Results 171 to 180 of about 502,314 (315)

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

Brain neuronal CG9593/ANGPTL4 activation mediates paternally acquired motor disorders. [PDF]

open access: yesSci Adv
Zhang J   +13 more
europepmc   +1 more source

Data-driven clustering of combined Functional Motor Disorders based on the Italian registry. [PDF]

open access: yesFront Neurol, 2022
Mostile G   +40 more
europepmc   +1 more source

Clinical neurophysiology of motor neuron diseases /

open access: yes, 2004
Includes bibliographical references and index.Print version record.Foreword. List of Contributors. 1. Overview (A. Eisen).I. Anatomy and Physiology of the Human Motor System. 2. Comparative anatomy of the motor system: differences in the organization of
Eisen, Andrew
core  

Aging Is a Key Driver for Adult Acute Myeloid Leukemia

open access: yesAging and Cancer, EarlyView.
Acute myeloid leukemia (AML) is a classical age‐related hematologic malignancy, and a key driver of AML is aging, which profoundly regulates intrinsic factors such as genomic instability, epigenetic reprogramming, and metabolic dysregulation, and alters bone marrow microenvironment.
Rong Yin, Haojian Zhang
wiley   +1 more source

Behavior of KCNQ Channels in Neural Plasticity and Motor Disorders. [PDF]

open access: yesMembranes (Basel), 2022
Singh SP, William M, Malavia M, Chu XP.
europepmc   +1 more source

Mutant NPM1 in Acute Myeloid Leukemia Initiation and Maintenance

open access: yesAging and Cancer, EarlyView.
NPM1 mutations drive acute myeloid leukemia by acting as neomorphic transcriptional regulators that cooperate with Menin–MLL and XPO1 to sustain HOX/MEIS1 expression and block differentiation. Targeting these mutant‐specific transcriptional dependencies provides a rational therapeutic strategy for NPM1‐mutated AML.
Yanan Jiang   +3 more
wiley   +1 more source

Clinical features of adolescent-onset functional motor disorders in tertiary movement disorders centers. [PDF]

open access: yesJ Neurol
Geroin C   +45 more
europepmc   +1 more source

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi   +2 more
wiley   +1 more source

Characterising alexithymia in individuals with functional motor disorders: a cross-sectional analysis of the Italian Registry of Functional Motor Disorders. [PDF]

open access: yesJ Neurol Neurosurg Psychiatry
Ostuzzi G   +32 more
europepmc   +1 more source

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