Results 31 to 40 of about 2,774 (200)
Glycogen storage disease type IIIa in pregnant women: A guide to management
JIMD Reports, 2022 Glycogen storage disease type IIIa (GSD‐IIIa) is an autosomal recessive disorder that impairs glycogenolysis, producing ketotic hypoglycaemia, hepatomegaly, cardiac and skeletal myopathy.
Demi Beneru +3 more
doaj +1 more source
Different sieving methods for determining the physical characteristics in ground corn
Acta Scientiarum: Animal Sciences, 2021 We evaluated various sieving methods to estimate particle size (PS) and geometric standard deviation (GSD) of ground corn. The corn had been previously divided in six fractions and each one ground in a hammermill (1-, 2-, 3-, 4-, 5- or 12-mm sieves ...
Heverton Michael Biazzi +4 more
doaj +1 more source
Orphanet Journal of Rare Diseases, 2020 Background Glycogen storage diseases (GSDs) with liver involvement are complex disorders with similar manifestations. Currently, the main diagnostic methods such as tissue diagnosis, either histopathology or enzyme assay, are invasive.
Zahra Beyzaei +2 more
doaj +1 more source
Scale issues for geoheritage 3D mapping: The case of Lesvos Geopark, Greece
International Journal of Geoheritage and Parks, 2022 A geopark can be composed of many individual geosites of various geographical scales, thus, categorization according to cartographic scale is crucial for their 3D mapping. The UNESCO Global Geopark of the island of Lesvos in the north-east Aegean, Greece,
Ermioni Eirini Papadopoulou +6 more
doaj +1 more source
Remote Sensing Applications in Sugarcane Cultivation: A Review
Remote Sensing, 2021 A large number of studies have been published addressing sugarcane management and monitoring to increase productivity and production as well as to better understand landscape dynamics and environmental threats.
Jaturong Som-ard +4 more
doaj +1 more source
GLUCOGENOSIS AS A CAUSE OF INTRAHEPATIC CHOLESTASIS
Annals of Hepatology, 2022 Introduction and Objectives: Hepatic glycogen storage pathologies are very rare diseases among inborn errors of metabolism caused by the alteration of the enzymes involved in the metabolism of glycogen.
K.Y. Santoyo López +1 more
doaj +1 more source
A Modified Enzymatic Method for Measurement of Glycogen Content in Glycogen Storage Disease Type IV
, 2016 Deficiency of glycogen branching enzyme in glycogen storage disease type IV (GSD IV) results in accumulation of less-branched and poorly soluble polysaccharides (polyglucosan bodies) in multiple tissues.
Yi, Haiqing +9 more
core +1 more source
, 2016 Patients with progressive hepatic form of GSD IV often die of liver failure in early childhood. We tested the feasibility of using recombinant human acid-α glucosidase (rhGAA) for treating GSD IV. Weekly intravenously injection of rhGAA at 40 mg/kg for 4
Yi, Haiqing +4 more
core +1 more source
Advanced Science, EarlyView.The configurational‐entropy strategy enables rapid and sensitive ethanol detection using a multicomponent oxide. The high‐entropy (InSnFeZnW)Ox provides enriched oxygen vacancies and diverse adsorption sites that strengthen surface reactivity. The sensor achieves a 5135% ethanol response with fast kinetics and stable long‐term operation.
Gi Baek Nam +19 more
wiley +1 more source
Liver transplantation for glycogen storage disease types I, III, and IV [PDF]
, 1999 Glycogen storage disease (GSD) types I, III, and IV can be associated with severe liver disease. The possible development of hepatocellular carcinoma and/or hepatic failure make these GSDs potential candidates for liver transplantation.
Matern, D +11 more
core +1 more source