Results 211 to 220 of about 37,346 (289)
Normal Gain with Corrective Saccades in the Video Head Impulse Test: Clinical Implications and Diagnostic Considerations. [PDF]
Choe G, Kim CH, Lee DH.
europepmc +1 more source
Abstract Opioids are prescribed widely for chronic pain despite well‐recognised risks and variable long‐term benefit, reflecting the lack of effective alternatives for many patients. Combination therapies offer a promising strategy to enhance efficacy whilst reducing side effects.
André Mouraux +26 more
wiley +1 more source
Quantifying cortex-wide traveling brain waves of complex patterns with a graph-based algorithm. [PDF]
Ho KT, Onoe H, Isa T, Chen CY.
europepmc +1 more source
Early Visual Development in Albinism
ABSTRACT Background Visual system development is incomplete at birth, and while fixation and tracking usually emerge within the first weeks of life, some infants show delayed visual development (DVDev). This is frequently observed in infants with albinism, yet the timing of visual attentiveness and subsequent visual acuity development remains unclear ...
Catelijne Maria Neijzen +6 more
wiley +1 more source
In pursuit of saccade awareness: Limited volitional control and minimal conscious access to catch-up saccades during smooth pursuit eye movements. [PDF]
Klanke JN, Ohl S, Esen AN, Rolfs M.
europepmc +1 more source
ABSTRACT A hive of recent policy and legislative activity in Australian family law has emphasized the importance of children's right to participate in decision‐making following parental separation. Yet a powerful tension persists between supporting children's right to participation and protecting children from parental conflict.
Georgina Dimopoulos +3 more
wiley +1 more source
A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy
PIP5K1C‐related lethal congenital contracture syndrome with hyperinsulinism and optic atrophy. ABSTRACT Lethal congenital contracture syndrome 3 (LCCS3, MIM #611369) is a rare autosomal recessive neuromuscular disorder caused by biallelic loss‐of‐function (LOF) variants in PIP5K1C, reported in only two families to date.
Tameemi Abdalla Moady +3 more
wiley +1 more source

