmc   +1 more source

Copy Number Variants and Their Association With Intracerebral Hemorrhage Risk: A Case–Control Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Intracerebral Hemorrhage (ICH) is a leading cause of morbidity and mortality worldwide and lacks effective therapeutic interventions. Despite previous studies, the genetic underpinnings of ICH remain poorly understood. We sought to investigate the role of copy number variants (CNVs) in ICH pathophysiology to identify novel ...
Savvina Prapiadou   +12 more
wiley   +1 more source

The Complex Pathway of Conventional Investigations before the Diagnosis of Functional Motor Disorders. [PDF]

open access: yesMov Disord Clin Pract
Ercoli T   +43 more
europepmc   +1 more source

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