Late-onset Pompe Disease with Elevated Liver Transaminases: A Case Report
Pompe disease or type II glycogen storage disease is a rare autosomal hereditary disease. The prevalence of the disease is about 1 in 40,000 to 1 in 300,000 population. It usually occurs as a result of glycogen accretion following acid maltase deficiency.
Maryam Bagheri +2 more
doaj
The nutritional and therapeutic properties of Moringa oleifera cannot be overemphasized, since all the parts of the plant (leaves, seeds, root, bark, pods etc.) have been reported to possess antibiotic, anti-hypertensive, anti-tumor and anti-oxidative ...
I. O Igwilo +5 more
doaj
Isolated IgG elevation in patients with persistently normal transaminases does not affect the outcome of autoimmune hepatitis: or just a little bit? [PDF]
Grossar L +4 more
europepmc +1 more source
Glutamic Aspartic Transaminase
W. Terry Jenkins, Irwin W. Sizer
openaire +1 more source
Drug-induced liver injury in inflammatory bowel disease: Challenges in diagnosis and monitoring. [PDF]
Singh A +5 more
europepmc +1 more source
Extraneurological Presentations of Tick-Borne Encephalitis Virus: A Rare Case of TBEV-Associated Myocarditis With Fever and Bicytopenia and a Systematic Literature Review. [PDF]
Seneghini M +4 more
europepmc +1 more source
People living with HIV co-infected with HBV at the Nkembo Outpatient Treatment Center, Gabon: prevalence and associated factors. [PDF]
Moukanda-Ifoundou R +13 more
europepmc +1 more source
Prolonged Cholestatic Hepatitis A in an Unvaccinated International Traveler. [PDF]
Bomfim EYM +4 more
europepmc +1 more source

