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Publikováno v:
Journal of Diabetes and Endocrine Practice. :75-82
Background: Hypothyroidism is a common endocrine disorder that is managed by a wide range of physicians. There are no data on the pattern of clinical management of hypothyroidism in the Middle East and Africa (MEA) region. Objectives: We sought to do
Publikováno v:
Hämostaseologie. 40:642-648
Objective This article aims to analyze the phenotype and genotype of an inherited dysfibrinogenemia pedigree associated with a heterozygous mutation in the FGA gene, and to investigate the pathogenesis of this disease. Clinical Presentation The proba
Autor:
Priyanka Samal, Prantar Chakrabarti
Publikováno v:
Indian Journal of Medical and Paediatric Oncology. 41:596-601
Waldenström macroglobulinemia (WM) is an indolent B-cell neoplasm in which lymphoplasmacytic cells are accumulated in the bone marrow. This rare disease is incurable with the available treatments and its management is generally based on risk-adapted
Publikováno v:
Journal of Pediatric Infectious Diseases. 15:238-241
Objective Central venous catheter (CVC) colonization is a common problem in the pediatric oncology department. Initial colonization of CVC by coagulase-negative staphylococci (CoNS), Staphylococcus aureus, and enterococci is followed by the growth of
Autor:
Pavel Kalinin, Ludmila Astaf’eva, Ludmila Valentinovna Shishkina, Galina Melnichenko, Oleg Sharipov, Boris A. Kadashev, Dariia Tserkovnay
Publikováno v:
Asian Journal of Neurosurgery
Introduction: Currently, cabergoline therapy is the main treatment for prolactinomas. The use of the drug in most cases leads to regression of the tumor, normalization of prolactin (PRL) levels, and restoration of gonadotropic function. The mechanism
Publikováno v:
Zeitschrift für Gastroenterologie. 58:63-67
We report the case of a 65-year-old female patient with hepatic alveolar echinococcosis (AE) caused by Echinococcus multilocularis. This infrequent zoonosis has a considerable morbidity and mortality. The malignant appearing hepatic mass was initiall
Publikováno v:
Journal of Neuroanaesthesiology and Critical Care (2020)
Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency of the enzyme phenylalanine hydroxylase which results in accumulation of phenylalanine. Patients of PKU presents with seizures, mental retardation, and organ damage and pos
Autor:
Sarah K. Dotters-Katz, Victoria L. Bae-Jump, Chunxiao Zhou, Matthew R. Grace, Tracy A. Manuck, Kim A. Boggess
Publikováno v:
American Journal of Perinatology Reports, Vol 09, Iss 02, Pp e138-e143 (2019)
AJP Reports
AJP Reports
Objective This study was aimed to measure the effects of a high-fat diet and metformin on placental mechanistic target of rapamycin (mTOR) signaling in mice. Study Design Pregnant friend virus B (FVB)-strain mice were allocated on embryonic day (e) 0
Publikováno v:
Asian Journal of Neurosurgery
Herein, we describe a fatal case of central nervous system (CNS) pseudallescheriasis following near-drowning. A 13-year-old boy, who had been successfully resuscitated after near-drowning, presented with a transient episode of mental confusion during
Publikováno v:
Journal of Health and Allied Sciences NU. :11-14
Background: Diabetes Mellitus (DM) has become an epidemic in the 21st century where India leads the world with largest number of patients. There is increasing evidence that inflammation is closely involved in the pathogenesis of type 2 diabetes and a