Results 91 to 100 of about 25,555 (216)
Awareness in Apraxia and Agnosia
Disconnected awareness in a diagonistic dyspraxic patient and degraded awareness in a visually agnosic patient were investigated. The first case was a male patient with disconnection syndrome including diagonistic dyspraxia. Speech regulation of interruptive actions in his left hand was introduced for the purpose of reorganization of bimanual activity.
openaire +3 more sources
Lesion network mapping of eye-opening apraxia
Apraxia of eyelid opening (or eye-opening apraxia) is characterized by the inability to voluntarily open the eyes because of impaired supranuclear control.
Pardis Zarifkar +11 more
core +1 more source
Apraxia verbal: una patología multidimensional [PDF]
Acquired apraxia of speech is an alteration of the production of speech that results of a cerebral wound. In the last ten years it has enlarged the interest by the description and understanding of its nature.
Melle Hernández, Natalia
core +1 more source
Unraveling a Diagnostic Enigma: A TECPR2 Case Solved Through Multi‐Omic Genomics
ABSTRACT TECPR2 is a key regulator of autophagy, encoded by the TECPR2 gene. Pathogenic variants in this gene have been linked to a rare hereditary sensory and autonomic neuropathy with intellectual disability (HSAN9). We report a teenage female with a syndromic intellectual disability disorder associated with neuromuscular abnormalities.
Teresa Zhao +123 more
wiley +1 more source
Background Gait apraxia, characterized by difficulties initiating and coordinating walking despite preserved conceptual movement abilities, is a distinct entity from lower limb apraxia.
Kota Igari +4 more
doaj +1 more source
Development of an oral apraxia diagnostic tool for 4-to-5-year-old children
Introduction: The majority of children with articulation disorders attending speech therapy centers typically don’t demonstrate the well-known pathologic signs of articulation disorders (such as oral structural abnormity, environmental deprivation ...
Naser Zareie shamsabadi +3 more
doaj +1 more source
The Clinical Spectrum of Ataxia with Oculomotor Apraxia Type 2 [PDF]
International audienceAtaxia with oculomotor apraxia type 2 (AOA2) is an inherited disorder caused by mutations within both alleles of the senataxin gene. First symptoms are usually recognized before the age of 30.
Brugger, Florian +18 more
core +1 more source
ABSTRACT Background Glutamate is the main excitatory neurotransmitter in the brain, and extracellular levels of glutamate and glycerol (a breakdown product of cell damage) increase after severe acute brain injury. Previous studies report that increased intracerebral glutamate—measured using cerebral microdialysis (CMD)—is associated with unfavorable ...
Trine Hjorslev Andreasen +7 more
wiley +1 more source
TOOL USE DISORDERS AFTER LEFT BRAIN DAMAGE
In this paper we review studies that investigated tool use disorders in left-brain damaged (LBD) patients over the last thirty years. Four tasks are classically used in the field of apraxia: Pantomime of tool use, single tool use, real tool use and ...
Josselin eBaumard +4 more
doaj +1 more source
Developmental stuttering with common and complex phenotypes
Abstract Aim To describe the phenotypic spectrum associated with stuttering. Method Individuals with current or resolved developmental stuttering self‐referred. Surveys assessed stuttering characteristics (onset, negative impact, family history) and health (early development, other conditions).
Sarah E. Horton +6 more
wiley +1 more source

