Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
THE ROLE OF RADIODIAGNOSIS OF NECROTIZING ENTEROCOLITIS IN PREMATURE INFANTS.
Georgian Med News
January 2024
K.Y. Farajeva Research Institute of Pediatrics, Baku, Azerbaijan Republic.
Necrotizing enterocolitis (NEC) is the most often encountered pathology of newborns and always requires an emerging surgery in cases of perforation. An active study of more important diagnostic factors at early stages of a disease is one of the first aims of neonatologists and pediatric surgeons. This study was therefore designed to examine the state of diagnostic problems in patients presenting with Necrotizing enterocolitis, identification of possible ways of the improvement of a patient's diagnosis suffering from Necrotizing enterocolitis and patients with perforated enterocolitis, definition of the possibilities of roentgenologic methods for the determination of a disease stage of Necrotizing enterocolitis.
View Article and Find Full Text PDFBlount disease and familial inheritance in Ghana, area cross-sectional study.
BMJ Paediatr Open
February 2022
Orthopaedic Surgery, Maastricht University Medical Centre+, Maastricht, The Netherlands.
Objective: The objective of this study is to study familial inheritance for Blount disease to create better understanding of the aetiology of Blount disease.
Methods: After reviewing patient files and conventional roentgenologic imaging, 139 patients with Blount disease were included in this cross-sectional study, of which 102 patients were interviewed. During the interviews, patient characteristics and family history were collected.
FGF23-related hypophosphatemic rickets/osteomalacia: diagnosis and new treatment.
J Mol Endocrinol
February 2021
Fujii Memorial Institute of Medical Sciences, Institute of Advanced Medical Sciences, Tokushima University, Tokushima, Tokushima, Japan.
FGF23 is a phosphaturic hormone produced by bone. FGF23 reduces serum phosphate by suppressing proximal tubular phosphate reabsorption and intestinal phosphate absorption. After the identification of FGF23, several kinds of hypophosphatemic rickets/osteomalacia such as X-linked hypophosphatemia (XLH) and tumor-induced osteomalacia (TIO) have been shown to be caused by excessive actions of FGF23.
View Article and Find Full Text PDF[IgG4-related sclerosing disease of the larynx].
Vestn Otorinolaringol
July 2017
M.F. Vladimirov Moscow Regional Research Clinical Institute, Moscow, Rusia, 129110.
IgG4-related sclerosing disease of the larynx (IgG4-SD) is a recently described immunodependent systemic pathology characterized by diffusive or focal inflammatory infiltration of the affected organs and tissues by plasma cells expressing IgG4; it is accompanied by the subsequent development of obliterative phlebitis and fibrosclerosis associated with the increase of the serum IgG4 level. According to the recently published materials, the disease can also develop in the respiratory system. The present article describes the first documented case of IgG4-related sclerosing disease with the isolated lesion of the larynx.
View Article and Find Full Text PDF[Radiodiagnostics of odontogenic maxillary sinusitis].
Vestn Otorinolaringol
July 2017
I.M. Sechenov First Moscow State Medical University, Moscow, Russia, 119991.
The objective of the present study was to analyze the potential of such techniques as X-ray, multi-slice computed tomography (MSCT), and cone-beam computed tomography (CBCT) for diagnostics of odontogenic maxillary sinusitis. The secondary objective was to describe changes in maxillary sinuses identifiable with the help of the above methods. The study included 166 patients at the age varying from 21 to 81 years presenting with odontogenic maxillary sinusitis.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!