Results 31 to 40 of about 42,181 (224)

Medication-Induced Hypokalemia [PDF]

open access: yes, 2015
The authors present an introduction to hypokalemia and then discuss a case report on a patient with medication-induced ...
Mason, Carly, Veltri, Keith
core   +1 more source

Remarkable Hypokalemia among Sudanese Patients with Jaundice [PDF]

open access: yes, 2019
Background: Impairment of potassium levels is common in clinical practice, mainly encountered among hospitalized patients with a wide spectrum of sickness. Hypokalemia is a potentially dangerous irregularity that may have pernicious actuates.
Mohamed, Bashir   +1 more
core   +2 more sources

Potassium wasting nephropathy in the setting of tizanidine overdose: a case report

open access: yesJournal of Medical Case Reports, 2021
Background Hypokalemia has been rarely attributed to tizanidine, although the precise mechanism is unclear. Severe hypokalemia is a well-established cause of abnormalities involving cardiac conduction. Given this agent’s well-known cardiac arrhythmogenic
Michael J. Brucculeri, Juan Garcia
doaj   +1 more source

Hypokalemia and rhabdomyolysis

open access: yesJournal of Pharmacology and Pharmacotherapeutics, 2015
The adverse drug event manager of the Capital Region of Denmark received a report of a 65-year-old male with type II diabetes and long-lasting treatment with indapamide. In addition, he had a history of a high consumption of licorice. For 2 weeks, the patient suffered from myalgia, which the general practitioner suspected to be polymyalgia rheumatica ...
Horwitz, Henrik   +3 more
openaire   +4 more sources

Risk factors for postoperative hypokalemia in patients undergoing endoscopic pituitary adenoma resection: a retrospective cohort study [PDF]

open access: yesPeerJ
Background Currently, endoscopic transsphenoidal surgery is the primary approach for treating pituitary tumors. While endoscopic surgery offers numerous advantages, it also comes with a series of potential surgical complications.
Maoxiang Li   +7 more
doaj   +2 more sources

A Novel NR3C1 Frameshift Variant Associated With Familial Glucocorticoid Resistance Syndrome: An Integrated Analysis of Steroid Profiling and Structural Modeling

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Glucocorticoid resistance syndrome (GRS) is a rare hereditary disorder caused by pathogenic variants in NR3C1, characterized by marked phenotypic heterogeneity and frequent misdiagnosis as primary aldosteronism or subclinical Cushing's syndrome.
Sufang Yun   +7 more
wiley   +1 more source

A Case Report of Recurrent Hypokalemia During Pregnancies Associated With Nonaldosterone-Mediated Renal Potassium Loss

open access: yesCanadian Journal of Kidney Health and Disease, 2021
Rationale: Geller et al reported a rare mutation in the mineralocorticoid receptor (MR) resulting in constitutive MR activity. Progesterone, normally an MR antagonist, acts as a potent agonist with this mutation. Progesterone levels can increase 100-fold
Pairach Pintavorn, Stephanie Munie
doaj   +1 more source

Analysis of ADRs with Hypokalaemia for Severity, Preventability and Causality in a Tertiary Care Centre in South India

open access: yesPharmacology and Clinical Pharmacy Research, 2023
Hypokalemia is one of the most frequently seen electrolyte disturbances in clinical practice. Various drugs are known to induce hypokalemia, such as furosemide, thiazides, dicloxacillin, ampicillin, etc.
Shiva Murthy Nanjundappa   +3 more
doaj   +1 more source

Immune Modulatory Therapy for Severe Dengue Hemorrhagic Fever in a Patient With Mitochondrial Complex I Deficiency: A Case Report

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Dengue virus (DENV) poses a serious global health challenge, particularly in cases of dengue hemorrhagic fever (DHF). Patients with preexisting mitochondrial disorders may be at increased risk for complications due to the specific impact of DENV on mitochondrial‐dependent cellular processes and immune function.
Audra N. Iness   +11 more
wiley   +1 more source

Genetic Variants of Na+,K+‐ATPase Associated With Neurological Disorders: A Systematic Review

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Neurological disorders encompass a wide range of severe symptoms and manifestations, many of which are associated with genetic variants that affect ionic homeostasis. Na+,K+‐ATPase, a transmembrane enzyme responsible for maintaining electrochemical gradients in cells, plays a crucial role in neuronal excitability and brain function.
Giovana Kummer da Rosa   +3 more
wiley   +1 more source

Home - About - Disclaimer - Privacy