Results 61 to 70 of about 79,532 (296)
Therapeutic Apheresis and Dialysis, EarlyView.ABSTRACT Background Maintenance hemodialysis (MHD) patients frequently suffer from frailty, characterized by reduced physical function and poor prognosis. Myokines, such as myonectin, secreted by muscle, are emerging regulators of systemic health. This study investigated the relationship between serum myonectin, adipokines (adiponectin, omentin), and ...
Kenichi Kono +7 more
wiley +1 more source
Non-syndromic sagittal synostosis [PDF]
, 2015 Non-syndromic sagittal synostosis.
Darvann, Tron A +5 more
core
Journal of Pharmacy and Bioallied Sciences, 2023 Facial development involves an intricate regulatory mechanism that accounts for numerous craniofacial abnormalities, common being orofacial clefts. Although cleft in the secondary palate accounts for one-third of orofacial clefts stills remains an under ...
Prathibha Prasad +6 more
doaj +1 more source
Therapeutic Apheresis and Dialysis, EarlyView.ABSTRACT Background Chronic micro‐inflammation in patients with end‐stage renal disease (ESRD) is a significant driver of cardiovascular complications and diminished quality of life. While standard hemodialysis (SHD) effectively manages small‐molecule clearance, its ability to remove medium‐to‐large uremic toxins—the primary catalysts of systemic ...
Hongwei Zuo +5 more
wiley +1 more source
PAX9 polymorphism in non-syndromic hypodontia in the Malaysian population [PDF]
, 2020 Non-syndromic hypodontia is the developmental absence of more than one tooth that appears as an independent congenital oral trait. Genetic mutations responsible for tooth agenesis have been identified in paired box 9 (PAX9) and muscle segment homeobox 1 (
Lestari, Widya +4 more
core
Molecular Insights into Craniosynostosis: A Review
Journal of Education, Health and SportIntroduction and Purpose Craniosynostosis (CS), the premature fusion of one or more calvarial sutures, is a common congenital skull malformation affecting 1 in 2000–2500 live births.
Aleksandra Kutaj, Zuzanna Adamowicz
doaj +1 more source
Neurodevelopmental Problems in Non-Syndromic Craniosynostosis
Journal of Korean Neurosurgical Society, 2016 Craniosynostosis is the premature fusion of calvarial sutures, resulting in deformed craniofacial appearance. Hence, for a long time, it has been considered an aesthetic disorder. Fused sutures restrict growth adjacent to the suture, but compensatory skull growth occurs to accommodate the growing brain.
Shim, Kyu-Won +4 more
openaire +3 more sources
Organoids in pediatric cancer research
FEBS Letters, EarlyView.Organoid technology has revolutionized cancer research, yet its application in pediatric oncology remains limited. Recent advances have enabled the development of pediatric tumor organoids, offering new insights into disease biology, treatment response, and interactions with the tumor microenvironment.
Carla Ríos Arceo, Jarno Drost
wiley +1 more source
Report of Non Syndromic Mental Retardation In Three Sisters [PDF]
Ravānshināsī-i Afrād-i Istis̠nāyī, 2011 This case report is Significantly important, Due to the fact, that so far no documeted report has shown the presence of three female members of the same family having mental retardation. History and Mental status examination and physical examination was
Alireza Moghadas
doaj
Non-syndromic monogenic male infertility.
Acta bio-medica : Atenei Parmensis, 2019 Infertility is a widespread clinical problem affecting 8-12% of couples worldwide. Of these, about 30% are diagnosed with idiopathic infertility since no causative factor is found. Overall 40-50% of cases are due to male reproductive defects. Numerical or structural chromosome abnormalities have long been associated with male infertility.
Guerri G. +8 more
openaire +3 more sources