Results 81 to 90 of about 671,192 (298)
Long‐Term Follow‐Up of Chemotherapy‐Associated Biological Aging in Women With Early Breast Cancer
Aging and Cancer, EarlyView.Women threated with adjuvant chemotherapy for early breast cancer have sustained long‐term increase in p16INK4a,, a robust marker of cell senescence, suggesting a chemotherapy‐associated age acceleration. p16INK4a as well as other biomarkers may identify patients at greatest risk for senescence‐related diseases of aging.
Hyman B. Muss +12 more
wiley +1 more source
Κατάγματα βάσεως πρώτου μετακαρπίου (κατάγματα Bennett) θεραπευμένα με κλειστή ανάταξη και σταθεροποίηση με βελόνες Kirschner: αποτελέσματα μετά 16-25 έτη [PDF]
Epistīmonika Chronika, 2017 Το κάταγμα Bennett είναι το κάταγμα-εξάρθρημα της βάσης του πρώτου μετακαρπίου, που προκαλείται από βία αξονικής συμπίεσης αυτού ενώ βρίσκεται σε ελαφρά κάμψη. Υπάρχουν διαφορετικοί τρόποι αντιμετώπισης.
Α. Ακριώτης +3 more
doaj
Annals 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
Fluid Biomarkers of Disease Burden and Cognitive Dysfunction in Progressive Supranuclear Palsy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Identifying objective biomarkers for progressive supranuclear palsy (PSP) is crucial to improving diagnosis and establishing clinical trial and treatment endpoints. This study evaluated fluid biomarkers in PSP versus controls and their associations with regional 18F‐PI‐2620 tau‐PET, clinical, and cognitive outcomes.
Roxane Dilcher +10 more
wiley +1 more source
MATEC Web of Conferences, 2016 In this study, 60 wt% Ce0.8Sm0.2O2–δ–Ba0.95La0.05Zr0.1Fe0.9–xCoxO3–δ (SDC–BLZFC, x = 0–0.4) dual–phase oxygen transport membranes were prepared by a combined EDTA–citrate complexing sol–gol method. The effects of partial substitution of iron by cobalt on
Wang Pengfei +5 more
doaj +1 more source
Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM
Annals of Clinical and Translational Neurology, EarlyView.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
Annals of Clinical and Translational Neurology, EarlyView.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
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To explore how cerebral hypoxia and Normal‐Appearing White Matter (NAWM) integrity affect MS lesion burden and clinical course. Methods Seventy‐nine MS patients, including 13 clinically isolated syndrome (CIS) patients and 66 relapsing–remitting multiple sclerosis (RRMS) patients, and 44 healthy controls (HCs) were recruited from ...
Xinli Wang +8 more
wiley +1 more source
2 επιστολές της Ευανθίας Δ. Κουρτζή σ τη Μυρσινιώ Κουρτζή
, 1909 Πρόκειται για 2 επιστολές της Ευανθίας Δ. Κουρτζή προς τη Μυρσινιώ Κουρτζή σχετικά με το προξενιό της Λιόλιας Κούππα με τον Μίτσα Κουρτζή.Το τεκμήριο βρίσκεται σε καλή ...
Κουρτζή, Ευανθία Δ.
core
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
Annals of Clinical and Translational Neurology, EarlyView.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