Results 51 to 60 of about 1,039,444 (298)

Lateral Preferences and Cerebral Speech Dominance

open access: yesCortex, 1983
Four types of lateral preference (hand, foot, eye, ear) were measured in 73 patients, who underwent sodium Amytal speech testing. In 63 cases, speech was on the left side whereas in 10, speech was on the right. All of the patients with right hemisphere lesions had speech represented in the left hemisphere.
E, Strauss, J, Wada
openaire   +2 more sources

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

Sex and lateral dominance effects on learning a complex gymnastic skill

open access: yesPhysical Education of Students
Background and Study Aim. The development of motor skills is influenced by various biological and biomechanical factors. Among these, sex-based characteristics and lateral dominance are known to shape movement strategies and performance outcomes. Despite
Sunčica Delaš Kalinski   +2 more
doaj   +1 more source

The Queen of the Paper Wasp Polistes jokahamae (Vespidae: Polistinae) Is Not Aggressive but Maintains Her Reproductive Priority

open access: yesSociobiology, 2019
The behaviors performed on the nest by the foundress queen and workers of the paper wasp Polistes jokahamae were observed in three colonies in the field and one colony in a cage set in the field.
Hideto Yoshimura   +2 more
doaj   +1 more source

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach   +23 more
wiley   +1 more source

Dominance learning in diploid genetic algorithms for dynamic optimization problems [PDF]

open access: yes, 2006
Copyright @ 2006 YangThis paper proposes an adaptive dominance mechanism for diploidy genetic algorithms in dynamic environments. In this scheme, the genotype to phenotype mapping in each gene locus is controlled by a dominance probability, which is ...
Yang, S   +2 more
core   +1 more source

Spatial and Volumetric Characteristics of Glioblastoma: Associations With Clinical Presentation and Survival

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aim to comprehensively analyze how regional tumor and edema characteristics are associated with clinical presentations and survival outcomes in a large cohort of glioblastoma patients. Methods Patients with IDH‐wildtype glioblastoma who received brain MRI from 2010 to 2023 were included.
Daniel J. Zhou   +16 more
wiley   +1 more source

TESTING FOR RESTRICTED STOCHASTIC DOMINANCE [PDF]

open access: yes
Asymptotic and bootstrap tests are studied for testing whether there is a relation of stochastic dominance between two distributions. These tests have a null hypothesis of nondominance, with the advantage that, if this null is rejected, then all that is ...
Jean-Yves Duclos, Russell Davidson
core   +2 more sources

Evaluation of Digital Technologies for Home‐Based Assessment in People With Amyotrophic Lateral Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Digital technologies hold promise for transforming healthcare by enhancing personalized treatments and offer valuable opportunities to improve patient care. Here, we evaluated several novel, self‐administered, home‐based, digital endpoints for their association with corresponding conventional standard clinical measures (primary) in ...
Arne Mueller   +14 more
wiley   +1 more source

Autosomal dominant juvenile amyotrophic lateral sclerosis [PDF]

open access: yesBrain, 1999
Juvenile amyotrophic lateral sclerosis (ALS) is a form of chronic motor neuron disease characterized by combined upper and lower motor neuron symptoms and signs with onset prior to age 25 years. We report the clinical and electrodiagnostic findings in 49 affected family members and neuropathological findings from two autopsies of a Maryland kindred ...
B A, Rabin   +5 more
openaire   +2 more sources

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