Results 161 to 170 of about 130,693 (343)
Oral manifestations in glycogen storage disease type 1b
, 1995 Glycogen storage disease type 1b is a rare metabolic disorder which affects the transport system of glucose‐6‐phosphatase metabolism. As a result, hepatomegaly, failure to thrive, renal dysfunction and recurrent infections occur in affected patients.
Drogari, E. +4 more
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Portal diversion in glycogen storage disease [PDF]
, 1969 Two children with glycogen storage disease were treated with portacaval transposition. The first is alive and in good health more than 5 years later. She underwent a rapid increase in growth after the operation, while the liver remained the same size ...
Brown, BI +3 more
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Studies of liver phosphorylase in hepatic injuries. I. Alteration in enzyme activity
, 1978 Phosphorylase activities (total and a form) were determined in the livers of experimental hepatic injuries with carbon tetrachloride or galactosamine and the livers of patients with liver diseases.
Kobayashi, Michio
core +1 more source
Entomologia Experimentalis et Applicata, EarlyView.We evaluated Lasiocampa quercus as an overwintering host for the koinobiont larval endoparasitoid Glyptapanteles porthetriae by exposing parasitized larvae to different environmental conditions and comparing parasitoid development with that in the primary host Lymantria dispar.
Thomas Zankl, Christa Schafellner
wiley +1 more source
Glycogen Storage Disease [PDF]
Proceedings of the Royal Society of Medicine, 1965 openaire +2 more sources
Diagnosis and management of equine metabolic syndrome
Equine Veterinary Education, EarlyView.Summary Equine metabolic syndrome (EMS) is a prevalent endocrine disorder that increases the risk of hyperinsulinaemia‐associated laminitis (HAL), the most common and clinically significant form of laminitis. The central pathological feature of EMS is insulin dysregulation (ID), which encompasses basal or postprandial hyperinsulinaemia and tissue ...
F. R. Bertin
wiley +1 more source
Immunology, EarlyView.Calcium oxalate monohydrate (COM) crystals cause changes in the secretion of 29 proteins from neutrophil‐like cells, including those involved in neutrophil immune activation and intracellular metabolic adaptation. The neutrophil secreted proteins (secretome) also inhibit calcium oxalate crystallisation and crystal growth, but promote crystal ...
Chanettee Lertprapai +2 more
wiley +1 more source
Neonatal Glycogen Storage Disease Ia
Pediatrics and Neonatology, 2015 Jinping Zhang, Wenjing Shi, Chao Chen
doaj +1 more source
Glycogen-storage Disease of Liver [PDF]
BMJ, 1956 C C, KAPILA, S, KAUL, B C, CHATTERJEE
openaire +2 more sources