Results 61 to 70 of about 26,695 (224)
Journal of the Formosan Medical Association, 2020 Background/Purpose: Our previous study found 284 gastric parietal cell antibody (GPCA)-positive atrophic glossitis (AG) patients (so-called GPCA+AG patients in this study) in a group of 1064 AG patients.
Chun-Pin Chiang +5 more
doaj +1 more source
Journal of Inherited Metabolic Disease, Volume 48, Issue 6, November 2025.ABSTRACT Liver transplantation (LTx) has become, over the years, an increasingly used therapeutic option in patients with inherited metabolic diseases (IMD). Initially performed for Tyrosinemia Type I and ornithine transcarbamylase deficiency, it now accounts as the second indication for pediatric transplants worldwide. The use of LTx has been extended
Andrea Pietrobattista +3 more
wiley +1 more source
Pediatric autoimmune gastritis: An international, multicentric study
Journal of Pediatric Gastroenterology and Nutrition, Volume 81, Issue 5, Page 1142-1150, November 2025.Abstract Objectives Autoimmune gastritis (AIG) has been poorly described in childhood. We sought to identify the patterns of manifestations of pediatric AIG at onset and to describe its laboratory, clinical, and histopathological features. Methods This was a retrospective, longitudinal, multicenter, cohort study enrolling histologically proven AIG ...
Marco Vincenzo Lenti +40 more
wiley +1 more source
Journal of the Formosan Medical Association, 2018 Background/Purpose: Atrophic glossitis (AG) patients are prone to have anemia, hematinic deficiencies, hyperhomocysteinemia, and serum gastric parietal cell antibody (GPCA) positivity.
Chun-Pin Chiang +5 more
doaj +1 more source
An uncommon presentation of hyperhomocysteinemia and vitamin B12 deficiency: a case report
Journal of Medical Case Reports, 2019 Introduction Cerebral venous thrombosis is relatively rare and characterized by a wide spectrum of clinical features. It is more common in young adults with women affected more than men.
Vinay Kapur +2 more
doaj +1 more source
The Role of Genetics in Stroke Risk and Outcome: A Review of Current Evidence
Brain and Behavior, Volume 15, Issue 10, October 2025.This study delineates the multiple pathways leading to stroke, encompassing genetic risk factors such as lipid/cholesterol metabolism, blood pressure regulation genes, and endothelial dysfunction. The report includes genetic pathways such as Val66Met polymorphism, prothrombin G20210A, interleukin‐6 and tumor necrosis factor gene variant, along with ...
Mega Obukohwo Oyovwi +3 more
wiley +1 more source
Cell Death and Disease, 2016 Hyperhomocysteinemia (HHcy) is a well-known risk factor for stroke; however, its underlying molecular mechanism remains unclear. Using both mouse and cell culture models, we have provided evidence that impairment of autophagy has a central role in HHcy ...
Madhulika Tripathi +6 more
semanticscholar +1 more source
Molecular Genetics and Metabolism Reports, 2015 Hyperhomocysteinemia results from hepatic metabolism dysfunction and is characterized by a high plasma homocysteine level, which is also an independent risk factor for cardiovascular disease.
Alizée Latour +9 more
doaj +1 more source
Український журнал серцево-судинної хірургії, 2020 To date, it has been established that in the progression of coronary artery disease (CAD) and its complications, an increase in the level of homocysteine and hypovitaminosis D are essential. However, medical publications do not adequately cover the study
O. S. Nikonenko +4 more
doaj +1 more source
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Although cerebral venous thrombosis and stroke are rare extra‐intestinal manifestations of Ulcerative colitis, if present, they increase the risk for morbidity and mortality. As such, physicians dealing with a case of Ulcerative colitis should always be vigilant about the potential for venous or arterial thrombosis.
Niranjan KC +4 more
wiley +1 more source