Results 61 to 70 of about 469,744 (362)
Congenital adrenal hyperplasia [PDF]
Dermato-Endocrinology, 2009 Congenital adrenal hyperplasia consists of a heterogenous group of inherited disorders due to enzymatic defects in the biosynthetic pathway of cortisol and/or aldosterone. This results in glucocorticoid deficiency, mineralocorticoid deficiency, and androgen excess. 95% of CAH cases are due to 21-hydroxylase deficiency.
Andreas Katsambas, Cleo Dessinioti
openaire +3 more sources
Advanced Healthcare Materials, Volume 14, Issue 7, March 14, 2025.This review highlights emerging bioengineering strategies for treating neointimal hyperplasia in the peripheral vasculature, focusing on approaches that promote re‐endothelialization, modulate smooth muscle cell phenotype, reduce inflammation, mitigate oxidative stress, and optimize biomechanical compliance.
Nikita Wilson John +5 more
wiley +1 more source
AACE Clinical Case Reports, 2022 Background/Objective: Nonclassic congenital adrenal hyperplasia (NCCAH) may be overlooked or mistaken for polycystic ovarian syndrome. Unlike congenital adrenal hyperplasia (CAH), the enzymatic activities of 21-hydroxylase or 11β-hydroxylase in NCCAH are
Eric D. Frontera, DO +3 more
doaj
Diagnosis and treatment of pituitary incidentalomas
Chinese Journal of Contemporary Neurology and Neurosurgery, 2022 Pituitary incidentalomas (PIs) are defined as previously unexpected pituitary lesions which are accidentally discovered during imaging examinations performed for unrelated reasons, including pituitary adenoma, craniopharyngioma, Rathke's cyst, pituitary ...
LIU Xiao⁃hai +3 more
doaj +1 more source
Database Annotation with few Examples: An Atlas-based Framework using Diffeomorphic Registration of 3D Trees [PDF]
arXiv, 2020 Automatic annotation of anatomical structures can help simplify workflow during interventions in numerous clinical applications but usually involves a large amount of annotated data. The complexity of the labeling task, together with the lack of representative data, slows down the development of robust solutions.
arxiv
Journal of Clinical Endocrinology and Metabolism, 2010 OBJECTIVE We developed clinical practice guidelines for congenital adrenal hyperplasia (CAH). PARTICIPANTS The Task Force included a chair, selected by The Endocrine Society Clinical Guidelines Subcommittee (CGS), ten additional clinicians experienced ...
P. Speiser +11 more
semanticscholar +1 more source
Advanced Healthcare Materials, EarlyView.This study introduces a controllable degradation system for Mg‐based biomaterials using sputtering technology, marking a significant advancement in nerve regeneration research. The Mg‐sputtered nerve conduits demonstrate enhanced biocompatibility, biofunctionality, mechanical compatibility, and precise magnesium release, resulting in improved axonal ...
Hyewon Kim +12 more
wiley +1 more source
Spontaneously Improving Occipitocondylar Hyperplasia: A Case Report
Journal of Neurological Surgery Reports, 2014 This case report presents a pediatric patient with the extremely rare craniovertebral junction anomaly of occipitocondylar hyperplasia. This 4-year old boy presented with macrocephaly and mild to moderate pontomedullary compression from the unilateral ...
Laszlo Nagy, Coby Ray
doaj +1 more source
Obstetrics and Gynecology, 2017 OBJECTIVE To assess efficacy of the levonorgestrel-releasing intrauterine device (LNG-IUD) for treatment of complex atypical hyperplasia or low-grade endometrial cancer.
N. Pal +12 more
semanticscholar +1 more source
Advanced Healthcare Materials, EarlyView.This study addresses bacterial biofilm resistance by developing mesoporous Fe3O4 nanoparticles loaded with photosensitizer IR‐820, enabling combined antimicrobial photodynamic therapyand magnetic hyperthermia therapy. The system achieves magnetic targeting, heat‐triggered drug release under alternating magnetic fields, and near‐infrared‐induced ROS ...
Yuange Li +8 more
wiley +1 more source