Results 271 to 280 of about 87,827 (343)

Outcomes and Adverse Events of WHO Shorter Regimen in the Treatment of Multi‐Drug Resistant Tuberculosis in Bhutan: A Longitudinal Study

open access: yesHealth Science Reports, Volume 8, Issue 9, September 2025.
ABSTRACT Background and Aims Bhutan first introduced the Shorter Regimen, consisting of a combination of Amikacin, Clofazamine, Ethionamide, Ethambutol, high dose Isoniazid, Moxifloxacin and Pyrazinamide, for the treatment of rifampicin or multidrug resistant tuberculosis (RR/MDR‐TB) in 2018.
Gaki Nima   +3 more
wiley   +1 more source

A relapse of acute group B streptococcus meningitis in a healthy adult: Case report and review of the literatures

open access: yesJournal of General and Family Medicine, Volume 26, Issue 5, Page 485-489, September 2025.
Abstract Streptococcus agalactiae (GBS) is a rare cause of meningitis in healthy adults. We report the case of a healthy 33‐year‐old man with acute GBS meningitis who experienced relapsed high‐grade fever and increased intracranial pressure following completing intravenous antibiotics.
Wannisa Wongpipathpong   +3 more
wiley   +1 more source

Sensorineural hearing loss and retinopathy in sickle cell patients. [PDF]

open access: yesJ Surg Case Rep
Ewusi-Wilson RK   +3 more
europepmc   +1 more source

Sensorineural Hearing Loss [PDF]

open access: yesOccupational and Environmental Medicine, 1972
openaire   +1 more source

Treatment of Inborn Errors by Product Replacement: The Example of Inborn Errors of Bile Acid Synthesis

open access: yesJournal of Inherited Metabolic Disease, Volume 48, Issue 5, September 2025.
ABSTRACT Many inborn errors of metabolism affect pathways involved in the synthesis of a metabolite that has an important biochemical or physiological function, and adverse effects of the disorder can be attributed to the lack of this metabolite. Thus, there is the opportunity for treatment by ‘product replacement’. One of the disorders in the pathways
Peter T. Clayton   +2 more
wiley   +1 more source

Successful Treatment of Severe Hepatopulmonary Syndrome as a Rare Complication of Zellweger Spectrum Disorder

open access: yesJIMD Reports, Volume 66, Issue 5, September 2025.
ABSTRACT We report the case of an 11‐year‐old girl who developed hepatopulmonary syndrome (HPS) as a rare complication of Zellweger spectrum disorder and was successfully treated with liver transplantation. Our patient presented with neonatal sensorineural hearing loss.
Riya Mary Tharakan   +2 more
wiley   +1 more source

Hearing loss secondary to novel variants of the KCNQ4 gene. [PDF]

open access: yesEur Arch Otorhinolaryngol
González-Aguado R   +3 more
europepmc   +1 more source

Glycine N‐Acyltransferase Deficiency due to a Homozygous Nonsense Variant in the GLYAT: A Novel Inborn Error of Metabolism

open access: yesJIMD Reports, Volume 66, Issue 5, September 2025.
ABSTRACT The enzyme glycine N‐acyltransferase (GLYAT) plays a crucial role in detoxifying both xenobiotic and endogenous compounds that contain a carboxylic acid group, such as benzoic acid. Data on the impact of human GLYAT on the glycine conjugation pathway is limited and difficult to determine.
Mona Nourbakhsh   +13 more
wiley   +1 more source

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