Autologous fat grafting in a case of Parry-Romberg syndrome: a case report. [PDF]
Sarda B, Nere S, Madke B, Singh A.
europepmc +1 more source
ABSTRACT Objective Cognitive decline is a disabling and variable feature of Parkinson disease (PD). While cholinergic system degeneration is linked to cognitive impairments in PD, most prior research reported cross‐sectional associations. We aimed to fill this gap by investigating whether baseline regional cerebral vesicular acetylcholine transporter ...
Taylor Brown +6 more
wiley +1 more source
Dental Effects of Discordant Thumb-Sucking in Monozygotic Twins: A Case Report. [PDF]
Brunstein K, Hu E, Shute J.
europepmc +1 more source
Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina +11 more
wiley +1 more source
Sex-specific alterations of cerebral blood flow in subjective tinnitus patients: an arterial spin labeling study. [PDF]
Zhang Y, Zhao Y, Luan J, Ma G, Han H.
europepmc +1 more source
ABSTRACT Background Emerging evidence suggests that low‐frequency neural oscillations are dynamically regulated by consciousness levels, with the recovery of low cortical activity potentially serving as a neurophysiological substrate for conscious emergence. Targeted enhancement of these low‐frequency rhythms in patients with disorders of consciousness
Chuan Xu +10 more
wiley +1 more source
The characteristics of lower extremity muscle activity and static balance of Chinese elite trampoline athletes during net contact phase. [PDF]
Liu K, Zhu Z, Yang T, Yin J.
europepmc +1 more source
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
Educational rights: twenty-five years of constitutional experience
Ángel J. Gómez Montoro.
doaj +1 more source
Advancing Climate Mitigation, Adaptation, and Equity Simultaneously: The Transformative Potential of Investments in Gender Equality. [PDF]
Heymann J +3 more
europepmc +1 more source

